Safety and efficacy of tisotumab vedotin with cervical cancers: A systematic review and meta-analysis.

IF 1.6 4区 医学 Q3 OBSTETRICS & GYNECOLOGY
Muhammed Edib Mokresh, Omar Alomari, Abdullah Varda, Goncagul Akdag, Hatice Odabas
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引用次数: 0

Abstract

Background: Tisotumab vedotin (TV) holds promise for treating recurrence or metastatic cervical cancer (r/mCC), with recent FDA approval for second-line use in recurrent or metastatic cases. Our research aims to evaluate TV's efficacy and safety in these patients, focusing on overall survival (OS) and progression-free survival (PFS) outcomes.

Methods: We searched five electronic databases in February 2024, retrieved articles, screened them based on inclusion and exclusion criteria, and assessed their quality. A meta-analysis of the extracted data was performed and applied a random-effects model for our analysis.

Results: The search identified 86 articles, with six meeting the inclusion criteria. Meta-analysis revealed 80.8% and 48.0% OS at 6 and 12 months, and a 29.9% PFS at 6 months. Combined treatment with carboplatin or pembrolizumab showed 33.0% PFS at 1 year and 15.1% at 2 years. The objective response rate (ORR) was 21.0%, reaching 43.3% with combined treatment. Confirmed disease control rate (CDCR) was 70.0% overall and in combination. The median duration of response (DOR) was 6.1 months, increasing to 9.5 months in combined treatment, with a consistent time to response (TTR) of 1.4 months. Adverse events included ocular issues (conjunctivitis 30.3%, dry eye 18.7%) and common side effects (nausea 38.4%, epistaxis 35.7%).

Conclusion: This systematic review and meta-analysis highlights the potential of TV as a treatment option for r/mCC patients. However, healthcare providers must communicate safety profiles and recommend prophylactic measures for optimal patient outcomes. Further studies, particularly assessing combination treatments, are needed to clarify TV's role in treatment algorithms and improve clinical outcomes.

替索单抗维多汀治疗宫颈癌的安全性和有效性:系统回顾与荟萃分析。
背景:蒂索单抗维多汀(Tisotumab vedotin,TV)有望治疗复发或转移性宫颈癌(r/mCC),最近美国食品药品管理局(FDA)已批准该药用于复发或转移性病例的二线治疗。我们的研究旨在评估 TV 对这些患者的疗效和安全性,重点关注总生存期(OS)和无进展生存期(PFS)的结果:我们搜索了 2024 年 2 月的五个电子数据库,检索了文章,根据纳入和排除标准对文章进行了筛选,并评估了文章的质量。我们对提取的数据进行了荟萃分析,并采用随机效应模型进行分析:搜索共发现 86 篇文章,其中 6 篇符合纳入标准。荟萃分析显示,6个月和12个月的OS分别为80.8%和48.0%,6个月的PFS为29.9%。卡铂或彭博利珠单抗联合治疗显示,1年的PFS为33.0%,2年的PFS为15.1%。客观反应率(ORR)为21.0%,联合治疗后达到43.3%。总体和联合治疗的确诊疾病控制率(CDCR)为70.0%。中位应答持续时间(DOR)为6.1个月,联合治疗时增至9.5个月,一致的应答时间(TTR)为1.4个月。不良反应包括眼部问题(结膜炎 30.3%、干眼症 18.7%)和常见副作用(恶心 38.4%、鼻衄 35.7%):这项系统综述和荟萃分析强调了电视作为一种治疗方法对乳腺癌/乳癌患者的潜力。然而,医疗服务提供者必须传达安全性信息,并建议采取预防措施,以优化患者的治疗效果。还需要进一步的研究,尤其是对联合治疗的评估,以明确电视在治疗算法中的作用并改善临床疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.10
自引率
0.00%
发文量
376
审稿时长
3-6 weeks
期刊介绍: The Journal of Obstetrics and Gynaecology Research is the official Journal of the Asia and Oceania Federation of Obstetrics and Gynecology and of the Japan Society of Obstetrics and Gynecology, and aims to provide a medium for the publication of articles in the fields of obstetrics and gynecology. The Journal publishes original research articles, case reports, review articles and letters to the editor. The Journal will give publication priority to original research articles over case reports. Accepted papers become the exclusive licence of the Journal. Manuscripts are peer reviewed by at least two referees and/or Associate Editors expert in the field of the submitted paper.
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