前列腺癌中的 PARP 抑制剂--了解当前形势

Karine Tawagi, M. Schmolze, Brandon Nguyen, Aaron Laviana, Natalie M Reizine
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摘要

多聚(ADP[二磷酸腺苷]-核糖]聚合酶抑制剂(PARPi)是目前治疗转移性去势抵抗性前列腺癌(mCRPC)患者的标准疗法之一,mCRPC 是指在使用常规一线雄激素剥夺疗法治疗后仍继续恶化的前列腺癌。PARPi的功能是针对前列腺癌细胞中导致细胞毒性双链DNA断裂(DSB)积累的同源重组修复途径。虽然 PARPi 作为 mCRCP 单药治疗方案的疗效已在临床上得到证实,但 PARPi 与其他抗癌药物联合使用的额外效用仍在探索之中。本文将回顾 PARP 抑制剂背后的科学原理,讨论对确定 PARPi 疗效预测生物标志物至关重要的种系突变和体细胞突变检测,并介绍目前已获批准的 PARPi 联合疗法及其适应症。本综述还将探讨 PARPi 药物毒性的发生率和处理方法,总结正在进行的试验,并提出未来的研究领域。
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PARP Inhibitors in Prostate Cancer – Understanding the Current Landscape
Poly (ADP [adenosine diphosphate]-ribose) polymerase inhibitors (PARPi) are a current standard of care treatment option for patients with metastatic castration resistant prostate cancer (mCRPC), defined as prostate cancers that continue to progress despite treatment with the usual first-line androgen-deprivation therapies. PARPi’s function by targeting faulty homologous recombination repair pathways that result in cytotoxic double strand DNA break (DSB) accumulation in prostate cancer cells. While the efficacy of PARPi’s as a monotherapy option in mCRCP has been demonstrated clinically, the added utility of PARPi’s in combination with other anti-cancer agents is still being explored. This article will review the scientific rationale behind PARP-inhibitors, discuss the germline and somatic mutation testing critical to identifying predictive biomarkers for PARPi efficacy, and present the currently approved PARPi combination therapies and their indications. This review will also examine the incidence and management of PARPi toxicity, summarize ongoing trials, and propose areas of future study.
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