Landscape and Predictive Significance of the Structural Classification of Mutations in Chinese NSCLCs: A Real-World Study.

J Clin Med

Department of Shanghai Lung Cancer Center, Shanghai Chest Hospital, School of Medicine, Shanghai Jiao Tong University, 241 Huaihai West Road, Shanghai 200030, China.

Published: December 2022

AI Article Synopsis

  • Non-classical mutations in non-small cell lung cancer (NSCLC) lead to varied and reduced responses to EGFR tyrosine kinase inhibitors (TKIs), leaving patients with atypical mutations with few treatment options.
  • A study classified these mutations into four categories—classical-like, T790M-like, PACC, and Ex20ins-L—to better predict their response to TKI treatment using data from 837 tumor samples from Chinese NSCLC patients.
  • The findings indicated that patients with PACC mutations benefited more from second-generation TKIs compared to first-generation TKIs, highlighting the potential for structural classification to inform effective treatment choices.

Article Abstract

Non-classical mutations demonstrate heterogeneous and attenuated responsiveness to EGFR TKIs. Non-small cell lung cancer (NSCLC) patients with atypical mutations have limited therapeutic options. A recent study established a novel structural-based classification of mutations and showed its value in predicting the response to TKI. We sought to interrogate the distribution of different structural types and to validate the predictive value in Chinese NSCLCs. A total of 837 tumor samples were retrospectively recruited from 522 patients with unresectable -mutant NSCLC. mutations were classified into four groups: classical-like, T790M-like, Ex20ins-L, and PACC. Treatment information and clinical outcomes were obtained from 436 patients. The time to treatment failure (TTF) was determined on a per-sample basis. : Of the 837 -mutant samples, 67.9%, 18.5%, 9.0%, and 3.1% harbored classical-like, T790M-like, PACC, and Ex20ins-L mutations, respectively. Thirteen (1.6%) samples carried mutations beyond the four types. Among the 204 samples with atypical mutations, 33.8%, 36.7%, 12.7%, and 10.3% were classical-like, PACC, Ex20ins-L, and T790M-like, respectively. In patients with PACC mutations, second-generation TKIs demonstrated a significantly longer TTF than first-generation TKIs (first-line: 15.3 vs. 6.2 months, = 0.009; all-line: 14.7 vs. 7.1 months, = 0.003), and a trend of longer TTF than third-generation TKIs (all-line: 14.7 vs. 5.1 months, = 0.135). Our study depicted the landscape of structural types of mutations in Chinese NSCLC patients. Our results also suggest that the structural classification can serve as a predictive marker for the efficacy of various EGFR TKIs, which would guide therapeutic decision making.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9821726PMC
http://dx.doi.org/10.3390/jcm12010236DOI Listing

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