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首页> 外文期刊>Clinical Pharmacology and Therapeutics >Pharmacokinetics of high-dose oral calcitriol: results from a phase 1 trial of calcitriol and paclitaxel.
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Pharmacokinetics of high-dose oral calcitriol: results from a phase 1 trial of calcitriol and paclitaxel.

机译:大剂量口服骨化三醇的药代动力学:来自骨化三醇和紫杉醇的1期试验结果。

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OBJECTIVES: The data reported are from a trial designed to determine, in patients with advanced cancer, the maximum tolerated dose and pharmacokinetics of calcitriol when administered with paclitaxel, an agent whose antitumor activity in in vitro and in vivo studies has been shown to be enhanced by calcitriol. An additional goal was to evaluate the relationship between calcitriol dose and hypercalcemia. METHODS: Calcitriol was given orally for 3 consecutive days each week, and paclitaxel (80 mg/m(2)) was given intravenously weekly. Thirty-six patients were treated in cohorts composed of 3 to 9 patients, at escalating dose levels of calcitriol. The starting dose of calcitriol was 4 microg for 3 consecutive days each week, and the maximum dose administered was 38 microg for 3 consecutive days each week. The preparation of calcitriol used in this trial was a commercially available caplet (0.5 microg per caplet). Serum calcitriol concentrations were measured by radioimmunoassay. Detailed assessments of calcitriol pharmacokinetics were performed in 26 patients. RESULTS: There was substantial interpatient variation in peak serum calcitriol concentrations (C(max)), time to reach C(max), and area under the concentration versus time curve (AUC). Serum calcitriol AUC was not proportional to calcitriol dose (P =.0014). AUC for the 24-hour period after calcitriol administration [AUC (0-24)] at 38 microg was only 4 times that at 4 microg, instead of the 9.5-fold increase expected for a proportional relationship. Calcitriol plasma concentrations of 600 to 1440 pg/mL were achieved. No dose-limiting toxicity occurred in this trial. CONCLUSIONS: Despite variability in absorption, very high doses of calcitriol can be safely administered with paclitaxel. The high calcitriol serum concentrations achieved in this study approach those that, both in vitro and in vivo, potentiate the cytotoxicity of taxanes and platinum analogs.
机译:目的:报告的数据来自一项旨在确定患有晚期癌症的患者与紫杉醇联合使用时,骨化三醇的最大耐受剂量和药代动力学的研究,该药物的体外和体内研究显示其抗肿瘤活性增强由骨化三醇。另一个目标是评估骨化三醇剂量与高钙血症之间的关系。方法:每周连续3天口服骨化三醇,每周静脉内注射紫杉醇(80 mg / m(2))。三十六名患者接受了三至九名患者的按三醇剂量递增的治疗。骨化三醇的起始剂量是每周连续3天为4微克,并且给药的最大剂量是每周连续3天为38微克。在该试验中使用的骨化三醇的制剂是可商购的囊片(每囊0.5微克)。通过放射免疫测定法测定血清骨化三醇浓度。对26名患者进行了骨化三醇药代动力学的详细评估。结果:患者的血清钙三醇峰值浓度(C(max)),达到C(max)的时间以及浓度与时间曲线下的面积(AUC)存在较大的患者差异。血清骨化三醇AUC与骨化三醇剂量不成正比(P = .0014)。骨化三醇给药后24小时内的AUC [AUC(0-24)]为38微克,仅为4微克的4倍,而不是比例关系预期的9.5倍增加。骨化三醇血浆浓度达到600至1440 pg / mL。在该试验中未发生剂量限制性毒性。结论:尽管吸收存在差异,但紫杉醇可以安全地给予很高剂量的骨化三醇。在这项研究中达到的高钙三醇血清浓度接近于在体外和体内均能增强紫杉烷类和铂类似物的细胞毒性的浓度。

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