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;
D O I
暂无
中图分类号
学科分类号
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.
引用
收藏
页码:1720 / 1724
页数:4
相关论文
共 50 条
  • [41] Randomized multicenter phase II trial of two different schedules of irinotecan combined with capecitabine as first-line treatment in metastatic colorectal carcinoma
    Bajetta, E
    Di Bartolomeo, M
    Mariani, L
    Cassata, A
    Artale, S
    Frustaci, S
    Pinotti, G
    Bonetti, A
    Carreca, I
    Biasco, G
    Bonaglia, L
    Marini, G
    Iannelli, A
    Cortinovis, D
    Ferrario, E
    Beretta, E
    Lambiase, A
    Buzzoni, R
    CANCER, 2004, 100 (02) : 279 - 287
  • [42] Capecitabine and irinotecan as first-line treatment of advanced colorectal cancer
    Punt, Cornelis J. A.
    Koopman, Miriam
    JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (11) : 1907 - 1908
  • [43] Capecitabine/oxaliplatin as first-line treatment for metastatic colorectal cancer: a meta-analysis
    Zhao, G.
    Gao, P.
    Yang, K. H.
    Tian, J. H.
    Ma, B.
    COLORECTAL DISEASE, 2010, 12 (07) : 615 - 623
  • [44] A triplet combination with capecitabine/oxaliplatin/irinotecan (XELOXIRI) plus cetuximab as first-line therapy for patients with metastatic colorectal cancer: a dose escalation study
    Sato, Yasushi
    Hirakawa, Masahiro
    Ohnuma, Hiroyuki
    Takahashi, Minoru
    Okamoto, Tetsuro
    Okamoto, Koichi
    Miyamoto, Hiroshi
    Muguruma, Naoki
    Furuhata, Tomohisa
    Takemasa, Ichiro
    Kato, Junji
    Takayama, Tetsuji
    CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2017, 80 (06) : 1133 - 1139
  • [45] Randomized multicenter phase II trial of oxaliplatin plus irinotecan versus raltitrexed as first-line treatment in advanced colorectal cancer
    Scheithauer, W
    Kornek, GV
    Raderer, M
    Ulrich-Pur, H
    Fiebiger, W
    Gedlicka, C
    Schüll, B
    Brugger, S
    Schneeweiss, B
    Lang, F
    Lenauer, A
    Depisch, D
    JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (01) : 165 - 172
  • [46] A triplet combination with capecitabine/oxaliplatin/irinotecan (XELOXIRI) plus cetuximab as first-line therapy for patients with metastatic colorectal cancer: a dose escalation study
    Yasushi Sato
    Masahiro Hirakawa
    Hiroyuki Ohnuma
    Minoru Takahashi
    Tetsuro Okamoto
    Koichi Okamoto
    Hiroshi Miyamoto
    Naoki Muguruma
    Tomohisa Furuhata
    Ichiro Takemasa
    Junji Kato
    Tetsuji Takayama
    Cancer Chemotherapy and Pharmacology, 2017, 80 : 1133 - 1139
  • [47] Irinotecan or oxaliplatin for first-line treatment of advanced colorectal cancer?
    Punt, CJA
    ANNALS OF ONCOLOGY, 2005, 16 (06) : 845 - 846
  • [48] A phase I/II study of capecitabine (X), irinotecan (I) and oxaliplatin (O) as first-line therapy in patients (PTS) with advanced or metastatic colorectal cancer (MCRC)
    Maroun, Jean A.
    Jonker, Derek
    Goel, Rakesh
    Cripps, Christine
    Lister, Diane
    Chiritescu, Gabriela
    ANNALS OF ONCOLOGY, 2006, 17 : 119 - 119
  • [49] Multicenter Phase II Study of Oxaliplatin, Irinotecan, and S-1 as First-Line Treatment for Patients with Recurrent or Metastatic Biliary Tract Cancer
    Yoo, Changhoon
    Han, Boram
    Kim, Hyeong Su
    Kim, Kyu-pyo
    Kim, Deokhoon
    Jeong, Jae Ho
    Lee, Jae-Lyun
    Kim, Tae Won
    Kim, Jung Han
    Choi, Dae Ro
    Ha, Hong Il
    Seo, Jinwon
    Chang, Heung-Moon
    Ryoo, Baek-Yeol
    Zang, Dae Young
    CANCER RESEARCH AND TREATMENT, 2018, 50 (04): : 1324 - 1330
  • [50] Irinotecan or oxaliplatin combined with leucovorin and 5-fluorouracil as first-line treatment in advanced colorectal cancer: a multicenter, randomized, phase II study
    Kalofonos, HP
    Aravantinos, G
    Kosmidis, P
    Papakostas, P
    Economopoulos, T
    Dimopoulos, M
    Skarlos, D
    Bamias, A
    Pectasides, D
    Chalkidou, S
    Karina, M
    Koutras, A
    Samantas, E
    Bacoyiannis, C
    Samelis, GF
    Basdanis, G
    Kalfarentzos, F
    Fountzilas, G
    ANNALS OF ONCOLOGY, 2005, 16 (06) : 869 - 877