Department of Obstetrics and Gynecology, Section of Gynecologic Oncology, The University of Chicago, Chicago, IL, United States.
Department of Gynecologic Oncology and Reproductive Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Pharmacol Ther. 2020 Sep;213:107588. doi: 10.1016/j.pharmthera.2020.107588. Epub 2020 May 23.
Poly (ADP-ribose) polymerase (PARP) inhibitors have transformed the therapeutic management of solid tumors, particularly ovarian cancer. Initially studied in BRCA deficient tumors, the Food and Drug Administration (FDA) indications have expanded to include other homologous recombination deficient tumors as well as biomarker-wildtype tumors. They have also gained momentum not only as a treatment strategy, but as a maintenance strategy as well. While PARP inhibitors were initially ev aluated in the recurrent setting, they have now moved to frontline therapy. This review will discuss the current FDA indications of the clinically available PARP inhibitors for treatment and maintenance therapies. We will then review the recently completed and ongoing clinical trials which may inform future clinical approvals.
聚(ADP-核糖)聚合酶(PARP)抑制剂改变了实体瘤的治疗管理方式,尤其是卵巢癌。最初在 BRCA 缺陷型肿瘤中进行研究,食品和药物管理局(FDA)的适应证已扩展到包括其他同源重组缺陷型肿瘤以及生物标志物野生型肿瘤。它们不仅作为一种治疗策略,而且作为一种维持策略也获得了发展势头。虽然 PARP 抑制剂最初在复发环境中进行评估,但现在已转移到一线治疗。本综述将讨论目前 FDA 批准的临床上可用的 PARP 抑制剂用于治疗和维持治疗的适应证。然后,我们将回顾最近完成和正在进行的临床试验,这些试验可能为未来的临床批准提供信息。