4.7 Article

Transcription Strikes Back: Clinical Utility of Lung Adenocarcinoma Subtypes

Journal

CLINICAL CANCER RESEARCH
Volume 27, Issue 4, Pages 913-915

Publisher

AMER ASSOC CANCER RESEARCH
DOI: 10.1158/1078-0432.CCR-20-3914

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Funding

  1. Cancer Prevention and Research Institute of Texas Individual Investigator Research Award [RP200287, P50-CA70907-21]
  2. Rexanna's Foundation for Fighting Lung Cancer

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Transcriptional profiling identified three robust subtypes of nonsquamous non-small cell lung cancer, regardless of initiating oncogenic driver events. Differential sensitivity to MEK 1/2 inhibitors was reported among the subtypes, and an interaction involving the mucinous subtype, STKII/LKBI genomic alterations, and inferior clinical outcomes with atezolizumab in the OAK clinical trial was identified.
Using transcriptional profiling, three robust subtypes of nonsquamous non-small cell lung cancer were defined, independently of initiating oncogenic driver events. Subtype-specific differential sensitivity to MEK 1/2 inhibitors was reported and an interaction between the mucinous subtype, STKII/LKBI genomic alterations, and inferior clinical outcomes with atezolizumab in the OAK clinical trial was identified.

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