Clinicopathological characteristics and eligibility for adjuvant olaparib of germline BRCA1/2 mutation carriers with HER2-negative early breast cancer

被引:0
作者
Morganti, Stefania [1 ,2 ,3 ,4 ]
Jin, Qingchun [5 ]
Vincuilla, Julie [2 ]
Buehler, Ryan [6 ]
Ryan, Sean [1 ,2 ]
Stokes, Samantha [4 ]
Parker, Tonia [1 ,2 ]
Mittendorf, Elizabeth A. [2 ,3 ,7 ]
King, Tari A. [2 ,3 ,7 ]
Weiss, Anna [2 ,3 ,7 ,10 ]
Partridge, Ann H. [1 ,2 ,3 ]
Bychkovsky, Brittany L. [1 ,2 ,3 ,6 ]
Curigliano, Giuseppe [8 ,9 ]
Tayob, Nabihah [3 ,5 ]
Lin, Nancy U. [1 ,2 ,3 ]
Garber, Judy E. [1 ,2 ,3 ,6 ]
Tolaney, Sara M. [1 ,2 ,3 ]
Lynce, Filipa [1 ,2 ,3 ]
机构
[1] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02215 USA
[2] Dana Farber Brigham Canc Ctr, Breast Oncol Program, Boston, MA 02115 USA
[3] Harvard Med Sch, Boston, MA 02115 USA
[4] Broad Inst MIT & Harvard, Boston, MA USA
[5] Dana Farber Canc Inst, Dept Data Sci, Boston, MA USA
[6] Dana Farber Canc Inst, Div Canc Genet & Prevent, Boston, MA USA
[7] Brigham & Womens Hosp, Dept Surg, Div Breast Surg, Boston, MA USA
[8] Univ Milan, Dept Oncol & Hemato Oncol, Milan, Italy
[9] European Inst Oncol IRCCS, Milan, Italy
[10] Univ Rochester, Med Ctr, Div Surg Oncol, Rochester, NY USA
关键词
D O I
10.1038/s41523-024-00632-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Following the survival benefit demonstrated in the OlympiA trial, one year of adjuvant olaparib is now recommended for all patients with germline BRCA1/2 pathogenic/likely pathogenic variants (PV) and high-risk, HER2-negative early breast cancer after chemotherapy. However, optimal identification of high-risk patients who may derive benefit from this genomically-directed therapy is debated. In this study, we sought to characterize the real-world proportion of gBRCA1/2 PV carriers eligible for adjuvant olaparib according to the OlympiA criteria, and to compare clinicopathologic characteristics and outcomes between eligible and ineligible patients.
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页数:6
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