Genomic characterization of NSCLC harboring oncogenic / likely oncogenic MET TKD mutations in cohort #1 and #2. Genomic characteristics of 44 NSCLC cases harboring oncogenic / likely oncogenic MET TKD mutations from cohort #1: (A) concurrent driver alterations and (B) concurrent MET amplification status (information unavailable for 4 cases). Genomic characteristics of 129 NSCLC cases harboring oncogenic / likely oncogenic MET TKD mutations from cohort #2: (C) concurrent driver alterations and (D) concurrent MET amplification status.
No takes yet. Share an insight, caveat, or question.
Pecci et al. (2024) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: