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Should men with DNA break repair mutations (BRCA1, BRCA2, ATM, etc) found on a genetic test, but who otherwise have low-risk disease, be considered for surveillance? What is the data?
1. Who should get routine molecular testing at the time of diagnosis of NSCLC and what genes should be included in the molecular panel?
2. What is the proper timing of testing and sequencing of available therapies?
3. What treatment options are available...
Nominations are now open for candidates...