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Treatment patterns and outcomes in KRAS G12C -positive advanced NSCLC patients previously treated with immune checkpoint inhibitors: A Canada-wide real-world, multi-center, retrospective cohort study.

Authors :
Barghout SH
Zhan LJ
Raptis S
Al-Agha F
Esfahanian N
Popovacki A
Kasymjanova G
Proulx-Rocray F
Chan SWS
Richardson M
Brown MC
Patel D
Dean ML
Navani V
Moore E
Carvery L
Yan E
Goldshtein D
Cleary-Gosine J
Gibson AJ
Hubley L
Balaratnam K
Ngo T
Gill A
Black M
Sacher A
Bradbury PA
Shepherd FA
Leighl N
Cheema P
Kuruvilla S
Agulnik J
Banerji S
Juergens R
Blais N
Cheung W
Wheatley-Price P
Liu G
Snow S
Source :
Lung cancer (Amsterdam, Netherlands) [Lung Cancer] 2024 Aug; Vol. 194, pp. 107898. Date of Electronic Publication: 2024 Jul 25.
Publication Year :
2024

Abstract

Objectives: KRAS mutations, particularly KRAS <superscript>G12C</superscript> , are prevalent in non-small cell lung cancer (NSCLC). Immune checkpoint inhibitors (ICIs) have been a frontline treatment, but recently developed KRAS <superscript>G12C</superscript> -selective inhibitors, such as sotorasib, present new therapeutic options. We conducted a multi-center retrospective cohort study to gain insights into real-world treatment patterns and outcomes in patients with KRAS <superscript>G12C</superscript> -positive advanced NSCLC receiving systemic therapy post-ICI treatment.<br />Methods: From the CAnadian CAncers With Rare Molecular Alterations-Basket Real-world Observational Study (CARMA-BROS), a cohort of 102 patients with KRAS <superscript>G12C</superscript> -positive advanced NSCLC across 9 Canadian centers diagnosed between 2015 and 2021 was analyzed. Clinico-demographic and treatment data were obtained from electronic health records. Survival outcomes were assessed using Kaplan-Meier curves and Cox proportional hazards models.<br />Results: The patients (median age 66 years; 58 % female; 99 % current/former tobacco exposure; 59 % PD-L1 ≥ 50 %), exhibited heterogeneous treatment patterns post-ICI. Most patients received ICIs as a first-line therapy, with varying subsequent lines including chemotherapy and targeted therapy. In patients receiving systemic therapy post-ICI, median overall survival was 12.6 months, and real-world progression-free survival was 4.7 months. KRAS <superscript>G12C</superscript> -selective targeted therapy post-ICI (n = 20) showed longer real-world progression-free survival compared to single-agent chemotherapy (aHR = 0.39, p = 0.012).<br />Conclusion: This study contributes valuable real-world data on KRAS <superscript>G12C</superscript> -positive advanced NSCLC post-ICI treatment. The absence of a standard treatment sequencing post-ICI underscores the need for further investigation and consensus-building in the evolving landscape of KRAS <superscript>G12C</superscript> -targeted therapies.<br />Competing Interests: Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: The study was supported by Amgen. The authors have no other conflicts of interest to declare.<br /> (Copyright © 2024 Elsevier B.V. All rights reserved.)

Details

Language :
English
ISSN :
1872-8332
Volume :
194
Database :
MEDLINE
Journal :
Lung cancer (Amsterdam, Netherlands)
Publication Type :
Academic Journal
Accession number :
39074423
Full Text :
https://doi.org/10.1016/j.lungcan.2024.107898