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肾细胞癌中免疫检查点抑制剂与抗血管内皮生长因子联合治疗的风险效益比平衡:一项系统评价和荟萃分析

Balancing the Risk-Benefit Ratio of Immune Checkpoint Inhibitor and Anti-VEGF Combination Therapy in Renal Cell Carcinoma: A Systematic Review and Meta-Analysis.

作者信息

Tao Li, Zhang Huiyun, An Guangyu, Lan Haoning, Xu Yaoqi, Ge Yang, Yao Jiannan

机构信息

Beijing Chaoyang Hospital, Capital Medical University, Beijing, China.

Department of Oncology, Beijing Chaoyang Hospital, Capital Medical University, Beijing, China.

出版信息

Front Oncol. 2021 Oct 14;11:739263. doi: 10.3389/fonc.2021.739263. eCollection 2021.

Abstract

BACKGROUND

Although immune checkpoint inhibitors (ICIs) combined with vascular endothelial growth factor receptor (VEGFR)-targeted therapy and sunitinib monotherapy have been widely applied to metastatic renal cell carcinoma (mRCC), effectiveness and safety data are still lacking. To optimize clinical decision-making, we conducted a systematic review and meta-analysis of published randomized clinical trials to characterize the efficacy and the risk of adverse events (AEs) in patients treated with ICIs plus anti-VEGF therapy.

MATERIALS AND METHODS

We used PubMed, EMBASE, and the Cochrane Library to retrieve randomized controlled trials (RCTs) published before March 27, 2021. The efficacy outcomes were progression-free survival (PFS), overall survival (OS), and objective response rate (ORR). The pooled risk ratio (RR) and 95% confidence intervals (CI) of AEs were calculated in the safety analysis.

RESULTS

Six RCTs involving 4,227 patients were identified after a systematic search. For OS, ICI and anti-VEGF combination therapy decreased mortality approximately 30% in the intention-to-treat population (ITT) (hazard ratio (HR) = 0.70, 95% CI: 0.57-0.87), but there was no statistical difference in patients evaluated as "favorable" by the International Metastatic Renal-Cell Carcinoma Database Consortium (IMDC) criteria compared with monotherapy (HR = 0.90, 95% CI: 0.55-1.46,  = 0.66). In terms of PFS, the progression risk for all participants declined 35% (HR = 0.65, 95% CI: 0.50-0.83) and patients evaluated as "poor" by IMDC benefited further (HR = 0.46, 95% CI: 0.36-0.58). No evident divergence was found in age and sex subgroups. The RRs of all-grade hypertension, arthralgia, rash, proteinuria, high-grade (grades 3-5) arthralgia, and proteinuria developed after combination therapy were increased compared with sunitinib. The risk of high-grade hypertension and rash showed no statistical difference. However, the risk of hand-foot skin reaction (HFSR), stomatitis, and dysgeusia decreased in combination therapy groups.

CONCLUSIONS

Compared with sunitinib, OS, PFS, and ORR were significantly improved in patients receiving ICI and anti-VEGF combination therapy at the expense of increased specific AEs. More attention should be paid to individualized application of these combination therapies to achieve the best benefit-risk ratio in the clinic.

SYSTEMATIC REVIEW REGISTRATION

[https://inplasy.com/] INPLASY: 202130104.

摘要

背景

尽管免疫检查点抑制剂(ICIs)联合血管内皮生长因子受体(VEGFR)靶向治疗及舒尼替尼单药治疗已广泛应用于转移性肾细胞癌(mRCC),但有效性和安全性数据仍较为缺乏。为优化临床决策,我们对已发表的随机临床试验进行了系统评价和荟萃分析,以明确接受ICIs联合抗血管生成素(VEGF)治疗患者的疗效及不良事件(AE)风险。

材料与方法

我们使用PubMed、EMBASE和Cochrane图书馆检索2021年3月27日前发表的随机对照试验(RCT)。疗效指标为无进展生存期(PFS)、总生存期(OS)和客观缓解率(ORR)。安全性分析中计算AE的合并风险比(RR)及95%置信区间(CI)。

结果

系统检索后共纳入6项RCT,涉及4227例患者。对于OS,在意向性治疗人群(ITT)中,ICIs联合抗VEGF治疗使死亡率降低约30%(风险比(HR)=0.70,95%CI:0.57 - 0.87),但根据国际转移性肾细胞癌数据库联盟(IMDC)标准评估为“预后良好”的患者与单药治疗相比无统计学差异(HR = 0.90,95%CI:0.55 - 1.46,P = 0.66)。在PFS方面,所有参与者的疾病进展风险下降35%(HR = 0.65,95%CI:0.50 - 0.83),IMDC评估为“预后不良”的患者获益更大(HR = 0.46,95%CI:0.36 - 0.58)。年龄和性别亚组未发现明显差异。与舒尼替尼相比,联合治疗后所有级别的高血压、关节痛、皮疹、蛋白尿、3 - 5级关节痛和蛋白尿的RR均升高。3级及以上高血压和皮疹的风险无统计学差异。然而,联合治疗组手足皮肤反应(HFSR)、口腔炎和味觉障碍的风险降低。

结论

与舒尼替尼相比,接受ICIs联合抗VEGF治疗的患者OS、PFS和ORR显著改善,但代价是特定AE增加。临床中应更加关注这些联合治疗的个体化应用,以实现最佳的效益风险比。

系统评价注册

[https://inplasy.com/] INPLASY:202130104 。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a5f/8552014/90702269a649/fonc-11-739263-g001.jpg

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