MacDonald J R, Pegg D G
Department of Pathology and Experimental Toxicology, Parke-Davis Pharmaceutical Research Division of Warner-Lambert Company, Ann Arbor, MI 48105.
Cancer Chemother Pharmacol. 1993;32(5):365-7. doi: 10.1007/BF00735920.
Severe soft-tissue ulceration is known to result from inadvertent extravasation of a number of anticancer drugs, including tubulin-binding vinca alkaloids, during intravenous administration. CI-980 is a novel anticancer drug candidate that also inhibits mitosis by binding to tubulin. Intradermal administration of CI-980 to mice at doses of 0.02 and 0.05 mg produced ulcerative lesions in 3/5 and 2/5 animals, respectively, that were significantly smaller than those produced in all animals at vinblastine doses of 0.05 and 0.1 mg. Ulcerative lesions resulting from CI-980 treatment were also less persistent, resolving in 2-8 days versus 7-16 days following vinblastine administration. As based on the common dose of 0.05 mg, CI-980 appears to have significantly less vesicant activity than vinblastine.
已知在静脉给药过程中,多种抗癌药物(包括与微管蛋白结合的长春花生物碱)意外外渗会导致严重的软组织溃疡。CI-980是一种新型抗癌候选药物,它也通过与微管蛋白结合来抑制有丝分裂。以0.02和0.05毫克的剂量对小鼠进行CI-980皮内给药,分别在3/5和2/5的动物中产生了溃疡性病变,这些病变明显小于在所有动物中以0.05和0.1毫克长春花碱剂量产生的病变。CI-980治疗引起的溃疡性病变持续时间也较短,在给药后2-8天消退,而长春花碱给药后为7-16天。基于0.05毫克的常用剂量,CI-980似乎比长春花碱的发泡活性明显更低。