Management of Hereditary Breast Cancer: American Society of Clinical Oncology, American Society for Radiation Oncology, and Society of Surgical Oncology Guideline

Nadine Tung(Beth Israel Deaconess Medical Center), Judy C. Boughey(Mayo Clinic in Arizona), Lori J. Pierce(University of Michigan), Mark E. Robson(Memorial Sloan Kettering Cancer Center), Isabelle Bedrosian(The University of Texas MD Anderson Cancer Center), Jill R. Dietz(University School), Anthony Dragun(Cooper University Hospital), Judith Balmaña Gelpí(Vall d'Hebron Hospital Universitari), Erin Hofstatter(Yale Cancer Center), Claudine Isaacs(Georgetown University), Ismail Jatoi(The University of Texas at San Antonio Health Science Center), Elaine Kennedy(Facing Our Risk of Cancer Empowered), Jennifer K. Litton(The University of Texas MD Anderson Cancer Center), Nina A. Mayr(University of Washington), Rubina Qamar(Aurora Health Care), Mark Trombetta(Allegheny Health Network), Brittany Harvey(American Society of Clinical Oncology), Mark R. Somerfield(American Society of Clinical Oncology), Dana Zakalik(Beaumont Health)
Journal of Clinical Oncology
April 3, 2020
Cited by 319Open Access
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Abstract

PURPOSE To develop recommendations for management of patients with breast cancer (BC) with germline mutations in BC susceptibility genes. METHODS The American Society of Clinical Oncology, American Society for Radiation Oncology, and Society of Surgical Oncology convened an Expert Panel to develop recommendations based on a systematic review of the literature and a formal consensus process. RESULTS Fifty-eight articles met eligibility criteria and formed the evidentiary basis for the local therapy recommendations; six randomized controlled trials of systemic therapy met eligibility criteria. RECOMMENDATIONS Patients with newly diagnosed BC and BRCA1/ 2 mutations may be considered for breast-conserving therapy (BCT), with local control of the index cancer similar to that of noncarriers. The significant risk of a contralateral BC (CBC), especially in young women, and the higher risk of new cancers in the ipsilateral breast warrant discussion of bilateral mastectomy. Patients with mutations in moderate-risk genes should be offered BCT. For women with mutations in BRCA1/ 2 or moderate-penetrance genes who are eligible for mastectomy, nipple-sparing mastectomy is a reasonable approach. There is no evidence of increased toxicity or CBC events from radiation exposure in BRCA1/ 2 carriers. Radiation therapy should not be withheld in ATM carriers. For patients with germline TP53 mutations, mastectomy is advised; radiation therapy is contraindicated except in those with significant risk of locoregional recurrence. Platinum agents are recommended versus taxanes to treat advanced BC in BRCA carriers. In the adjuvant/neoadjuvant setting, data do not support the routine addition of platinum to anthracycline- and taxane-based chemotherapy. Poly (ADP-ribose) polymerase (PARP) inhibitors (olaparib and talazoparib) are preferable to nonplatinum single-agent chemotherapy for treatment of advanced BC in BRCA1/ 2 carriers. Data are insufficient to recommend PARP inhibitor use in the early setting or in moderate-penetrance carriers. Additional information available at www.asco.org/breast-cancer-guidelines .


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