Gemcitabine (GEM) plus oxaliplatin, folinic acid, and 5-fluorouracil (FOLFOX-4) in patients with advanced gastric cancer

被引:28
作者
Correale, P
Fulfaro, F
Marsili, S
Cicero, G
Bajardi, E
Intrivici, C
Vuolo, G
Carli, AF
Caraglia, M
Del Prete, S
Greco, E
Gebbia, N
Francini, G
机构
[1] Univ Siena, Sch Med, Human Pathol & Oncol Dept, Sect Med Oncol, I-53100 Siena, Italy
[2] Univ Palermo, Div Oncol, Palermo, Italy
[3] Univ Siena, Surg Sci Div, I-53100 Siena, Italy
[4] Frattamaggiore Hosp, Oncol Operat Unit, Naples, Italy
[5] Lamezia Terme Hosp, Oncol Operat Unit, Lamezia Terme, Italy
关键词
gastric cancer; gemcitabine; oxaliplatin; 5-fluorouracil; folinic acid;
D O I
10.1007/s00280-005-1024-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background and aims: oxaliplatin in combination with folinic acid (FA) and infusional 5-fluorouracil (5-FU) has shown significant anti-tumor activity in gastric cancer patients (FOLFOX). Previous studies have shown that gemcitabine ( GEM), a new fluorinated anti-metabolite, enhances the individual anti-tumor activity of either 5-FU or oxaliplatin. We have therefore designed a multi-center phase II trial in order to test a novel GEM + FOLFOX-4 regimen in patients with metastatic gastric cancer. Methods: we enrolled 36 patients, 28 males and 8 females, with an average age of 64.4 years ( range 37 - 78), who received bi-weekly treatment with GEM ( 1,000 mg/m(2) on day 1), levo-FA ( 100 mg/m(2) on days 1 and 2), a 5-FU ( 400 mg/m(2)) bolus injection followed by 22-h continuous infusion ( 800 mg/ m 2) on days 1 and 2, and oxaliplatin 85 mg/ m 2 in a 4 6 h intravenous (i.v.) infusion before the second FUFA administration on day 2. Results: the most frequent side effect was grade 1 - 2 hematological toxicity and late sensorial neurotoxicity. Two patients developed hypersensitivity to oxaliplatin while another developed an aseptic eosinophilic pneumonitis. Two patients refused to continue the treatment after two cycles of chemotherapy and were lost at the follow-up. Among the remaining 34 patients four achieved a complete response, 15 a partial response, 12 had a stable disease and three progressed. Conclusions: these results may grant the rationale to evaluate this multi-drug combination in randomized phase III trials in advanced gastric cancer.
引用
收藏
页码:563 / 568
页数:6
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