A multicenter phase II study of the combination of oxaliplatin, irinotecan and capecitabine in the first-line treatment of metastatic colorectal cancer

被引:0
|
作者
E Vasile
G Masi
L Fornaro
S Cupini
F Loupakis
S Bursi
I Petrini
S Di Donato
I M Brunetti
S Ricci
A Antonuzzo
S Chiara
D Amoroso
M Andreuccetti
A Falcone
机构
[1] UO Oncologia Medica,Dipartimento di Oncologia
[2] Azienda USL 6,undefined
[3] Istituto Toscano Tumori,undefined
[4] Viale Alfieri 36,undefined
[5] UO Oncologia Medica,undefined
[6] Azienda Ospedaliera Pisana,undefined
[7] Istituto Toscano Tumori,undefined
[8] Via Roma 55,undefined
[9] Sez. Oncologia Medica,undefined
[10] Azienda USL 6,undefined
[11] Piombino (LI),undefined
[12] Istituto Toscano Tumori,undefined
[13] UO Oncologia Medica,undefined
[14] Istituto Tumori IST,undefined
[15] UO Oncologia Medica,undefined
[16] Ospedale della Versilia,undefined
[17] Istituto Toscano Tumori,undefined
[18] dei Trapianti e delle Nuove Tecnologie in Medicina,undefined
[19] Università degli studi di Pisa,undefined
[20] Via Roma 55,undefined
来源
British Journal of Cancer | 2009年 / 100卷
关键词
first-line treatment; metastatic colorectal cancer; triple drug combination; XELOXIRI;
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摘要
The triple drug combination consisting of irinotecan, oxaliplatin and 5-fluorouracil (FOLFOXIRI) has demonstrated higher activity and efficacy compared to the doublet FOLFIRI. 5-Fluorouracil could be substituted in FOLFOXIRI regimen by capecitabine, an oral fluoropyrimidine with similar efficacy. Recently, a dose-finding trial has demonstrated the feasibility of the combination of irinotecan, oxaliplatin and capecitabine (XELOXIRI) and established their recommended doses. The aim of this study was to evaluate the activity of XELOXIRI. A total of 36 patients with unresectable metastatic colorectal cancer received irinotecan 165 mg m−2 and oxaliplatin 85 mg m−2 on day 1 plus capecitabine 2000 mg m−2 per day orally in two doses from day 1 to day 7, every 2 weeks. Grade 3–4 toxicities were infrequent, expect for neutropenia and diarrhoea, which were each observed in 30% of patients. Two complete and twenty-two partial responses were obtained, corresponding to an overall response rate of 67% (95% CI 51.4–82%). After a median follow-up of 17.7 months, the median progression-free and overall survival were 10.1 and 17.9 months, respectively.
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页码:1720 / 1724
页数:4
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