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聚(ADP - 核糖)聚合酶抑制剂:最新进展与未来发展

Poly (ADP-ribose) polymerase inhibitors: recent advances and future development.

作者信息

Scott Clare L, Swisher Elizabeth M, Kaufmann Scott H

机构信息

Clare L. Scott, Walter and Eliza Hall Institute of Medical Research and Royal Melbourne Hospital, Parkville, Victoria, Australia; Elizabeth M. Swisher, University of Washington, Seattle, WA; and Scott H. Kaufmann, Mayo Clinic, Rochester, MN.

出版信息

J Clin Oncol. 2015 Apr 20;33(12):1397-406. doi: 10.1200/JCO.2014.58.8848. Epub 2015 Mar 16.

Abstract

Poly (ADP-ribose) polymerase (PARP) inhibitors have shown promising activity in epithelial ovarian cancers, especially relapsed platinum-sensitive high-grade serous disease. Consistent with preclinical studies, ovarian cancers and a number of other solid tumor types occurring in patients with deleterious germline mutations in BRCA1 or BRCA2 seem to be particularly sensitive. However, it is also becoming clear that germline BRCA1/2 mutations are neither necessary nor sufficient for patients to derive benefit from PARP inhibitors. We provide an update on PARP inhibitor clinical development, describe recent advances in our understanding of PARP inhibitor mechanism of action, and discuss current issues in the development of these agents.

摘要

聚(ADP - 核糖)聚合酶(PARP)抑制剂在上皮性卵巢癌中已显示出有前景的活性,尤其是复发性铂敏感的高级别浆液性疾病。与临床前研究一致,在BRCA1或BRCA2中存在有害种系突变的患者中发生的卵巢癌和许多其他实体瘤类型似乎特别敏感。然而,也越来越清楚的是,种系BRCA1/2突变对于患者从PARP抑制剂中获益既不是必需的也不是充分的。我们提供了PARP抑制剂临床开发的最新情况,描述了我们对PARP抑制剂作用机制理解的最新进展,并讨论了这些药物开发中的当前问题。

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