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Lifileucel,一种自体 TIL(肿瘤浸润淋巴细胞)单药治疗,用于对免疫检查点抑制剂耐药的晚期非小细胞肺癌患者

英文原题:Lifileucel, an Autologous Tumor-Infiltrating Lymphocyte Monotherapy, in Patients with Advanced Non-Small Cell Lung Cancer Resistant to Immune Checkpoint Inhibitors.

PubMed 2024/08/02(内容时间) Cancer Discov Q1 · IF 29.5(JCR 2025)

研究概要

客观缓解率为21.4%(6/28)。

中文摘要

在这项2期多中心研究中,我们评估了lifileucel(LN-145)——一种自体TIL(肿瘤浸润淋巴细胞)细胞疗法——在既往接受过免疫治疗且最近一次治疗进展的转移性非小细胞肺癌(mNSCLC)患者中的疗效和安全性。既往全身治疗的中位数为2线(范围,1-6)。Lifileucel使用来自不同解剖部位(主要为肺)的肿瘤组织成功制备。客观缓解率为21.4%(6/28)。缓解出现在通常对免疫治疗耐药的肿瘤特征中,如PD-L1阴性、低肿瘤突变负荷和STK11突变。截至数据截止时,有两例缓解仍在持续,包括一例PD-L1阴性肿瘤中的完全代谢缓解。不良事件总体符合预期且可管理。两例患者死于治疗中出现的不良事件:心力衰竭和多器官衰竭。Lifileucel是既往治疗难治的mNSCLC患者的一种潜在治疗选择。意义:自体TIL(肿瘤浸润淋巴细胞)疗法lifileucel被用于28例经重度预治疗的转移性非小细胞肺癌(mNSCLC)患者。在具有驱动突变以及不同肿瘤突变负荷和PD-L1表达的患者中观察到了缓解,可能满足既往治疗难治的mNSCLC患者中未被满足的医疗需求。参见Lotze等人的相关评论,第1366页。

展开英文摘要原文

In this phase 2 multicenter study, we evaluated the efficacy and safety of lifileucel (LN-145), an autologous tumor-infiltrating lymphocyte cell therapy, in patients with metastatic non-small cell lung cancer (mNSCLC) who had received prior immunotherapy and progressed on their most recent therapy. The median number of prior systemic therapies was 2 (range, 1-6). Lifileucel was successfully manufactured using tumor tissue from different anatomic sites, predominantly lung. The objective response rate was 21.4% (6/28). Responses occurred in tumors with profiles typically resistant to immunotherapy, such as PD-L1-negative, low tumor mutational burden, and STK11 mutation. Two responses were ongoing at the time of data cutoff, including one complete metabolic response in a PD-L1-negative tumor. Adverse events were generally as expected and manageable. Two patients died of treatment-emergent adverse events: cardiac failure and multiple organ failure. Lifileucel is a potential treatment option for patients with mNSCLC refractory to prior therapy. Significance: Autologous tumor-infiltrating lymphocyte therapy lifileucel was administered to 28 patients with heavily pretreated metastatic non-small cell lung cancer (mNSCLC). Responses were observed in patients with driver mutations, and various tumor mutational burdens and PD-L1 expression, potentially addressing an unmet medical need in patients with mNSCLC refractory to prior therapy. See related commentary by Lotze et al., p. 1366.

论文信息

作者
Schoenfeld AJ、Lee SM、Doger de Spéville B、Gettinger SN、Häfliger S、Sukari A、Papa S、Rodríguez-Moreno JF
第一作者单位
Division of Solid Tumor Oncology, Department of Medicine, Thoracic Oncology Service, Memorial Sloan Kettering Cancer Center, New York, New York.United States
通讯作者单位
Division of Medical Oncology, Department of Internal Medicine, Thoracic Oncology Program, Ohio State University, Columbus, Ohio.United States
文献类型
II 期临床试验 · 多中心研究
期刊
Cancer discovery2024 Aug 2
原文标识
PubMed 38563600 · DOI 10.1158/2159-8290.CD-23-1334