Harrison S D, Stevens J J, Waud W R, Dykes D J, Schmid S M, Griswold D P
Chemotherapy and Toxicology Research Department, Southern Research Institute, Birmingham, Alabama 35255-5305.
J Biol Response Mod. 1990 Aug;9(4):395-400.
This investigation was conducted to provide preclinical in vivo tumor response data collected under standardized conditions with a range of clinically useful drugs combined with type I (alpha/beta) or type II (gamma) interferon. Murine tumor models used were P388 leukemia, Meth A sarcoma, and B16 melanoma. Eleven cytotoxic drugs were studied. Interferon combinations with cytosine arabinoside provided consistent indications of activity greater than that of the respective single agents. Doxorubicin and cisplatin each prolonged the time to treatment failure, relative to single-agent results, when they were combined with gamma-interferon in the Meth A and B16 models. Interferon combinations with methotrexate, 6-mercaptopurine, 6-thioguanine, ampligen, suramin, 5-fluorouracil, cyclophosphamide, and vinblastine yielded no evidence of any positive therapeutic interactions under the conditions of this study.
进行这项研究是为了提供在标准化条件下收集的临床前体内肿瘤反应数据,这些数据涉及一系列临床常用药物与I型(α/β)或II型(γ)干扰素联合使用的情况。所使用的小鼠肿瘤模型有P388白血病、Meth A肉瘤和B16黑色素瘤。研究了11种细胞毒性药物。干扰素与阿糖胞苷的联合使用始终显示出比各自单一药物更强的活性迹象。在Meth A和B16模型中,当阿霉素和顺铂与γ干扰素联合使用时,相对于单一药物的结果,它们各自都延长了治疗失败的时间。在本研究条件下,干扰素与甲氨蝶呤、6-巯基嘌呤、6-硫鸟嘌呤、氨普立糖、苏拉明、5-氟尿嘧啶、环磷酰胺和长春碱的联合使用未显示出任何积极治疗相互作用的证据。