Here is a table I found which was not part of the pdf of the article I had. This appendix of the article shows PFS and OS According to MET GCN Status. This supports my thesis that increased MET GCN may not be a such a good biomarker for tivantinib.
To confuse things further, the authors say that [based on the data presented in this table and ...]
[...], given that tivantinib was initially identified from a cellbased screen, we cannot rule out that the demonstrated anticancer activity of the compound relies on additional mechanisms other than MET inhibition.
Wow!!
Even with all these negative reasons cited. I still think the NSCLC trial has a good chance of early unblinding.
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