首页> 外文期刊>Tumori. >Suramin in combination with 5-fluorouracil (5-FU) and leucovorin (LV) in metastatic colorectal cancer patients resistant to 5-FU+LV-based chemotherapy.
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Suramin in combination with 5-fluorouracil (5-FU) and leucovorin (LV) in metastatic colorectal cancer patients resistant to 5-FU+LV-based chemotherapy.

机译:苏拉明与5-氟尿嘧啶(5-FU)和亚叶酸(LV)联合用于对基于5-FU + LV的化疗耐药的转移性结直肠癌患者。

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AIMS AND BACKGROUND: 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. METHODS AND STUDY DESIGN: 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. RESULTS: 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. CONCLUSIONS: 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.
机译:目的和背景:苏拉明已被证明是潜在的新型抗癌剂,因为它具有抑制多种生长因子与其受体结合并抑制体外癌细胞生长的能力。由于在结直肠癌中已证明涉及涉及被苏拉明拮抗的生长因子的多自分泌环,因此我们先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,三名在服用苏拉明后接受5-FU + LV的患者尽管接受了氟嘧啶的大量预处理,但获得了客观的应答。该观察结果很有趣,因为苏拉明可能改变了肿瘤的生物学特性,使其对5-FU + LV敏感。因此,我们进行了本研究以调查苏拉明可能克服对5-FU + LV的耐药性的可能性。方法和研究设计:只有在基于5-FU + LV的化疗过程中发生转移和进行性疾病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八周,该算法使用贝叶斯药代动力学将苏拉明血浆浓度维持在200-250微克/毫升。在苏拉明起始后的一周开始的两小时内,I-LV 250 mg / m2的输注两小时中途每周以450 mg / m2的剂量给药5-FU,最多持续26周。结果:治疗的耐受性相对较好,但在试验的第一阶段招募了13名患者后,未观察到客观反应。因此,根据最初的两阶段抽样设计,该试验被中断。结论:本研究不支持苏拉明可能克服5-FU + LV耐药性的假设,不建议将其用于结直肠癌。

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