A significant response to sorafenib in a woman with advanced lung adenocarcinoma and a BRAF non-V600 mutation

Lung adenocarcinoma includes recurrent activating oncogenic mutations (EGFR, EML4-ALK, ROS1) that have been associated with response to EGFR and ALK inhibitors. Platinum-based chemotherapy is the standard therapy for non-oncodrivers population. Sorafenib is a small molecule that blocks the activatio...

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Veröffentlicht in:Anti-cancer drugs 2015-10, Vol.26 (9), p.1004-1007
Hauptverfasser: Sereno, María, Moreno, Victor, Moreno Rubio, Juan, Gómez-Raposo, César, García Sánchez, Sagrario, Hernández Jusdado, Rebeca, Falagan, Sandra, Zambrana Tébar, Francisco, Casado Sáenz, Enrique
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Sprache:eng
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Zusammenfassung:Lung adenocarcinoma includes recurrent activating oncogenic mutations (EGFR, EML4-ALK, ROS1) that have been associated with response to EGFR and ALK inhibitors. Platinum-based chemotherapy is the standard therapy for non-oncodrivers population. Sorafenib is a small molecule that blocks the activation of C-RAF, B-RAF, c-KIT, FLT-3, RET, VEGFR-2, VEGFR-3 and PDGFR approved for advanced renal cell and hepatocellular carcinoma (b, c). Many studies have evaluated sorafenib in advanced non-small-cell lung cancer (NSCLC), with different results. We present a case report of a patient with NSCLC and the BRAF G469R mutation who showed a dramatic response to sorafenib.
ISSN:0959-4973
1473-5741
DOI:10.1097/CAD.0000000000000277