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Authors | M. Heinrich, R. Jones, P. Schoffski, S. Bauer, M. von Mehren, F. Eskens, P. Cassier, O. MIr, H. Shi, T. Alvarez-Diez, M.E. Healy, B. Wolf, S. George | ||||||||||||
Title | Preliminary safety and activity in a first-in-human phase 1 study of BLU-285, a potent, highly-selective inhibitor of KIT and PDGFRa activation loop mutants in advanced gastrointestinal stromal tumor (GIST) | ||||||||||||
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URL | https://colectivogist.files.wordpress.com/2016/12/2016_1201_blu-285-slides.pdf | ||||||||||||
Abstract Text | https://colectivogist.files.wordpress.com/2016/12/2016_1201_blu-285-slides.pdf |
Molecular Profile | Treatment Approach |
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Gene Name | Source | Synonyms | Protein Domains | Gene Description | Gene Role |
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Therapy Name | Drugs | Efficacy Evidence | Clinical Trials |
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Drug Name | Trade Name | Synonyms | Drug Classes | Drug Description |
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Gene | Variant | Impact | Protein Effect | Variant Description | Associated with drug Resistance |
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Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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KIT exon17 | gastrointestinal stromal tumor | sensitive | Avapritinib | Phase I | Actionable | In a Phase I trial, Ayvakit (avapritinib) demonstrated preliminary antitumor activity in gastrointestinal stromal tumor patients harboring KIT mutations, with reduced tumor burden in 38% (5/13) of patients, including 1 partial response and 4 stable diseases, and 3 of the 5 responding patients harbored KIT exon 17 mutations (EORTC-NCI-AACR 2016, Abs 6LBA). | detail... |