Prados-Carvajal Rosario, Irving Elsa, Lukashchuk Natalia, Forment Josep V
DDR Biology, Bioscience, Oncology R&D, AstraZeneca, Cambridge CB4 0WG, UK.
Translational Medicine, Oncology R&D, AstraZeneca, Cambridge CB4 0WG, UK.
Cancers (Basel). 2021 Dec 23;14(1):44. doi: 10.3390/cancers14010044.
Poly(ADP-ribose) polymerase (PARP) inhibitors (PARPi) are now a first-line maintenance treatment in ovarian cancer and have been approved in other cancer types, including breast, pancreatic and prostate. Despite their efficacy, and as is the case for other targeted therapies, resistance to PARPi has been reported clinically and is generating a growing patient population of unmet clinical need. Here, we discuss the mechanisms of resistance that have been described in pre-clinical models and focus on those that have been already identified in the clinic, highlighting the key challenges to fully characterise the clinical landscape of PARPi resistance and proposing ways of preventing and overcoming it.
聚(ADP-核糖)聚合酶(PARP)抑制剂(PARPi)现已成为卵巢癌的一线维持治疗药物,并已在其他癌症类型中获批,包括乳腺癌、胰腺癌和前列腺癌。尽管它们具有疗效,但与其他靶向治疗一样,临床上已报道对PARPi存在耐药性,并且产生了越来越多有未满足临床需求的患者群体。在此,我们讨论临床前模型中已描述的耐药机制,并重点关注临床中已确定的耐药机制,强调全面表征PARPi耐药临床情况的关键挑战,并提出预防和克服耐药的方法。