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NEW YORK (GenomeWeb) – The US Food and Drug Administration on Friday approved the first lung cancer immunotherapy drug for a molecularly defined subset of patients.

Merck's anti-PD-1 drug Keytruda (pembrolizumab) is indicated for advanced non-small cell lung cancer patients who have progressed despite receiving platinum-containing chemotherapy or agents targeting EGFR or ALK tumor mutations, and whose tumors are positive for PD-L1 expression.

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Jul
23

This webinar will discuss how the Molecular Pathology Laboratory at the University of Oklahoma (OUMP) is using a new quality improvement model to support molecular testing of oncology patients.