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

Claudine J Isaacs, Dana Zakalik, Mark R Somerfield, Brittany E Harvey, Mark G Trombetta, Rubina D Qamar, Nina A Mayr, Jennifer K Litton, Elaine Kennedy, Ismail Jatoi, Nadine M Tung, Erin W Hofstatter, Judith Balmana Gelpi, Anthony Dragun, Jill R Dietz, Isabelle Bedrosian, Mark E Robson, Lori J Pierce, Judy C Boughey

Journal: Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2021;38(18):2080-2106

PMID: 32243226

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 / 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 / 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 / carriers. Radiation therapy should not be withheld in carriers. For patients with germline 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 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 / 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.

Address: Beth Israel Deaconess Medical Center, Boston, MA.; Mayo Clinic, Rochester, MN.; Rogel Cancer Center, University of Michigan, Ann Arbor, MI.; Memorial Sloan Kettering Cancer Center, New York, NY.; The University of Texas MD Anderson Cancer Center, Houston, TX.; Case Western Reserve University School of Medicine and University Hospitals, Cleveland, OH.; MD Anderson-Cooper University Hospital, Camden, NJ.; Vall d'Hebron University Hospital, Barcelona, Spain.; Yale Cancer Center, New Haven, CT.; Georgetown University, Washington, DC.; University of Texas Health Science Center at San Antonio, San Antonio, TX.; FORCE, Washington, DC.; University of Washington, Seattle, WA.; Advocate Aurora Health, Milwaukee, WI.; Allegheny Health Network, Pittsburgh, PA.; American Society of Clinical Oncology, Alexandria, VA.; Beaumont Health, Royal Oak, MI.
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