The FDA granted approval to pembrolizumab (Keytruda, Merck), an anti-PD-1 checkpoint immunotherapy, for first-line treatment of patients with stage III non-small cell lung cancer (NSCLC) that is PD-L1-positive and is not amenable to surgery or chemo-radiation treatment.
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Meet Dr. Julie Brahmer, Scientific Advisory Board member at LCFA and leader in immunotherapy research.