A dose finding and pharmacokinetic study of capecitabine in combination with oxaliplatin and irinotecan in metastatic colorectal cancer

被引:14
作者
Fornaro, Lorenzo [1 ]
Masi, G. [1 ]
Bursi, S. [1 ]
Loupakis, F. [1 ]
Vasile, E. [1 ]
Antonuzzo, A. [2 ]
Chiara, S. [3 ]
Pfanner, E. [4 ]
Di Paolo, A. [5 ]
Bocci, G. [5 ]
Del Tacca, M. [5 ]
Falcone, A. [1 ,6 ]
机构
[1] Ist Toscano Tumori, Azienda Livorno USL6, Dept Oncol, I-57124 Livorno, Italy
[2] Ist Toscano Tumori, Azienda Livorno USL6, Day Hosp Med Oncol Piombino, I-57124 Livorno, Italy
[3] Ist Nazl Ric Canc, I-16132 Genoa, Italy
[4] Azienda Osped Univ Pisa, Ist Toscano Tumori, Dept Oncol, Pisa, Italy
[5] Univ Pisa, Dept Internal Med, Div Pharmacol & Chemotherapy, Pisa, Italy
[6] Univ Pisa, Dept Oncol Transplants & New Technol Med, Pisa, Italy
关键词
Metastatic colorectal cancer; Capecitabine; Oxaliplatin; Irinotecan; Triplet regimen; Dose finding; 1ST-LINE TREATMENT; PLUS OXALIPLATIN; PHASE-III; INFUSIONAL FLUOROURACIL; LEUCOVORIN; CHEMOTHERAPY; TRIAL; 5-FLUOROURACIL/LEUCOVORIN; FOLFOXIRI; THERAPY;
D O I
10.1007/s00280-008-0840-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The GONO-FOLFOXIRI regimen demonstrated higher activity and efficacy than FOLFIRI in metastatic colorectal cancer patients. The aim of this study was to determine the maximum tolerated dose of capecitabine, in substitution of 5-fluorouracil, combined with oxaliplatin and irinotecan and to evaluate the pharmacokinetics of the drugs. We treated 15 patients with escalating doses of capecitabine (from day 1 to 7) and fixed doses of oxaliplatin (85 mg/m(2)) plus irinotecan (165 mg/m(2)) (both administered on day 1), repeated every 2 weeks. Pharmacokinetic analysis was performed on plasma samples collected at the first cycle of treatment. The maximum tolerated dose of capecitabine resulted 2,000 mg/m(2)/day, with diarrhea being the only dose-limiting toxicity. Large interpatient variability in the pharmacokinetic parameters of investigated drugs was observed. Results in terms of activity are promising. At the maximum tolerated dose of capecitabine of 2,000 mg/m(2)/day the combination is feasible with promising activity and deserves further investigations.
引用
收藏
页码:965 / 969
页数:5
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