Capecitabine in combination with irinotecan (XELIRI), administered as a 2-weekly schedule, as first-line chemotherapy for patients with metastatic colorectal cancer: a phase II study of the Spanish GOTI group

被引:22
作者
Garcia-Alfonso, P. [1 ]
Munoz-Martin, A. [1 ]
Mendez-Urena, M. [2 ]
Quiben-Pereira, R. [2 ]
Gonzalez-Flores, E. [3 ]
Perez-Manga, G. [1 ]
机构
[1] Hosp Gen Univ Gregorio Maranon, Med Oncol Serv, Madrid 28007, Spain
[2] Hosp Univ Mostoles, Med Oncol Serv, Madrid 28935, Spain
[3] Hosp Univ Virgen Nieves, Med Oncol Serv, Granada 18014, Spain
关键词
capecitabine; colorectal cancer; combined modality therapy; irinotecan; FLUOROURACIL PLUS LEUCOVORIN; ORAL CAPECITABINE; INTRAVENOUS FLUOROURACIL; RANDOMIZED-TRIAL; 5-FLUOROURACIL/LEUCOVORIN; FLUOROPYRIMIDINES; PREFERENCE; CARCINOMA; EFFICACY; THERAPY;
D O I
10.1038/sj.bjc.6605261
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: Combination chemotherapy is standard treatment for metastatic colorectal cancer (MCRC). The aim of this study was to determine the efficacy and safety of capecitabine_irinotecan (2-weekly schedule), as first-line therapy of MCRC. METHODS: Patients received irinotecan 175 mg m(-2) on day 1 and oral capecitabine 1000 mg m(-2) twice daily on days 2-8 every 2 weeks. For patients aged >= 65 years, the starting doses of irinotecan and capecitabine were reduced to 140 and 750 mg m(-2), respectively. RESULTS: A total of 53 patients were enrolled: 29 (55%) were >= 65 years old. In an intention-to-treat analysis, complete response was achieved in three patients for an overall response rate (ORR) of 32%. The disease control rate (ORR + stable disease) was 66% and the median duration of response was 7.3 months. Median time to progression and overall survival were 9.0 and 19.2 months, respectively. Grade 4 neutropenia was reported in one patient: no other grade 4 toxicities were recorded. Grade 3 diarrhoea occurred in 8 (15%) patients and grade 1-2 hand-foot syndrome in 7 (13%) patients. CONCLUSION: Capecitabine and irinotecan, given every 2 weeks, as first-line treatment of MCRC is an active regimen with a manageable toxicity profile, even in older patients. British Journal of Cancer ( 2009) 101, 1039-1043. doi:10.1038/sj.bjc.6605261 www.bjcancer.com Published online 8 September 2009 (C) 2009 Cancer Research UK
引用
收藏
页码:1039 / 1043
页数:5
相关论文
共 29 条
[11]  
Garcia-Alfonso P., 2003, EJC Supplements, V1, pS73, DOI 10.1016/S1359-6349(03)90270-9
[12]   Comparison of oral capecitabine versus intravenous fluorouracil plus leucovorin as first-line treatment in 605 patients with metastatic colorectal cancer: Results of a randomized phase III study [J].
Hoff, PM ;
Ansari, R ;
Batist, G ;
Cox, J ;
Kocha, W ;
Kuperminc, M ;
Maroun, J ;
Walde, D ;
Weaver, C ;
Harrison, E ;
Burger, HU ;
Osterwalder, B ;
Wang, AO ;
Wong, R .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (08) :2282-2292
[13]  
Hwang Jimmy J, 2004, Oncology (Williston Park), V18, P26
[14]   Multicenter phase II study of oral capecitabine plus irinotecan as first-line chemotherapy in advanced colorectal cancer: A Korean Cancer Study Group Trial [J].
Kim, TW ;
Kang, WK ;
Chang, HM ;
Park, JO ;
Ryoo, BY ;
Ahn, JS ;
Zang, DY ;
Lee, KH ;
Kang, YK ;
Kim, SR ;
Kim, HK .
ACTA ONCOLOGICA, 2005, 44 (03) :230-235
[15]   Irinotecan combined with infusional 5-fluorouracil/folinic acid or capecitabine plus celecoxib or placebo in the first-line treatment of patients with metastatic colorectal cancer.: EORTC study 40015 [J].
Koehne, C.-H. ;
De Greve, J. ;
Hartmann, J. T. ;
Lang, I. ;
Vergauwe, P. ;
Becker, K. ;
Braumann, D. ;
Joosens, E. ;
Mueller, L. ;
Janssens, J. ;
Bokemeyer, C. ;
Reimer, P. ;
Link, H. ;
Spath-Schwalbe, E. ;
Wilke, H. -J. ;
Bleiberg, H. ;
Van den Brande, J. ;
Debois, M. ;
Bethe, U. ;
Van Cutsem, E. .
ANNALS OF ONCOLOGY, 2008, 19 (05) :920-926
[16]   Sequential versus combination chemotherapy with capecitabine, irinotecan, and oxaliplatin in advanced colorectal cancer (CAIRO): a phase III randomised controlled trial [J].
Koopman, Miriam ;
Antonini, Ninja F. ;
Douma, Joep ;
Wals, Jaap ;
Honkoop, Aafke H. ;
Erdkamp, Frans L. G. ;
de Jong, Robert S. ;
Rodenburg, Cees J. ;
Vreugdenhil, Gerard ;
Loosveld, Olaf J. L. ;
van Bochove, Aart ;
Sinnige, Harm A. M. ;
Creemers, Geert-Jan M. ;
Tesselaar, Margot E. T. ;
Slee, Peter H. Th J. ;
Werter, Marjon J. B. P. ;
Mol, Linda ;
Dalesio, Otilia ;
Punt, Cornelis J. A. .
LANCET, 2007, 370 (9582) :135-142
[17]   Patient preferences for oral versus intravenous palliative chemotherapy [J].
Liu, G ;
Franssen, E ;
Fitch, MI ;
Warner, E .
JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (01) :110-115
[18]   Oral fluoropyrimidines in the treatment of colorectal cancer [J].
Meropol, NJ .
EUROPEAN JOURNAL OF CANCER, 1998, 34 (10) :1509-1513
[19]   A PROSPECTIVE RANDOMIZED TRIAL COMPARING THE INFECTIOUS AND NONINFECTIOUS COMPLICATIONS OF AN EXTERNALIZED CATHETER VERSUS A SUBCUTANEOUSLY IMPLANTED DEVICE IN CANCER-PATIENTS [J].
MUELLER, BU ;
SKELTON, J ;
CALLENDER, DPE ;
MARSHALL, D ;
GRESS, J ;
LONGO, D ;
NORTON, J ;
RUBIN, M ;
VENZON, D ;
PIZZO, PA .
JOURNAL OF CLINICAL ONCOLOGY, 1992, 10 (12) :1943-1948
[20]   First-line chemotherapy with irinotecan plus capecitabine for advanced colorectal cancer [J].
Park, SH ;
Bang, SM ;
Cho, EK ;
Baek, JH ;
Oh, JH ;
Im, SA ;
Park, YS ;
Shin, DB ;
Lee, JH .
ONCOLOGY, 2004, 66 (05) :353-357