KEYNOTE-189 tested chemo ± Keytruda is first-line non-squamous NSCLC for patients with any PD-L1 status. The hazard ratio for OS/PFS and other details will be presented at an unspecified medical conference (probably ASCO).
Success in KEYNIOTE-189 allows MRK to convert the accelerated approval from the small KEYNOTE-021G study (#msg-131249474) into a full FDA approval.
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