Management of breast diseases 2nd ed

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Management of breast diseases 2nd ed

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Ismail Jatoi Achim Rody Editors Management of Breast Diseases Second Edition 123 Management of Breast Diseases Ismail Jatoi Achim Rody • Editors Management of Breast Diseases Second Edition 123 Editors Ismail Jatoi Department of Surgery University of Texas Health Science Center San Antonio, TX USA ISBN 978-3-319-46354-4 DOI 10.1007/978-3-319-46356-8 Achim Rody Obstetrics and Gynecology University Medical Center Schleswig-Holstein Lübeck Germany ISBN 978-3-319-46356-8 (eBook) Library of Congress Control Number: 2016951967 1st edition: © Springer-Verlag Berlin Heidelberg 2010 2nd edition: © Springer International Publishing Switzerland 2016 This work is subject to copyright All rights are reserved by the Publisher, whether the whole or part of the material is concerned, specifically the rights of translation, reprinting, reuse of illustrations, recitation, broadcasting, reproduction on microfilms or in any other physical way, and transmission or information storage and retrieval, electronic adaptation, computer software, or by similar or dissimilar methodology now known or hereafter developed The use of general descriptive names, registered names, trademarks, service marks, etc in this publication does not imply, even in the absence of a specific statement, that such names are exempt from the relevant protective laws and regulations and therefore free for general use The publisher, the authors and the editors are safe to assume that the advice and information in this book are believed to be true and accurate at the date of publication Neither the publisher nor the authors or the editors give a warranty, express or implied, with respect to the material contained herein or for any errors or omissions that may have been made Printed on acid-free paper This Springer imprint is published by Springer Nature The registered company is Springer International Publishing AG The registered company address is: Gewerbestrasse 11, 6330 Cham, Switzerland Preface In 2002, Lippincott published the Manual of Breast Diseases, edited by Prof Ismail Jatoi That book was expanded and a larger text entitled Management of Breast Diseases was published by Springer in 2010, edited by Prof Jatoi and Prof Manfred Kaufmann of the Goethe-University of Frankfurt Professor Kaufmann subsequently retired, and the current text is the second edition of the Springer text, with Prof Achim Rody of the University Hospital Schleswig-Holstein in Lübeck, Germany now serving as co-editor Many of the chapters have been extensively revised and numerous other authors have been added to the second edition of this text We hope that this updated text will continue to serve as a useful guide to the wide spectrum of clinicians who treat benign and malignant diseases of the breast: surgeons, gynecologists, medical oncologists, radiation oncologists, internists, and general practitioners Today, the management of breast diseases, and particularly breast cancer, is predicated upon the results of large randomized prospective trials The authors of the various chapters in this text have highlighted the major trials that have contributed to our improved understanding and treatment of breast diseases Many of these trials have, in particular, revolutionized the treatment of breast cancer Indeed, there has been a very rapid decline in breast cancer mortality throughout the industrialized world since 1990, due largely to the implementation of the results of landmark randomized trials For this progress to continue, we will need to design innovative trials in the future, and recruit large numbers of women into those trials We should always be grateful to the thousands of women throughout the world who have participated in clinical trials, and thereby enabled progress in the treatment of breast cancer We are deeply indebted to all the investigators who have contributed chapters to this text They have diverse interests, but all share the common goal of reducing the burden of breast diseases We would also like to thank the editorial staff of the Springer publishing company for their continued assistance with updating this text In particular, we are most grateful to Portia Levasseur of the Springer publishing company Without Portia’s persistence and diligence, this second edition would not have been possible We hope that clinicians will continue to find this text to be an informative guide to the management of breast diseases San Antonio, USA Lübeck, Germany Ismail Jatoi Achim Rody v Contents Anatomy and Physiology of the Breast Martha C Johnson and Mary L Cutler Congenital and Developmental Abnormalities of the Breast Kristin Baumann and Telja Pursche 41 Nipple Discharge Jill R Dietz 57 Mastalgia Amit Goyal and Robert E Mansel 73 Management of Common Lactation and Breastfeeding Problems Lisa H Amir and Verity H Livingstone 81 Evaluation of a Breast Mass 105 Alastair M Thompson and Andrew Evans Breast Cancer Epidemiology 125 Alicia Brunßen, Joachim Hübner, Alexander Katalinic, Maria R Noftz, and Annika Waldmann Breast Cancer Screening 139 Ismail Jatoi Breast Imaging 157 Anne C Hoyt and Irene Tsai 10 Premalignant and Malignant Breast Pathology 179 Hans-Peter Sinn 11 Breast Cancer Molecular Testing for Prognosis and Prediction 195 Nadia Harbeck 12 Molecular Classification of Breast Cancer 203 Maria Vidal, Laia Paré, and Aleix Prat 13 Ductal Carcinoma In Situ 221 Ian H Kunkler 14 Surgical Considerations in the Management of Primary Invasive Breast Cancer 229 Carissia Calvo and Ismail Jatoi 15 Management of the Axilla 247 John R Benson and Vassilis Pitsinis 16 Breast Reconstructive Surgery 273 Yash J Avashia, Amir Tahernia, Detlev Erdmann, and Michael R Zenn vii viii 17 The Role of Radiotherapy in Breast Cancer Management 291 Mutlay Sayan and Ruth Heimann 18 Adjuvant Systemic Treatment for Breast Cancer: An Overview 311 Rachel Nirsimloo and David A Cameron 19 Endocrine Therapy 323 Olivia Pagani and Rosaria Condorelli 20 Systemic Therapy 335 Frederik Marmé 21 HER2-Targeted Therapy 391 Phuong Dinh and Martine J Piccart 22 Inflammatory and Locally Advanced Breast Cancer 411 Tamer M Fouad, Gabriel N Hortobagyi, and Naoto T Ueno 23 Neoadjuvant Systemic Treatment (NST) 437 Cornelia Liedtke and Achim Rody 24 Metastatic Breast Cancer 451 Berta Sousa, Joana M Ribeiro, Domen Ribnikar, and Fátima Cardoso 25 Estrogen and Breast Cancer in Postmenopausal Women: A Critical Review 475 Joseph Ragaz and Shayan Shakeraneh 26 Estrogen and Cardiac Events with all-cause Mortality A Critical Review 483 Joseph Ragaz and Shayan Shakeraneh 27 Breast Diseases in Males 491 Darryl Schuitevoerder and John T Vetto 28 Breast Cancer in the Older Adult 519 Emily J Guerard, Madhuri V Vithala, and Hyman B Muss 29 Breast Cancer in Younger Women 529 Manuela Rabaglio and Monica Castiglione 30 Psychological Support for the Breast Cancer Patient 565 Donna B Greenberg 31 Management of the Patient with a Genetic Predisposition for Breast Cancer 575 Sarah Colonna and Amanda Gammon 32 Chemoprevention of Breast Cancer 593 Jack Cuzick 33 Design, Implementation, and Interpretation of Clinical Trials 601 Carol K Redmond and Jong-Hyeon Jeong 34 Structure of Breast Centers 637 David P Winchester Index 649 Contents Contributors Lisa H Amir Judith Lumley Centre, La Trobe University, Melbourne, VIC, Australia; Breastfeeding service, Royal Women’s Hospital, Melbourne, Australia Yash J Avashia Surgery, Duke University Medical Center, Durham, NC, USA Kristin Baumann Clinic for Gynaecology and Obstetrics, University Medical Centre Schleswig-Holstein Campus Lübeck, Lübeck, Schleswig-Holstein, Germany John R Benson Cambridge Breast Unit, Addenbrooke’s Hospital, Cambridge University Hospitals NHS Trust, Cambridge, UK Alicia Brunßen Department of Surgery, University of Texas Health Science Center at San Antonio, San Antonio, TX, USA Carissia Calvo Department of Surgery, University of Texas Health Science Center, San Antonio, TX, USA David A Cameron Edinburgh Cancer Research Centre, Western General Hospital, University of Edinburgh, Edinburgh, UK Fátima Cardoso Breast Unit, Champalimaud Clinical Center, Lisbon, Portugal Monica Castiglione Coordinating Center, International Breast Cancer Study Group (IBCSG), Berne, Switzerland Sarah Colonna Oncology, Huntsman Cancer Institute, Salt Lake City, UT, USA Rosaria Condorelli Department of Medical Oncology, Institute of Oncology of Southern Switzerland, Bellinzona, Switzerland Mary L Cutler Department of Pathology, Uniformed Services University, Bethesda, MD, USA Jack Cuzick Wolfson Institute of Preventive Medicine, Queen Mary University of London, Centre for Cancer Prevention, London, UK Jill R Dietz Surgery, University Hospitals Seidman Cancer Center, Bentleyville, OH, USA Phuong Dinh Westmead Hospital, Westmead, NSW, Australia Detlev Erdmann Surgery, Duke University Medical Center, Durham, NC, USA Andrew Evans Division of Imaging and Technology, University of Dundee, Dundee, Scotland, UK Tamer M Fouad Department of Breast Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA ix x Amanda Gammon High Risk Cancer Research, Huntsman Cancer Institute, Salt Lake City, UT, USA Amit Goyal Royal Derby Hospital, Derby, UK Donna B Greenberg Department of Psychiatry, Harvard Medical School, Massachusetts General Hospital, MGH Cancer Center, Boston, MA, USA Emily J Guerard Medicine, Division of Hematology Oncology, University of North Carolina, Chapel Hill, NC, USA Nadia Harbeck Breast Center, University of Munich, Munich, Germany Ruth Heimann Department of Radiation Oncology, University of Vermont Medical Center, Burlington, VT, USA Gabriel N Hortobagyi Department of Breast Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA Anne C Hoyt Department of Radiological Sciences, UCLA, Los Angeles, CA, USA Joachim Hübner Institute for Social Medicine and Epidemiology, University of Luebeck, Luebeck, Schleswig-Holstein, Germany Ismail Jatoi Division of Surgical Oncology and Endocrine Surgery, University of Texas Health Science Center, San Antonio, TX, USA Jong-Hyeon Jeong Department of Biostatistics, University of Pittsburgh, Pittsburgh, PA, USA Martha C Johnson Department of Anatomy, Physiology and Genetics, Uniformed Services University, Bethesda, MD, USA Alexander Katalinic Institute for Social Medicine and Epidemiology, University of Luebeck, Luebeck, Schleswig-Holstein, Germany Ian H Kunkler Institute of Genetics and Molecular Medicine (IGMM), University of Edinburgh, Edinburgh, Scotland, UK Cornelia Liedtke Department of Obstetrics and Gynecology, University Hospital Schleswig-Holstein/Campus Lübeck, Luebeck, Schleswig-Holstein, Germany Verity H Livingstone Department of Family Practice, The Vancouver Breastfeeding Centre, University of British Columbia, Vancouver, BC, Canada Robert E Mansel Cardiff University, Monmouth, UK Frederik Marmé Department of Gynecologic Oncology, National Center of Tumor Diseases, Heidelberg University Hospital, Heidelberg, Germany Hyman B Muss Medicine, Division of Hematology Oncology, University of North Carolina, Chapel Hill, NC, USA Rachel Nirsimloo Edinburgh Cancer Centre, NHS LOTHIAN, Edinburgh, UK Maria R Noftz Institute for Social Medicine and Epidemiology, University of Luebeck, Luebeck, Schleswig-Holstein, Germany Olivia Pagani Institute of Oncology and Breast Unit of Southern Switzerland, Ospedale San Giovanni, Bellinzona, Ticino, Switzerland Laia Paré Translational Genomics and Targeted Therapeutics in Solid Tumors Lab, August Pi I Sunyer Biomedical Research Institute (IDIBAPS), Barcelon, Spain Contributors Contributors xi Martine J Piccart Medicine Department, Institut Jules Bordet, Bruxelles, Belgium Vassilis Pitsinis Breast Unit, Ninewells Hospital and Medical School, NHS Tayside, Dundee, UK Aleix Prat Medical Oncology, Hospital Clinic of Barcelona, Barcelona, Spain Telja Pursche Clinic for Gynaecology and Obstetrics, University Medical Centre Schleswig-Holstein Campus Lübeck, Lübeck, Schleswig-Holstein, Germany Manuela Rabaglio Department of Medical Oncology, University Hospital/Inselspital and IBCSG Coordinating Center, Berne, Switzerland Joseph Ragaz School of Population and Public Health, University of British Columbia, North Vancouver, BC, Canada Carol K Redmond Department of Biostatistics, University of Pittsburgh, Pittsburgh, PA, USA Joana M Ribeiro Breast Unit, Champalimaud Clinical Center, Lisbon, Portugal Domen Ribnikar Medical Oncology Department, Institute of Oncology Ljubljana, Ljubljana, Slovenia Achim Rody Department of Obstetrics and Gynecology, University Schleswig-Holstein/Campus Lübeck, Luebeck, Schleswig-Holstein, Germany Hospital Mutlay Sayan Department of Radiation Oncology, University of Vermont Medical Center, Burlington, VT, USA Darryl Schuitevoerder Department of Surgery, Oregon Health & Science University, Portland, OR, USA Shayan Shakeraneh Infection Prevention and Control, Providence Health Care, Vancouver, BC, Canada; School of Population and Public Health, University of British Columbia, Vancouver, BC, Canada Hans-Peter Sinn Department of Pathology, University of Heidelberg, Heidelberg, Baden-Württemberg, Germany Berta Sousa Breast Unit, Champalimaud Clinical Center, Lisbon, Portugal Amir Tahernia Plastic and Reconstructive Surgery, Beverly Hills, CA, USA Alastair M Thompson Department of Breast Surgical Oncology, University of Texas MD Anderson Cancer Center, Houston, TX, USA Irene Tsai Department of Radiological Sciences, UCLA, Los Angeles, CA, USA Naoto T Ueno Department of Breast Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA John T Vetto Department of Surgery, Division of Surgical Oncology, Oregon Health & Science University, Portland, OR, USA Maria Vidal Medical Oncology, Hospital Clinic of Barcelona, Barcelona, Spain Madhuri V Vithala Duke University, Durham