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抗血管生成药物联合化疗治疗铂敏感/耐药卵巢癌的疗效与安全性:一项随机对照试验的Meta分析及试验序贯分析

Efficacy and safety of anti-angiogenic drugs combined with chemotherapy in the treatment of platinum-sensitive/resistant ovarian cancer: a meta-analysis with trial sequential analysis of randomized controlled trials.

作者信息

He Haining, Zhou Fei

机构信息

Department of Obstetrics and Gynaecology, Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, China.

出版信息

Front Pharmacol. 2024 Nov 21;15:1446403. doi: 10.3389/fphar.2024.1446403. eCollection 2024.

Abstract

BACKGROUND

With the emergence of new anti-angiogenic treatments and the ongoing updates to clinical guidelines, the effectiveness and safety of these agents in treating platinum-sensitive/resistant ovarian cancer (OC) are yet to be fully determined. Therefore, we conducted a meta-analysis to evaluate the efficacy and safety of anti-angiogenic drugs combined with chemotherapy (CT) for platinum-sensitive OC (PSOC) or platinum-resistant OC (PROC).

METHODS

A comprehensive literature search was conducted across several databases, including PubMed, Web of Science, Embase, and the Cochrane Library, encompassing all pertinent randomized controlled trials (RCTs) up to 31 May 2024. The primary outcomes for the meta-analysis were progression-free survival (PFS) and overall survival (OS), while the objective response rate (ORR), adverse events (AEs) of any grade, and grade ≥3 AEs were considered secondary endpoints. Data synthesis involved the computation of hazard ratio (HR), relative risk (RR), along with their 95% confidence interval (CI) and prediction interval (PI). Trial sequential analysis was carried out using STATA 12.0, R software 4.3.1, and TSA v0.9.5.10 Beta software.

RESULTS

This meta-analysis encompassed 15 RCTs. The overall analysis revealed that compared to CT alone (or plus placebo), anti-angiogenic drugs combined with CT significantly improved PFS (HR [95% CI] = 0.573 [0.518-0.633], 95% PI: 0.383-0.876) and ORR (RR [95% CI] = 1.362 [1.260-1.472], 95% PI: 0.824-2.251), but also increased the incidence of grade ≥3 AEs (RR [95% CI] = 1.115 [1.070-1.162], 95% PI: 0.870-1.422) in PSOC patients. For PROC patients, this combination therapy notably improved PFS (HR [95% CI] = 0.542 [0.475-0.619], 95% PI: 0.322-0.930), OS (HR [95% CI] = 0.752 [0.646-0.875], 95% PI: 0.554-0.997), and ORR (RR [95% CI] = 2.141 [1.702-2.694], 95% PI: 0.839-5.307), whilst simultaneously elevating the risk of grade ≥3 AEs (RR [95% CI] = 1.487 [1.216-1.819], 95% PI: 0.755-2.828).

CONCLUSION

Our research verified the advantages of combining anti-angiogenic agents with CT in enhancing PFS and ORR for patients with PSOC, and also confirmed improvements in PFS, OS, and ORR for those with PROC. It is crucial for medical practitioners to remain alert to the potential occurrence of AEs when implementing this combined therapeutic approach in a clinical milieu.

SYSTEMATIC REVIEW REGISTRATION

https://www.crd.york.ac.uk/PROSPERO/, identifier CRD42024552010.

摘要

背景

随着新型抗血管生成治疗方法的出现以及临床指南的不断更新,这些药物在治疗铂敏感/耐药卵巢癌(OC)中的有效性和安全性尚未完全确定。因此,我们进行了一项荟萃分析,以评估抗血管生成药物联合化疗(CT)治疗铂敏感OC(PSOC)或铂耐药OC(PROC)的疗效和安全性。

方法

在多个数据库中进行了全面的文献检索,包括PubMed、Web of Science、Embase和Cochrane图书馆,涵盖截至2024年5月31日的所有相关随机对照试验(RCT)。荟萃分析的主要结局是无进展生存期(PFS)和总生存期(OS),而客观缓解率(ORR)、任何级别的不良事件(AE)和≥3级AE被视为次要终点。数据合成涉及计算风险比(HR)、相对风险(RR)及其95%置信区间(CI)和预测区间(PI)。使用STATA 12.0、R软件4.3.1和TSA v0.9.5.10 Beta软件进行试验序贯分析。

结果

该荟萃分析纳入了15项RCT。总体分析显示,与单纯CT(或加安慰剂)相比,抗血管生成药物联合CT显著改善了PSOC患者的PFS(HR [95% CI] = 0.573 [0.518 - 0.633],95% PI:0.383 - 0.876)和ORR(RR [95% CI] = 1.362 [1.260 - 1.472],95% PI:0.824 - 2.251),但也增加了≥3级AE的发生率(RR [95% CI] = 1.115 [1.070 - 1.162],95% PI:0.870 - 1.422)。对于PROC患者,这种联合治疗显著改善了PFS(HR [95% CI] = 0.542 [0.475 - 0.619],95% PI:0.322 - 0.930)、OS(HR [95% CI] = 0.752 [0.646 - 0.875],95% PI:0.554 - 0.997)和ORR(RR [95% CI] = 2.141 [1.702 - 2.694],95% PI:0.839 - 5.307),同时增加了≥3级AE的风险(RR [95% CI] = 1.487 [1.216 - 1.819],95% PI:0.755 - 2.828)。

结论

我们的研究证实了抗血管生成药物联合CT在提高PSOC患者PFS和ORR方面的优势,也证实了PROC患者在PFS、OS和ORR方面的改善。在临床环境中实施这种联合治疗方法时,医生必须警惕AE的潜在发生,这一点至关重要。

系统评价注册

https://www.crd.york.ac.uk/PROSPERO/,标识符CRD42024552010。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c7f/11617189/fdc14336bd33/fphar-15-1446403-g001.jpg

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