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PD1/PDL1 抑制剂联合放疗和抗血管生成治疗实体瘤的疗效和安全性:系统评价和荟萃分析。

Efficacy and safety of PD1/PDL1 inhibitors combined with radiotherapy and anti-angiogenic therapy for solid tumors: A systematic review and meta-analysis.

机构信息

Department of Oncology, Nanchong Central Hospital, The Second Clinical Institute of North Sichuan Medical College, Nanchong, China.

School of Medicine, University of Electronic Science and Technology of China, Chengdu, China.

出版信息

Medicine (Baltimore). 2023 Mar 10;102(10):e33204. doi: 10.1097/MD.0000000000033204.

Abstract

BACKGROUND

The triple combination of programmed cell death 1 (PD1)/programmed cell death ligand 1 (PDL1) inhibitors, radiotherapy (RT), and anti-angiogenesis agents has been widely used in the treatment of solid tumors and has shown positive efficacy. We conducted a meta-analysis to evaluate the efficacy and safety of PD1/PDL1 inhibitors combined with anti-angiogenic agents and RT for the treatment of solid cancers.

METHODS

A systematic search of PubMed, Embase, Cochrane Library, and Web of Science databases was conducted from inception to October 31, 2022. Studies involving patients with solid cancers who received PD1/PDL1 inhibitors combined with RT and anti-angiogenic agents treatment that reported overall response rate, complete remission rate, disease control rate, and adverse events (AEs) were included. A random-effects or fixed-effects model was used for the pooled rates, and 95% confidence intervals (CIs) were determined for all outcomes. The quality of the included literature was assessed using the methodological index for nonrandomized studies critical appraisal checklist. Egger test was used to assess the publication bias in the included studies.

RESULTS

Ten studies (4 nonrandomized controlled trials and 6 single-arm trials), including 365 patients, were identified and included in the meta-analysis. The pooled overall response rate after treatment with PD1/PDL1 inhibitors combined with RT and anti-angiogenic agents was 59% (95% CI: 48-70%), whereas the disease control rate and complete remission rate were 92% (95% CI: 81-103%) and 48% (95% CI: 35-61%), respectively. Moreover, the meta-analysis showed that compared with triple-regimen, monotherapy or dual-combination treatment did not improve overall survival (hazard ratio = 0.499, 95% CI: 0.399-0.734) and progression-free survival (hazard ratio = 0.522, 95% CI: 0.352-0.774). The pooled rate of grade 3 to 4 AEs was 26.9% (95% CI: 7.8%-45.9), and the common AEs to triple therapy included leukopenia (25%), thrombocytopenia (23.8%), fatigue (23.2%), gastrointestinal discomfort (22%), increased alanine aminotransferase (22%), and neutropenia (21.4%).

CONCLUSION

In the treatment of solid tumors, PD1/PDL1 inhibitors combined with RT and anti-angiogenic drugs achieved a positive response and better survival benefits than monotherapy or dual therapy. In addition, combination therapy is tolerable and safe.

REGISTRATION

PROSPERO ID: CRD42022371433.

摘要

背景

程序性细胞死亡蛋白 1(PD-1)/程序性细胞死亡配体 1(PD-L1)抑制剂、放疗(RT)和抗血管生成药物的三联疗法已广泛应用于实体瘤的治疗,并显示出积极的疗效。我们进行了一项荟萃分析,以评估 PD-1/PD-L1 抑制剂联合抗血管生成药物和 RT 治疗实体癌的疗效和安全性。

方法

系统检索 PubMed、Embase、Cochrane 图书馆和 Web of Science 数据库,检索时间从建库至 2022 年 10 月 31 日。纳入接受 PD-1/PD-L1 抑制剂联合 RT 和抗血管生成药物治疗且报告总缓解率、完全缓解率、疾病控制率和不良反应(AE)的实体癌患者的研究。采用随机效应或固定效应模型对汇总率进行合并,所有结局的 95%置信区间(CI)均采用。使用非随机研究方法学指数评估纳入文献的质量评估检查表。采用 Egger 检验评估纳入研究的发表偏倚。

结果

共纳入 10 项研究(4 项非随机对照试验和 6 项单臂试验),包括 365 例患者,纳入荟萃分析。PD-1/PD-L1 抑制剂联合 RT 和抗血管生成药物治疗后的总缓解率为 59%(95%CI:48-70%),疾病控制率和完全缓解率分别为 92%(95%CI:81-103%)和 48%(95%CI:35-61%)。此外,荟萃分析显示,与三联疗法相比,单药或双联疗法并未改善总生存期(风险比=0.499,95%CI:0.399-0.734)和无进展生存期(风险比=0.522,95%CI:0.352-0.774)。3 级和 4 级 AE 的汇总发生率为 26.9%(95%CI:7.8%-45.9%),三联治疗的常见 AE 包括白细胞减少症(25%)、血小板减少症(23.8%)、疲劳(23.2%)、胃肠道不适(22%)、丙氨酸氨基转移酶升高(22%)和中性粒细胞减少症(21.4%)。

结论

在实体瘤治疗中,PD-1/PD-L1 抑制剂联合 RT 和抗血管生成药物比单药或双药治疗具有更积极的反应和更好的生存获益。此外,联合治疗是可耐受且安全的。

登记

PROSPERO 注册号:CRD42022371433。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/781c/9997836/cb1906a7f999/medi-102-e33204-g001.jpg

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