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Comparative Efficacy of Adagrasib and Sotorasib in KRAS G12C-Mutant NSCLC: Insights from Pivotal Trials

Overview
Journal Cancers (Basel)
Publisher MDPI
Specialty Oncology
Date 2024 Nov 9
PMID 39518114
Authors
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Abstract

: The KRAS G12C mutation, prevalent in various malignancies, including non-small cell lung cancer (NSCLC), represents a unique therapeutic target. Adagrasib and sotorasib, two FDA-approved agents specifically targeting this mutation, have shown promise in clinical trials. This study aims to compare their efficacy in treating KRAS G12C-mutated NSCLC, drawing insights from pivotal clinical trials. : We analyzed data from three key clinical trials: KRYSTAL-1, CodeBreak100, and CodeBreak200. Our methodology involved reconstructing individual patient data from published Kaplan-Meier curves using the IPDfromKM tool (Version 0.1.10). The primary endpoints were progression-free survival (PFS) and overall survival (OS), evaluated through hazard ratios (HRs) and the restricted mean survival time (RMST) method. : The HR for PFS favored adagrasib (HR: 0.90 [95% CI: 0.69, 1.19], = 0.473), suggesting a non-significant trend toward better disease control compared to sotorasib. For OS, the HR was 0.99 [95% CI: 0.75, 1.33] ( = 0.969), indicating no significant difference between the two drugs. RMST analysis supported these findings, with adagrasib showing a consistently higher RMST in PFS at 6, 12, and 18 months. However, OS benefits converged over time, with adagrasib marginally surpassing sotorasib by the 18-month mark. : This comprehensive analysis reveals that while adagrasib may offer a slight advantage in PFS, both drugs demonstrate comparable efficacy in OS for KRAS G12C-mutated NSCLC. The subtle differences observed, particularly in PFS, could inform clinical decision-making, emphasizing the need for personalized treatment strategies. Future research should focus on long-term effects and identifying patient subgroups that may benefit more from one drug over the other.

Citing Articles

The Reconstructed Individual Patient Data from Kaplan-Meier (IPDfromKM) Method for Non-Inferiority Analyses: A New Potential Application.

Piragine E, Trippoli S, Veneziano S, Messori A, Calderone V Methods Protoc. 2025; 8(1).

PMID: 39997637 PMC: 11857869. DOI: 10.3390/mps8010013.

References
1.
Huang B . Some statistical considerations in the clinical development of cancer immunotherapies. Pharm Stat. 2017; 17(1):49-60. DOI: 10.1002/pst.1835. View

2.
Tsiouda T, Domvri K, Boutsikou E, Bikos V, Kyrka K, Papadaki K . Prognostic Value of KRAS Mutations in Relation to PDL1 Expression and Immunotherapy Treatment in Adenocarcinoma and Squamous Cell Carcinoma Patients: A Greek Cohort Study. J Pers Med. 2024; 14(5). PMC: 11121847. DOI: 10.3390/jpm14050457. View

3.
de Langen A, Johnson M, Mazieres J, Dingemans A, Mountzios G, Pless M . Sotorasib versus docetaxel for previously treated non-small-cell lung cancer with KRAS mutation: a randomised, open-label, phase 3 trial. Lancet. 2023; 401(10378):733-746. DOI: 10.1016/S0140-6736(23)00221-0. View

4.
Naei V, Monkman J, Sadeghirad H, Mehdi A, Blick T, Mullally W . Spatial proteomic profiling of tumor and stromal compartments in non-small-cell lung cancer identifies signatures associated with overall survival. Clin Transl Immunology. 2024; 13(7):e1522. PMC: 11257771. DOI: 10.1002/cti2.1522. View

5.
Liu N, Zhou Y, Lee J . IPDfromKM: reconstruct individual patient data from published Kaplan-Meier survival curves. BMC Med Res Methodol. 2021; 21(1):111. PMC: 8168323. DOI: 10.1186/s12874-021-01308-8. View