5-fluorouracil and folinic acid with or without CPT-11 in advanced colorectal cancer patients: A multicenter randomised phase II study of the Southern Italy Oncology Group

被引:29
作者
Maiello, E
Gebbia, V
Giuliani, F
Paoletti, G
Gebbia, N
Cigolari, S
Fortunato, S
Pedicini, T
Borsellino, N
Lopez, M
Colucci, G
机构
[1] Inst Oncol, Med & Expt Oncol Unit, I-70125 Bari, Italy
[2] La Maddalena Oncol Hosp, Med Oncol Unit, Palermo, Italy
[3] Regina Elena Oncol Inst, Div Med Oncol, Rome, Italy
[4] Univ Palermo, Serv Chemotherapy, Palermo, Italy
[5] Univ Naples, Serv Oncol, Naples, Italy
[6] Oncol Ctr Anal, Catania, Italy
[7] Fatebenefratelli Hosp, Benevento, Italy
关键词
colorectal cancer; combination therapy; folinic acid; fluorouracil; irinotecan;
D O I
10.1023/A:1008342928408
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: The combination regimen CPT-11 plus bolus and infusion 5-fluorouracil (5-FU) with high-dose leucovorin (hybrid regimen LV5FU2) has been tested for activity and toxicity against advanced colorectal carcinoma in a randomised, multicenter phase II trial. Patients and methods: A total of 102 chemotherapy-naive patients were randomised in a 1 : 2 fashion to receive: leucovorin 100 mg/m(2) administered as a two-hour infusion before 5-FU 400 mg/m(2) as an intravenous bolus, and FU 600 mg/m(2) as a 22-hour infusion immediately after 5-FU bolus injection repeated on days 1 and 2 (LV5FU2 regimen, arm A, 34 patients) or CPT-11 at 180 mg/m(2) (150 mg/m(2) for patients of age greater than or equal to 70 and < 75 years) only on day 1 immediately before LV5FU2 therapy (LV5FU2 + CPT-11 regimen, arm B 68 patients). Both treatments were repeated every two weeks. The presence of a calibration arm assured consistency and more realistic evaluation of results achieved with the LV5FU2 + CTP-11 regimen. Results: Thirty-three and sixty-four patients were evaluable in arm A and B, respectively. The overall response rate was 18% in arm A (95% CI: 7%-34%) and 40% in arm B (95% CI: 28%-52%). Median time to progression, median duration of response and survival were similar in both groups. Responders (CR + PR) survived statistically longer than non-responders only in arm B (20 vs. 10 months, P = 0.0016). All patients were evaluable for toxicity which was mild in both groups; gastrointestinal disturbances were the most common. There were no treatment-related deaths. Grade 3-4 toxicity was uncommon in both arms. Conclusions: The addition of CPT-11 to the hybrid LV5FU2 regimen provided a significant overall response rate (40%) with relatively mild toxicity. The overall response rate was 18% in patients treated with LV5FU2 alone in the calibration arm. Thus, considering other encouraging data from the literature, the CPT-11 + FU-LV combination therapy can be regarded as a new, very effective treatment option for first-line treatment of advanced colorectal cancer patients.
引用
收藏
页码:1045 / 1051
页数:7
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