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比较低危型妊娠滋养细胞肿瘤患者应用放线菌素 D 和甲氨蝶呤的疗效和安全性:一项随机和高质量非随机研究的荟萃分析。

Direct comparisons of efficacy and safety between actinomycin-D and methotrexate in women with low-risk gestational trophoblastic neoplasia: a meta-analysis of randomized and high-quality non-randomized studies.

机构信息

Department of Obstetrics and Gynecology, The First Affiliated Hospital of Xi'an Jiaotong University, 277 West Yanta Road, Xi'an, Shaanxi, China.

Department of Urology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.

出版信息

BMC Cancer. 2021 Oct 18;21(1):1122. doi: 10.1186/s12885-021-08849-7.

Abstract

BACKGROUND

Actinomycin-D (Act-D) and Methotrexate (MTX) are both effective first-line agents for low-risk gestational trophoblastic neoplasia (LRGTN) with no consensus regarding which is more effective or less toxic. The primary objective of this meta-analysis is to compare Act-D with MTX in the treatment of LRGTN.

METHODS

We systematically searched electronic databases, conferences abstracts and trial registries for randomized controlled trials (RCTs) and high-quality non-randamized controlled trials (non-RCTs), comparing Act-D with MTX for patients with LRGTN. Studies were full-text screened for quality assessment and data extraction. Eligible studies must have reported complete remission rate. A fixed-effects meta-analysis was conducted to quantify the efficacy and safety of Act-D and MTX on odds ratios (ORs) and 95% confidence intervals (95%CIs), respectively.

RESULTS

A total of 8 RCTs and 9 non-RCTs (1674 patients) were included. In terms of efficacy, Act-D is superior to MTX in complete remission (80.2% [551/687] vs 65.1% [643/987]; OR 2.15, 95%CI 1.70 to 2.73). In the stratified analysis, patients from RCTs and non-RCTs both had a better complete remission from Act-D-based regimen (RCTs: 81.2% [259/319] vs 66.1% [199/301], OR 2.17, 95%CI 1.49 to 3.16; non-RCTs: 79.3% [292/368] vs 65.0% [444/686], OR 2.14, 95%CI 1.57 to 2.92). In terms of safety, patients receiving Act-D had higher risks of suffering nausea (OR 2.35, 95%CI 1.68 to 3.27), vomiting (OR 2.40, 95%CI 1.63 to 3.54), and alopecia (OR 2.76, 95%CI 1.60 to 4.75). Notably, liver toxicity (OR 0.38, 95%CI 0.19 to 0.76) was the only one that was conformed to have a higher risk for patients receiving MTX. In addition, the pooled results showed no significant difference of anaemia, leucocytopenia, neutropenia, thrombocytopnia, constipation, diarrhea, anorexia, and fatigue between Act-D and MTX.

CONCLUSIONS

Our meta-analysis suggests that Act-D had better efficacy profile in general, and MTX had less toxicities in LRGTN. Future clinical trials should be better orchestrated to provide more valid data on efficacy and toxicity.

摘要

背景

放线菌素 D(Act-D)和甲氨蝶呤(MTX)均为低危型妊娠滋养细胞肿瘤(LRGTN)的一线有效药物,但哪一种更有效或毒性更小尚无共识。本荟萃分析的主要目的是比较 Act-D 与 MTX 在 LRGTN 治疗中的疗效。

方法

我们系统地检索了电子数据库、会议摘要和试验注册处的随机对照试验(RCT)和高质量非随机对照试验(non-RCT),比较了 Act-D 与 MTX 治疗 LRGTN 的患者。对研究进行全文筛选以进行质量评估和数据提取。合格的研究必须报告完全缓解率。采用固定效应荟萃分析分别以比值比(OR)和 95%置信区间(95%CI)定量评估 Act-D 和 MTX 的疗效和安全性。

结果

共纳入 8 项 RCT 和 9 项 non-RCT(1674 例患者)。在疗效方面,Act-D 优于 MTX 的完全缓解率(80.2%[551/687]vs 65.1%[643/987];OR 2.15,95%CI 1.70 至 2.73)。在分层分析中,来自 RCT 和 non-RCT 的患者均接受 Act-D 为基础的方案治疗有更好的完全缓解率(RCT:81.2%[259/319]vs 66.1%[199/301],OR 2.17,95%CI 1.49 至 3.16;non-RCT:79.3%[292/368]vs 65.0%[444/686],OR 2.14,95%CI 1.57 至 2.92)。在安全性方面,接受 Act-D 的患者恶心(OR 2.35,95%CI 1.68 至 3.27)、呕吐(OR 2.40,95%CI 1.63 至 3.54)和脱发(OR 2.76,95%CI 1.60 至 4.75)的风险更高。值得注意的是,肝脏毒性(OR 0.38,95%CI 0.19 至 0.76)是唯一接受 MTX 治疗的患者风险更高的毒性。此外,汇总结果显示,Act-D 与 MTX 之间在贫血、白细胞减少症、中性粒细胞减少症、血小板减少症、便秘、腹泻、厌食症和疲劳方面无显著差异。

结论

本荟萃分析表明,Act-D 总体疗效更好,而 MTX 在 LRGTN 中毒性更小。未来的临床试验应更好地协调,以提供关于疗效和毒性的更有效数据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bdbe/8524874/4631bed57769/12885_2021_8849_Fig1_HTML.jpg

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