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维持治疗奥拉帕利与安慰剂在晚期恶性肿瘤中的特异性毒性:系统评价和荟萃分析。

Specific Toxicity of Maintenance Olaparib Placebo in Advanced Malignancies: A Systematic Review and Meta-analysis.

机构信息

Department of Experimental, Diagnostic and Specialty Medicine, S. Orsola-Malpighi University Hospital, Bologna, Italy

Department of Experimental, Diagnostic and Specialty Medicine, S. Orsola-Malpighi University Hospital, Bologna, Italy.

出版信息

Anticancer Res. 2020 Feb;40(2):597-608. doi: 10.21873/anticanres.13989.

Abstract

BACKGROUND/AIM: We performed a systematic review and meta-analysis to investigate the safety of maintenance with olaparib after platinum-based chemotherapy in cancer patients.

MATERIALS AND METHODS

Eligible studies included randomized controlled trials (RCTs) regarding the clinical role of olaparib maintenance therapy versus placebo in BRCA-mutated, advanced cancers. Safety profile from each selected study was investigated for all-grade and G3-G4 haematological and non-haematological adverse drug events (ADEs).

RESULTS

Four RTCs that involved 1099 patients were included in the analysis. Overall incidences of all-grade and G3-4 ADEs in olaparib group were 97.6% and 41%, respectively. Patients treated with maintenance olaparib showed higher risk of all-grade and G3-G4 anaemia, all-grade neutropenia and thrombocytopenia. Moreover, all-grade and G3-G4 fatigue, all-grade vomiting, diarrhoea, nausea and decreased appetite were more common in the olaparib group compared to placebo.

CONCLUSION

Despite an increased risk and incidence of several haematological and non-haematological toxicities, olaparib is a relatively safe agent for the treatment of advanced solid tumors. Prompt identification of ADEs is mandatory to avoid therapy discontinuation and optimize treatment.

摘要

背景/目的:我们进行了一项系统评价和荟萃分析,以调查在铂类化疗后使用奥拉帕利维持治疗癌症患者的安全性。

材料和方法

合格的研究包括关于奥拉帕利维持治疗与安慰剂在 BRCA 突变、晚期癌症中的临床作用的随机对照试验(RCT)。从每个选定的研究中调查所有等级和 G3-G4 血液学和非血液学不良药物事件(ADE)的安全性概况。

结果

纳入了四项涉及 1099 名患者的 RCT 进行分析。奥拉帕利组的所有等级和 G3-4 ADE 的总发生率分别为 97.6%和 41%。接受维持奥拉帕利治疗的患者发生所有等级和 G3-G4 贫血、所有等级中性粒细胞减少和血小板减少的风险更高。此外,与安慰剂相比,奥拉帕利组更常见所有等级和 G3-G4 疲劳、所有等级呕吐、腹泻、恶心和食欲下降。

结论

尽管几种血液学和非血液学毒性的风险和发生率增加,但奥拉帕利是治疗晚期实体瘤的相对安全药物。必须及时识别 ADE,以避免停药和优化治疗。

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