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Pembrolizumab 联合高剂量 IL-2 治疗晚期透明细胞肾细胞癌:一项 2 期试验的六年生存结局与分子特征

英文原题:Pembrolizumab plus high-dose IL-2 in advanced clear cell renal cell carcinoma: six-year survival outcomes and molecular signatures from a phase 2 trial.

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Pembrolizumab plus high-dose IL-2 in advanced clear cell renal cell carcinoma: six-year survival outcomes and molecular signatures from a phase 2 trial.

PubMed 2026/05/25(内容时间) Nat Commun Q1 · IF 18.1(JCR 2025)

研究概要

该研究达到了其主要终点,ORR超过预先设定的45%阈值。

中文摘要

晚期透明细胞肾细胞癌(ccRCC)的标准治疗仍为长期或无限期全身治疗,常导致累积毒性和治疗负担。我们开展了一项固定疗程抗PD1帕博利珠单抗联合高剂量白细胞介素-2治疗初治晚期ccRCC的单臂2期试验(ClinicalTrials.gov标识符:NCT02964078)。安全性和缓解的主要目标此前已报告。该研究达到主要终点,总缓解率超过预设的45%阈值。在此我们报告长期随访(中位随访76.4个月)结果,包括总缓解、无进展生存、无治疗间期以及相关性分析。在26例接受治疗的患者中,客观缓解率为73%,其中42%的患者达到完全缓解。中位总生存期>84个月,5年限制性平均生存时间为48.6个月。中位无进展生存期为19.3个月,中位无治疗间期为23.8个月。42%的患者在5年时间点仍无需治疗。未发生5级不良事件,且无持续疾病控制的患者出现持续性≥2级毒性。相关性分析确定了与持久获益相关的探索性免疫模式,包括CD16⁺NK 细胞富集、PD-1⁺T细胞频率抑制,以及趋化因子、补体和PKC/TGF-β通路的协同激活。

展开英文摘要原文

Prolonged or indefinite systemic therapy remains standard for advanced clear cell renal cell carcinoma (ccRCC), often resulting in cumulative toxicities and treatment burden. We conducted a single-arm phase 2 trial (ClinicalTrials.gov identifier: NCT02964078) of a fixed-duration regimen of anti-PD1 pembrolizumab plus high-dose interleukin-2 in treatment-naive advanced ccRCC. Primary objectives of safety and response were previously reported. The study met its primary endpoint with an overall response rate exceeding the pre-specified threshold of 45%. Here we report long-term follow-up (median follow-up of 76.4 months) including overall response, progression-free survival, treatment-free interval, and correlative analysis. Among 26 patients treated, the objective response rate was 73%, with complete responses in 42% of patients. Median overall survival was >84 months with a 5-year restricted mean survival time of 48.6 months. Median progression-free survival was 19.3 months, and median treatment-free interval was 23.8 months. 42% of patients remained treatment-free at the 5-year timepoint. No grade 5 adverse events occurred, and no patients with durable disease control experienced persistent grade ≥2 toxicities. Correlative analyses identified exploratory immune patterns associated with durable benefit, including enrichment of CD16⁺ natural killer cells, suppression of PD-1⁺ T-cell frequencies, and coordinated chemokine, complement, and PKC/TGF-β pathway activation.

论文信息

作者
Johnson JS、Miller JW、Hatoum F、Schell MJ、Yu X、Roman Souza G、Mizelle S、Gullapalli K
第一作者单位
Department of Genitourinary Oncology, H. Lee Moffitt Cancer Center, Tampa, FL, USA.United States
通讯作者单位
Department of Genitourinary Oncology, Orlando Health Cancer Institute, Orlando, FL, USA. Jad.Chahoud@orlandohealth.com.United States
文献类型
II 期临床试验
期刊
Nature communications2026 May 25
原文标识
PubMed 42185255 · DOI 10.1038/s41467-026-73336-1