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

Authors :
Schoenfeld AJ
Lee SM
Doger de Spéville B
Gettinger SN
Häfliger S
Sukari A
Papa S
Rodríguez-Moreno JF
Graf Finckenstein F
Fiaz R
Catlett M
Chen G
Qi R
Masteller EL
Gontcharova V
He K
Source :
Cancer discovery [Cancer Discov] 2024 Aug 02; Vol. 14 (8), pp. 1389-1402.
Publication Year :
2024

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.<br /> (©2024 The Authors; Published by the American Association for Cancer Research.)

Details

Language :
English
ISSN :
2159-8290
Volume :
14
Issue :
8
Database :
MEDLINE
Journal :
Cancer discovery
Publication Type :
Academic Journal
Accession number :
38563600
Full Text :
https://doi.org/10.1158/2159-8290.CD-23-1334