A phase II trial of gemcitabine in combination with 5-fluorouracil (24-hour) and folinic acid in patients with chemonaive advanced pancreatic cancer

被引:43
作者
Oettle, H
Arning, M
Pelzer, U
Arnold, D
Stroszczynski, C
Langrehr, J
Reitzig, P
Kindler, M
Herrenberger, J
Musch, R
Korsten, FW
Huhn, D
Riess, H
机构
[1] Humboldt Univ, Fak Med, Med Klin & Poliklin S Hamatol & Onkol, D-13353 Berlin, Germany
[2] Univ Dusseldorf, Med Klin & Poliklin S Hamatol & Onkol, D-4000 Dusseldorf, Germany
[3] Humboldt Univ, Fac Med, Strahlenklin & Poliklin, Berlin, Germany
[4] Humboldt Univ, Fak Med, Chirurg Klin & Poliklin, D-1040 Berlin, Germany
[5] Oskar Ziethen Krankenhaus, Berlin, Germany
[6] Onkol Schwerpunktpraxis, Berlin, Germany
[7] Wenckebach Krankenhaus, Berlin, Germany
[8] Krankenhaus, Grevenbroich, Germany
关键词
chemotherapy; 5-FU; folinic acid; gemcitabine; Gemzar (R); pancreas cancer;
D O I
10.1023/A:1008364018881
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Gemcitabine (Gemzar(R)) and 5-fluorouracil (5-FU) plus folinic acid (FA) both have proven activity in the treatment of patients with advanced pancreatic cancer. The present study was initiated to investigate the efficacy of gemcitabine in combination with 5-FU-FA. Patients and methods: Thirty-eight patients, median age 60 years (range 34-70) with inoperable, stage IV, pancreatic cancer were enrolled into the study and treated on an outpatient basis. All except one patient received at least one cycle of treatment with gemcitabine (1000 mg/m(2)), followed by FA (200 mg/m(2)) and 5-FU (750 mg/m(2)) administered as a 24-hour continuous infusion on days 1, 8, 15 and 22 of a 42-day schedule. No patient had received prior chemotherapy or radiotherapy. All 38 patients were assessed for efficacy, toxicity and time to progressive disease. Results: Two patients (5%), achieved a partial response and thirty-four patients (89%) achieved stable disease. There were two early deaths (less than or equal to4 weeks). The median time to progression was 7.1 months (range 0.4-18.1+; 95% confidence interval (95% CI): 5.3-7.9 months). Three patients had a progression-free interval of greater than 12 months and 12 of 38 patients (32%) survived longer than 12 months. The median overall survival was 9.3 months (range 0.5-26.5; 95% CI: 7.3-13.0 months). The incidence of grade 3 and 4 toxicities was low. Conclusions: The combination of gemcitabine and 5-FU-FA is active and well tolerated and seems to offer an improvement in progression-free interval over both gemcitabine monotherapy and 5-FU-FA therapy.
引用
收藏
页码:1267 / 1272
页数:6
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