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The use of intratumor heterogeneity and clonal evolution to predict clinical outcomes in patients with early-stage non–small-cell lung cancer (NSCLC) has had limited exploration in large prospective studies. To determine the prognostic value of these factors, investigators conducted a prospective, multicenter, cohort study (TRACERx) in which whole-exome sequencing was performed on 327 regions of 100 resected NSCLC tumors.
Results were as follows:
Extensive intratumor heterogeneity was present; a median 30% of somatic mutations were subclonal, and a median 48% of copy-number alterations were subclonal.
There was wide variation between tumors, with a range of 2 to 2310 subclonal mutations and a range of 0.06% to 81% tumor involvement by subclona…