Adjuvant Olaparib for Germline BRCA Carriers With HER2-Negative Early Breast Cancer: Evidence and Controversies

Author:

Morganti Stefania123456,Bychkovsky Brittany L1237,Poorvu Philip D123,Garrido-Castro Ana C1234,Weiss Anna8,Block Caroline C123,Partridge Ann H123,Curigliano Giuseppe56,Tung Nadine M39,Lin Nancy U123,Garber Judy E1237,Tolaney Sara M123,Lynce Filipa123ORCID

Affiliation:

1. Department of Medical Oncology, Dana-Farber Cancer Institute , Boston, MA , USA

2. Breast Oncology Program, Dana-Farber Brigham Cancer Center , Boston, MA , USA

3. Harvard Medical School , Boston, MA , USA

4. Broad Institute of MIT and Harvard , Boston, MA , USA

5. Division of New Drugs and Early Drug Development, European Institute of Oncology, IRCCS , Milan , Italy

6. Department of Oncology and Hemato-Oncology, University of Milan , Milan , Italy

7. Division of Genetics and Prevention Program, Dana-Farber Cancer Institute , Boston, MA , USA

8. Department of Surgery, Division of Surgical Oncology, University of Rochester , Rochester, NY , USA

9. Division of Hematology-Oncology, Beth Israel Deaconess Medical Center , Boston, MA , USA

Abstract

AbstractIn the OlympiA study, 1 year of adjuvant olaparib significantly extended invasive disease-free survival and overall survival. The benefit was consistent across subgroups, and this regimen is now recommended after chemotherapy for germline BRCA1/2 mutation (gBRCA1/2m) carriers with high-risk, HER2-negative early breast cancer. However, the integration of olaparib in the landscape of agents currently available in the post(neo)adjuvant setting—ie, pembrolizumab, abemaciclib, and capecitabine—is challenging, as there are no data suggesting how to select, sequence, and/or combine these therapeutic approaches. Furthermore, it is unclear how to best identify additional patients who could benefit from adjuvant olaparib beyond the original OlympiA criteria. Since it is unlikely that new clinical trials will answer these questions, recommendations for clinical practice can be made through indirect evidence. In this article, we review available data that could help guide treatment decisions for gBRCA1/2m carriers with high-risk, early-stage breast cancer.

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Triple-negative breast cancers;Expert Review of Anticancer Therapy;2023-09-14

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