Falcone A, Pfanner E, Brunetti I, Allegrini G, Lencioni M, Galli C, Masi G, Danesi R, Antonuzzo A, Del Tacca M, Conte P F
U.O. Oncologia Medica, Dipartimento di Oncologia, Ospedale S. Chiara, Pisa, Italy.
Tumori. 1998 Nov-Dec;84(6):666-8. doi: 10.1177/030089169808400610.
Suramin has been shown to be of interest as a potential new anticancer agent because of its capacity to inhibit the binding of several growth factors to their receptors and to inhibit the growth of cancer cells in vitro. Since multi-autocrine loops involving growth factors which are antagonized by suramin have been demonstrated in colorectal cancer, we previously evaluated the activity of suramin in patients with advanced colorectal cancer. Interestingly, in this study three patients who had received 5-FU+LV after suramin, although heavily pretreated with fluoropyrimidines, obtained an objective response. This observation was intriguing as it might have been that suramin had changed the biology of the tumor, making it sensitive to 5-FU+LV. We therefore conducted the present study to investigate the possibility that suramin might overcome the resistance to 5-FU+LV.
Only colorectal cancer patients with metastatic and progressive disease during 5-FU+LV-based chemotherapy were eligible for this study. Suramin was administered for eight weeks at doses determined by means of a computer-assisted dosing algorithm that used Bayesian pharmacokinetics to maintain suramin plasma concentrations of 200-250 microg/ml. 5-FU was administered weekly at a dosis of 450 mg/m2 halfway through a two-hour infusion of I-LV 250 mg/m2 starting one week after the initiation of suramin for a maximum of 26 weeks.
Treatment was relatively well tolerated, but no objective responses were observed after the accrual of 13 patients in the first stage of the trial. Consequently, the trial was interrupted according to the initial two-stage sampling design.
The present study does not support the hypothesis that suramin might overcome resistance to 5-FU+LV and its use in colorectal cancer is not recommended.
苏拉明已被证明是一种潜在的新型抗癌药物,因为它能够抑制多种生长因子与其受体的结合,并在体外抑制癌细胞的生长。由于在结直肠癌中已证实存在涉及生长因子的多自分泌环路,而苏拉明可拮抗这些生长因子,我们之前评估了苏拉明在晚期结直肠癌患者中的活性。有趣的是,在这项研究中,三名在接受苏拉明治疗后接受5-氟尿嘧啶+亚叶酸钙治疗的患者,尽管之前已大量接受氟嘧啶类药物治疗,但仍获得了客观缓解。这一观察结果很有趣,因为可能是苏拉明改变了肿瘤的生物学特性,使其对5-氟尿嘧啶+亚叶酸钙敏感。因此,我们进行了本研究,以探讨苏拉明是否可能克服对5-氟尿嘧啶+亚叶酸钙的耐药性。
只有在基于5-氟尿嘧啶+亚叶酸钙的化疗期间出现转移和病情进展的结直肠癌患者才有资格参加本研究。苏拉明以计算机辅助给药算法确定的剂量给药8周,该算法使用贝叶斯药代动力学来维持苏拉明血浆浓度在200-250微克/毫升。从苏拉明开始给药一周后开始,5-氟尿嘧啶每周给药一次,剂量为450毫克/平方米,在两小时内输注亚叶酸钙250毫克/平方米,最多持续26周。
治疗耐受性相对较好,但在试验第一阶段纳入13例患者后未观察到客观缓解。因此,根据最初的两阶段抽样设计,试验中断。
本研究不支持苏拉明可能克服对5-氟尿嘧啶+亚叶酸钙耐药性的假设,不建议在结直肠癌中使用苏拉明。