Négrier S, Mercatello A, Bret M, Merrouche Y, Coronel B, Favrot M, Gaspard M, Dorez D, Philip I, Lanier F
Medical Oncology Department, Centre León Bérard, Lyon, France.
J Immunother Emphasis Tumor Immunol. 1995 Jan;17(1):62-8. doi: 10.1097/00002371-199501000-00008.
We conducted a Phase II trial using an intensive regimen combining interleukin-2 (IL2), interferon-alfa-2b (IFN), and lymphokine-activated killer (LAK) cells. The aim of this study was to evaluate the toxicity and the efficacy of this combination in selected patients with metastatic renal cell carcinoma. Thirty-one assessable patients were treated with at least one cycle of a regimen consisting of 20 x 10(6) IU/day s.c. IFN for 5 days, followed 2 days later by i.v. injections of 24 x 10(6) IU/m2/day IL2 every 8 h together with i.v. bolus of 5 x 10(6) IU/m2/day IFN every 8 h during 5 days. After a 6-day break, during which four leukophereses were performed, this i.v. combination was administered along with the LAK cell reinjections for a maximum of 5 days. Twenty-seven patients underwent the two parts of the first course of treatment; respectively, 42% and 46% of the planned dose of IL2 and IFN were administered. Several severe toxicities were observed including two treatment-related deaths. Significant tumor responses were observed in seven patients, including two complete remissions. Two of these patients remain alive without evidence of disease 36 and 40 months after treatment, respectively. This intensive regimen of IL2 together with IFN and LAK cells cannot be recommended even in selected patients with metastatic renal cell carcinoma. In addition, our results argue against the concept of a dose-response relationship in this setting.
我们开展了一项II期试验,使用了包含白细胞介素-2(IL2)、干扰素-α-2b(IFN)和淋巴因子激活的杀伤细胞(LAK)的强化方案。本研究的目的是评估该联合方案对选定的转移性肾细胞癌患者的毒性和疗效。31例可评估患者接受了至少一个周期的方案治疗,该方案包括皮下注射20×10⁶IU/天的IFN,持续5天,2天后开始,静脉注射24×10⁶IU/m²/天的IL2,每8小时一次,同时在5天内每8小时静脉推注5×10⁶IU/m²/天的IFN。在为期6天的休息期(在此期间进行了4次白细胞分离术)后,静脉联合用药与LAK细胞回输一起进行,最长持续5天。27例患者接受了第一疗程的两个部分;分别给予了计划剂量42%的IL2和46%的IFN。观察到了几种严重毒性,包括两例与治疗相关的死亡。7例患者观察到显著的肿瘤反应,包括2例完全缓解。其中2例患者分别在治疗后36个月和40个月仍存活,无疾病证据。即使是选定的转移性肾细胞癌患者,也不推荐使用这种IL2联合IFN和LAK细胞的强化方案。此外,我们的结果反对在这种情况下存在剂量反应关系的概念。