Clark R H, Dimitrov N V, Axelson J A, Charamella L J
J Biol Response Mod. 1984 Dec;3(6):613-9.
In vitro and in vivo studies utilizing a combination of leukocyte interferon-alpha (IFN) and chlorambucil (CLB) were done to investigate possible synergism between a biological response modifier and a chemotherapy drug. In vitro studies utilized a human myeloid leukemia cell line (K-562) pretreated with IFN and then exposed to CLB. The combination resulted in significant depression of cell growth compared with use of IFN or CLB alone. In vivo studies involved eight heavily pretreated patients given 6 million units IFN for 5 days followed by oral CLB (16 mg/m2) for 5 days repeated every 4 weeks. Three myeloma patients had reduction in immunoglobulins and experienced clinical responses. Three of four patients with Hodgkin's disease responded after relatively short periods of treatment. One patient with a diffuse lymphocytic lymphoma had a complete unmaintained remission lasting 6 months. Toxicity was minimal, with mild fever, nausea, and vomiting. These preliminary studies suggest that IFN may be a biological response modifier when used in combination with a cytotoxic agent.
利用白细胞α-干扰素(IFN)和苯丁酸氮芥(CLB)联合进行了体外和体内研究,以探讨一种生物反应调节剂与一种化疗药物之间可能存在的协同作用。体外研究采用一种经IFN预处理后再暴露于CLB的人髓性白血病细胞系(K-562)。与单独使用IFN或CLB相比,联合使用导致细胞生长显著受抑。体内研究涉及8例经过大量预处理的患者,给予600万单位IFN,持续5天,随后口服CLB(16mg/m²),持续5天,每4周重复一次。3例骨髓瘤患者的免疫球蛋白降低并出现临床反应。4例霍奇金病患者中有3例在相对较短的治疗期后出现反应。1例弥漫性淋巴细胞淋巴瘤患者获得了持续6个月的完全未维持缓解。毒性极小,有轻度发热、恶心和呕吐。这些初步研究表明,IFN与细胞毒性药物联合使用时可能是一种生物反应调节剂。