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当前免疫肿瘤学时代晚期皮肤黑色素瘤中 TIL 疗法的疗效:更新的系统评价和荟萃分析。

Efficacy of TIL therapy in advanced cutaneous melanoma in the current immuno-oncology era: updated systematic review and meta-analysis.

机构信息

Department of Medical Oncology, Vall d'Hebron University Hospital, Barcelona; Departamento de Ciencias Médicas Básicas, Facultad de Medicina, Universidad San Pablo-CEU, CEU Universities, Madrid, Spain.

Department of Oncology, National Center for Cancer Immune Therapy (CCIT-DK), Copenhagen University Hospital, Herlev, Denmark.

出版信息

Ann Oncol. 2024 Oct;35(10):860-872. doi: 10.1016/j.annonc.2024.07.723. Epub 2024 Jul 23.

Abstract

BACKGROUND

Adoptive cell therapy with tumor-infiltrating lymphocytes (TIL-ACT) has consistently shown efficacy in advanced melanoma. New results in the field provide now the opportunity to assess overall survival (OS) after TIL-ACT and to examine the effect of prior anti-programmed cell death protein 1/programmed death-ligand 1 [anti-PD-(L)1] therapy on its efficacy.

METHODS

A comprehensive search was conducted in PubMed up to 29 February 2024. Ιn this meta-analysis we focused on studies including high-dose interleukin 2, doubling the patient numbers from our previous meta-analysis conducted up to December 2018 and using OS as the primary endpoint. Objective response rate (ORR), complete response rate (CRR), and duration of response were secondary endpoints. Findings are synthesized using tables, Kaplan-Meier plots, and forest plots. Pooled estimates for ORR and CRR were derived from fixed or random effects models.

RESULTS

A total of 13 high-dose interleukin 2 studies were included in this updated meta-analysis, with OS information available for 617 patients. No difference was found in median OS between studies with prior anti-PD-(L)1 treatment {n = 238; 17.5 months [95% confidence interval (CI) 13.8-20.5 months]} and without [n = 379; 16.3 months (95% CI 14.2-20.6 months)] (log-rank P = 0.53). ORR was estimated to be 34% (95% CI 16%-52%) and 44% (95% CI 37%-51%), for the studies with and without prior anti-PD-(L)1, respectively. The pooled estimate for CRR was 10% for both groups. No statistically significant difference was observed between the two groups, either for ORR (P = 0.15) or CRR (P = 0.45).

CONCLUSIONS

Prior anti-PD-(L)1 treatment has no effect on the clinical response or survival benefit from TIL-ACT in advanced cutaneous melanoma. The benefit of TIL therapy in the second-line setting is also present after anti-PD-(L)1 treatment. Our data reinforce the evidence that TIL-ACT should be considered as a treatment of choice in second line for metastatic melanoma patients failing anti-PD-(L)1 therapy.

摘要

背景

肿瘤浸润淋巴细胞(TIL-ACT)过继细胞疗法在晚期黑色素瘤中始终显示出疗效。该领域的新成果现在提供了评估 TIL-ACT 后总生存期(OS)的机会,并检查了先前抗程序性细胞死亡蛋白 1/程序性死亡配体 1 [抗 PD-(L)1]治疗对其疗效的影响。

方法

在 PubMed 上进行了全面搜索,截至 2024 年 2 月 29 日。在这项荟萃分析中,我们专注于包括高剂量白细胞介素 2在内的研究,将我们之前截至 2018 年 12 月进行的荟萃分析的患者数量增加一倍,并将 OS 作为主要终点。客观缓解率(ORR)、完全缓解率(CRR)和缓解持续时间是次要终点。使用表格、Kaplan-Meier 图和森林图综合发现。ORR 和 CRR 的汇总估计值来自固定或随机效应模型。

结果

这项更新的荟萃分析共纳入了 13 项高剂量白细胞介素 2 研究,其中 617 名患者可提供 OS 信息。在先前接受抗 PD-(L)1 治疗的研究(n=238;中位 OS 17.5 个月[95%置信区间 (CI) 13.8-20.5 个月])和未接受治疗的研究之间(n=379;中位 OS 16.3 个月[95% CI 14.2-20.6 个月]),中位 OS 无差异(对数秩 P=0.53)。有和没有先前抗 PD-(L)1 治疗的研究中,ORR 分别估计为 34%(95% CI 16%-52%)和 44%(95% CI 37%-51%)。两组的 CRR 汇总估计值均为 10%。两组之间在 ORR(P=0.15)或 CRR(P=0.45)方面均未观察到统计学显著差异。

结论

先前的抗 PD-(L)1 治疗对晚期皮肤黑色素瘤中 TIL-ACT 的临床反应或生存获益没有影响。在二线治疗中,TIL 治疗的获益在接受抗 PD-(L)1 治疗后也存在。我们的数据加强了证据,即 TIL-ACT 应该被认为是抗 PD-(L)1 治疗失败的转移性黑色素瘤患者二线治疗的首选治疗方法。

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