Detalle Publicación

ARTÍCULO

Randomized phase II trial of non-platinum induction or consolidation chemotherapy plus concomitant chemoradiation in stage III NSCLC patients: Mature results of the Spanish Lung Cancer Group 0008 study

Autores: Garrido, P. (Autor de correspondencia); Rosell, R.; Arellano, A.; Andreu, F. ; Domine, M.; Perez-Casas, A. ; Cardenal, F.; Arnaiz, M. D.; Moran, T. ; Morera, R.; Isla, D.; Valencia, J.; Cobo, M.; Delgado, R. ; Garcia-Gomez, R. ; Calvo Manuel, Felipe; Zamora, J.; Ramos, A.; Massuti, B.
Título de la revista: LUNG CANCER
ISSN: 0169-5002
Volumen: 81
Número: 1
Páginas: 84 - 90
Fecha de publicación: 2013
Resumen:
The optimal schedule and regimen of chemotherapy (CT) in association with chemoradiation has not been established in stage III non-small-cell lung cancer (NSCLC). We have compared three schedules of non-platinum-based cr plus either radiotherapy or chemoradiation. From May 2001 to June 2006, 158 patients with unresectable stage III NSCLC were enrolled in a randomized phase II trial with overall response rate (ORR) as the primary endpoint. The initial design included three arms: sequential CT followed by thoracic radiation (TRT); concurrent CT/TRT followed by consolidation CT; and induction CT followed by concurrent CT/TRT. However, based on the preliminary results of the RTOG 9410 trial, the sequential arm was closed when 19 patients had been enrolled. All patients received two cycles of docetaxel 40 mg/m(2) days 1 and 8 plus gemcitabine 1200 mg/m(2) days 1 and 8, as either induction or consolidation therapy. Concurrent CT/TRT consisted of docetaxel 20 mg/m(2) and carboplatin AUC 2 weekly plus 60 Gy TRT. No differences were found in ORR between the two arms (56% and 57%). Hematological toxicity was mild but significantly superior with consolidation Cl'; the esophagitis rate was similar in both arms (16% and 15%). Wlth a median follow-up of 57 months, no differences were found in median survival (13.07 and 13.8 months) or 5-year survival (16.4% and 22%). This regimen cannot be recommended as an alternative to platinum-based CT/TRT although it has an acceptable toxicity profile and encouraging long-term survival data (ClinicalTrials.gov NCT01652820). (C) 2013 Elsevier Ireland Ltd. All rights reserved.