PD-L1/PD-1 immunotherapy is coming to NSCLC, but the question arises will it take market share from known driver mutations such as EGFRm (15% ADC) or ALK (5% ADC), or is the PD-L1/PD-1 population (50% NSCLC) substantially independent, i.e. consisting mostly of the 45% driver-unknown population? Two studies below suggest conflicting answers:
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