奥拉帕利、尼拉帕利、卢卡帕利疗法对新诊断和复发卵巢癌的影响——系统评价与荟萃分析

Impact of Olaparib, Niraparib, Rucaparib therapies on Newly Diagnosed and Relapsed Ovarian Cancer -Systematic Review and Meta-Analysis.

作者信息

Devi Seeta, Chandrababu Ramesh

机构信息

Department of Obstetrics and Gynecological Nursing, Symbiosis College of Nursing (SCON), Symbiosis International University (SIDU), Pune, India.

Department of Medical Surgical Nursing, Sri Ramachandra Faculty of Nursing, Sri Ramachandra Institute of Higher Education and Research, Deemed to be University, Porur, Chennai, India.

出版信息

Asian Pac J Cancer Prev. 2025 Jun 1;26(6):1931-1941. doi: 10.31557/APJCP.2025.26.6.1931.

Abstract

OBJECTIVE

This review aims to examine the effect of PARP inhibitors on PFS, OS, and adverse events in women with advanced ovarian cancer (OC).

METHODS

The PRISMA 2020 guidelines are followed while conducting this comprehensive review. Data from 17 randomized control trails (RCT) published between 2014 and June 2024 were included. These trials compared PARPi maintenance therapy to placebo women with newly diagnosed and recurrent advanced OC. The specific keywords were used to search relevant studies in databases including PubMed, SCOPUS, Cochrane library, and WoS. The main outcomes were the Progression free survival (PFS), overall survival (OS), or adverse events (AEs). The combined hazard ratios (HRs) and risk ratios (RRs) were determined, together with 95% confidence intervals (CIs). Each of the analyses were conducted using a model with random effects.

RESULTS

Despite high heterogeneity, the meta-analysis found that poly (ADP-ribose) polymerase inhibitors (PARPi) maintenance therapy ominously improved PFS compared to placebo, with a combined HR of 1.33 (95% CI: 1.10-1.61) in newly diagnosed cases and 0.88 (95% CI: 0.59-1.30) in relapsed cases. However, the OS improvement was not significantly substantial, with a collective HR of 1.06 (95% CI: 0.99-1.13). AEs are considerably higher in the PARPi groups, notably hematologic toxicities including anaemia, thrombocytopenia, and neutropenia. However, these adverse effects may be controlled with dosage modifications, and therapy was discontinued only in few cases.

CONCLUSION

PARPi are an effective therapy in both newly discovered and relapsed. Although there is a modest rise in the frequency of severe adverse reactions, they are usually handled well.

摘要

目的

本综述旨在研究聚(ADP - 核糖)聚合酶(PARP)抑制剂对晚期卵巢癌(OC)女性患者无进展生存期(PFS)、总生存期(OS)及不良事件的影响。

方法

本全面综述遵循PRISMA 2020指南。纳入了2014年至2024年6月期间发表的17项随机对照试验(RCT)的数据。这些试验将PARP抑制剂维持治疗与新诊断和复发的晚期OC女性患者的安慰剂进行了比较。使用特定关键词在包括PubMed、SCOPUS、Cochrane图书馆和WoS在内的数据库中搜索相关研究。主要结局为无进展生存期(PFS)、总生存期(OS)或不良事件(AE)。确定了合并风险比(HRs)和风险率(RRs)以及95%置信区间(CIs)。每项分析均使用随机效应模型进行。

结果

尽管异质性较高,但荟萃分析发现,与安慰剂相比,聚(ADP - 核糖)聚合酶抑制剂(PARPi)维持治疗显著改善了PFS,新诊断病例的合并HR为1.33(95%CI:1.10 - 1.61),复发病例为0.88(95%CI:0.59 - 1.30)。然而,OS的改善并不显著,总体HR为1.06(95%CI:0.99 - 1.13)。PARPi组的不良事件明显更高,尤其是血液学毒性,包括贫血、血小板减少和中性粒细胞减少。然而,这些不良反应可通过调整剂量得到控制,仅在少数情况下停止治疗。

结论

PARPi在新诊断和复发患者中均为有效治疗方法。尽管严重不良反应的发生率略有上升,但通常处理良好。

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