PARP Inhibitors for Breast Cancer: Germline BRCA1/2 and Beyond

被引:26
作者
Menezes, Maria Clara Saad [1 ]
Raheem, Farah [2 ]
Mina, Lida [2 ]
Ernst, Brenda [2 ]
Batalini, Felipe [2 ]
机构
[1] Harvard TH Chan Sch Publ Hlth, 677 Huntington Ave, Boston, MA 02115 USA
[2] Mayo Clin Arizona, 5777 E Mayo Blvd, Phoenix, AZ 85054 USA
关键词
breast cancer; PARPi; BRCA1; BRCA2; PALB2; homologous recombination repair; HRD; HOMOLOGOUS RECOMBINATION DEFICIENCY; ADVANCED SOLID TUMORS; OLAPARIB TABLET FORMULATION; PATIENT-REPORTED OUTCOMES; PHASE-I TRIAL; POLY(ADP-RIBOSE) POLYMERASE; MAINTENANCE THERAPY; OVARIAN-CARCINOMA; JAPANESE PATIENTS; ANTITUMOR-ACTIVITY;
D O I
10.3390/cancers14174332
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary Poly-adenosine diphosphate ribose polymerase (PARP) inhibitors (PARPi) are effective against tumors with mutations in DNA repair genes, most commonly in the BRCA1 and BRCA2 genes. Because these tumors are unable to repair their DNA, PARPi have been used to target DNA repair pathways and are useful in the treatment of breast cancers with some of these alterations. There are two FDA-approved PARPi for patients with breast cancer-olaparib and talazoparib. The data on olaparib and talazoparib in the treatment of breast cancer are summarized in this review, and we also explore potential future applications of PARPi beyond inherited BRCA mutations. Poly-adenosine diphosphate ribose polymerase (PARP) inhibitors (PARPi) are approved for BRCA1/2 carriers with HER2-negative breast cancer in the adjuvant setting with a high risk of recurrence as well as the metastatic setting. However, the indications for PARPi are broader for patients with other cancer types (e.g., prostate and ovarian cancer), involving additional biomarkers (e.g., ATM, PALB2, and CHEK) and genomic instability scores. Herein, we summarize the data on PARPi and breast cancer and discuss their use beyond BRCA carriers.
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页数:18
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