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Efficacy of Dabrafenib Plus Trametinib Combination in Patients with BRAF V600E-Mutant NSCLC in Real-World Setting: GFPC 01-2019.
Auliac, Jean-Bernard; Bayle, Sophie; Do, Pascal; Le Garff, Gwenaëlle; Roa, Magali; Falchero, Lionel; Huchot, Eric; Quéré, Gilles; Jeannin, Gaëlle; Métivier, Anne-Cécile; Hobeika, Joëlle; Guisier, Florian; Chouaid, Christos.
Afiliación
  • Auliac JB; Department of Pneumology, CHI de Créteil, 94000 Créteil, France.
  • Bayle S; Department of Pneumology, CHU de Saint-Etienne, 42055 Saint-Etienne, France.
  • Do P; Department of Pneumology, Centre Baclesse, 14076 Caen, France.
  • Le Garff G; Department of Pneumology, CH de Saint Brieuc, 22027 Saint-Brieuc, France.
  • Roa M; Department of Pneumology, CHI de de Fréjus Saint Raphael, 83600 Fréjus, France.
  • Falchero L; Department of Pneumology, Hôpital Nord Ouest de Villefranche-sur-Saône, 69400 Gleizé, France.
  • Huchot E; Department of Pneumology, CHU Réunion Site Sud, 97448 Saint-Pierre, France.
  • Quéré G; Department of Pneumology, CHU de Brest, 29200 Brest, France.
  • Jeannin G; Department of Pneumology, CHU de Clermont-Ferrand, 63000 Clermont-Ferrand, France.
  • Métivier AC; Department of Pneumology, Hôpital Foch, 92150 Suresnes, France.
  • Hobeika J; Department of Pneumology, CHI de Créteil, 94000 Créteil, France.
  • Guisier F; Department of Pneumology, CHU Charles Nicolle, 76000 Rouen, France.
  • Chouaid C; Department of Pneumology, CHI de Créteil, 94000 Créteil, France.
Cancers (Basel) ; 12(12)2020 Dec 02.
Article en En | MEDLINE | ID: mdl-33276639
ABSTRACT
Dabrafenib plus trametinib combination is approved in Europe for BRAF V600E-mutant metastatic non-small-cell lung cancer (NSCLC). The objective of this study was to assess efficacy and safety of this combination in a real-world setting. This retrospective multicentric study included 40 patients with advanced NSCLC harboring BRAF V600E mutation and receiving dabrafenib plus trametinib. The median progression-free survival (PFS) and overall survival (OS) were 17.5 (95% CI 7.1-23.0) months and 25.5 (95% CI 16.6-not reached) months in the entire cohort, respectively. For the 9 patients with first-line treatment, median PFS was 16.8 (95% CI 6.1-23.2) months and median OS was 21.8 (95% CI 1.0-not reached) months; for the 31 patients with second-line or more treatments, median PFS and OS were 16.8 (95% CI 6.1-23.2) months and 25.5 (95% CI 16.6-not reached) months, respectively. Adverse events led to permanent discontinuation in 7 (18%) patients, treatment interruption in 8 (20%) and dose reduction in 12 (30%). In conclusion, these results suggest that efficacy and safety of dabrafenib plus trametinib combination in patients with BRAF V600E metastatic NSCLC are comparable in a real-world setting and in clinical trials for both previously untreated and treated patients.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Clinical_trials Idioma: En Revista: Cancers (Basel) Año: 2020 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Clinical_trials Idioma: En Revista: Cancers (Basel) Año: 2020 Tipo del documento: Article País de afiliación: Francia
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