Veteran Affairs, Durham, NC, USA Annika Waldmann Institute for Social Medicine and Epidemiology, University of Luebeck, Luebeck, Schleswig-Holstein, Germany David P Winchester American College of Surgeons, Chicago, IL, USA Michael R Zenn Surgery, Duke University Medical Center, Durham, NC, USA 648 • • • • • • • • • • • D.P Winchester – Needle biopsy—palpable – Image guided—Stereotactic – Image guided—Ultrasound – Image guided—MRI (if available) Pathology – Report completeness/CAP protocols – Radiology-Pathology correlation – Prognostic and predictive indicators – Gene studies (if available) Interdisciplinary Conference – Pre-and Post-treatment interdisciplinary discussion – History and findings – Imaging studies – Pathology Patient Navigation – Facilitates navigation of patient through system Genetic Evaluation and Management – Risk assessment – Genetic counseling – Genetic testing Surgical Care – Surgical correlation with imaging/concordance – Preoperative planning after biopsy for surgical care – Breast biopsy: lumpectomy or mastectomy – Lymph node surgery: SNB/ALND – Post-initial surgical correlation/treatment planning Plastic Surgery Consultation/Treatment – Tissue expander/Implants – TRAM/Latissimus flaps – DIEP flap/free flaps (if available) Nursing – Nurses with specialized knowledge and skills in diseases of the breast Medical Oncology Consultation/Treatment – Hormone therapy – Chemotherapy – Biologics – Chemoprevention Radiation Oncology Consultation/Treatment – Whole breast irradiation with or without boost – Regional nodal irradiation – Partial breast irradiation treatment or protocols – Palliative radiation for bone or systemic metastasis – Stereotactic radiation for isolated or limited brain metastasis Data Management – Data collection and submission Research – Cooperative trials – Institutional original research – Industry sponsored trials • Education, Support, and Rehabilitation – Education (nurse) along continuum of care (pre-treatment, during, post-treatment) – Psychosocial Support Individual Support Family Support Support Groups – Symptom management – Physical therapy (e.g., lymphedema management) • Outreach and Education – Community education: at large (including low-income/medically underserved) – Patient education – Physician education • Quality Improvement – Continuous quality improvement through annual studies • Survivorship Program – Follow-up surveillance – Rehabilitation – Health promotion/risk reduction References American Cancer Society Cancer Facts and Figures 2015, Atlanta: American Cancer Society; 2015 Silverstein MJ The Van Nuys Breast Center The first free-standing multidisciplinary breast center Surg Oncol Clin North Am 2003;9 (2):159–76 AJCC Cancer Staging Manual Seventh Edition Springer, New York; 2010 College of American Pathologists Reporting on Cancer Specimens, Northfield, IL 2005; 16 American Society of Breast Surgeons [Internet] Columbia, MD: The Society, c 2015 [cited 2016 May 13] Guidelines and quality measures Available from: http://www.breastsurgeons.org/new_ layout/about/statements/#quality_measures Kaufman CS, Shockney L, Rabinowitz B, et al National Quality Measures for Breast Centers (NQMBC): a robust quality tool: breast center quality measures Ann Surg Oncol 2010;17(2):377–85 doi:10.1245/s10434-009-0729-5 Epub 2009 Oct 16 NQF Cancer Project Report from 2012 “Cancer endorsement summary.” National Quality Forum October 2012 [cited 2016 May 20] Available from: http://www.qualityforum.org/WorkArea/linkit aspx?LinkIdentifier=id&ItemID=72130 The American College of Surgeons [Internet] Chicago, IL; The College, c 1996–2016 [cited 2016 May 13] National Cancer Data Base Breast Cancer Benchmarks Available from: https://www.facs org/quality-programs/cancer/ncdb/qualitytools National Accreditation Program for Breast Centers (NAPBC) Standards Manual, 2014 ed American College of Surgeons, Chicago, IL; 2014 Index Note: Page numbers followed by “f” and “t” indicate figures and tables respectively A Acute myelogeneous leukemia (AML), 340 Adjuvant accelerated partial breast irradiation (ABPI), 225 Adjuvant hormonal therapy, 225–226 Adjuvant radiotherapy, 189, 223–225 Adjuvant systemic therapy, 149, 311, 522 adjuvant bisphosphonates, 317 adjuvant chemotherapy, 312 anthracyclines, 312–314 single agent or combination chemotherapy, 312 taxanes, 314 adjuvant endocrine therapy, 315 aromatase inhibitors, 315–316 aims of, 311 cancer stem cells, 311 immunogenicity, 312 micro-metastatic disease, 311 ER- and PR-negative tumour, 524 genomic testing, 317–318 HER-2 negative tumors, 523 HER-2 positive tumors, 523–524 monoclonal antibodies, 316–317 ovarian suppression, 317 treatment benefit, 522 treatment selection, 522–523 trials in older patients, 318–319 Adjuvant therapy, 324 GnRHa for ovarian protection, 326 neoadjuvant therapy, 327 postmenopausal patients, 328 postmenopausal women, 326–327 premenopausal patients, 324, 327 aromatase inhibitors (AIs), 325–326 ovarian function suppression (OFS), 324–325 tamoxifen, 324 Ado-trastuzumab emtansine (T-DM1), 358–359, 397–398, 459 Afatinib, 354t Aflibercept, 362t, 364 Alkylating agents, 347, 348t bendamustine, 348–349, 348t cyclophosphamide, 347–348, 348t Alloplastic vs autogenous reconstruction alloplastic, 276–277 implant complications reconstruction, 279–280 implant types, 277–278 permanent tissue expander, 279 single stage reconstruction implants, 278–279 two stage expander, 278 ALTTO (Adjuvant Lapatinib and/or Trastuzumab Treatment Optimisation) trial, 402 design of, 441f Amastia/athelia, 44, 46 American Cancer Society (ACS), 147, 632, 637 American Joint Committee on Cancer (AJCC) staging system, 160 Anastrozole, 53, 325, 326, 328, 368, 395, 457 Anatomy and physiology, factors, 2, 3t, 25, 27 gross anatomy changes, lifespan, 6–7 lymphatic drainage, 5–6, 7f nerve supply, 4–5 relationships and quadrants, 2, vascular supply, 5, 6f histology basement membrane (BM), 9, 13 3-D reconstruction, parenchyma, lactiferous duct, low power micrograph, 8f nipple and areola, parenchyma, 9–13 stroma, 13–15 hormones estrogen and progesterone, 15–17 GnRH, 15 hypothalamo–hypophyseal-gonadal axis, 16f menstrual cycle, 15, 16f oxytocin (OXT), 17, 27 mammary gland-related mouse gene knockouts, 3t mammary gland structure and function adult premenopausal breast, 22–23 birth-puberty development, 20 lactation, 25–28 postlactational involution, 28 postmenopausal involution, 28–29 pregnancy, 23–25 prenatal development, 18–19 puberty, 20–22 other regulators, breast development, 17–18 Angiogenesis inhibitors, 417–418 Angiosarcoma, 189 Anthracyclines, 312–314, 335 acute myelogeneous leukemia (AML), 340 in adjuvant chemotherapy and alternative anthracycline-free regimens, 340–341 © Springer International Publishing Switzerland 2016 I Jatoi and A Rody (eds.), Management of Breast Diseases, DOI 10.1007/978-3-319-46356-8 649 650 avoiding, 401 cardiotoxicity, 339–340 chemotherapy, 419 liposomal anthracyclines, 341–342 myelodysplastic syndromes (MDS), 340 Antiangiogenic agents, 359, 361t aflibercept, 364 antiangiogenic tyrosine kinase inhibitors (TKIs), 364 sorafenib, 361t, 364 sunitinib, 361t, 364 bevacizumab, 359–363, 361t ramucirumab, 364–365 trebananib, 365 VEGF-Trap, 364 Antiangiogenic tyrosine kinase inhibitors (TKIs), 364 sorafenib, 361t, 364 sunitinib, 361t, 364 Antidepressant medications, 569, 570t syndromes treated by, 569t Antimetabolites, 350, 351t capecitabine, 352 5-fluourouracil (5-FU), 352 gemcitabine, 352–353 methotrexate (MTX), 350 Anxiety disorder, 566–567 APHINITY trial, 402 Architectural distortion, 165 Aromatase inhibitors, 315–316, 366–367, 596 efficacy, 596 side effects, 596–597 Aromatase inhibitors (AIs), 325–326, 521, 523 Arterial supply, Ataxia-telangiectasia (AT), 150 Atypical ductal hyperplasia (ADH), 182–183 Atypical lobular hyperplasia (ALH), 173, 184 Autogenous reconstruction abdominal perforator flaps, 284–285 gluteal musculocutaneous and perforator flaps, 286 latissimus dorsi musculocutaneous flap, 285–286 myocutaneous flaps, 280 TRAM flaps, 282 bipedicled, 282 free, 283–284 midabdominal, 283 pedicled/unipedicled flap, 281–282, 281f, 282f Autologous fat grafting, 287 Axilla management axillary relapse, 237–238 lymph node classification, 236 partial ALND, 237 radiotherapy, 241 skip metastases, 237 staging, 238–239 survival, 237 Axillary dissection, 231, 253, 546 Axillary lymph node dissection (ALND), 230, 236–237, 251 axillary relapse, 252–253 completion, 257–259 overall survival, 252 partial, 237 surgical aspects, 251–252 Axillary lymph nodes, anatomy of, 248, 249f Axillary node sampling, 253 blue dye-assisted node sampling (BDANS), 253–254 four-node axillary sampling, 253 Index B Bacterial infection of nipple, 97 Basal-like subtype, 209 biological and epidemiological implications, 209–211 Bayesian approach, 610 Bazedoxifen, 488–489 Beam arrangement for the supraclavicular and axillary apex area, 296f Bendamustine, 348–349, 348t Bevacizumab, 359–363, 361t, 403, 537 in neoadjuvant chemotherapy, 445 Biomarkers, 195 predictive, 195 prognostic, 195 Bisphosphonates (BPs), 371 adjuvant, 317, 374–375 nitrogenous, 372–374 nonnitrogenous, 372 Blue dye-assisted node sampling (BDANS), 247, 253–254 Body mass index (BMI), 130 Bone metastasis, 463 locoregional therapy of, 464–465 systemic therapy of, 463–464 Bone mineral density (BMD), 146 Bone-targeted agents, 371, 372t adjuvant use of, 374 adjuvant bisphosphonates, 374–375 adjuvant denosumab, 375 bisphosphonates (BPs), 371 nitrogenous bisphosphonates, 372–374 nonnitrogenous bisphosphonates, 372 rank ligand (RANKL) inhibitors, 374 denosumab, 374 Brain metastasis, 465 general recommendations, 465 radiotherapy for, 465–466 systemic therapy of, 465 Breast cancer aetiology alcohol, 131 body fat distribution, 130 body mass index (BMI), 130 breast density and benign breast disease, 131 diet, 131 endogenous sex hormones, 130 exogenous sex hormones, 131 height, 130 inheritance, 128–130 ionising radiation, 131 lifestyle, 131 physical activity, 131 reproductive factors, 130 risk factors, 127–131 diagnosis, 531–532 epidemiology, 529–530 extended family members, 588–589 family history, 578–580 fertility preservation American Society of Clinical Oncology, 541 embryo cryopreservation, 542 ovagenesis, 541 ovarian tissue cryopreservation, 543 fetal exposure, staging procedures axillary dissection, 546 chemotherapy, 546–547 granulocyte colony-stimulating factor (G-CSF), 548 mastectomy, 546 Index methotrexate avoidance, 548 pregnancy, surgery safety, 545 radiation therapy, 546 genetic testing education and counseling, 582–583 interpretation, 583 high risk gene mutation carriers, medical management of, 585 high-risk individuals, medical management chemoprevention, 586 mutation carriers diagnosis, 588 ovarian cancer, screening, 584 predisposition gene mutation carriers, 585 risk-reducing mastectomy, 587–588 risk-reducing salpingo-oophorectomy, 586–587 screening, men and women, 584, 585 without identifiable mutation, 584 incidence and mortality rates, 125–127 lactation BRCA2 mutation, 543 fine-needle aspiration (FNA), 544–545 gestational/pregnancy-associated breast cancer, 543 management/treatment (see Lactation) sonography, 544 management/treatment, 539 moderate risk gene mutation carriers, medical management of, 585 monoclonal antibodies, 539 vascular endothelial growth factor (VEGF), 537 PARP1 [poly(ADP-ribose) polymerase-1], 538 pedigree symbols, 579f personal health history, 580 pregnancy after breast cancer, 549–550 prevalence, 127 primary prevention, 131–133 psychological support anxiety disorder, 566–567 cognitive difficulties, 568 diagnosis, 565 estrogen deficiency and depression, 568–569 fatigue, 569 hormonal medication adherence, 566 hormonal treatment effect, 566 insomnia, 567, 567t major depressive disorder (MDD), 569 psychotic illness, 570 treatment, 569–570 psychosocial, familial and professional aspects, 550–551 risk assessment absolute risk, 580 BRCA gene mutation, BRCAPro and BOADICEA, 581 Gail model and Claus tables, 581 relative risk, 580 risk factors/prognosis BRCA1/BRCA2 mutations, 530 fetal estrogen, 531 oral contraceptive, 530 secondary prevention/screening, 133 side effects radiation therapy, 540–541 surgery, 539 systemic treatment, 539–540 somatic and germline genetics, 575–576 survivors care, 541 syndromes BRCA1/BRCA2 mutation, 575, 577 Li-Fraumeni disorder, 583 tumor characteristics, 532–533 651 tyrosine kinase inhibitors, 538 vaccines, 538–539 5-year survival, 133 Breast Cancer Index (BCI), 199 Breast cancer in males (BCM) associated factors and conditions, 494–496 vs BCF, 504–507 breast lump diagnosis, 498 factors associated with development of, 495t family history and genetics, 496 global distribution, 494 histologies, 497 imaging, 498 physical findings, 498 prognostic factors, 503–504 staging, 497 survivorship issues, 507–508 family members, testing of, 507 follow-up, 507 psychological issues/resources/support groups, 508 tumor registry, 507 treatment and outcomes adjuvant chemotherapy, 502–503 hormone therapy, 503 palliative therapy, 503 prognostic factors, 503–504 radiation therapy (RT), 502 surgery, 501–502 tumor biology, 497 U.S incidence, 494 Breast cancer screening benefits, 139, 140t breast self-examination (BSE), 147, 148 breast ultrasound, 146 clinical breast examination (CBE), 147–148 breast cancer detection and demonstration project (BCDDP), 147 CNBSS, 147–148 mammography screening, 141 Canadian trials, 143 vs diagnostic mammography, 141 Edinburgh trial, 143 effect of age, 145–146 health insurance plan (HIP) trial, 142 meta-analyses, 144 randomized controlled trials characteristics, 142t Swedish trials, 142–143 United Kingdom age trial, 143–144 MRI, 146–147 potential hazards, 149 cost, 151–152 false positives, 150 lead time, 150 over-diagnosis, 151 radiation exposure, 150–151 principles, 139 detectable preclinical phase (DPCP), 139–140 lead-time bias, 140 length and selection bias, 