Labianca R, Giaccon G, Barni S, Ambrosini G, Iirillo A, Fiorentini G, Duro M, Piazza E, Oliani C, Pancera G
Division of Medical Oncology, San Carlo Borromeo Hospital, Milan, Italy.
Eur J Cancer. 1994;30A(11):1611-6. doi: 10.1016/0959-8049(94)00190-g.
In advanced colorectal cancer the addition of folinic acid (FA) has been shown to lead to increased activity, at least in terms of response rate, in comparison with 5-fluorouracil (5FU) alone. Similarly, interferon-alpha (IFN) is able to potentiate 5FU, although high doses cause heavy toxicity. Given the different mechanisms of action of the two agents, the double modulation of 5FU deserves clinical evaluation. In a multicenter study (involving both primary care and referral institutions) 63 patients with advanced colorectal cancer, previously untreated with chemotherapy, received, in an outpatient setting, FA (200 mg/m2 i.v. bolus) + 5FU (400 mg/m2 i.v. in 15 min) for 5 consecutive days every 4 weeks + IFN 3 x 10(6) U on alternate days, starting 1 week before chemotherapy. During the 5 days of 5FU + FA, IFN was administered daily. The antitumour activity, the impact on response duration and survival and toxicity of the combination were evaluated according to WHO criteria. Of the 63 enrolled patients, 56 were evaluable: there were 2 complete responses (3%) and 13 partial responses (21%), giving an objective response rate of 24% (95% confidence interval 13-35%); no change was observed in 17 cases and progressive disease in 24. Median duration of response was 9 months and median survival (all patients) 13 months. Toxicity was acceptable, even though 4 patients presented reversible grade 4 side-effects (2 mucositis and 2 diarrhoea). With this schedule and these doses, addition of IFN did not lead to any increase in the activity of 5FU + FA. In colorectal cancer, further clinical studies with these drugs should be based on a deeper experimental knowledge of their mechanisms of interaction.
在晚期结直肠癌中,与单独使用5-氟尿嘧啶(5FU)相比,添加亚叶酸(FA)已显示出至少在缓解率方面能提高活性。同样,α干扰素(IFN)能够增强5FU的作用,尽管高剂量会导致严重毒性。鉴于这两种药物的作用机制不同,5FU的双重调节值得临床评估。在一项多中心研究(涉及基层医疗和转诊机构)中,63例先前未接受过化疗的晚期结直肠癌患者在门诊接受治疗,每4周连续5天静脉推注FA(200mg/m²)+静脉滴注5FU(400mg/m²,15分钟内滴完),并在化疗前1周开始隔日给予IFN 3×10⁶U。在5FU+FA治疗的5天期间,每天给予IFN。根据世界卫生组织标准评估联合治疗的抗肿瘤活性、对缓解持续时间和生存的影响以及毒性。在63例入组患者中,56例可评估:有2例完全缓解(3%)和13例部分缓解(21%),客观缓解率为24%(95%置信区间13 - 35%);17例无变化,24例病情进展。中位缓解持续时间为9个月,中位生存期(所有患者)为13个月。毒性是可接受的,尽管有4例患者出现可逆的4级副作用(2例黏膜炎和2例腹泻)。按照这个方案和这些剂量,添加IFN并未导致5FU+FA的活性增加。在结直肠癌中,使用这些药物的进一步临床研究应基于对其相互作用机制更深入的实验认识。