[聚(adp -核糖)聚合酶(PARP-)抑制剂作为转移性去势抵抗性前列腺癌(mCRPC)的基因精准治疗]。

Der Urologe. Ausg. A Pub Date : 2022-02-01 Epub Date: 2022-01-10 DOI:10.1007/s00120-021-01754-8
Isabel Heidegger, Christoph Becker, Igor Tsaur, Tilman Todenhöfer
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引用次数: 0

摘要

有了PARP抑制剂,转移性去势抵抗性前列腺癌(mCRPC)的治疗前景自2020年11月以来已经扩大了一个新的物质类别。目前,这种创新疗法的适应症需要存在BRCA1/2基因突变和先前的激素治疗。这篇简短的综述解释了PARP的分子背景,并总结了目前PARP抑制的临床试验,以及与其他治疗策略的结合。鉴于被引用研究的阳性数据和具有“可操作”突变的患者比例相对较高,BRCA1/2突变依赖性PARP抑制mCRPC的个性化治疗理念现在反映在包括S3指南在内的各种指南中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Poly(ADP-ribose) polymerase (PARP-)inhibitors as genetically based precision therapy in metastatic castration-resistent prostate cancer (mCRPC)].

With PARP inhibitors, the therapeutic landscape for metastatic castration-resistant prostate cancer (mCRPC) has been expanded by a new substance class since November 2020. Currently, the indication for this innovative therapy requires the presence of a mutation in one of the BRCA1/2 genes and prior hormonal therapy. This short review explains the molecular background and summarizes current clinical trials on PARP inhibition-also in combination with other therapy strategies. In view of positive data from the cited studies and the relatively high proportion of patients with "actionable" mutations, the personalized therapy concept of BRCA1/2 mutation-dependent PARP inhibition for mCRPC is now reflected in various guidelines including S3 guidelines.

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