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要与不要:抗血管生成药物联合免疫检查点抑制剂是否在晚期或转移性肾细胞癌的治疗中必要。

To be or not to be: whether anti-angiogenic agent combined with immune checkpoint inhibitoris necessary in the treatment of advanced or metastatic renal cell carcinoma.

机构信息

The First Clinical Medical College of Zhejiang, Chinese Medical University, Hangzhou, 310053, Zhejiang, China.

Department of Medical Oncology, The First Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou, 310006, Zhejiang, China.

出版信息

Med Oncol. 2020 Feb 1;37(2):15. doi: 10.1007/s12032-020-1340-7.

Abstract

Although it's widely known that targeted therapy against angiogenesis and immunotherapy agents showed survival benefit over chemoradiotherapy in advanced or metastatic renal cell carcinoma, some patients still cannot receive a satisfied prognosis. We performed a systematic review and meta-analysis to explore the efficacy and safety of anti-angiogenic agents combined with immune checkpoint inhibitors. We conducted a search for randomized controlled trials in Pubmed, Embase, Cochrane, and major conference. Enrolled eligible studies and extracted data were completed by two investigators to compare OS, PFS, and ORR both in PD-L1 and ITT subset. Then, we calculated the pooled RR and 95% CI of all-grade and high-grade adverse effects to study its safety. Besides, we assessed the heterogeneity through subgroup and sensitivity analysis. A total of three RCTs covering 2662 patients were enrolled. In PFS analysis, the estimated HR for ITT subset was 0.74 with 95% CI of 0.65 to 0.84 and for PD-L1 subset was 0.65 with 95% CI of 0.56 to 0.76. And in OS analysis, the result was 0.74 with 95% CI of 0.53 to 1.03 in ITT subset and 0.74 with 95% CI of 0.56 to 0.96 in PD-L1 subset. As for ORR analysis, combination therapy showed advantage rather than monotherapy in ITT subset (RR 1.54; 95% CI 1.11 to 2.14), but conversely in PD-L1 positive subset (RR 1.64; 95% CI 0.94 to 2.84). Additionally, combination therapy failed to show obvious safety in most immune-related adverse events, whatever in all-grade or high grade.

摘要

虽然靶向血管生成和免疫治疗药物在晚期或转移性肾细胞癌中的疗效优于化疗和放疗已广为人知,但仍有部分患者无法获得满意的预后。我们进行了一项系统评价和荟萃分析,以探讨抗血管生成药物联合免疫检查点抑制剂的疗效和安全性。我们在 Pubmed、Embase、Cochrane 和主要会议上进行了随机对照试验的检索。由两名研究者完成了合格研究的纳入和数据提取,以比较 PD-L1 和 ITT 亚组的 OS、PFS 和 ORR。然后,我们计算了所有级别和高级别不良事件的汇总 RR 和 95%CI,以研究其安全性。此外,我们还通过亚组和敏感性分析评估了异质性。共纳入三项 RCT,涵盖 2662 名患者。在 PFS 分析中,ITT 亚组的估计 HR 为 0.74,95%CI 为 0.65 至 0.84,PD-L1 亚组为 0.65,95%CI 为 0.56 至 0.76。在 OS 分析中,ITT 亚组的结果为 0.74,95%CI 为 0.53 至 1.03,PD-L1 亚组为 0.74,95%CI 为 0.56 至 0.96。对于 ORR 分析,与单药治疗相比,联合治疗在 ITT 亚组中显示出优势(RR 1.54;95%CI 1.11 至 2.14),但在 PD-L1 阳性亚组中则相反(RR 1.64;95%CI 0.94 至 2.84)。此外,联合治疗在大多数免疫相关不良事件中并未显示出明显的安全性,无论是在所有级别还是高级别。

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