Capecitabine and irinotecan with bevacizumab 2-weekly for metastatic colorectal cancer: the phase II AVAXIRI study.


Por: Garcia-Alfonso P, Chaves M, Muñoz A, Salud A, García-Gonzalez M, Grávalos C, Massuti B, González-Flores E, Queralt B, López-Ladrón A, Losa F, Gómez MJ, Oltra A and Aranda E

Publicada: 29 abr 2015 Ahead of Print: 29 abr 2015
Resumen:
BACKGROUND: The optimal sequence of chemotherapeutic agents is not firmly established for the treatment of metastatic colorectal cancer (mCRC). This phase II multi-centre study investigated the efficacy and tolerability of a standard capecitabine plus irinotecan (XELIRI) regimen with bevacizumab in previously untreated patients with mCRC. METHODS: Patients received intravenous irinotecan 175 mg/m(2) on day 1 and oral capecitabine 1000 mg/m(2) (800 mg/m(2) for patients >65 years of age) twice daily on days 2-8, followed by a 1-week rest, and bevacizumab 5 mg/kg as an intravenous infusion on day 1 every 2 weeks. RESULTS: Seventy-seven patients were included in the intention-to-treat and safety populations. Progression-free survival at 9 months was 61%. The overall response and disease control rates were 51% and 84%, respectively. Median progression-free and overall survival times were 11.9 and 24.8 months, respectively. 48 patients (62%) had at least one grade 3/4 adverse event, the most common being asthenia, diarrhoea and neutropenia. Quality of life varied little over the study period with mean visual analogue scale general health scores ranging from 71 to 76 over cycles 1-11. CONCLUSION: Our study found irinotecan and capecitabine administered fortnightly with bevacizumab in patients with mCRC to be an effective and tolerable regimen. TRIAL REGISTRATION: clinicaltrials.gov identifier NCT00875771. Trial registration date: 04/02/2009.

Filiaciones:
Garcia-Alfonso P:
 Servicio de Oncología, Hospital Universitario Gregorio Marañón, C/Maiquez 7, 2nd floor, 28007, Madrid, Spain.

Chaves M:
 Servicio de Oncología, Hospital Virgen del Rocío, 41004, Sevilla, Spain.

Salud A:
 Servicio de Oncología, Hospital Lleida Arnau de Vilanova, 25198, Barcelona, Spain.

García-Gonzalez M:
 Servicio de Oncología, Hospital Universitario de Burgos, 09005, Burgos, Spain.

Grávalos C:
 Servicio de Oncología, Hospital 12 Octubre, 28041, Madrid, Spain.

:
 Servicio de Oncología, Hospital General Universitario, 03011, Alicante, Spain.

González-Flores E:
 Servicio de Oncología, Hospital Virgen de las Nieves, 18014, Granada, Spain.

Queralt B:
 Servicio de Oncología, ICO. Hospital. Josep Trueta, 17007, Gerona, Spain.

López-Ladrón A:
 Servicio de Oncología, Hospital Nuestra Señora de Valme, 41014, Sevilla, Spain.

Losa F:
 Servicio de Oncología, Hospital General de L'Hospitalet, 08906, Barcelona, Spain.

Gómez MJ:
 Servicio de Oncología, Hospital Puerta del Mar, 11009, Cádiz, Spain.

Oltra A:
 Servicio de Oncología, Hospital Virgen de los Lirios, 03804, Alicante, Spain.

Aranda E:
 Reina Sofía Hospital, University of Córdoba, Maimonides Institute of Biomedical Research (IMIBIC). Spanish Cancer Network (RTICC), Instituto de Salud Carlos III, Córdoba, Spain.
ISSN: 14712407





BMC Cancer
Editorial
BIOMED CENTRAL LTD, 236 GRAYS INN RD, FLOOR 6, LONDON WC1X 8HL, ENGLAND, Reino Unido
Tipo de documento: Article
Volumen: 15 Número:
Páginas: 327-327
WOS Id: 000354016400002
ID de PubMed: 25925749

MÉTRICAS