140–141 total preclinical phase (TPCP), 139 Breast cancer screening programs (BSC), 133 Breast cancer specific survival (BCSS), 198 Breast center accreditation award matrix, 647 breast program staff education, 646 center leadership cancer conference, 640 652 evaluation and management guidelines, 641 level of responsibility and accountability, 639–640 responsibility and accountability level, 639–640 clinical management AJCC staging, 642 benign breast disease, evaluation and management, 644 breast cancer surveillance, 642 breast conservation, 641–642 diagnostic imaging, 642–643 educational resources, 644 genetic evaluation and management, 643–644 interdisciplinary patient management, 641 medical oncology, 643 needle biopsy, 643 nursing, 643 pathology reports, 642 patient navigation, 641 radiation oncology, 643 reconstructive surgery, 644 sentinel node biopsy, 641 stereotactic core needle biopsy, 643 support and rehabilitation, 643 ultrasonography, 643 community outreach, 645–646 member organizations, 638t National Accreditation Program for Breast Centers (NAPBC) accredited center benefits, 647 mission objectives, 639, 639t standards, 639 prevention and early detection programs, 646 quality improvement, 646 research clinical trial accrual, 645 clinical trial information, 645 survey process, 646–647 Breast conserving surgery (BCS) appropriate surgical therapy, 234 axillary surgery, 236 factors, 232 frequency, 234 ipsilateral breast tumor recurrences, 231 preoperative chemotherapy, 234 vs radical mastectomy, 232 RT administration, 232 tumor size, 233 Breast-conserving therapy (BCT), 273, 299, 546, 533 Breastfeeding, benefits of, 81–82 Breastfeeding and lactation problems intrapartum period, 85 galactopoiesis failure, 87 hospital discharge planning, 90 in-hospital risk assessment, 90 lactation establishment, 85 lactogenesis failure, 86–87 mammogenesis failure, 85–86 maternal psychosocial health, 90 milk intake, 90 milk transfer, 87–89 postpartum period, 91 clinical breastfeeding assessment, 91 insufficient milk syndrome, 92–93 maternal hyperlactation syndrome, 93–96 medicines, 99 relactation, 99 sore nipples, 96–98 prenatal period, 81 Index anticipatory guidance, 84–85 breastfeeding benefits, 81–82 infant formula hazards, 82 informed choice, 81 prenatal breast examination, 84 prenatal education, 82 prenatal lactation assessment, 82–83 screening for risk factors, 83–84 Breast imaging breast ultrasound cystic masses, 169–170 normal anatomy, 169 core needle biopsy (CNB), 172 indications, relative, contraindications and complications, 173 postcore biopsy, 113 magnetic resonance imaging, 173–175 mammography abnormality location, 163, 164f calcifications, 164–165, 166f craniocaudal (CC), 157, 158f diagnostics, 160 false-negative mammograms, 168 indirect and secondary signs of malignancy, 165, 167f, 168 masses, 164 mediolateral oblique (MLO), 157, 158f report, 161–163 screening, potential adverse consequences, 168 radionuclide imaging, 175 screening, 171–172 solid masses, 170–171, 170f technical advances, 169 ultrasonography, 157 Breast imaging reporting and data system (BI-RADS), 157, 162–163 Breast lift procedure, 287 Breast mass evaluation, 105 benign breast masses, 120–121 benign nodularity, 121 breast sepsis, 122 breast ultrasound, 112, 113f–114f clinical examination, 107–110 abnormalities detection, 108 bilateral axillary examination, 110 inspection and palpation, 108 left breast cancer, 110f, 112f craniocaudal mammograms, 111, 112f, 117f cysts, 112, 113f, 114f, 121 fat necrosis, 123 fibroadenoma, 112, 116f, 119 history of presentation, 106 bleeding nipple discharge, 106, 107f features, 106, 106t nipple retraction, cancer, 108f, 110f patient age and diagnosis, 106t patient’s record, 109t skin nodules, 106, 108f intraduct papilloma, 122 investigation, 110 magnetic resonance imaging (MRI), 115–116, 117f–18f magnification views, 113f mammography, 114–115 medio-lateral oblique views, 112f, 1111 other lesions, 123 pathology diagnosis core needle, fibroadenoma, 119f cytology scoring, 118 fine needle aspiration cytology, 120f Index malignant cells, 114 needle localisation, 120f X-ray image, cores, 119, 119f patient plan, 120 phyllodes tumour, 121 positron emission tomography/computerised tomography (PET/CT), 116–117 pregnancy and lactation, 121 presentation routes, 105 incidental detection, 106 screening, 106 symptomatic, 105–106 skin lesions, 122 Breast program leadership (BPL), 639–642 Breast quadrants, 4, 4f Breast reconstructive surgery, 273 alloplastic vs autogenous, 276–280 autogenous reconstruction, 280–286 chemotherapy, 288 indications, 274 nipple–areola reconstruction, 286–287 radiation, 287–288 skin-sparing mastectomy, 274 timing, 275–276 Breast self-examination (BSE), 133 Breast ultrasound cystic masses, 169–170 normal anatomy, 169 screening, 171–172 solid masses, 170–171, 170f technical advances, 169 Bromocriptine, 51, 77 C Calcifications, 164–165, 166f Calcium metabolism, during lactation, 27–28 Canadian National Breast Screening Study (CNBSS), 141, 143, 147–148, 150 Cancer Chemotherapy National Service Center (CCNSC), 602–603 The Cancer Genome Atlas (TCGA) Project, 204 Cancer stem cells, 311 Candida albicans, 97 Candidiasis, 97–98 Capecitabine, 344, 351t, 352, 362, 394, 397, 462 Carboplatin, 349–350, 350t, 415–416, 444 Cardiac events and timing hypothesis, 483–484 Cardiff Breast Pain Chart, 74f, 77 Cardiotoxicity, 339–340 CD8 + T cells, 312 Chapped nipples, 97 Chemoprevention of breast cancer, 593 chemoprevention agents, 593 aromatase inhibitors, 596–597 tamoxifen, 593–596 prevention trials, 597 exemestane, using, 599 International Breast Cancer Intervention Study-II, 597–599 new agents, 599 Chemotherapy, adjuvant, 312 anthracyclines, 312–314 single agent or combination chemotherapy, 312 taxanes, 314 Chemotherapy (CT), 453 Chest wall tenderness, 75–76, 76f Chlorpromazine, 99 653 Cisplatin, 349, 350t Claudin-low tumors, 211 Clinical breast examination (CBE), 133 Clinical trials baseline outcome rates, 612 clinical significance vs statistical significance, 611–612 competing risks, design under, 629–630 design considerations control group choice, 610 definition, 609–610 masking and placebos, 610–611 precision and eliminating bias, 608–609 disease-free survival (DFS), 628 ethical concerns, 618 evolution, 601–602 Food and Drug Administration (FDA), 617 fundamental features collaboration, 603–604 explanatory and pragmatic considerations, 606–608 new drug development and testing, 605 primary question selection, 608 history of cancer cooperative groups, 602–603 intention-to-treat (ITT) analysis, 625 interpretation, 630–631 Kaplan-Meier life-table, 626 1-KM method vs nonparametric cumulative incidence approach, 628–629 log-rank test, 626 loss of power and sample size, 629–630 multiplicity considerations, 628 multivariable models, 627–628 National Institutes of Health (NIH), 616 NSABP Biostatistical Center, 625 NSABP Protocol B-06 data integrity, 620–621 ethical controversies, 618 Greco-Latin square design, 618–620 interim data monitoring, 621–625 International Conference on Harmonization (ICH), 622 lumpectomy, 618–619 manual of operations (MOP), 621 prerandomization approach, 619–620 population measures of variability, 612 prediction model, validation and building, 630 randomization methods biased coin algorithm, 615–616 phase III cancer trial, 614 pseudorandom sequence, 615 regression, on cumulative incidence function, 629 sample size adjustments, 613 statistical analysis, 623 statistical inference and sample size considerations, 597–598 statistical significance and study power, 612 time-to-event outcomes, 612–613 two-sample considerations, 629 type I (a) and type II (ß) error, 612 Clodronate, 372t, 373 Cognitive behavioral therapy (CBT), 570 Cognitive difficulties, 568 Colloid carcinoma See Mucinous carcinoma Comprehensive geriatric assessment (CGA), 525 Congenital and developmental abnormalities anatomy, 41 breast masses biopsy, 41 gynecomastia, 52–53 polymastia/polythelia, 42–43 654 congenital breast hypoplasia/aplasia, 43 amastia/athelia, 44, 46 Poland syndrome, 46 tubular/tuberous breast, 46–49 embryonic development, mammary glands, 46 gigantomastia, 50, 51–52 intrauterine development, 46 inverted nipples, 49–52, 50f nipple-areolar complex (NAC), 41 premature thelarche, 42 puberty, 42 Conjugated Equine synthetic Estrogen (CEE), 485 Connective tissue growth factor (CTGF), 18 Consolidated Standards of Reporting Trials (CONSORT) statement, 631 Contralateral breast, 287 Contralateral breast cancer, 596, 597f Contralateral prophylactic mastectomy (CPM), 235 Contrast-enhanced breast MRI, 175 Cooper’s ligament, 42 Core needle biopsy (CNB), 172–173 Cox proportional hazards model, 627 Craniocaudal mammograms, 111, 112f, 117f Cribriform carcinoma, 189 Cyclin-dependent kinases (CDKs), 458 Cyclophosphamide, 347–348, 348t Cyclophosphamide, methotrexate and 5-fluorouracil (CMF), 312 CYP 2D6, 200 Cytotoxic agents, systemic therapy, 335 alkylating agents, 347, 348t bendamustine, 348–349 cyclophosphamide, 347–348 antimetabolites, 350 capecitabine, 352 5-fluourouracil (5-FU), 352 gemcitabine, 352–353 methotrexate (MTX), 350 platinum-based chemotherapeutic agents, 349–350 topoisomerase II inhibitors, 335, 336t anthracyclines, 335–342 tubulin inhibitors, 342 epothilones (ixabepilone), 344 eribulin, 347 taxanes, 342–344 vinca alkaloids (vinorelbine), 346–347 D Danazol, 77 Danish Osteoporosis Prevention Study (DOPS), 484 Deep circumflex iliac artery (DCIA), 281 Deep inferior epigastric (artery) perforator (DIEP), 236 flap, 284, 285f Deep inspiration breath-hold (DIBH) technique, 295 Denosumab, 372t, 374, 464 Denosumab, adjuvant, 375 Department of Defense (DoD) healthcare system, 234 Dermatitis of nipple, 98 Detectable preclinical phase (DPCP), 139–40 Diagnostic mammography, 160 Digital breast tomosynthesis (DBT), 157, 160–161 Docetaxel, 342, 343, 345t Domperidone, 99 Dose distribution in the breast, 295f Doxorubicin, 314, 318, 336t, 339, 341 Drug-induced gigantomastia, 51–52 Index Ductal carcinoma cribriform carcinoma, 189 Elston–Ellis modification, 189 mammography, 64 medullary carcinoma, 189 metaplastic carcinoma, 189 tubular carcinoma, 189 variants, invasive breast cancer, 189 Ductal carcinoma in situ (DCIS), 151, 179, 180–182, 261, 297–299 adjuvant hormonal therapy, 225–226 adjuvant radiotherapy, 223–225 biology, 221–222 breast treatment local recurrence rate, 224–225 mastectomy, 222 wide local excision, 223 diagnosis, 222 follow-up, 221, 226 grading and risk assessment, 180–181 incidence and clinical presentation, 180 molecular pathology and special types, 181 mortality, 180 MRI utility, 222 natural history, 180, 221 partial breast irradiation, 225 pathologic working up of, 181–182 presentation, 222, 225 recurrence treatment, 223–224 surgery, 222–223 E Early breast cancer (EBC) decision-making in, 199–200 multigene assays in, 196–199, 197t therapy concepts in, 196f Early Breast Cancer Treatment Collaborative Group (EBCTCG), 631 Early Breast Cancer Trialists Collaborative Group (EBCTCG), 232, 312, 521, 522 Early stage breast cancer ductal carcinoma in situ, 297–299 invasive breast cancer breast-conserving therapy, 299–304 contraindications, 300 local recurrence, 301 mutations, 301 neoadjuvant chemotherapy, 305 postmastectomy radiation, 302–304 radiation and breast reconstruction, 304 E-cadherin, 185, 214, 425 Edinburgh trial, 143, 147 Elderly breast cancer adjuvant systemic therapy ER- and PR-negative tumour, 524 HER-2 negative tumors, 523 HER-2 positive tumors, 523–524 treatment benefit, 522 treatment selection, 522–523 chemoprevention of breast cancer, 520 clinical assessment, 519–520 clinical trials, 525 epidemiology, 519 metastatic disease, 524–525 primary breast cancer treatment axilla management, 521–522 radiation therapy, 521 Index surgery/endocrine therapy, 521 screening, 520–521 Embryo cryopreservation, 542 Endocrine therapy, 323 adjuvant therapy, 315, 324 aromatase inhibitors, 315–316 GnRHa for ovarian protection, 326 neoadjuvant therapy, 327 postmenopausal women, 326–327, 328 premenopausal patients, 324, 327 metastatic therapy, 328 HR+/HER2+, 330–331 postmenopausal patients, 329–330 premenopausal patients, 328–329 overcoming endocrine resistance, 331–332 Endocrine therapy (ET), 365 aromatase inhibitors, 366–367 combination of endocrine therapies, 368 fulvestrant, 367–368 gonadotropin-releasing hormone (GnRH) analogs, 368–369 selective estrogen receptor modulators (SERMs), 365 tamoxifen, 365–366 targeted agents used in combination with, 369 everolimus, 369 palbociclib and Cdk4/6 inhibitors, 370–371 PIK3CA inhibitors, 369–370 Endogenous sex hormones, 130 Endopredict, 198–199 English OPTIMA program, 199 Eosinophils, 14 EPclin, 198 Epidermal growth factor receptors (EGFRs), 17 Epirubicin, 336t Epothilones (ixabepilone), 344 EPrognosis website, 519 ER+HER2 negative ABC, treatment of, 454 biological and endocrine resistance, 457–458 chemotherapy, 458 endocrine therapy, 454–457 Eribulin, 346t, 347, 394 ER-positive and -negative breast cancer, 534–535 Estrogen and breast cancer in postmenopausal women, 475 Women’s Health Initiative (WHI) HRT trials, 476–477 design, 477 E + P vs placebo, 477–478 follow-up, 478–480 methodology, 480–481 Estrogen and cardiac events with all-cause mortality, 483 cardiac events and timing hypothesis, 483–484 estrogen and biochemical surrogates, 486–488 HRT agent selection and cardiac outcome, 484–485 HRT and breast cancer patients with BRCA mutations, 489 HRT developments, 488 tibolone and bazedoxifen, 488–489 WHI HRT trials and cardiac outcomes, 485–486 Estrogen deficiency and depression, 568–569 Estrogen receptor (ER), 12, 15 Estrogen receptor cross-talk pathways, 455f European Organization for Research and Treatment of Cancer (EORTC), 423, 534 Everolimus, 360t, 369, 538 Exemestane, 360t, 599 Exogenous sex hormones, 131 Exploratory anti-HER2 blockade strategies, 405–406 ExteNET, 402 Extracellular matrix (ECM), 10, 15 655 F Feedback inhibitor of lactation (FIL), 85 Fetal exposure by staging procedures, 545t Fibrocystic disease, 61 Fine needle aspirate (FNA), 412, 414, 499–501, 500f FinHer trial, 400 First-line single-agent therapy, 392–393 Fluconazole, 98 Fluorine-18 2-deoxy-2-fluoro-D-glucose (FDG), 175 5-fluourouracil (5-FU), 351t, 352 Follicle stimulating hormone (FSH), 15, 27 Formalin-fixed paraffin-embedded (FFPE), 198 Four-node axillary sampling, 253 Frequently mutated genes in breast cancer, 213 lobular breast cancer, 214 Fulvestrant, 360t, 367–368, 455–457 G Gail model and Claus tables, 581 Galactopoiesis process, 85, 87 Galactorrhea, 60, 61t Gemcitabine, 351t, 352–353, 394 21 Gene Assay, 196–198 70 Gene Assay, 198 Gene expression profiling, 203 Gene expression vs histopathology, intrinsic subtyping based on, 204–205 Genome-wide association studies (GWAS), 130 Genomic testing, 317–318 Gentian violet, 98 GeparQuinto study, 403 GeparQuinto trial, 417, 418 GeparSixto trial, 415 GeparTrio study, 416 Geriatric assessment (GA), 519–520 German GeparQuinto trial, 417, 418 Glandular failure, 86 GnRHa for ovarian protection, 326 Gonadotropin releasing hormone (GnRH), 15, 27, 542 analogs, 368–369 Goserelin (Zoladex), 77, 360t Gravid-induced gigantomastia, 51 Gross anatomy changes, lifespan, 6–7 lymphatic drainage, 5, 7f dye microinjection, internal mammary nodes, 5, pectoralis major, pectoralis minor, nerve supply cutaneous and intercostal nerves, 4–5 sympathetic fibers, relationships and quadrants, 2, 4, 4f sagittal section, lactating breast, 4f vascular supply, 5, 6f Gynecomastia, 52–53, 491–493 bilateral, 53f causes of, 53t conditions associated with, 492t drugs associated with, 492t H ‘Halstedian’ hypothesis, 249 Health insurance plan (HIP) trial, 142, 143, 147 656 Hepatic cytochrome P450 2D2, 200 HER2, 13 overexpression, 134 HER+ABC, treatment of, 458 first-line therapy, 459–461 progression beyond second line therapy, 462 second-line therapy, 461–462 treatment of HER2+/HR+ disease, 462 unanswered questions for management HER2 positive disease, 462–463 HERA trial, 399–400 Hereditary breast cancer, 575 genes associated with, 576 predispositions high-risk, 577–578 moderate-risk, 578 HER2-enriched subtype, 207–209 HER2-positive breast cancer, 440–441 High-risk individuals chemoprevention, 586 mutation carriers diagnosis, 588 ovarian cancer, screening, 584 predisposition gene mutation carriers, 585 risk-reducing mastectomy, 587–588 risk-reducing salpingo-oophorectomy, 586–587 screening, men and women, 584, 585 without identifiable mutation, 584 Hormonal medication adherence, 566 Hormonal treatment effect, 566 Hormone receptor positive/human epidermal growth factor receptor 2-positive breast cancer (HR+/HER2+), 330–331 Hormone replacement therapy (HRT), 131, 475, 481 Hormone replacement trial agent selection and cardiac outcome, 484–485 and breast cancer patients with BRCA mutations, 489 developments, 488 Human chorionic gonadotropin (hCG) hormones, 24–25 Human epidermal growth factor receptor (HER2)-targeted therapies, 353, 354t ado-trastuzumab emtansine, T-DM1, 358–359 lapatinib, 354t, 356–357 new HER2-directed agents and combinations under investigation, 359 pertuzumab, 354t, 357–358 trastuzumab, 353–356, 354t Human epidermal growth factor receptor-2 (HER2) targeted therapy, 383–384, 272 accurate identification, 391 adjuvant setting, trastuzumab anthracyclines, avoiding, 401 BCIRG 006 trial, 399–400 combined American NSABP-B31 and NCCTG-N9831 trials, 399, 400 duration, 400–401 efficacy in trial, 398–399 FinHer trial, 400 HERA trial, 399–400 safety in trial, 399 sequencing and timing, 400 small HER2+ tumors, 401 ado-trastuzumab emtansine (T-DM1), 397–398 ASCO/CAP Updated Recommendations, 392 bevacizumab, 403 dual HER2 targeted therapies, neoadjuvant trials of, 404t EGFR inhibitors, 382–383 exploratory anti-HER2 blockade strategies, 405–406 Index lapatinib, 402 metastatic HER2+ breast cancers, algorithm for treating, 398 first-line therapy, 398 second-line therapy, 398 third-line therapy and beyond, 398 metastatic setting, trastuzumab after disease progression, 395 combination with chemotherapy, 393–394 combination with hormonal therapy, 394–395 first-line single-agent therapy, 392–393 single-agent therapy, 392 neoadjuvant HER2+ approaches, 403 lapatinib-based neoadjuvant regimens, 403–405 neratinib-based neoadjuvant regimens, 405 pertuzumab-based neoadjuvant regimens, 405 trastuzumab, neoadjuvant, 403 neratinib, 402–403 oncogene hypothesis, 391 pertuzumab, 402 4-Hydroxytamoxifen (4-OHT), 77 Hyperplasia of breast, 50–52 I Ibandronate, 372t, 373 Immediate reconstruction, 275–276 Immunogenicity, 312 Inflammatory and locally advanced breast cancer, 420f diagnosis and staging, 412–415 different presentations, 413f epidemiology, 411–412 flow diagram describing management of, 429f local therapy, 421–424 management, 415, 428 molecular biology, 424–425 prognostic factors, 426 survival, 426–429 systemic therapy anthracycline-based chemotherapy, 419 immunotherapy, 418 for inflammatory breast cancer, 418–421 investigational therapy, 417–418 neoadjuvant chemotherapy, 415–416 neoadjuvant endocrine therapy, 417 and pCR, 418 preoperative HER2-directed therapy, 416–417 Inframammary fold (IMF), 275, 277 Insomnia, 567, 567t Insufficient milk syndrome, 92–93, 93f Insulin-like growth factors (IGFs), 17–18 Integrins, 12, 13, 15 Intensity-modulated radiation therapy (IMRT), 293 Intercostobrachial nerve (ICBN), 251 Interim data monitoring breast cancer prevention trial (BCPT), 624 data monitoring committee (DMC), 622–623 herceptin, 624 mechanism, 622 quality assurance, 622 statistical methods, 623 Internal mammary chain (IMC), 249 Internal mammary node biopsy, 265–266 Internal mammary nodes (IMN), 296 International Agency for Research on Cancer (IARC), 133 International Breast Cancer Intervention Study-II, 597–599 International (Ludwig) Breast Cancer Study Group (IBCSG), 534 Index Intra-operative node assessment, 259–260 Intrinsic subtypes, main molecular features of, 205 basal-like subtype, 209 biological and epidemiological implications, 209–211 claudin-low tumors, 211 HER2-enriched subtype, 207–209 luminal disease, 205–207 Intrinsic subtypes in metastatic setting, 213 Intrinsic subtyping based on gene expression vs histopathology, 204–205 Invasive breast cancer breast-conserving therapy, 299–304 contraindications, 300 local recurrence, 301 mutations, 301 neoadjuvant chemotherapy, 305 postmastectomy radiation, 302–304 radiation and breast reconstruction, 304 Invasive carcinoma, 185 breast cancer classification and grading, 185 invasive lobular carcinoma (ILC), 187–189 no special type (NST), 186–187 sarcoma and malignant phyllodes tumors, 189 special types, 189 tumor grading, 189–190 Ionizing radiation, 292 Ipsilateral breast, 231–232 Ipsilateral breast tumor recurrence (IBTR), 426 Ixabepilone, 344, 346t J Japan Strategic Anti-cancer Randomized Trial (J-START), 146 Juvenile hypertrophy, 50–51 K Kaplan-Meier survival rate representation, 427f KATHERINE trial, 418 King’s/Cambridge trials, 230–231 L Lactation, 81 calcium metabolism, 27–28 effects, nursing mother, 27 events, 25–26 hormones, 27 IgA, 26, 27 lipid droplets, 26 management/treatment breast conserving vs mastectomy, 533–534 cellular mechanisms, 536 chemotherapy, 534–535 endocrine, 535–536 radiation, 534 paracellular pathway, 27 proteinaceous material, 26 regulatory factors, 20 secretory process, 26–27 Laminin, 10, 13 Lapatinib, 354t, 356–357, 402, 417, 459 Lapatinib-based neoadjuvant regimens, 403–405 Lapatinib dual kinase inhibitor, 538 Letrozol, 326, 328, 360t Leuprorelin, 360t 657 Li-Fraumeni syndrome, 496 Linear accelerator (LINAC), 292f Liposomal anthracyclines, 341–342 Liposomal doxorubicin, 336t Liver metastasis, 466 Lobular breast cancer, 214 Lobular carcinoma in situ (LCIS), 173, 183, 184–185, 185f Lobular neoplasia (LN), 183–185 Locally advanced breast cancers (LABC), 403 Local-regional recurrence (LRR), 426 Locoregional therapy of bone metastases, 464–465 Loss of heterozygosity (LOH), 213 Luminal disease, 205–207 Luminal epithelial cells, 23, 26 Luminal tumours, 134 Lumpectomy, 231, 233, 238 Luteal phase, 22 Luteinizing hormone (LH), 15, 27 Lymphatic plexuses, Lymphatic system of the breast, 248–251 Lymphedema, 297, 540–541 M Magnetic resonance imaging (MRI), 115–116, 117f, 234, 544 Major depressive disorder (MDD), 569 Major histocompatibility complex class (MHC1), 312 Male breast diseases benign breast conditions, 493 breast cancer adjuvant chemotherapy, 502–503 associated factors and conditions, 494–496 vs BCF, 504–507 family history and genetics, 496 global distribution, 494 histologies, 497 hormone therapy, 503 imaging, 498 palliative therapy, 503 physical findings, 498 prognostic factors, 503–504 radiation therapy (RT), 502 staging, 497 surgery, 501–502 survivorship issues, 507–508 tumor biology, 497 U.S incidence, 494 differential diagnosis of breast masses, 498–501 gynecomastia, 491–493 malignant breast conditions in males, 499t Mammogenesis, 85–86 Mammography report BI-RADS, 161 breast tissue composition, 162 final assessment categories, 162–163 findings, 162 Manual stripping, 95 Mastalgia breast cancer, 75 chest wall pain, 74–75 classification, 73, 74t clinical assessment and investigations, 75–76 cyclical mastalgia, 73 agnus castus, 76 non-steroidal anti-inflammatory drugs (NSAIDs), 77 oral contraceptive method, 76 658 premenstrual syndrome (PMS), 74 etiology, 73 management algorithm, 77–78 non-chest wall pain, 73, 75 non-cyclical mastalgia, 73, 77 psychosocial factors, 75 Mastopexy, 287 Maternal hyperlactation syndrome, 93 acute mastitis, 94 breast abscess, 95 chronic mastitis, 94 clinical spectrum, 93 decreased milk retention, 95 infection treatment, 95–96 milk stasis, 94 milk synthesis, 95 obstruction removal, 95 recurrence prevention, 96 supportive measures, 96 white spot, 94 Matrix metalloproteinases (MMPs), 10 Mediolateral oblique (MLO), 157, 158f Medullary carcinoma, 189 Memorial Sloan-Kettering Cancer Center, 502, 505, 507 Metaplastic carcinoma, 189 Metastatic breast cancer, 451 epidemiology, 451 future perspectives, 467 new biology insights, 451–452 role of imaging, nuclear medicine, and other technology, 452 supportive care and survivorship issues, 466–467 treatment, 452 bone metastasis, 463 brain metastasis, 465–466 of ER+HER2 negative ABC, 454–458 general principles, 452–454 of HER+ABC, 458–463 liver metastasis, 466 locoregional therapy of bone metastases, 464–465 systemic therapy of bone metastases, 463–464 of triple negative ABC, 463 Metastatic breast cancer (mBC), 451 Metastatic disease, 524–525 Metastatic HER2+ breast cancers, algorithm for treating, 398 first-line therapy, 398 second-line therapy, 398 third-line therapy and beyond, 398 Metastatic therapy, 328 HR+/HER2+, 330–331 postmenopausal patients, 329–330 premenopausal patients, 328–329 Methotrexate (MTX), 350, 351t Metoclopramide, 99 Microarray in node-negative disease may avoid chemotherapy trial (MINDACT), 198, 533 Microdochectomy, 67 Micromastia, 44f, 45f Micro-metastatic disease, 311 Micropapillary carcinoma, 189 MicroRNAs (MiRNAs), 424–425 Milk intake duration and factors, 89, 90 frequency, 89 pattern, breast usage, 90 Milk synthesis, maternal, 92f Milk transfer Index breastfeeding skills, 88 impeding milk transfer, 88–89 milk ejection reflex, 87, 88 positioning, 88 suckling, 88 MISCAN (microsimulation screening analysis), 145 Mitoxantrone, 336t and other topoisomerase II inhibitors, 341–342 Molecular classification of breast cancer, 203 frequently mutated genes in breast cancer, 213 lobular breast cancer, 214 intrinsic subtypes, main molecular features of, 205 basal-like subtype, 209–211 claudin-low tumors, 211 HER2-enriched subtype, 207–209 luminal disease, 205–207 intrinsic subtypes in metastatic setting, 213 intrinsic subtyping based on gene expressionvs histopathology, 204–205 novel subgroups, 212 Molecular subtypes in breast cancer and therapy concepts, 195–196 Molecular testing for therapy prediction, 200 Monoclonal antibodies, 316–317 Montgomery’s tubercles, 62 MTOR inhibitors, 418 Mucinous carcinoma, 186t Multifocal and multicentric tumours, 261 Multigene assays, 196, 197t clinical use of, 199–200 Endopredict, 198–199 21 Gene Assay, 196–198 70 Gene Assay, 198 Prosigna (PAM50), 199 Multileaf collimator (MLC), 293, 293f Myelodysplastic syndromes (MDS), 340 Myocardial infarction (MI), 151 Myoepithelial cells, 10–11 N Nab-paclitaxel, 342, 344, 345t National Accreditation Program for Breast Centers (NAPBC), 637–639 accredited center benefits, 647 mission objectives, 638 standards, 639 National Cancer Data Base (NCDB), 501, 502, 637 National Cancer Institute (NCI), 415, 602 National Surgical Adjuvant Breast and Bowel Project (NSABP), 222, 223, 415, 422, 601, 615 National Surgical Adjuvant Breast Project (NSABP), 312 National Surgical Adjuvant Breast Project-04 (NSABP-04), 230 Neoadjuvant chemotherapy, 262, 415–416 noncross-resistant agents, 416 platinum agents, 415–416 preoperative anthracycline and taxane, 415 sentinel lymph node biopsy after, 263–265 sentinel lymph node biopsy prior to, 263 Neo-adjuvant chemotherapy setting, axillary surgery in, 241–242 Neoadjuvant endocrine therapy, 417 Neoadjuvant HER2+ approaches, 403 lapatinib-based neoadjuvant regimens, 403–405 neratinib-based neoadjuvant regimens, 405 pertuzumab-based neoadjuvant regimens, 405 trastuzumab, neoadjuvant, 403 NeoAdjuvant Lapatinib and/or Trastuzumab Optimization (NeoALTTO) trial, 404 Index Neoadjuvant systemic treatment (NST), 437 biomarkers in, 438 individual molecular biomarkers of resistance, 439 tumor cell proliferation, 439 tumor-infiltrating lymphocytes, 439 choice of chemotherapy regimens in, 439 bevacizumab, use of, 533 biomarkers for prediction of platinum efficacy in TNBC, 444 HER2-positive breast cancer, 440–441 patients with TNBC, 441–444 indications for, 437 neoadjuvant endocrine approaches, 