Lifileucel, an Autologous Tumor-infiltrating Lymphocyte Monotherapy, in Patients with Advanced Non-small Cell Lung Cancer Resistant to Immune Checkpoint Inhibitors

医学 肺癌 淋巴细胞 免疫系统 癌症研究 癌症 免疫检查点 肿瘤科 免疫学 免疫疗法 内科学
作者
Adam J. Schoenfeld,Sylvia M. Lee,Bernard Doger de Spéville,Scott Gettinger,Simon Häfliger,Ammar Sukari,Sophie Papa,Juan F. Rodríguez-Moreno,Friedrich Graf Finckenstein,Rana Fiaz,Melissa Catlett,Guang Chen,Rongsu Qi,Emma L. Masteller,Viktoria Gontcharova,Kai He
出处
期刊:Cancer Discovery [American Association for Cancer Research]
卷期号:14 (8): 1389-1402 被引量:32
标识
DOI:10.1158/2159-8290.cd-23-1334
摘要

Abstract 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
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