Goey S H, Gratama J W, Primrose J N, Ward U, Mertelsmann R H, Osterwalder B, Verweij J, Stoter G
Department of Medical Oncology, Rotterdam Cancer Institute (Daniel den Hoed Kliniek, The Netherlands.
Br J Cancer. 1996 Dec;74(12):2018-23. doi: 10.1038/bjc.1996.670.
Treatment using a combination of 5-fluorouracil (5-FU), interferon-alpha (IFN alpha-2a) and interleukin 2 (IL-2) has been shown to mediate disease regression in selected patients with advanced colorectal cancer. This phase II study was designed to evaluate the anti-tumour activity and toxicity of the combination of IL-2, IFN alpha-2a and 5-FU in patients with advanced colorectal cancer. Forty-four patients with metastatic colorectal cancer were treated, predominantly on an outpatient basis, with subcutaneous IFN alpha-2a and IL-2 three times per week followed by once a week bolus intravenous 5-FU injections. There were six (14%) partial responses among the 43 evaluable patients [95% confidence interval (CI) 5-28%]. Twenty-four patients had stable disease (56%) and 13 patients (30%) showed progressive disease. The median time to progressive disease in 43 patients was 19 weeks (range 2-72 weeks) and in responders 34 weeks (range 24-30 weeks). The median overall survival was 47 weeks (range 2-85 weeks) and in responders 60 weeks (range 35-71 weeks). Treatment-related toxic effects included fatigue, nausea and vomiting. Granulocytopenia was the main reason for the dose reductions or treatment interruptions in 32 out of 44 patients. One patient died of toxicity due to renal failure. Serial assessments of immunophenotyping and cytolytic activities of peripheral blood lymphocytes did not show changes in the numbers of circulating natural killer (NK) cells or in the levels of NK and lymphokine-activated killer (LAK) cytolytic activities. This regimen of IL-2 and IFN alpha-2a with 5-FU has only modest anti-tumour activity in advanced colorectal cancer.
已证明,使用5-氟尿嘧啶(5-FU)、α-干扰素(IFNα-2a)和白细胞介素2(IL-2)联合治疗可使部分晚期结直肠癌患者的病情出现缓解。本II期研究旨在评估IL-2、IFNα-2a和5-FU联合方案对晚期结直肠癌患者的抗肿瘤活性和毒性。44例转移性结直肠癌患者接受了治疗,主要为门诊治疗,皮下注射IFNα-2a和IL-2,每周3次,随后每周1次静脉推注5-FU。43例可评估患者中有6例(14%)出现部分缓解[95%置信区间(CI)5%-28%]。24例患者病情稳定(56%),13例患者(30%)病情进展。43例患者病情进展的中位时间为19周(范围2-72周),缓解者为34周(范围24-30周)。总生存期中位时间为47周(范围2-85周),缓解者为60周(范围35-71周)。与治疗相关的毒性反应包括疲劳、恶心和呕吐。44例患者中有32例因粒细胞减少而减量或中断治疗。1例患者因肾衰竭毒性死亡。外周血淋巴细胞免疫表型和细胞溶解活性的系列评估未显示循环自然杀伤(NK)细胞数量或NK及淋巴因子激活杀伤(LAK)细胞溶解活性水平有变化。IL-2、IFNα-2a与5-FU联合方案对晚期结直肠癌的抗肿瘤活性有限。