445 pathohistological complete remission (pCR), 438 definitions of, 438 prognostic significance, 438 post-neoadjuvant therapy, dynamic biomarkers, and “window studies,” 445–446 radiotherapy after, 447 surgical considerations in, 446 sentinel node biopsy, 446–447 NeoALTTO trial, 417, 440f Neratinib, 402–403, 538 Neratinib-based neoadjuvant regimens, 405 Neuregulin, 17 Neuropeptides, New drug development and testing phase I trial, 605 phase II trial, 605 phase III trial, 605 Nipple and areola, Nipple aspirate fluid (NAF), 56–57, 57–58, 66 Nipple discharge algorithm, 69f anatomy and physiology, 57 biochemical markers, 66 breast cancer, 66, 68 characteristics and etiology, 59–63 bloody discharge, 62 carcinoma, 63 cysts communication, 61 cytologic evaluation, 62 duct ectasia, 61 fibrocystic disease, 61 galactorrhea, 60, 61t Montgomery’s tubercles, 62 nonpathologic nipple discharge, 60 opalescent physiologic discharge, 60 papillomas, 62 pathologic and physiologic nipple discharge, 58 cytology, 66–67 definition, 57–58 diagnostic evaluation, 64 ductal imaging, 66–67, 66f follow-up, 68–69 incidence, 58–59 magnetic resonance imaging (MRI), 65 mammary ductoscopy, 67–68 mammography, 64 occult blood, 65 surgical evaluation and treatment, 67 ultrasound, 64–65 Nipple-sparing mastectomy (NSM), 274–275 Nipple trauma, 96–97 Nitrogenous bisphosphonates, 372–374 Non-chest wall pain, 73, 75 Non-cyclical mastalgia, 73 659 Nonnitrogenous bisphosphonates, 372 Nonpathologic nipple discharge, 60t Non-sentinel lymph nodes (NSLN), 254 Novel subgroups of breast cancer, 212 NSABP Protocol B-06 data integrity, 620–621 Greco-Latin square design, 618 interim data monitoring, 621–625 International Conference on Harmonization (ICH), 622 lumpectomy, 618–619 manual of operations (MOP), 621 prerandomization approach, 619–620 Nystatin suspension, 98 O 4-OHT See 4-Hydroxytamoxifen Oncogene hypothesis, 391 OncotypeDx 523 Oocyte cryopreservation, 542 Ovarian function suppression (OFS), 324–325 Ovarian protection, GnRHa for, 326 Ovarian suppression, 317 Ovarian tissue cryopreservation, 543 Overcoming endocrine resistance, 331–332 Oxford overview analysis, 225 Oxytocin (OXT), 17, 27 P Paclitaxel, 342, 345t nab-paclitaxel, 344 Paget’s disease, 98, 108f, 184 Palbociclib, 361t Palbociclib and Cdk4/6 inhibitors, 370–371 PAM50, 199 Pamidronate, 372t, 373 Papillomas, 62 Parathyroid hormone-related peptide (PTHrP), 19, 28 Parenchyma luminal epithelial cells, 9–10 myoepithelial cells, 10–11 stem cells definitions and terms, 11 mammary stem cells, 11–12 regulation factors, 12–13 structure and function, 11 PARP-inhibitors, 371 Partial breast irradiation, 225 Pathohistological complete remission (pCR), 438 definitions of, 438 prognostic significance, 438 Pathological complete response (pCR), 426 prognosis in patients who not achieve, 426 Pathologic nipple discharge (PND), 58, 59f, 60t, 62t, 64 P-cadherin, 10 Pegylated liposomal doxorubicin, 336t Perforator flaps, 284 Pertuzumab, 354t, 357–358, 402, 416, 459, 537 Pertuzumab-based neoadjuvant regimens, 405 p53 gene, 425 Photons, 291 Phyllodes tumors, 189 Physiologic nipple discharge, 58, 58f, 60t PIK3CA inhibitors, 369–370 PIK3CA mutations, 200 660 p27kip1, 425 Platinum-based chemotherapeutic agents, 349–350, 350t Poland syndrome, 46 classification, 46t Poly (ADP-ribose) polymerase (PARP), 463 Poly(ADP-ribose) polymerase (PARP) inhibitors, 418 Polymastia, 42–43, 43f Polythelia, 42–43 Positron emission tomography (PET), 175, 176f, 294 Postglandular, 86, 87 Postmastectomy radiation/radiotherapy (PMRT), 276, 287, 288 Precision and eliminating bias random errors, 608 systematic errors, 608 Prediction Analysis of Microarray 50 (PAM50), 318 Predictive markers, 195 Preglandular, 86, 87 Pregnancy cellular hypertrophy and hyperplasia, 23 development of breast cancer during, 262 hormones, 24–25 lobuloalveolar structure, 23 luminal cells, 23 luminal epithelial cells, 23, 26 other regulatory factors, 25 Pregnancy-specific mammary nuclear factor (PMF), 86 Premalignant and malignant breast pathology basal phenotype, 189 HER2, oncogene protein, 184 invasion and metastases, 189 invasive carcinoma, 185 breast cancer classification and grading, 185 invasive lobular carcinoma (ILC), 187–189 no special type (NST), 186–187 sarcoma and malignant phyllodes tumors, 189 special types, 189 tumor grading, 189–190 lobular carcinoma, 184 malignant tumors, stroma origin, 189 premalignant lesions, 179 atypical ductal hyperplasia (ADH), 182–183 atypical lobular hyperplasia (ALH), 184 ductal carcinoma in situ (DCIS), 180–182 lobular carcinoma in situ (LCIS), 183, 184–185 Premenstrual syndrome (PMS), 74 Prenatal breast development epithelial ingrowth, 18 fetal period, 18 genes, transcription factors and growth factors, 19 hormonal regulation, 19 stages, 18 Prenatal lactation assessment anticipatory guidance, 84–95 prenatal breast examination nipple graspability, 84 size and symmetry, 84 risk factors, screening biological factors, infant and maternal, 83 psychological, 83 social, 83–84 Preoperative HER2-directed therapy, 416–417 lapatinib, 417 pertuzumab, 416 trastuzumab, 416 Primary invasive breast cancer axilla management, 236–239 Index breast conserving surgery (BCS), 230 Halstedian concept, 229 local recurrences, 231–232 radiotherapy (RT) techniques, 230 sentinel lymph node biopsy, 239–242 surgical options, 232 appropriate surgical therapy, 234 breast reconstructive surgery, 235–236 contralateral prophylactic mastectomy (CPM), 235 extended tylectomy, 233 factors, 234t mammograms, 234 nipple-areola complex, 234 quadrantectomy, 233 reconstructive surgery, 235–236 Virchow’s hypothesis, 229 Primary operable breast cancers (POBC), 403 PROACT trial, 417 Problem solving mammography See Diagnostic mammography Progenitor cells, 11 Progesterone receptor (PR), 11, 17 Prognostic markers, 195 Prolactin (PRL), 17, 27, 85 Prosigna (PAM50), 199 Prosthetic reconstruction, 276 Proton therapy, 295 Protons, 293 Provera, 480–481 Psoriasis, 98 Puberty hormonal regulation, 21–22 inactive human breast, 21f mammary gland duct system, 20 regulatory factors, 21–22 terminal end buds (TEBs), 20 Pygo2, 12 Q Quadrantectomy, 233 R Radiation oncology adverse effects, 295–297 radiation, surgery and chemotherapy, 293 radiation therapy, physics, 291–293 technical aspects, 293–295 Radical mastectomy, 229–230, 232 Radioisotope, 257 Radionuclide imaging, 175 Radiosurgery, 465 Radiotherapy, 262 after neoadjuvant systemic treatment, 447 Radiotherapy for brain metastases, 465–466 Raloxifene, 520 prevention trials using, 596t Ramucirumab, 362t, 364–365 Randomized controlled studies, 159 Rank ligand (RANKL) inhibitors, 374 denosumab, 374 Raynaud’s phenomenon, 98 Residual cancer burden (RCB), 438 Reverse transcriptase polymerase chain reaction (RT-PCR), 257 Role of radiotherapy early stage breast cancer, 297–304 Index locally advanced breast cancer, 304–305 palliation, 305 radiation oncology, 291–297 S Salvage mastectomy, 231 Sarcoma and malignant phyllodes tumors, 189 Schonberg index, 519 Sebaceous glands, Selective estrogen receptor modulators (SERMs), 131–132, 365, 548 tamoxifen, 365–366 Sensory fibers, Sentinel lymph node biopsy (SLNB), 239–242, 247, 254, 423, 521–522, 546 after neoadjuvant chemotherapy, 263–265 vs axillary lymph node dissection, 240–241 completion axillary lymph node dissection, 257–259 indications for, 260 ductal carcinoma in situ, 261 elderly patients, 262 multifocal and multicentric tumours, 261 pregnancy, 262 repeat, 262 prior to neoadjuvant chemotherapy, 263 technical aspects, 255–257 Sentinel lymph nodes, 5–6 sentinel lymphadenectomy, SLNE, 446–447 “SENTinel Neo-Adjuvant” (SENTINA) study, 242 Sentinel node biopsy, 446–447 Serum tumour biomarkers, 452 Sex hormones endogenous, 130 exogenous, 131 Sialyl-Lewis X/A-deficient MUCI, 425 Single-agent therapy, 392 Single nucleotide polymorphisms, 130 Skeletal-related events (SREs), 373 Skin-sparing mastectomy, 274, 275f Snoopy-nose deformity, 47 Society of surgical oncology, 274 Somatic and germline genetics, 575–576 Sorafenib, 361t, 364 Sore nipples bacterial infection, 97 candidiasis, 97–98 chapped nipples, 97 dermatitis, 98 nipple trauma, 96–97 Paget’s disease, 98 psoriasis, 98 vasospasm/Raynaud’s phenomenon, 98 Stage migration effect, 237 Staphylococcus aureus, 97, 98 Stem cells definitions and terms, 11 mammary stem cells, 11–12 regulation factors, 12–13 structure and function, 11 Stereotactic radiosurgery (SRS), 465 Stroma adipocytes, 13, 14 epithelial-stromal interactions, 13 extracellular matrix (ECM), 14 fibroblasts, 13–14 interstitial cell of Cajal (ICC), 14 661 macrophages, 13, 14 Stromal fibronectin, 15 Subclavian artery supply disruption sequence, 46 Subcutaneous turnover flaps, 50f Sunitinib, 361t, 364 Superficial inferior epigastric artery (SIEA) perforator flap, 284–285 Suppression of ovarian function trial (SOFT), 536 Systemic therapy, 335 cytotoxic agents, 335 alkylating agents, 347–349, 348t antimetabolites, 350–353 platinum-based chemotherapeutic agents, 349–350 topoisomerase II inhibitors, 335–342, 336t tubulin inhibitors, 342–347 targeted therapies, 353 antiangiogenic agents, 359–365 bone-targeted agents, 371–375, 372t endocrine therapy (ET), 365–371 human epidermal growth factor receptor (HER2)-targeted therapies, 353–359 PARP-inhibitors, 371 Systemic therapy of bone metastases, 463–464 Systemic therapy of brain metastases, 465 T Tamoxifen, 52, 77, 225–226, 324, 360t, 365–366, 454–455, 521, 593–596 breast cancer prevention trials using, 594t Tangential beam arrangement, 294f Targeted therapies, 353 antiangiogenic agents, 359 aflibercept, 364 antiangiogenic tyrosine kinase inhibitors (TKIs), 364 bevacizumab, 359–363 ramucirumab, 364–365 trebananib, 365 VEGF-Trap, 364 bone-targeted agents, 371, 372t adjuvant use of bone-targeted agents, 374–375 bisphosphonates (BPs), 371–374 rank ligand (RANKL) inhibitors, 374 endocrine therapy (ET), 365 aromatase inhibitors, 366–367 combination of endocrine therapies, 368 fulvestrant, 367–368 further targeted agents used in combination with endocrine therapies, 369–371 gonadotropin-releasing hormone (GnRH) analogs, 368–369 selective estrogen receptor modulators (SERMs), 365–366 human epidermal growth factor receptor (HER2)-targeted therapies, 353 ado-trastuzumab emtansine, T-DM1, 358–359 lapatinib, 356–357 new HER2-directed agents and combinations under investigation, 359 pertuzumab, 357–358 trastuzumab, 353–356 PARP-inhibitors, 371 Taxanes, 314, 342, 393, 548 docetaxel and paclitaxel, 342 nab-paclitaxel, 344 T-DM1 (Trastuzumab Emtansine), 537 TEACH trial, 402 Terminal ductal lobular units (TDLUs), 8–9, 9f, 57 Thelarche, 6, 41–42 662 premature, 42 Tibolone, 485, 488–489 Tietze syndrome, 75 Tipifarnib, 421 Tissue growth factor α/β, 20 Topoisomerase II alpha, 200 Topoisomerase II inhibitors, 335, 336t anthracyclines, 335 acute myelogeneous leukemia (AML), 340 in adjuvant chemotherapy and alternative anthracycline-free regimens, 340–341 cardiotoxicity, 339–340 liposomal anthracyclines, 341–342 myelodysplastic syndromes (MDS), 340 Total preclinical phase (TPCP), 139 Touch imprint cytology (TIMC), 260 Tracer agents, sites of injection of, 256f Transverse rectus abdominis muscle/myocutaneous (TRAM) flap, 236, 273 Trastuzumab, 353–356, 354t, 416, 459, 548 adjuvant setting anthracyclines, avoiding, 401 BCIRG 006 trial, 399–400 combined American NSABP-B31 and NCCTG-N9831 trials, 399, 400 duration, 400–401 efficacy in trial, 398–399 FinHer trial, 400 HERA trial, 399–400 safety in trial, 399 sequencing and timing, 400 small HER2+ tumors, 401 combined with EGFR inhibitors, 382–383 large adjuvant trastuzumab trials longer term follow-up from, 400t reports from, 399t metastatic setting after disease progression, 395 capecitabine, 394 combination with hormonal therapy, 394–395 first-line single-agent therapy, 392–393 gemcitabine, 394 platinum salts, 393–394 polychemotherapy, 394 single-agent therapy, 392 taxanes, 393 vinorelbine, 394 Trastuzumab, neoadjuvant, 403 Trastuzumab-Emtansin (T-DM1), 354t Trebananib, 365 Triple negative ABC, treatment of, 463 Triple-negative breast cancer (TNBC), 213, 437, 441–444, 535 TRYPHAENA trial, 416 Index TRYPHENA, 405 Tubular breast deformity, 47f Tubulin inhibitors, 342 epothilones (ixabepilone), 344 eribulin, 347 taxanes, 342 docetaxel and paclitaxel, 342–344 vinca alkaloids (vinorelbine), 346–347 Tumor grading, 189–190 Tumor-infiltrating lymphocytes, 439 U Ultrasound, 64–65, 112, 113f–114f Ultrasound-guided fine needle aspiration, 64–65 V Vacuum-assisted biopsies (VAB), 119–120 Vascular supply, 5, 6f Vasospasm/Raynaud’s phenomenon, 98 VEGF-Trap, 364 Venous drainage, Vinblastine, 346 Vinca alkaloids (vinorelbine), 346–347 Vincristine, 346 Vindesine, 346 Vinflunin, 346 Vinorelbine, 346, 346–347, 346t, 394 Virchow’s hypothesis, 229 W WECARE (Women’s Environment, Cancer, and Radiation Epidemiology) study, 530 Witches milk, 60 WNT-1-induced secreted protein (Wisp 3), 425 Wnt/β-catenin signaling, 12 Women’s environment, cancer, and radiation epidemiology (WECARE), 530 Women’s Health Initiative (WHI) HRT trials, 476–477 design, 477 E + P vs placebo, 477–478 estrogen and invasive breast cancer, 478–480 methodology, 480–481 Women’s Health Initiative (WHI) trial hormone replacement trial 1, 483 WHI HRT trials and cardiac outcomes, 485–486 Z Zoledronate, 372t, 373 Zuska’s disease, 61 ... published the Manual of Breast Diseases, edited by Prof Ismail Jatoi That book was expanded and a larger text entitled Management of Breast Diseases was published by Springer in 2010, edited by Prof.. .Management of Breast Diseases Ismail Jatoi Achim Rody • Editors Management of Breast Diseases Second Edition 123 Editors Ismail Jatoi Department of Surgery University of Texas Health... and Prof Manfred Kaufmann of the Goethe-University of Frankfurt Professor Kaufmann subsequently retired, and the current text is the second edition of the Springer text, with Prof Achim Rody of

