HIGHLIGHTS
- What: The authors focused on the clinical characterization and outcomes of with rare molecular alterations: EGFR exon 20 insertion non-activating EGFR mutations BRAF V600E and non-V600 ROS1 and RET rearrangements MET ErbB2 and FGFR mutations. The authors focus on the rarest molecular subpopulations among the mandatory ten, describing their clinical features and outcomes according to the therapies approved in Italy for each subtype following the initial diagnosis. The authors describe the patients the rarest moThe data fro . the whole oncogene-addicted population of the with NEROnE study, a lecular, driver alterationsdata among the pivotal analysed . . .

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