In the NCI MATCH trial, Subprotocol H, which served as the basis for FDA approval of dabrafenib plus trametinib for tissue-agnostic indications, a high degree of tumor mutational heterogeneity was reported and trends toward differences in patient outcomes were observed, although these did not reach statistical significance ( 52 ).
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BRAF V600E-mutated metastatic Wilms tumor with complete response to targeted RAF/MEK inhibition: a post-treatment follow-up case report.
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