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  • Preface

  • Contents

  • Contributors

  • 1 Anatomy and Physiology of the Breast

    • 1.1 Gross Anatomy of the Breast

      • 1.1.1 Relationships and Quadrants

      • 1.1.2 Nerve Supply

      • 1.1.3 Vascular Supply

      • 1.1.4 Lymphatic Drainage

      • 1.1.5 Gross Anatomic Changes Throughout the Life span

    • 1.2 Histology

      • 1.2.1 Overview

      • 1.2.2 Nipple and Areola

      • 1.2.3 Parenchyma

        • 1.2.3.1 Luminal Epithelial Cells

        • 1.2.3.2 Myoepithelial Cells

        • 1.2.3.3 Stem Cells

      • 1.2.4 Basement Membrane

      • 1.2.5 Stroma

        • 1.2.5.1 Cells in Breast Stroma

        • 1.2.5.2 Extracellular Matrix

    • 1.3 Synopsis of Hormones and Other Factors that Regulate Breast Structure and Function

      • 1.3.1 Hormones

      • 1.3.2 Other Regulators of Breast Development

    • 1.4 Mammary Gland Structure and Function Throughout Life

      • 1.4.1 Prenatal Development of the Breast

        • 1.4.1.1 Events of Prenatal Breast Development

        • 1.4.1.2 Hormonal Regulation of Prenatal Breast Development

        • 1.4.1.3 Genes, Transcription Factors, and Growth Factors During Prenatal Breast Development

      • 1.4.2 Breast Development from Birth to Puberty

        • 1.4.2.1 Events in Breast Development from Birth to Puberty

        • 1.4.2.2 Hormones in Breast Development from Birth to Puberty

        • 1.4.2.3 Other Regulatory Factors in Breast Development from Birth to Puberty

      • 1.4.3 Puberty

        • 1.4.3.1 Events in the Breast During Puberty

        • 1.4.3.2 Hormonal Regulation of the Breast During Puberty

        • 1.4.3.3 Other Regulatory Factors in the Breast During Puberty

      • 1.4.4 The Adult Premenopausal Breast

        • 1.4.4.1 Cyclic Events in the Premenopausal Adult Breast

        • 1.4.4.2 Hormones Regulating the Adult Premenopausal Breast

        • 1.4.4.3 Other Factors Regulating the Adult Premenopausal Breast

      • 1.4.5 Pregnancy

        • 1.4.5.1 Events in the Breast During Pregnancy

        • 1.4.5.2 Hormones in the Breast During Pregnancy (Fig. 1.15)

        • 1.4.5.3 Other Regulatory Factors in the Breast During Pregnancy

      • 1.4.6 Lactation

        • 1.4.6.1 Events in the Lactating Breast

        • 1.4.6.2 The Process of Lactation

        • 1.4.6.3 Hormones During Lactation and Nursing

        • 1.4.6.4 Other Regulatory Factors During Lactation

        • 1.4.6.5 Effects of Lactation on the Nursing Mother

        • 1.4.6.6 Calcium Metabolism During Lactation

      • 1.4.7 Postlactational Involution

      • 1.4.8 Postmenopausal Involution

      • 1.4.9 Concluding Comments

    • Acknowledgments

    • Appendix

      • A Brief Comparison of Murine and Human Breast

    • References

  • 2 Congenital and Developmental Abnormalities of the Breast

    • 2.1 Embryology

    • 2.2 Early Development of the Mammary Gland

    • 2.3 Thelarche

    • 2.4 Anatomy of the Breast

    • 2.5 Premature Thelarche

    • 2.6 Accessory Breast Tissue: Polymastia/Polythelia

    • 2.7 Underdevelopment of the Mammary Corpus

      • 2.7.1 Breast Hypoplasia

      • 2.7.2 Amastia/Athelia

      • 2.7.3 Poland Syndrome

      • 2.7.4 Tubular/Tuberous Breast

    • 2.8 Inverted Nipples

    • 2.9 Hyperplasia of the Breast

    • 2.10 Gynecomastia

    • 2.11 Conclusion

    • References

  • 3 Nipple Discharge

    • 3.1 Introduction

    • 3.2 Anatomy and Physiology

    • 3.3 Definition

    • 3.4 Incidence

    • 3.5 Characteristics and Etiology

    • 3.6 Diagnostic Evaluation

    • 3.7 Mammography

    • 3.8 Ultrasound

    • 3.9 MRI

    • 3.10 Occult Blood

    • 3.11 Cytology

    • 3.12 Biochemical Markers

    • 3.13 Ductal Imaging

    • 3.14 Surgical Evaluation and Treatment

    • 3.15 Mammary Ductoscopy

    • 3.16 Follow-up

    • References

  • 4 Mastalgia

    • 4.1 Etiology

    • 4.2 Classification

    • 4.3 Cyclical Mastalgia

    • 4.4 Non-cyclical Mastalgia

    • 4.5 Chest Wall Pain

    • 4.6 Non-chest Wall Pain

    • 4.7 Mastalgia and Breast Cancer

    • 4.8 Psychosocial Factors

    • 4.9 Clinical Assessment and Investigations

    • 4.10 Treatment

      • 4.10.1 Cyclical Mastalgia

      • 4.10.2 Non-cyclical Mastalgia

    • 4.11 Management Algorithm

    • References

  • 5 Management of Common Lactation and Breastfeeding Problems

    • 5.1 Prenatal Period

      • 5.1.1 Informed Choice

      • 5.1.2 Benefits of Breastfeeding

      • 5.1.3 The Hazards of Infant Formula

      • 5.1.4 Prenatal Education

      • 5.1.5 Prenatal Lactation Assessment

      • 5.1.6 Screening for Risk Factors

        • 5.1.6.1 Maternal Biological Risk Factors for Successful Lactation

        • 5.1.6.2 Infant Biological Risk Factors for Successful Lactation

        • 5.1.6.3 Psychological Risk Factors

        • 5.1.6.4 Social Risk Factors

      • 5.1.7 Prenatal Breast Examination

        • 5.1.7.1 Size and Symmetry

        • 5.1.7.2 Nipple Graspability

      • 5.1.8 Anticipatory Guidance

    • 5.2 Intrapartum Period

      • 5.2.1 Establishing Lactation

      • 5.2.2 Factors that Help to Establish Lactation

      • 5.2.3 Factors that Interfere with Lactation

        • 5.2.3.1 Failure of Mammogenesis

        • 5.2.3.2 Failure of Lactogenesis

        • 5.2.3.3 Failure of Galactopoiesis

      • 5.2.4 Milk Transfer

        • 5.2.4.1 Factors that Help Milk Transfer

        • 5.2.4.2 Factors Impeding Milk Transfer

      • 5.2.5 Milk Intake

        • 5.2.5.1 Frequency

        • 5.2.5.2 Duration

        • 5.2.5.3 Pattern of Breast Use

        • 5.2.5.4 Factors that Help Milk Intake

        • 5.2.5.5 Factors that Impair Milk Intake

      • 5.2.6 Maternal Psychosocial Health

      • 5.2.7 In-Hospital Risk Assessment

      • 5.2.8 Hospital Discharge Planning

    • 5.3 Postpartum Period

      • 5.3.1 Clinical Breastfeeding Assessment

      • 5.3.2 Insufficient Milk Syndrome

      • 5.3.3 Maternal Hyperlactation Syndrome

        • 5.3.3.1 White Spot

        • 5.3.3.2 Milk Stasis

        • 5.3.3.3 Acute Mastitis

        • 5.3.3.4 Chronic Mastitis

        • 5.3.3.5 Breast Abscess

        • 5.3.3.6 Management Goals

      • 5.3.4 Sore Nipples

        • 5.3.4.1 Nipple Trauma

        • 5.3.4.2 Chapped Nipples

        • 5.3.4.3 Bacterial Infection of the Nipple

        • 5.3.4.4 Candidiasis

        • 5.3.4.5 Dermatitis

        • 5.3.4.6 Paget’s Disease

        • 5.3.4.7 Vasospasm or Raynaud’s Phenomenon

        • 5.3.4.8 Psoriasis

      • 5.3.5 Induced Lactation and Relactation

      • 5.3.6 Medicines and Breastfeeding

    • 5.4 Conclusion

    • References

  • 6 Evaluation of a Breast Mass

    • 6.1 Introduction

    • 6.2 Routes of Presentation

      • 6.2.1 Symptomatic breast mass

      • 6.2.2 Screening

      • 6.2.3 Incidental Detection of the Breast Mass on Clinical Examination

    • 6.3 History of Presentation

    • 6.4 Clinical Examination

    • 6.5 Investigation

    • 6.6 Imaging

    • 6.7 Breast Ultrasound

    • 6.8 Mammography

    • 6.9 Magnetic Resonance Imaging (MRI)

    • 6.10 Other Imaging Techniques

    • 6.11 Pathology Diagnosis

    • 6.12 Patient Plan

    • 6.13 Benign Breast Masses

      • 6.13.1 Benign Nodularity

      • 6.13.2 Changes Associated with Pregnancy and Lactation

      • 6.13.3 Fibroadenoma

      • 6.13.4 Phyllodes Tumour

      • 6.13.5 Cysts

      • 6.13.6 Breast Sepsis

      • 6.13.7 Intraduct Papilloma

      • 6.13.8 Skin Lesions

      • 6.13.9 Fat Necrosis

      • 6.13.10 Other Lesions

    • References

  • 7 Breast Cancer Epidemiology

    • 7.1 Descriptive Epidemiology

      • 7.1.1 Incidence

      • 7.1.2 Mortality

      • 7.1.3 Prevalence

    • 7.2 Risk Factors

      • 7.2.1 Sex and Age

      • 7.2.2 Genetic Predispositions

        • 7.2.2.1 Family History

        • 7.2.2.2 Molecular Genetic Substrates

      • 7.2.3 Anthropometric Measures

        • 7.2.3.1 Adult Height

        • 7.2.3.2 BMI and Body Fat Distribution

      • 7.2.4 Reproductive Factors

      • 7.2.5 Hormones

        • 7.2.5.1 Endogenous Hormones

        • 7.2.5.2 Exogenous Hormones

      • 7.2.6 Breast Density and Benign Breast Disease

      • 7.2.7 Ionizing Radiation

      • 7.2.8 Diet and Lifestyle

      • 7.2.9 Overview

    • 7.3 Prevention

      • 7.3.1 Primary Prevention

      • 7.3.2 Secondary Prevention

    • 7.4 Prognosis

    • References

  • 8 Breast Cancer Screening

    • 8.1 Cancer Screening Principles

      • 8.1.1 Lead-Time Bias

      • 8.1.2 Length Bias

      • 8.1.3 Selection Bias

    • 8.2 Mammography Screening

      • 8.2.1 Health Insurance Plan Trial

      • 8.2.2 Swedish Trials

      • 8.2.3 Edinburgh Trial

      • 8.2.4 Canadian Trials

      • 8.2.5 UK Age Trial

    • 8.3 Overview (Meta-analyses) of the Mammographic Screening Trials

    • 8.4 Effect of Age on Mammographic Screening

      • 8.4.1 Mammography Screening in Elderly Women

    • 8.5 Screening Breast Ultrasound

    • 8.6 Screening Breast MRI

    • 8.7 Screening by Clinical Breast Examination

    • 8.8 Screening by Breast Self-examination

    • 8.9 The Impact of Advances in Therapy on the Efficacy of Screening

    • 8.10 Potential Hazards of Screening

      • 8.10.1 Lead Time

      • 8.10.2 False-Positives

      • 8.10.3 Radiation Exposure

      • 8.10.4 Overdiagnosis

      • 8.10.5 Cost

    • 8.11 Conclusion

    • References

  • 9 Breast Imaging

    • 9.1 Introduction

    • 9.2 Mammography

      • 9.2.1 Screening Mammography

      • 9.2.2 Diagnostic Mammography

      • 9.2.3 Digital Breast Tomosynthesis

      • 9.2.4 The Mammography Report

        • 9.2.4.1 Reason for the Examination

        • 9.2.4.2 Breast Tissue Composition

        • 9.2.4.3 Description of Findings

        • 9.2.4.4 Comparison to Prior Examinations, if Appropriate

        • 9.2.4.5 Assessment Categories and Management

      • 9.2.5 Describing the Location of an Abnormality

      • 9.2.6 Masses

      • 9.2.7 Calcifications

      • 9.2.8 Indirect and Secondary Signs of Malignancy

      • 9.2.9 Potential Adverse Consequences of Screening

      • 9.2.10 False-Negative Mammograms

    • 9.3 Breast Ultrasound

      • 9.3.1 Technical Advances

      • 9.3.2 Normal Anatomy

      • 9.3.3 Cystic Masses

      • 9.3.4 Solid Masses

      • 9.3.5 Screening Ultrasound

    • 9.4 Core Needle Biopsy

      • 9.4.1 Indications, Relative Contraindications, and Complications

      • 9.4.2 Appropriate Post-core Needle Biopsy Follow-up

    • 9.5 Magnetic Resonance Imaging of the Breast

      • 9.5.1 Contrast-Enhanced Breast MRI for Screening in High-Risk Women

    • 9.6 Radionuclide Imaging

    • References

  • 10 Premalignant and Malignant Breast Pathology

    • 10.1 Introduction

    • 10.2 Premalignant Lesions

      • 10.2.1 Ductal Carcinoma in Situ

        • 10.2.1.1 Terminology

        • 10.2.1.2 Incidence and Clinical Presentation

        • 10.2.1.3 Natural History and Mortality of DCIS

        • 10.2.1.4 Grading and Risk Assessment of DCIS

        • 10.2.1.5 Molecular Pathology and Special Types of DCIS

        • 10.2.1.6 Pathologic Working Up of DCIS Specimens

      • 10.2.2 Atypical Ductal Hyperplasia (ADH)

        • 10.2.2.1 Terminology

        • 10.2.2.2 Molecular Similarity of ADH and DCIS

        • 10.2.2.3 Significance of ADH in Core Biopsy

      • 10.2.3 Lobular Neoplasia and Its Variants

        • 10.2.3.1 Incidence and Clinical Presentation

        • 10.2.3.2 Atypical Lobular Hyperplasia (ALH)

        • 10.2.3.3 Lobular Carcinoma In Situ (LCIS Classical Variant)

        • 10.2.3.4 High-Risk Variants of LCIS

      • 10.2.4 Immunohistology and Molecular Biology

    • 10.3 Invasive Carcinoma

      • 10.3.1 Breast Cancer Classification and Grading

      • 10.3.2 Invasive Carcinoma of No Special Type (NST)

      • 10.3.3 Invasive Lobular Carcinoma

        • 10.3.3.1 Clinical Presentation

        • 10.3.3.2 Classical and Variant Forms of ILC

        • 10.3.3.3 Prognostic Factors

      • 10.3.4 Other Special Types of Breast Cancer

      • 10.3.5 Sarcoma and Malignant Pyhllodes Tumors

      • 10.3.6 Tumor Grading

    • References

  • 11 Breast Cancer Molecular Testing for Prognosis and Prediction

    • 11.1 Biomarkers

      • 11.1.1 Prognostic Markers

      • 11.1.2 Predictive Markers

    • 11.2 Molecular Subtypes in Breast Cancer and Therapy Concepts

    • 11.3 Multigene Assays in Early Breast Cancer

      • 11.3.1 21-Gene Signature (Oncotype DX, Recurrence Score)

      • 11.3.2 70-Gene Signature (MammaPrint)

      • 11.3.3 Endopredict

      • 11.3.4 Prosigna (PAM50)

    • 11.4 Breast Cancer Index (BCI)

    • 11.5 Clinical Use of Multigene Assays for Decision-Making in Early Breast Cancer

    • 11.6 Molecular Testing for Therapy Prediction

    • 11.7 Conclusions

    • References

  • 12 Molecular Classification of Breast Cancer

    • 12.1 Introduction

    • 12.2 Intrinsic Subtyping Based on Gene Expression Versus Histopathology

    • 12.3 Main Molecular Features of the Intrinsic Subtypes

      • 12.3.1 Luminal Disease

      • 12.3.2 HER2-Enriched

      • 12.3.3 Basal-Like

        • 12.3.3.1 Basal-Like Classification: Biological and Epidemiological Implications

