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替索妥单抗维布妥昔治疗复发性/转移性宫颈癌的疗效与安全性:单臂研究的系统评价和荟萃分析

The efficacy and safety of Tisotumab vedotin in the treatment of recurrent/metastatic cervical cancer: a systematic review and meta-analysis of single-arm studies.

作者信息

Zeng Siyuan, Li Xin, Xiao Simin, Yang Peina, Lin Changsheng, Chen Huiling, Zhao Hu, Zhan Jun, Xiao Xue

机构信息

Department of Gynecology and Obstetrics, West China Second University Hospital, Sichuan University, Chengdu, China.

Key Laboratory of Birth Defects and Related Diseases of Women and Children, Ministry of Education, West China Second Hospital, Sichuan University, Chengdu, China.

出版信息

Front Pharmacol. 2025 May 19;16:1538980. doi: 10.3389/fphar.2025.1538980. eCollection 2025.

Abstract

OBJECTIVE

This study was conducted to evaluate the efficacy and safety of Tisotumab Vedotin (TV) in the treatment of recurrent/metastatic cervical cancer (r/m CC) through a systematic review and meta-analysis.

METHODS

The clinical studies on the monotherapy of TV for r/m CC were retrieved comprehensively from some databases, including PubMed, Embase, and Cochrane Library. The inclusion criteria encompassed observational studies and randomized controlled trials. Data analysis was performed using STATA 15.0. Besides, the median overall survival (OS), median progression-free survival (PFS), disease control rate (DCR), objective response rate (ORR), and the incidence of adverse events (AEs) and AEs at Grades 3-5 were calculated.

RESULTS

A total of 5 articles (covering 7 studies and 527 patients) were included in this study. The meta-analysis results revealed that the median OS, median PFS, ORR, and DCR were 11.83 months, 4.22 months, 29.9%, and 75.1%, respectively, for patients treated with TV. The incidence of AEs was 99.1%, and AEs at Grades 3-5 were reported in 61.7% of patients.

CONCLUSION

TV demonstrates significant efficacy as a second-line or third-line therapy for r/m CC, making it a promising therapeutic option. Nevertheless, large-scale randomized controlled trials are needed to validate these findings and optimize clinical application strategies.

SYSTEMATIC REVIEW REGISTRATION

https://www.crd.york.ac.uk/PROSPERO/view/CRD42024577046, identifier CRD42024577046.

摘要

目的

通过系统评价和荟萃分析,评估维迪西妥单抗(TV)治疗复发/转移性宫颈癌(r/m CC)的疗效和安全性。

方法

从PubMed、Embase和Cochrane图书馆等数据库全面检索TV单药治疗r/m CC的临床研究。纳入标准包括观察性研究和随机对照试验。使用STATA 15.0进行数据分析。此外,计算中位总生存期(OS)、中位无进展生存期(PFS)、疾病控制率(DCR)、客观缓解率(ORR)以及不良事件(AE)的发生率和3-5级AE的发生率。

结果

本研究共纳入5篇文章(涵盖7项研究和527例患者)。荟萃分析结果显示,接受TV治疗的患者中位OS、中位PFS、ORR和DCR分别为11.83个月、4.22个月、29.9%和75.1%。AE的发生率为99.1%,61.7%的患者报告了3-5级AE。

结论

TV作为r/m CC的二线或三线治疗方案显示出显著疗效,使其成为一种有前景的治疗选择。然而,需要大规模随机对照试验来验证这些发现并优化临床应用策略。

系统评价注册

https://www.crd.york.ac.uk/PROSPERO/view/CRD42024577046,标识符CRD42024577046。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6d6/12127362/6a79d50e017a/fphar-16-1538980-g001.jpg

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