Teyssonneau Diego, Thiery-Vuillemin Antoine, Dariane Charles, Barret Eric, Beauval Jean-Baptiste, Brureau Laurent, Créhange Gilles, Fiard Gaëlle, Fromont Gaëlle, Gauthé Mathieu, Ruffion Alain, Renard-Penna Raphaële, Mathieu Romain, Sargos Paul, Rouprêt Morgan, Ploussard Guillaume, Roubaud Guilhem
Department of Medical Oncology, Institut Bergonié, 33000 Bordeaux, France.
Department of Medical Oncology, Centre Hospitalier Universitaire Besançon, 25000 Besançon, France.
J Clin Med. 2022 Mar 21;11(6):1734. doi: 10.3390/jcm11061734.
Despite recent improvements in survival, metastatic castration-resistant prostate cancers (mCRPCs) remain lethal. Alterations in genes involved in the homologous recombination repair (HRR) pathway are associated with poor prognosis. Poly-ADP-ribose polymerase (PARP) inhibitors (PARPis) have demonstrated anti-tumoral effects by synthetic lethality in patients with mCRPCs harboring HRR gene alterations, in particular . While both olaparib and rucaparib have obtained government approvals for use, the selection of eligible patients as well as the prescription of these treatments within the clinical urology community are challenging. This review proposes a brief review of the rationale and outcomes of PARPi treatment, then a pragmatic vision of PARPi use in terms of prescription and the selection of patients based on molecular screening, which can involve potential genetic counseling in the case of associated germinal alterations.
尽管近期生存率有所提高,但转移性去势抵抗性前列腺癌(mCRPC)仍然是致命的。参与同源重组修复(HRR)途径的基因改变与预后不良相关。聚ADP核糖聚合酶(PARP)抑制剂(PARPis)已通过合成致死性在携带HRR基因改变的mCRPC患者中显示出抗肿瘤作用,尤其是。虽然奥拉帕利和卢卡帕利均已获得政府批准使用,但在临床泌尿外科领域选择符合条件的患者以及这些治疗的处方具有挑战性。本综述简要回顾了PARPi治疗的基本原理和结果,然后从处方和基于分子筛查的患者选择方面对PARPi的使用提出了务实的观点,在相关胚系改变的情况下可能涉及潜在的遗传咨询。