Lifileucel, an autologous tumor-infiltrating lymphocyte monotherapy, in patients with advanced non-small cell lung cancer resistant to immune checkpoint inhibitors Journal Article


Authors: Schoenfeld, A. J.; Lee, S. M.; de Spéville, B. D.; Gettinger, S. N.; Häfliger, S.; Sukari, A.; Papa, S.; Rodríguez-Moreno, J. F.; Finckenstein, F. G.; Fiaz, R.; Catlett, M.; Chen, G.; Qi, R.; Masteller, E. L.; Gontcharova, V.; He, K.
Article Title: Lifileucel, an autologous tumor-infiltrating lymphocyte monotherapy, in patients with advanced non-small cell lung cancer resistant to immune checkpoint inhibitors
Abstract: In this phase 2 trial, the tumor-infiltrating lymphocyte therapy lifileucel showed potential as a one-time treatment option for patients with metastatic non-small cell lung cancer who progressed after prior immunotherapy. 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
Keywords: adoptive transfer; therapy; interleukin-2; knockout; pd-1; metastatic melanoma; responses; naive; persistence; til
Journal Title: Cancer Discovery
Volume: 14
Issue: 8
ISSN: 2159-8274
Publisher: American Association for Cancer Research  
Date Published: 2024-08-01
Start Page: 1389
End Page: 1402
Language: English
ACCESSION: WOS:001283297200009
DOI: 10.1158/2159-8290.Cd-23-1334
PROVIDER: wos
PMCID: PMC11294887
PUBMED: 38563600
Notes: The MSK Cancer Center Support Grant (P30 CA008748) is acknowledge in the PDF -- Source: Wos
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