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Authors | AO. Siefker-Radtke, A Necchi, SH Park, J Garca-Donas, RA Huddart, EF Burgess, MT Fleming, A Rezazadeh, B Mellado, S Varlamov, M Joshi, I Duran, ST Tagawa, A OHagan, AN Avadhani, B Zhong, PD Porre, Y Loriot | ||||||||||||
Title | First results from the primary analysis population of the phase 2 study of erdafitinib (ERDA; JNJ-42756493) in patients (pts) with metastatic or unresectable urothelial carcinoma (mUC) and FGFR alterations (FGFRalt). | ||||||||||||
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URL | https://meetinglibrary.asco.org/record/160559/abstract | ||||||||||||
Abstract Text | J Clin Oncol 36, 2018 (suppl; abstr 4503) |
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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FGFR1 mutant | transitional cell carcinoma | predicted - sensitive | Erdafitinib | Phase II | Actionable | In a Phase II trial, Balversa (erdafitinib) treatment resulted in an objective response rate of 42% (40/96, 3 complete response, 37 partial response) and a disease control rate of 80% in patients with metastatic or unresectable urothelial carcinoma harboring FGFR alterations (J Clin Oncol 36, 2018 (suppl; abstr 4503); NCT02365597). | detail... |