Heidegger Isabel, Becker Christoph, Tsaur Igor, Todenhöfer Tilman
Department für Urologie, Medizinische Universität Innsbruck, Innsbruck, Österreich.
Forschungskoordination, Deutsche Gesellschaft für Urologie (DGU) e. V., Uerdinger Straße 64, 40474, Düsseldorf, Deutschland.
Urologe A. 2022 Feb;61(2):187-192. doi: 10.1007/s00120-021-01754-8. Epub 2022 Jan 10.
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.
自2020年11月以来,随着PARP抑制剂的出现,转移性去势抵抗性前列腺癌(mCRPC)的治疗领域因一种新的药物类别而得到扩展。目前,这种创新疗法的适应症要求BRCA1/2基因之一存在突变且之前接受过激素治疗。这篇简短综述解释了分子背景,并总结了目前关于PARP抑制(也包括与其他治疗策略联合)的临床试验。鉴于引用研究中的阳性数据以及“可操作”突变患者的比例相对较高,mCRPC基于BRCA1/2突变的PARP抑制的个性化治疗理念现已反映在包括S3指南在内的各种指南中。