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帕博利珠单抗治疗晚期肾细胞癌的 Meta 分析:提供 1a 级证据。

Pembrolizumab in advanced renal cell carcinoma: a meta-analysis providing level 1a evidence.

机构信息

Division of Experimental Oncology/Unit of Urology, URI, Urological Research Institute, IRCCS San Raffaele Scientific Institute, Milan, Italy.

Division of Experimental Oncology/Unit of Urology, URI, Urological Research Institute, IRCCS San Raffaele Scientific Institute, Milan, Italy.

出版信息

Curr Probl Cancer. 2022 Aug;46(4):100875. doi: 10.1016/j.currproblcancer.2022.100875. Epub 2022 Jun 1.

Abstract

The recent introduction of immunotherapy in the first line setting of advanced renal cell carcinoma (aRCC) has dramatically improved patients' prognosis. The aim of the current meta-analysis was to provide level 1a evidence supporting the use of pembrolizumab plus tyrosine kinase inhibitors (TKI) as first-line treatment for advanced RCC. All published randomized prospective trials including patients with advanced RCC treated with pembrolizumab in combination with TKIs vs Sunitinib were included in this meta-analysis. An algorithm was used to reconstruct survival data from the published Kaplan-Meier curves of overall survival (OS), progression free survival (PFS) and duration of response (DoR) from the included trials. Restricted mean survival time (RMST) with 95% confidence interval (CI) for comparison among the different regimens was calculated. Main outcomes were differences in RMST for OS, PFS and DoR for pembrolizumab plus TKIs vs sunitinib arm. Reconstructed survival data from 1,573 patients were retrieved from 2 trials (KEYNOTE-581 and KEYNOTE-426) comparing pembrolizumab plus TKI (lenvatinib or axitinib, respectively) to sunitinib. Patients who received pembrolizumab-lenvatinib or pembrolizumab-axinitinib had better OS (24-month ΔRMST of 1.79 months [95% CI: 0.12-2.50; P < 0.001]), PFS (24-month ΔRMST of 3.83 months [95% CI: 2.93-4.74; P < 0.001]) and DoR (24-month ΔRMST of 2.32 months [95% CI: 0.97-3.67; P < 0.001]) relative to sunitinib. Pembrolizumab-lenvatinib combination gave a marginal benefit in terms of OS, PFS and DoR relative to pembrolizumab-axitinib group. By relying on individual survival data, we provided a level-1a evidence supporting the use of pembrolizumab plus TKI for first-line aRCC treatment.

摘要

免疫疗法在晚期肾细胞癌(aRCC)一线治疗中的应用最近有了显著的进展,极大地改善了患者的预后。本荟萃分析的目的是提供 1a 级证据,支持使用派姆单抗联合酪氨酸激酶抑制剂(TKI)作为晚期 RCC 的一线治疗。本荟萃分析纳入了所有发表的随机前瞻性试验,包括接受派姆单抗联合 TKI 治疗的晚期 RCC 患者与舒尼替尼治疗的患者。使用算法从纳入试验的发表的总生存(OS)、无进展生存(PFS)和缓解持续时间(DoR)的 Kaplan-Meier 曲线中重建生存数据。计算不同方案之间 OS、PFS 和 DoR 的受限平均生存时间(RMST)及其 95%置信区间(CI)。主要结局是派姆单抗联合 TKI 与舒尼替尼组之间 OS、PFS 和 DoR 的 RMST 差异。从 2 项试验(KEYNOTE-581 和 KEYNOTE-426)中检索到 1573 例患者的重建生存数据,这些患者分别接受派姆单抗联合 TKI(仑伐替尼或阿昔替尼)与舒尼替尼治疗。接受派姆单抗-仑伐替尼或派姆单抗-阿昔替尼治疗的患者 OS 更好(24 个月 RMST 差值为 1.79 个月[95%CI:0.12-2.50;P < 0.001]),PFS 更好(24 个月 RMST 差值为 3.83 个月[95%CI:2.93-4.74;P < 0.001]),DoR 更好(24 个月 RMST 差值为 2.32 个月[95%CI:0.97-3.67;P < 0.001]),与舒尼替尼相比。派姆单抗-仑伐替尼联合治疗在 OS、PFS 和 DoR 方面相对于派姆单抗-阿昔替尼组略有优势。通过依赖于个体生存数据,我们提供了 1a 级证据,支持使用派姆单抗联合 TKI 作为晚期 RCC 的一线治疗。

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