      • 12.3.4 Claudin-Low

    • 12.4 Novel Subgroups of Breast Cancer

    • 12.5 Intrinsic Subtypes in the Metastatic Setting

    • 12.6 Frequently Mutated Genes in Breast Cancer

      • 12.6.1 Lobular Breast Cancer

    • 12.7 Conclusions

    • References

  • 13 Ductal Carcinoma In Situ

    • 13.1 Introduction

    • 13.2 Biology

    • 13.3 Presentation

    • 13.4 Diagnosis

    • 13.5 Surgery

    • 13.6 Adjuvant Radiotherapy

    • 13.7 Partial Breast Irradiation

    • 13.8 Adjuvant Hormonal Therapy

    • References

  • 14 Surgical Considerations in the Management of Primary Invasive Breast Cancer

    • 14.1 Introduction

    • 14.2 Historical Background

    • 14.3 Local Recurrences

    • 14.4 Surgical Options

      • 14.4.1 Contralateral Prophylactic Mastectomy

      • 14.4.2 Breast Reconstructive Surgery

    • 14.5 Management of the Axilla

      • 14.5.1 Survival

      • 14.5.2 Axillary Relapse

      • 14.5.3 Staging

    • 14.6 Sentinel Lymph Node Biopsy

      • 14.6.1 Sentinel Lymph Node Biopsy Versus Axillary Lymph Node Dissection

      • 14.6.2 Radiotherapy of the Axilla

      • 14.6.3 Axillary Surgery in the Neo-Adjuvant Chemotherapy Setting

    • 14.7 Conclusion

    • References

  • 15 Management of the Axilla

    • 15.1 Introduction

    • 15.2 Anatomy of the Axillary Lymph Nodes

    • 15.3 Lymphatic System of the Breast

    • 15.4 Axillary Lymph Node Dissection

      • 15.4.1 Surgical Aspects

      • 15.4.2 Overall Survival

      • 15.4.3 Axillary Relapse

    • 15.5 Methods for Axillary Node Sampling

      • 15.5.1 Four-Node Axillary Sampling

      • 15.5.2 Blue Dye-Assisted Node Sampling (BDANS)

    • 15.6 Sentinel Lymph Node Biopsy

      • 15.6.1 Technical Aspects

      • 15.6.2 Completion Axillary Lymph Node Dissection

    • 15.7 Intra-operative Node Assessment

    • 15.8 Indications for Sentinel Lymph Node Biopsy

      • 15.8.1 Ductal Carcinoma in Situ

      • 15.8.2 Multifocal and Multicentric Tumours

      • 15.8.3 Pregnancy

      • 15.8.4 Elderly Patients

      • 15.8.5 Repeat Sentinel Lymph Node Biopsy

    • 15.9 Neoadjuvant Chemotherapy

      • 15.9.1 Sentinel Lymph Node Biopsy Prior to Neoadjuvant Chemotherapy

      • 15.9.2 Sentinel Lymph Node Biopsy After Neoadjuvant Chemotherapy

    • 15.10 Internal Mammary Node Biopsy

    • 15.11 Conclusion

    • References

  • 16 Breast Reconstructive Surgery

    • 16.1 Introduction

    • 16.2 Indications for Reconstruction

    • 16.3 Skin-Sparing Mastectomy

    • 16.4 Nipple-Sparing Mastectomy

    • 16.5 Timing of Breast Reconstruction

    • 16.6 Alloplastic Versus Autogenous Reconstruction

      • 16.6.1 Alloplastic Reconstruction

      • 16.6.2 Implant Types

      • 16.6.3 Two-Stage Expander/Implant Reconstruction

      • 16.6.4 Single-Stage Reconstruction with Implants

      • 16.6.5 Permanent Tissue Expander/Implant Reconstruction

      • 16.6.6 Prosthetic Reconstruction with Acellular Dermal Matrix

      • 16.6.7 Complications of Implant Reconstruction

    • 16.7 Autogenous Reconstruction

      • 16.7.1 Pedicled TRAM Flap/Unipedicled Flap

      • 16.7.2 Bipedicled TRAM Flap

      • 16.7.3 Midabdominal TRAM Flap

      • 16.7.4 Free TRAM Flaps

      • 16.7.5 Abdominal Perforator Flaps

      • 16.7.6 Latissimus Dorsi Musculocutaneous Flap

      • 16.7.7 Gluteal Musculocutaneous and Perforator Flaps

    • 16.8 Secondary Breast Reconstruction

      • 16.8.1 Nipple–Areola Reconstruction

      • 16.8.2 Autologous Fat Grafting

      • 16.8.3 Contralateral Breast

    • 16.9 Radiation and Breast Reconstruction

    • 16.10 Chemotherapy

    • 16.11 Conclusion

    • References

  • 17 The Role of Radiotherapy in Breast Cancer Management

    • 17.1 Introduction to Radiation Oncology

      • 17.1.1 Physics of Radiation Therapy

      • 17.1.2 Radiation, Surgery, and Chemotherapy

      • 17.1.3 Technical Aspects of Radiation Planning and Delivery

      • 17.1.4 Adverse Effects of Radiation to the Breast

    • 17.2 Radiation Therapy in the Early-Stage Breast Cancer

      • 17.2.1 Ductal Carcinoma in Situ

      • 17.2.2 Invasive Breast Cancer

        • 17.2.2.1 Breast Conservation

    • 17.3 Locally Advanced Breast Cancer

    • 17.4 Radiation as Palliation

    • 17.5 Summary

    • References

  • 18 Adjuvant Systemic Treatment for Breast Cancer: An Overview

    • 18.1 Aims of Adjuvant Therapy

      • 18.1.1 Micro-Metastatic Disease

      • 18.1.2 Cancer Stem Cells

      • 18.1.3 Immunogenicity

    • 18.2 Adjuvant Chemotherapy: The Evidence

      • 18.2.1 Single Agent or Combination Chemotherapy

      • 18.2.2 Anthracyclines

      • 18.2.3 Taxanes

    • 18.3 Adjuvant Endocrine Therapy

      • 18.3.1 Aromatase Inhibitors

    • 18.4 Monoclonal Antibodies

    • 18.5 Adjuvant Bisphosphonates

    • 18.6 Ovarian Suppression

    • 18.7 Genomic Testing

    • 18.8 Trials in Older Patients

    • References

  • 19 Endocrine Therapy

    • 19.1 Introduction

    • 19.2 Adjuvant Therapy

      • 19.2.1 Premenopausal Patients

        • 19.2.1.1 Tamoxifen

        • 19.2.1.2 Ovarian Function Suppression (OFS)

        • 19.2.1.3 Aromatase Inhibitors (AIs)

      • 19.2.2 GnRHa for Ovarian Protection

      • 19.2.3 Postmenopausal Women

      • 19.2.4 Neoadjuvant Therapy

      • 19.2.5 Premenopausal Patients

      • 19.2.6 Postmenopausal Patients

    • 19.3 Metastatic Therapy

      • 19.3.1 Premenopausal Patients

      • 19.3.2 Postmenopausal Patients

      • 19.3.3 Hormone Receptor Positive/Human Epidermal Growth Factor Receptor 2-Positive Breast Cancer (HR+/HER2+)

    • 19.4 Overcoming Endocrine Resistance

    • 19.5 New Perspectives

    • References

  • 20 Systemic Therapy

    • 20.1 Cytotoxic Agents

      • 20.1.1 Topoisomerase II Inhibitors

        • 20.1.1.1 Anthracyclines

      • 20.1.2 Tubulin Inhibitors

        • 20.1.2.1 Taxanes

          • Docetaxel and Paclitaxel

        • 20.1.2.2 Epothilones (Ixabepilone)

        • 20.1.2.3 Vinca Alkaloids (Vinorelbine)

        • 20.1.2.4 Eribulin

      • 20.1.3 Alkylating Agents

        • 20.1.3.1 Cyclophosphamide

        • 20.1.3.2 Bendamustine

      • 20.1.4 Platinum-Based Chemotherapeutic Agents

      • 20.1.5 Antimetabolites

        • 20.1.5.1 Methotrexate (MTX)

        • 20.1.5.2 Capecitabine, 5-Fluourouracil (5-FU)

        • 20.1.5.3 Gemcitabine

    • 20.2 Targeted Therapies

      • 20.2.1 Human Epidermal Growth Factor Receptor 2 (HER2)-Targeted Therapies

        • 20.2.1.1 Trastuzumab

        • 20.2.1.2 Lapatinib

        • 20.2.1.3 Pertuzumab

        • 20.2.1.4 Ado-Trastuzumab Emtansine, T-DM1

        • 20.2.1.5 New HER2-Directed Agents and Combinations Under Investigation

      • 20.2.2 Antiangiogenic Agents

        • 20.2.2.1 Bevacizumab

        • 20.2.2.2 Antiangiogenic Tyrosine Kinase Inhibitors (TKIs) and Other Agents, Sorafenib, Sunitinib

          • Sunitinib (SUTENT®)

          • Sorafenib (NEXAVAR®)

        • 20.2.2.3 Aflibercept, VEGF-Trap (ZALTRAP®)

        • 20.2.2.4 Ramucirumab (CYRAMZA®)

        • 20.2.2.5 Trebananib (AMG386)

      • 20.2.3 Endocrine Therapy (ET)

        • 20.2.3.1 Selective Estrogen Receptor Modulators (SERMs), Tamoxifen

        • 20.2.3.2 Aromatase Inhibitors

        • 20.2.3.3 Fulvestrant—Selective Estrogen Receptor Downregulator (SERD)

        • 20.2.3.4 Combination of Endocrine Therapies

        • 20.2.3.5 Gonadotropin-Releasing Hormone (GnRH) Analogs

        • 20.2.3.6 Further Targeted Agents Used in Combination with Endocrine Therapies

          • Everolimus (Afinitor)

          • PIK3CA Inhibitors

          • Palbociclib (Ibrance™) and Cdk4/6 Inhibitors

      • 20.2.4 PARP-Inhibitors

      • 20.2.5 Bone-Targeted Agents

        • 20.2.5.1 Bisphosphonates

          • Nonnitrogenous Bisphosphonates

          • Nitrogenous Bisphosphonates (Amino-bisphosphonates)

        • 20.2.5.2 Rank Ligand (RANKL) Inhibitors

        • 20.2.5.3 Adjuvant Use of Bone-Targeted Agents

          • Adjuvant Bisphosphonates

          • Adjuvant Denosumab

    • References

  • 21 HER2-Targeted Therapy

    • 21.1 Introduction

    • 21.2 Targeting the HER2 Receptor

      • 21.2.1 ASCO/CAP Updated Recommendations for HER2 Testing

    • 21.3 Trastuzumab in the Metastatic Setting

      • 21.3.1 Single-Agent Therapy in Heavily Pretreated Patients

      • 21.3.2 First-Line Single-Agent Therapy

      • 21.3.3 Trastuzumab in Combination with Chemotherapy

        • 21.3.3.1 Trastuzumab and Taxanes

        • 21.3.3.2 Trastuzumab and Platinum Salts

        • 21.3.3.3 Trastuzumab Plus Vinorelbine

        • 21.3.3.4 Trastuzumab with Capecitabine

        • 21.3.3.5 Trastuzumab Plus Gemcitabine

        • 21.3.3.6 Trastuzumab and Eribulin

        • 21.3.3.7 Trastuzumab with Polychemotherapy

      • 21.3.4 Trastuzumab in Combination with Hormonal Therapy

      • 21.3.5 Trastuzumab After Disease Progression

      • 21.3.6 Trastuzumab and New Drugs

        • 21.3.6.1 Lapatinib

        • 21.3.6.2 Pertuzumab

        • 21.3.6.3 Ado-Trastuzumab Emtansine (T-DM1)

      • 21.3.7 The Algorithm for Treating Metastatic HER2+ Breast Cancers (ASCO 2014 Guidelines)

        • 21.3.7.1 First-Line Therapy

        • 21.3.7.2 Second-Line Therapy

        • 21.3.7.3 Third-Line Therapy and Beyond

    • 21.4 Trastuzumab in the Adjuvant Setting

      • 21.4.1 Adjuvant Trastuzumab Trials—Efficacy Results

      • 21.4.2 Adjuvant Trastuzumab Trials: Safety Results

      • 21.4.3 The Sequencing and Timing of Adjuvant Trastuzumab Treatment

      • 21.4.4 The Duration of Adjuvant Trastuzumab Treatment

      • 21.4.5 Avoiding Anthracyclines

      • 21.4.6 Small HER2+ Tumors

      • 21.4.7 Trastuzumab and/or Other Targeted Therapies

        • 21.4.7.1 Lapatinib

        • 21.4.7.2 Pertuzumab

        • 21.4.7.3 Neratinib

        • 21.4.7.4 Bevacizumab

    • 21.5 Neoadjuvant HER2+ Approaches

      • 21.5.1 Neoadjuvant Trastuzumab

      • 21.5.2 Lapatinib-Based Neoadjuvant Regimens

      • 21.5.3 Pertuzumab-Based Neoadjuvant Regimens

      • 21.5.4 Neratinib-Based Neoadjuvant Regimens

    • 21.6 Other Exploratory Anti-HER2 Blockade Strategies

    • 21.7 Conclusion

    • References

  • 22 Inflammatory and Locally Advanced Breast Cancer

    • 22.1 Introduction

    • 22.2 Epidemiology

    • 22.3 Diagnosis and Staging

    • 22.4 Management

    • 22.5 Systemic Therapy

      • 22.5.1 Neoadjuvant Chemotherapy

        • 22.5.1.1 Preoperative Anthracycline and Taxane

        • 22.5.1.2 Platinum Agents

        • 22.5.1.3 Other Noncross-Resistant Agents

      • 22.5.2 Preoperative HER2-Directed Therapy

        • 22.5.2.1 Trastuzumab

        • 22.5.2.2 Pertuzumab

        • 22.5.2.3 Lapatinib

      • 22.5.3 Neoadjuvant Endocrine Therapy

      • 22.5.4 Investigational Therapy

        • 22.5.4.1 Angiogenesis Inhibitors

        • 22.5.4.2 mTOR Inhibitors

        • 22.5.4.3 PARP Inhibitors

      • 22.5.5 Immunotherapy

      • 22.5.6 Systemic Therapy in Patients Who Do not Achieve PCR

      • 22.5.7 Systemic Therapy for Inflammatory Breast Cancer

    • 22.6 Local Therapy

    • 22.7 Molecular Biology of IBC

    • 22.8 Prognostic Factors of Locally Advanced Breast Cancer

      • 22.8.1 Pathological Complete Response (pCR)

      • 22.8.2 Prognosis in Patients Who Do not Achieve pCR

    • 22.9 Survival

    • References

  • 23 Neoadjuvant Systemic Treatment (NST)

    • 23.1 Indications for Neoadjuvant Chemotherapy

    • 23.2 Pathohistological Complete Remission (pCR) as a Surrogate Marker for Survival

