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Pharmacokinetics and Toxicity of Sodium Selenite in the Treatment of Patients with Carcinoma in a Phase I Clinical Trial: The SECAR Study

机译:I期临床试验中亚硒酸钠在治疗癌症患者中的药代动力学和毒性:SECAR研究

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摘要

Background: Sodium selenite at high dose exerts antitumor effects and increases efficacy of cytostatic drugs in multiple preclinical malignancy models. We assessed the safety and efficacy of intravenous administered sodium selenite in cancer patients’ refractory to cytostatic drugs in a phase I trial. Patients received first line of chemotherapy following selenite treatment to investigate altered sensitivity to these drugs and preliminary assessment of any clinical benefits. Materials and Methods: Thirty-four patients with different therapy resistant tumors received iv sodium selenite daily for consecutive five days either for two weeks or four weeks. Each cohort consisted of at least three patients who received the same daily dose of selenite throughout the whole treatment. If 0/3 patients had dose-limiting toxicities (DLTs), the study proceeded to the next dose-level. If 2/3 had DLT, the dose was considered too high and if 1/3 had DLT, three more patients were included. Dose-escalation continued until the maximum tolerated dose (MTD) was reached. MTD was defined as the highest dose-level on which 0/3 or 1/6 patients experienced DLT. The primary endpoint was safety, dose-limiting toxic effects and the MTD of sodium selenite. The secondary endpoint was primary response evaluation. Results and Conclusion: MTD was defined as 10.2 mg/m2, with a calculated median plasma half-life of 18.25 h. The maximum plasma concentration of selenium from a single dose of selenite increased in a nonlinear pattern. The most common adverse events were fatigue, nausea, and cramps in fingers and legs. DLTs were acute, of short duration and reversible. Biomarkers for organ functions indicated no major systemic toxicity. In conclusion, sodium selenite is safe and tolerable when administered up to 10.2 mg/m2 under current protocol. Further development of the study is underway to determine if prolonged infusions might be a more effective treatment strategy.
机译:背景:高剂量的亚硒酸钠在多种临床前恶性肿瘤模型中具有抗肿瘤作用,并能提高细胞抑制药物的功效。在一项I期临床试验中,我们评估了静脉注射亚硒酸钠对癌症患者难治细胞抑制药物的安全性和有效性。在亚硒酸盐治疗后,患者接受了一线化疗,以调查对这些药物敏感性的改变以及对任何临床益处的初步评估。材料和方法:34例具有不同治疗耐药性肿瘤的患者每天连续2天或连续4天连续5天接受亚硒酸钠静脉注射。每个队列至少由三名患者组成,他们在整个治疗过程中每天接受相同剂量的亚硒酸盐。如果0/3患者具有剂量限制性毒性(DLT),则研究将继续进行下一个剂量水平。如果2/3患有DLT,则认为剂量太高;如果1/3患有DLT,则包括三名患者。剂量递增一直持续到达到最大耐受剂量(MTD)为止。 MTD被定义为0/3或1/6患者经历DLT的最高剂量水平。主要终点是安全性,剂量限制性毒性作用和亚硒酸钠的MTD。次要终点是主要反应评估。结果与结论:MTD定义为10.2 mg / m 2 ,平均血浆半衰期为18.25 h。单剂量亚硒酸盐中硒的最大血浆浓度呈非线性增加。最常见的不良事件是手指,腿部疲劳,恶心和抽筋。 DLT急性发作,持续时间短且可逆。器官功能的生物标志物未显示主要的全身毒性。总之,按照目前的方案,亚硒酸钠的安全性和耐受性最高可达10.2 mg / m 2 。研究的进一步发展正在进行中,以确定延长输注是否可能是更有效的治疗策略。

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