Abstract

Testing for activating genomic mutations is recommended in all patients with advanced non-small cell lung cancer (aNSCLC), including ALK, BRAF, KRAS, EGFR, ROS1, as well as PD-L1 expression, to support optimal treatment decisions. Current real-world testing patterns of biomarkers in aNSCLC are not well known and testing rates may be lower than expected despite clinical guideline recommendations. The objective of this study was to measure real-world aNSCLC biomarker testing rates and characterize patient and clinical characteristics associated with testing.

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