I agree that MET matters and there might be consistent OS benefit for MET high patients versus the other sub-groups. However, see below.
The first, i.e., this group will also have MET high and MET low patients.
One apparent reason why certain patients were not evaluable was because the co decided to collect samples to evaluate the MET status later in the trial. So a good portion (1/4? 1/2? all?) of the 600 patients in this group would have no corresponding samples.
Were there other reasons (e.g., certain regions or certain hospitals could not collect samples?) I dont know. Did the tests fail for certain samples/patients? I dont know.
However, (which is my whole point), there might be a reason (other than pure extreme chance) why this last group (patients who were not evaluable for MET status) fared the worst.
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