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尼妥珠单抗联合放疗或放化疗治疗局部晚期头颈部癌的疗效和安全性的系统评价和荟萃分析。

Efficacy and Safety of Nimotuzumab in Combination with Radiotherapy or Chemoradiotherapy for Local Advanced Head and Neck Cancer: A Systematic Review and Meta-analysis.

机构信息

Department of Radiation Oncology, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/ Beijing), Peking University Cancer Hospital & Institute, Beijing, China.

Department of Radiation Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

出版信息

Curr Cancer Drug Targets. 2024;24(9):952-966. doi: 10.2174/0115680096281982240117114819.

Abstract

BACKGROUND

The present meta-analysis aimed to evaluate the efficacy and safety of adding nimotuzumab to radiotherapy (RT) or chemoradiotherapy (CRT).

METHODS

Prospective randomized controlled studies at EMBASE, PubMed, and the Cochrane Library from January 1, 2010, to October 1, 2022, were searched. Data on the overall survival (OS), progress-free survival (PFS), disease-free survival (DFS), complete response rate (CRR), objective response rate (ORR), and all grade adverse events were collected from the enrolled publications. OS was the primary measurement indicator. Pooled analysis was performed with relative risks (RRs), hazard risks (HRs), and their corresponding 95% confidence intervals (CIs) in the software Stata SE 16.0.

RESULTS

Six randomized controlled studies were included in the analysis of the overall pooled effect. As compared to the control group, the nimotuzumab intervention group exhibited improved OS by 21% (pooled HR=0.79,95% CI: 0.64-0.98, P=0.028), along with PFS up to 31% (HR=0.69, 95% CI: 0.55-0.86, P=0.001) and DFS up to 29% (HR=0.71, 95% CI: 0.56-0.91, P=0.006), increased CRR as 50% (RR=1.50, 95% CI:1.09-2.04; P=0.012), and ORR as 35% (RR=1.35, 95% CI:1.04-1.73; P=0.022). Regarding safety, nimotuzumab in combination with RT or CRT did not increase the incidence of all grade adverse events (pooled-RD=-1.27, 95% CI:-2.78-0.23, P=0.099).

CONCLUSION

The present meta-analysis has demonstrated that nimotuzumab, in combination with RT or CRT, could provide survival benefits and increase response rates. Its safety profile has been found to be controllable.

摘要

背景

本荟萃分析旨在评估尼莫单抗联合放疗(RT)或放化疗(CRT)的疗效和安全性。

方法

从 2010 年 1 月 1 日至 2022 年 10 月 1 日,在 EMBASE、PubMed 和 Cochrane 图书馆中搜索前瞻性随机对照研究。从纳入的出版物中收集总生存期(OS)、无进展生存期(PFS)、无病生存期(DFS)、完全缓解率(CRR)、客观缓解率(ORR)和所有等级不良事件的数据。OS 是主要测量指标。使用 Stata SE 16.0 软件进行相对风险(RR)、风险比(HR)及其相应的 95%置信区间(CI)的汇总分析。

结果

共纳入 6 项随机对照研究进行总体汇总效果分析。与对照组相比,尼莫单抗干预组的 OS 提高了 21%(汇总 HR=0.79,95%CI:0.64-0.98,P=0.028),PFS 提高了 31%(HR=0.69,95%CI:0.55-0.86,P=0.001),DFS 提高了 29%(HR=0.71,95%CI:0.56-0.91,P=0.006),CRR 提高了 50%(RR=1.50,95%CI:1.09-2.04;P=0.012),ORR 提高了 35%(RR=1.35,95%CI:1.04-1.73;P=0.022)。安全性方面,尼莫单抗联合 RT 或 CRT 并未增加所有等级不良事件的发生率(汇总 RD=-1.27,95%CI:-2.78-0.23,P=0.099)。

结论

本荟萃分析表明,尼莫单抗联合 RT 或 CRT 可带来生存获益,并提高缓解率。其安全性可控。

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