      • 23.2.1 Prognostic Significance of pCR

      • 23.2.2 Definitions of pCR

    • 23.3 Biomarkers in Neoadjuvant Systemic Therapy

      • 23.3.1 Tumor-Infiltrating Lymphocytes

      • 23.3.2 Individual Molecular Biomarkers of Resistance

      • 23.3.3 Tumor Cell Proliferation

    • 23.4 Choice of Chemotherapy Regimens in Neoadjuvant Systemic Therapy

      • 23.4.1 Choice of Therapy Regimens in HER2-Positive Breast Cancer

      • 23.4.2 Choice of Therapy Regimens in Patients with TNBC

      • 23.4.3 Biomarkers for Prediction of Platinum Efficacy in TNBC

      • 23.4.4 Use of Bevacizumab in Neoadjuvant Chemotherapy

    • 23.5 Neoadjuvant Endocrine Approaches

    • 23.6 Novel Therapeutic Concepts: Post-neoadjuvant Therapy, Dynamic Biomarkers, and “Window Studies”

    • 23.7 Surgical Considerations in the Context of Neoadjuvant Systemic Therapy

      • 23.7.1 Sentinel Node Biopsy in the Context of PST

    • 23.8 Radiotherapy After NST

    • References

  • 24 Metastatic Breast Cancer

    • 24.1 Introduction

      • 24.1.1 Epidemiology

      • 24.1.2 New Biology Insights

    • 24.2 The Role of Imaging, Nuclear Medicine, and Other Technology

    • 24.3 Treatment

      • 24.3.1 General Principles

      • 24.3.2 Treatment of ER+HER2 Negative ABC

        • 24.3.2.1 Endocrine Therapy

        • 24.3.2.2 Biological and Endocrine Resistance

        • 24.3.2.3 Chemotherapy

      • 24.3.3 Treatment of HER+ABC

        • 24.3.3.1 First-Line Therapy (See Table 24.2)

        • 24.3.3.2 Second-Line Therapy (See Table 24.2)

        • 24.3.3.3 Progression Beyond Second Line Therapy

        • 24.3.3.4 Treatment of HER2+/HR+ Disease

        • 24.3.3.5 Unanswered Questions for Management HER2 Positive Disease

      • 24.3.4 Treatment of Triple Negative ABC

      • 24.3.5 Treatment According to Special Sites

        • 24.3.5.1 Bone Metastasis

          • General Recommendations

        • 24.3.5.2 Systemic Therapy of Bone Metastases

        • 24.3.5.3 Locoregional Therapy of Bone Metastases

        • 24.3.5.4 Brain Metastasis

          • General Recommendations

          • Systemic Therapy of Brain Metastases

          • Radiotherapy for Brain Metastases

        • 24.3.5.5 Liver Metastasis

    • 24.4 Supportive Care and Survivorship Issues

    • 24.5 Future Perspectives

    • References

  • 25 Estrogen and Breast Cancer in Postmenopausal Women: A Critical Review

    • 25.1 Introduction

    • 25.2 Background: WHI Trials

      • 25.2.1 WHI Trials: Design

      • 25.2.2 WHI HRT Trial 1: E + P versus Placebo

      • 25.2.3 WHI HRT Trial 2: Estrogen Alone versus Placebo—The First 2004 Data

      • 25.2.4 Trial 2: Estrogen and Invasive Breast Cancer—WHI HRT Trial 2 Follow-up

      • 25.2.5 WHI Trials: Methodology

        • 25.2.5.1 Provera—A New Carcinogen or the Methodology?

        • 25.2.5.2 Methodology 1—Impact of Provera

        • 25.2.5.3 Methodology 2—Impact of Unblinding

      • 25.2.6 Could This Have Influenced the Results?

    • 25.3 Conclusion

    • References

  • 26 Estrogen and Cardiac Events with all-cause Mortality. A Critical Review

    • 26.1 Introduction

    • 26.2 Cardiac Events and the Timing Hypothesis

    • 26.3 HRT Agent Selection and Cardiac Outcome

    • 26.4 The WHI HRT Trials and the Cardiac Outcomes

    • 26.5 Estrogen and Biochemical Surrogates of Cardiac Events

    • 26.6 New HRT Developments

      • 26.6.1 TIBOLONE and BAZEDOXIFEN; and What to Do with BRCA 1 and 2 Mutations?

      • 26.6.2 Tibolone

      • 26.6.3 HRT and Breast Cancer Patients with BRCA Mutations

    • 26.7 Conclusion

    • References

  • 27 Breast Diseases in Males

    • 27.1 The Male Breast

    • 27.2 Gynecomastia

    • 27.3 Other Benign Breast Conditions

    • 27.4 Breast Cancer in Males

      • 27.4.1 Global Distribution

      • 27.4.2 U.S. Incidence

      • 27.4.3 Associated Factors and Conditions

      • 27.4.4 Family History and Genetics

      • 27.4.5 Histologies

      • 27.4.6 Tumor Biology

      • 27.4.7 Staging

      • 27.4.8 Physical Findings

      • 27.4.9 Imaging

    • 27.5 Differential Diagnosis of Breast Masses in Males

      • 27.5.1 Fine-Needle Aspiration-Based Evaluation of Breast Masses in Males

    • 27.6 Breast Cancer in Males: Treatment and Outcomes

      • 27.6.1 Surgery

      • 27.6.2 Radiation

      • 27.6.3 Adjuvant Chemotherapy

      • 27.6.4 Hormone Therapy

      • 27.6.5 Palliative Therapy

      • 27.6.6 Prognostic Factors

      • 27.6.7 Prognosis: Are BCM and BCF “Different” Diseases? A Critical Appraisal of the Literature

      • 27.6.8 Similarities and Differences Between BCM and BCF: A Summary (Table 27.7)

    • 27.7 Breast Cancer Survivorship Issues in Males

      • 27.7.1 Follow-Up

      • 27.7.2 Testing of Family Members

      • 27.7.3 Tumor Registry

      • 27.7.4 Psychological Issues/Resources/Support Groups

    • Acknowledgments

    • References

  • 28 Breast Cancer in the Older Adult

    • 28.1 Introduction and Epidemiology

    • 28.2 Clinical Assessment of the Older Adult with Breast Cancer

    • 28.3 Breast Cancer Prevention

      • 28.3.1 Screening

    • 28.4 Treatment of Primary Breast Cancer

      • 28.4.1 Surgery or Endocrine Therapy

      • 28.4.2 Radiation Therapy

      • 28.4.3 Management of the Axilla

    • 28.5 Adjuvant Systemic Therapy

      • 28.5.1 Treatment Benefit

      • 28.5.2 Selecting Treatment

      • 28.5.3 Treatment of Older Patients with Hormone Receptor Positive, HER-2 Negative Tumors

      • 28.5.4 Treatment of Older Patients with HER-2 Positive Tumors

      • 28.5.5 Treatment of Older Patients with ER- and PR-Negative and HER-2 Negative Tumors

    • 28.6 Treatment of Metastatic Disease

    • 28.7 Clinical Trials

    • 28.8 Conclusions

    • References

  • 29 Breast Cancer in Younger Women

    • 29.1 Introduction

    • 29.2 Epidemiology

    • 29.3 Risk Factors/Prognosis

    • 29.4 Diagnosis

    • 29.5 Tumor Characteristics/Biology

    • 29.6 Management/Treatment of Early Breast Cancer

      • 29.6.1 Surgery (Breast-Conserving Versus Mastectomy)

      • 29.6.2 Radiation

      • 29.6.3 Chemotherapy

      • 29.6.4 Endocrine Treatment

      • 29.6.5 Targeted Treatment

        • 29.6.5.1 Monoclonal Antibodies

        • 29.6.5.2 Tyrosine Kinase Inhibitors

        • 29.6.5.3 PARP1 [Poly(ADP-Ribose) Polymerase-1]—Inhibitors

        • 29.6.5.4 Vaccines and Immunotherapy

    • 29.7 Management/Treatment of Advanced Breast Cancer

    • 29.8 Side Effects of the Treatment

      • 29.8.1 Surgery

      • 29.8.2 Systemic Treatment

      • 29.8.3 Radiation Therapy

    • 29.9 Follow-up Recommendations and Survivors Care

    • 29.10 Fertility Preservation

    • 29.11 Breast Cancer Associated with Pregnancy (Lactation)

    • 29.12 Pregnancy After Breast Cancer

    • 29.13 Psychosocial, Familial, and Professional Aspects

    • 29.14 Conclusion

    • References

  • 30 Psychological Support for the Breast Cancer Patient

    • 30.1 Anxiety at Diagnosis

    • 30.2 Psychological Assessment

    • 30.3 Effect of Hormonal Treatment on Mood

    • 30.4 Adherence to Hormonal Medications

    • 30.5 Anxiety

    • 30.6 Sleep

    • 30.7 Cognitive Difficulties

    • 30.8 Overlap of Symptoms of Estrogen Deficiency and Depression

    • 30.9 Fatigue

    • 30.10 Prevalence of Major Depressive Disorder in Breast Cancer Patients

    • 30.11 Treatment

    • 30.12 Patients with Psychotic Illness

    • 30.13 Conclusion

    • References

  • 31 Management of the Patient with a Genetic Predisposition for Breast Cancer

    • 31.1 Hereditary Breast Cancer

      • 31.1.1 Somatic and Germline Genetics

    • 31.2 Genes Associated with Hereditary Breast Cancer

      • 31.2.1 Hereditary Breast Cancer Predispositions: High-Risk

      • 31.2.2 Hereditary Breast Cancer Predispositions: Moderate-Risk

    • 31.3 Identification of Individuals at Increased Risk for Breast Cancer

      • 31.3.1 Family History

      • 31.3.2 Personal Health History

    • 31.4 Risk Assessment

      • 31.4.1 Absolute Risk

      • 31.4.2 Relative Risk

      • 31.4.3 Predicting Development of Breast Cancer: Gail Model and Claus Tables

      • 31.4.4 Models for Predicting Presence of a Gene Mutation and Cancer Development: BRCAPro, BOADICEA, and Tyrer-Cuzick

    • 31.5 Genetic Testing

      • 31.5.1 Genetic Counseling

      • 31.5.2 Interpretation of Test Results

    • 31.6 Medical Management of Breast Cancer Risk

      • 31.6.1 Screening for Breast Cancer in Men

      • 31.6.2 Medical Management of a Woman with no Identifiable Mutation

      • 31.6.3 Medical Management of High Risk Gene Mutation Carriers

      • 31.6.4 Medical Management of Moderate Risk Gene Mutation Carriers

      • 31.6.5 Screening for Breast Cancer in Women

      • 31.6.6 Chemoprevention for Breast Cancer

      • 31.6.7 Risk-Reducing Salpingo-Oophorectomy

      • 31.6.8 Risk-Reducing Mastectomy

      • 31.6.9 Medical Management of Mutation Carriers Diagnosed with Breast Cancer

    • 31.7 Information for Extended Family Members

    • 31.8 In Summary

    • References

  • 32 Chemoprevention of Breast Cancer

    • 32.1 Chemoprevention of Breast Cancer

    • 32.2 Chemoprevention Agents

      • 32.2.1 Tamoxifen

      • 32.2.2 Aromatase Inhibitors

        • 32.2.2.1 Efficacy

        • 32.2.2.2 Side Effects

    • 32.3 Prevention Trials

      • 32.3.1 International Breast Cancer Intervention Study-II

      • 32.3.2 Map.3

      • 32.3.3 New Agents

    • 32.4 Conclusions

    • References

  • 33 Design, Implementation, and Interpretation of Clinical Trials

    • 33.1 Introduction

      • 33.1.1 Highlights in the Evolution of Clinical Trials

      • 33.1.2 History of Cancer Clinical Trial Cooperative Groups

    • 33.2 Fundamental Features

      • 33.2.1 Collaboration

      • 33.2.2 Phases in Development and Testing of New Drugs

      • 33.2.3 Explanatory and Pragmatic Considerations

      • 33.2.4 Selection of the Primary Question for Investigation

    • 33.3 Design Considerations

      • 33.3.1 Assuring Precision and Eliminating Bias

      • 33.3.2 Defining Study Outcomes

      • 33.3.3 Choice of Control Group

      • 33.3.4 Masking and Placebos

    • 33.4 Sample Size and Study Power

      • 33.4.1 Clinical Significance Versus Statistical Significance

      • 33.4.2 Statistical Significance and Study Power

      • 33.4.3 Baseline Outcome Rates and Population Measures of Variability

      • 33.4.4 Sample Sizes for Other Common Experimental Designs

      • 33.4.5 Time-to-Event Outcomes

      • 33.4.6 Sample Size Adjustments

    • 33.5 Randomization Methods

      • 33.5.1 An Example of Biased Coin Algorithm

    • 33.6 Ethical and Related Considerations

      • 33.6.1 Ethical Concerns Relating to Randomization

      • 33.6.2 Ethical Controversies in Randomization and NSABP Protocol B-06

      • 33.6.3 Data Integrity

    • 33.7 Conduct of the Clinical Trial

      • 33.7.1 Interim Data Monitoring

    • 33.8 General Analysis Considerations

      • 33.8.1 Modeling Treatment Effects with Multivariable Models

      • 33.8.2 Multiplicity Considerations

      • 33.8.3 Analysis of Multiple Outcomes Under Competing Risks

        • 33.8.3.1 One Sample Case

        • 33.8.3.2 Comparing 1-KM Method and Nonparametric Cumulative Incidence Approach in NSABP B-04 Data

        • 33.8.3.3 Two-Sample Comparison

        • 33.8.3.4 Regression on Cumulative Incidence Function

        • 33.8.3.5 Design Under Competing Risks; Sample Size and Loss of Power

      • 33.8.4 Building and Validating Prediction Models

      • 33.8.5 Interpretation

    • 33.9 Reporting and Publication

    • 33.10 Clinical Trial Overviews

    • References

  • 34 Structure of Breast Centers

    • 34.1 Introduction

    • 34.2 The National Accreditation Program for Breast Centers

    • 34.3 NAPBC Standards

    • 34.4 Center Leadership

      • 34.4.1 Level of Responsibility and Accountability

      • 34.4.2 Cancer Conference

      • 34.4.3 Evaluation and Management Guidelines

    • 34.5 Clinical Management

      • 34.5.1 Interdisciplinary Patient Management

      • 34.5.2 Patient Navigation

      • 34.5.3 Breast Conservation

      • 34.5.4 Sentinel Node Biopsy

      • 34.5.5 Breast Cancer Surveillance

      • 34.5.6 AJCC Staging

      • 34.5.7 Pathology Reports

      • 34.5.8 Diagnostic Imaging

      • 34.5.9 Needle Biopsy

      • 34.5.10 Ultrasonography

      • 34.5.11 Stereotactic Core Needle Biopsy

      • 34.5.12 Radiation Oncology

      • 34.5.13 Medical Oncology

      • 34.5.14 Support and Rehabilitation

      • 34.5.15 Genetic Evaluation and Management

      • 34.5.16 Educational Resources

      • 34.5.17 Reconstructive Surgery

      • 34.5.18 Evaluation and Management of Benign Breast Disease

      • 34.5.19 Breast Cancer Survivorship Care

    • 34.6 Research

      • 34.6.1 Clinical Trial Information

      • 34.6.2 Clinical Trial Accrual

    • 34.7 Community Outreach

      • 34.7.1 Education, Prevention, and Early Detection Programs

    • 34.8 Professional Education

      • 34.8.1 Breast Program Staff Education

    • 34.9 Quality Improvement

      • 34.9.1 Quality and Outcomes

    • 34.10 Survey Process

    • 34.11 Accreditation Awards

    • 34.12 Accreditation Award Matrix

    • 34.13 Benefits of Being a NAPBC-Accredited Center

    • Acknowledgments

    • Appendix

    • References

  • Index

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