Creagan E T, Hestorff R D, Suman V J, Mailliard J A, Nair S, Krook J E, Kugler J W, Marschke R F, Michalak J C, Tschetter L K
Mayo Clinic and Mayo Foundation, Rochester, Minnesota 55905, USA.
Am J Clin Oncol. 1998 Apr;21(2):139-41. doi: 10.1097/00000421-199804000-00008.
Adoptive immunotherapy (AI) with interleukin-2 (IL-2) and lymphokine-activated killer (LAK) cells is an antineoplastic modality in which immune-activated cells are administered to a host having cancer in an attempt to mediate tumor regression. Levamisole (LEV), an immune stimulant, has been suggested as having therapeutic effectiveness in a variety of cancers. After a phase I trial of recombinant IL-2 plus LEV, a phase II trial of this combination was conducted in patients who had advanced renal cell carcinoma. The regimen was IL-2 at 3 x 10(6) U/m2 daily x 5 plus LEV at 50 mg/m2 perorally three times a day x 5. Only one of the 22 eligible patients had a regression. It was a partial regression, 85 days in duration. The median time to treatment failure (refusal, progression, or off study because of toxicity) was 36 days. The only grade 4 toxicity reported was lethargy. This regimen is not recommended for further testing in patients who have advanced renal cell carcinoma.
采用白细胞介素-2(IL-2)和淋巴因子激活的杀伤细胞(LAK)进行过继性免疫治疗(AI)是一种抗肿瘤方法,即向患有癌症的宿主给予免疫激活细胞,试图介导肿瘤消退。左旋咪唑(LEV)是一种免疫刺激剂,已被认为在多种癌症中具有治疗效果。在进行了重组IL-2加LEV的I期试验后,对晚期肾细胞癌患者进行了该联合方案的II期试验。方案为IL-2 3×10⁶ U/m²每日×5天,加LEV 50 mg/m²口服每日三次×5天。22例符合条件的患者中只有1例出现消退。这是一次部分缓解,持续85天。治疗失败(因毒性而拒绝、病情进展或退出研究)的中位时间为36天。报告的唯一4级毒性是嗜睡。不建议在晚期肾细胞癌患者中对该方案进行进一步试验。