American Society of Clinical Oncology Clinical Practice Guideline: Update on Adjuvant Endocrine Therapy for Women With Hormone Receptor–Positive Breast Cancer

Author:

Burstein Harold J.1,Prestrud Ann Alexis1,Seidenfeld Jerome1,Anderson Holly1,Buchholz Thomas A.1,Davidson Nancy E.1,Gelmon Karen E.1,Giordano Sharon H.1,Hudis Clifford A.1,Malin Jennifer1,Mamounas Eleftherios P.1,Rowden Diana1,Solky Alexander J.1,Sowers MaryFran R.1,Stearns Vered1,Winer Eric P.1,Somerfield Mark R.1,Griggs Jennifer J.1

Affiliation:

1. From the Dana-Farber Cancer Institute, Boston, MA; American Society of Clinical Oncology, Alexandria, VA; Breast Cancer Coalition of Rochester; Interlakes Oncology and Hematology, Rochester; Memorial Sloan-Kettering Cancer Center, New York, NY; M. D. Anderson Cancer Center, Houston; Susan G. Komen for the Cure, Dallas, TX; University of Pittsburgh Cancer Institute, Pittsburgh, PA; British Columbia Cancer Agency, Vancouver, British Columbia, Canada; Greater Los Angeles Veterans Affairs Healthcare System,...

Abstract

PurposeTo develop evidence-based guidelines, based on a systematic review, for endocrine therapy for postmenopausal women with hormone receptor–positive breast cancer.MethodsA literature search identified relevant randomized trials. Databases searched included MEDLINE, PREMEDLINE, the Cochrane Collaboration Library, and those for the Annual Meetings of the American Society of Clinical Oncology (ASCO) and the San Antonio Breast Cancer Symposium (SABCS). The primary outcomes of interest were disease-free survival, overall survival, and time to contralateral breast cancer. Secondary outcomes included adverse events and quality of life. An expert panel reviewed the literature, especially 12 major trials, and developed updated recommendations.ResultsAn adjuvant treatment strategy incorporating an aromatase inhibitor (AI) as primary (initial endocrine therapy), sequential (using both tamoxifen and an AI in either order), or extended (AI after 5 years of tamoxifen) therapy reduces the risk of breast cancer recurrence compared with 5 years of tamoxifen alone. Data suggest that including an AI as primary monotherapy or as sequential treatment after 2 to 3 years of tamoxifen yields similar outcomes. Tamoxifen and AIs differ in their adverse effect profiles, and these differences may inform treatment preferences.ConclusionThe Update Committee recommends that postmenopausal women with hormone receptor–positive breast cancer consider incorporating AI therapy at some point during adjuvant treatment, either as up-front therapy or as sequential treatment after tamoxifen. The optimal timing and duration of endocrine treatment remain unresolved. The Update Committee supports careful consideration of adverse effect profiles and patient preferences in deciding whether and when to incorporate AI therapy.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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