Role of PARP inhibitors in prostate cancer.

IF 1.4 Q3 UROLOGY & NEPHROLOGY
Central European Journal of Urology Pub Date : 2024-01-01 Epub Date: 2024-10-28 DOI:10.5173/ceju.2024.72.R1
Julia Szczotka, Gabriela Szpila, Michał Hejduk, Ewa Mucha, Jolanta Rudel, Michał Kępiński, Julia Kaletka, Jakub Ryszawy, Piotr Zapala, Ichiro Tsuboi, Akihiro Matsukawa, Marcin Miszczyk, Tamas Fazekas, Fabio Zattoni, Piotr Bryniarski, Paweł Rajwa
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引用次数: 0

Abstract

Introduction: Olaparib, rucaparib, niraparib, and talazoparib are poly (ADP-ribose) polymerase (PARP) inhibitors (PARPi) targeted at recombination. To gain a comprehensive understanding of the mechanism of action of PARPi, scientists conducted research involving numerous studies that provided evidence regarding their efficacy and safety.

Material and methods: A literature review was performed using the PubMed® and Google Scholar databases. Articles were reviewed and categorized based on the most crucial and current information regarding the pharmacological properties and use of PARPi in treating metastatic castration-resistant prostate cancer (mCRPC), while also indicating the future therapeutic direction toward which these pharmaceuticals are progressing. Data were extracted, analyzed and summarized.

Results: PARP inhibitors like olaparib, rucaparib, niraparib, and talazoparib show promise in mCRPC, particularly for patients with specific genetic mutations (BRCA1/2, ATM). While they extend PFS and sometimes OS, side effects - especially anemia - are prevalent and impact treatment continuation.

Conclusions: Despite PARPi already being recognized as the standard treatment for mCRPC, further research is crucial to optimize their efficacy and safety, particularly in the context of combination therapies and use in the early stages of the disease.

PARP抑制剂在前列腺癌中的作用。
简介:奥拉帕尼、鲁卡帕尼、尼拉帕尼和塔拉唑帕尼是靶向重组的聚(adp -核糖)聚合酶(PARP)抑制剂(PARPi)。为了全面了解PARPi的作用机制,科学家们进行了大量的研究,为其有效性和安全性提供了证据。材料和方法:使用PubMed®和谷歌Scholar数据库进行文献综述。本文根据PARPi治疗转移性去势抵抗性前列腺癌(mCRPC)的药理学特性和应用的最重要和最新信息对文章进行了回顾和分类,同时也指出了这些药物未来的治疗方向。对数据进行提取、分析和汇总。结果:PARP抑制剂如奥拉帕尼、rucaparib、niraparib和talazoparib在mCRPC中显示出希望,特别是对于具有特定基因突变(BRCA1/2, ATM)的患者。虽然它们延长了PFS,有时延长了OS,但副作用——尤其是贫血——很普遍,并影响了治疗的持续。结论:尽管PARPi已被公认为mCRPC的标准治疗方法,但进一步的研究对于优化其疗效和安全性至关重要,特别是在联合治疗和疾病早期使用的背景下。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Central European Journal of Urology
Central European Journal of Urology UROLOGY & NEPHROLOGY-
CiteScore
2.30
自引率
8.30%
发文量
48
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