The primary objective of this study is to compare DFS in patients with completely resected (R0), stage I or IIA non-squamous NSCLC who are found to be at High or Intermediate Risk by the 14-Gene Prognostic Assay and who are subsequently either randomized to observation or randomized to and are willing to initiate adjuvant therapy with four cycles of a standard NSCLC platinum-based doublet (i.e., mITT population), so as to document the benefit of personalizing patient care based on molecular prognostic data.
