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恩度联合放化疗对比单纯放化疗治疗局部晚期宫颈癌的有效性和安全性:一项基于 PRISMA 指南的系统评价和荟萃分析。

Efficacy and safety of endostar combined with chemoradiotherapy versus chemoradiotherapy alone in locally advanced cervical cancer: A PRISMA-compliant systematic review and meta-analysis.

机构信息

Department of Four Comprehensive Internal Medicine, The First Affiliated Hospital of Xinjiang Medical University, Xinjiang, People's Republic of China.

出版信息

Medicine (Baltimore). 2022 Sep 9;101(36):e30170. doi: 10.1097/MD.0000000000030170.

DOI:10.1097/MD.0000000000030170
PMID:36086700
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10980378/
Abstract

BACKGROUND

To evaluate the role and safety of endostar in cervical cancer by comparing the efficacy and adverse reactions of endostar combined with concurrent chemoradiotherapy in patients with locally advanced cervical carcinoma.

METHODS

The quality of the included literature was evaluated by searching the database for the comparison of endostar combined with concurrent radiotherapy and chemotherapy in cervical cancer patients; objective response rate (ORR) and disease control rate (DCR) were used as the main outcome indicators, and statistical analysis was performed using RevMan5.3 and State15.3 software.

RESULTS

A total of 13 studies were included in this study, including 1057 patients with locally advanced cervical cancer, suggesting that endostar combined with chemoradiotherapy can significantly improve the objective response rate (ORR: odds ratio 3.88, 95% confidence interval 2.77-5.45, P < .00001) and disease control rate (DCR: odds ratio 4.43, 95% confidence interval 2.78-7.04; P < .00001), and there was no significant increase in treatment-related adverse reactions.

CONCLUSIONS

In this meta-analysis, endostar combined with concurrent chemoradiotherapy significantly improved ORR and DCR in patients with locally advanced cervical cancer without increasing toxicity. However, this study only analyzed the short-term efficacy of endostar, and its influence on overall survival and progression-free survival needs to be further verified in large randomized controlled trials with long-term follow-up.

摘要

背景

通过比较恩度联合同步放化疗治疗局部晚期宫颈癌患者的疗效和不良反应,评估恩度在宫颈癌中的作用和安全性。

方法

检索数据库,对恩度联合同步放化疗治疗宫颈癌患者的文献进行质量评价;以客观缓解率(ORR)和疾病控制率(DCR)为主要结局指标,采用 RevMan5.3 和 State15.3 软件进行统计学分析。

结果

共纳入 13 项研究,包含 1057 例局部晚期宫颈癌患者,结果表明恩度联合放化疗可显著提高客观缓解率(ORR:比值比 3.88,95%置信区间 2.77-5.45,P<0.00001)和疾病控制率(DCR:比值比 4.43,95%置信区间 2.78-7.04;P<0.00001),且未增加治疗相关不良反应。

结论

本荟萃分析表明,恩度联合同步放化疗可显著提高局部晚期宫颈癌患者的 ORR 和 DCR,且不增加毒性。但本研究仅分析了恩度的短期疗效,其对总生存和无进展生存的影响需要进一步在具有长期随访的大样本随机对照试验中加以验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff82/10980378/898af1962e5c/medi-101-e30170-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff82/10980378/d0d2e4c825d4/medi-101-e30170-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff82/10980378/7a4dddf9aa2f/medi-101-e30170-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff82/10980378/8049cd0dd908/medi-101-e30170-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff82/10980378/dee30df4b87d/medi-101-e30170-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff82/10980378/fb046b57e003/medi-101-e30170-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff82/10980378/898af1962e5c/medi-101-e30170-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff82/10980378/d0d2e4c825d4/medi-101-e30170-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff82/10980378/7a4dddf9aa2f/medi-101-e30170-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff82/10980378/8049cd0dd908/medi-101-e30170-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff82/10980378/dee30df4b87d/medi-101-e30170-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff82/10980378/fb046b57e003/medi-101-e30170-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff82/10980378/898af1962e5c/medi-101-e30170-g006.jpg

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