首页> 外文期刊>Transplantation: Official Journal of the Transplantation Society >A rational dosing algorithm for basiliximab (Simulect) in pediatric renal transplantation based on pharmacokinetic-dynamic evaluations.
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A rational dosing algorithm for basiliximab (Simulect) in pediatric renal transplantation based on pharmacokinetic-dynamic evaluations.

机译:一种基于药代动力学评估的巴利昔单抗(Simulect)在小儿肾移植中的合理剂量算法。

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BACKGROUND The pharmacokinetics and immunodynamics of basiliximab were assessed in 39 pediatric de novo kidney allograft recipients to rationally chose a dose regimen for this age group.METHODS In study part 1, patients were given 12 mg/m of basiliximab by bolus intravenous injection before surgery and on day 4. An interim pharmacokinetic evaluation supported a fixed-dose approach for study part 2 in which infants and children received two 10-mg doses and adolescents received two 20-mg doses. Blood samples were collected over a 12-week period for analysis of basiliximab and soluble interleukin-2 receptor concentrations, flow cytometry, and screening for anti-idiotype antibodies.RESULTS Basiliximab clearance in infants and children (n=25) was reduced by approximately half compared with adults from a previous study and was independent of age (1-11 years), weight (9-37 kg), and body surface area (0.44-1.20 m ). Clearance in adolescents (12-16 years, n=14) approached or reached adult values. CD25-saturating basiliximab concentrations were maintained for 31+/-12 days in study part 1 with mg/m dosing and for 36+/-14 days in study part 2 based on the fixed-dose regimen ( =0.31). A single patient experienced a rejection episode during CD25 saturation. The duration of CD25 saturation in patients who experienced a rejection episode after desaturation did not differ from those who remained rejection-free for the full 6-month period: 34+/-6 days (n=6) vs. 35+/-14 days (n=33 patients); =0.74. Anti-idiotype antibodies were detected in two patients; however, this did not influence the clearance of basiliximab or the duration of CD25 saturation.CONCLUSIONS To achieve similar basiliximab exposure as is efficacious in adults, pediatric patients <35 kg should receive two 10-mg doses and those >/=35 kg should receive two 20-mg doses of basiliximab by intravenous infusion or bolus injection. The first dose is given before surgery and the second on day 4 after transplantation.
机译:背景对39例小儿从头进行肾脏移植的接受者评估了巴西利昔单抗的药代动力学和免疫动力学,以合理地选择该年龄组的剂量方案。方法在研究的第一部分,患者在手术前通过静脉推注静脉给予巴利昔单抗12 mg / m。在第4天,中期药代动力学评估支持研究2的固定剂量方法,其中婴儿和儿童接受两次10毫克剂量,青少年接受两次20毫克剂量。在为期12周的时间内采集血样,分析巴利昔单抗和可溶性白细胞介素2受体的浓度,流式细胞仪并筛选抗独特型抗体。结果婴儿和儿童(n = 25)的Basiliximab清除率降低了约一半与先前研究的成年人相比,与年龄(1-11岁),体重(9-37 kg)和身体表面积(0.44-1.20 m)无关。青少年(12-16岁,n = 14)的清除率接近或达到成人值。基于固定剂量方案,在用mg / m剂量给药的研究部分1中,饱和CD25的巴利昔单抗浓度维持31 +/- 12天,在研究部分2中保持36 +/- 14天(= 0.31)。一名患者在CD25饱和期间经历了排斥反应。在去饱和后经历排斥反应的患者中CD25饱和的持续时间与那些在整个6个月内保持无排斥反应的患者没有区别:34 +/- 6天(n = 6)对35 +/- 14天(n = 33名患者); = 0.74。在两名患者中检测到抗独特型抗体。然而,这并不影响巴利昔单抗的清除率或CD25饱和的持续时间。结论为了达到与成人有效的巴利昔单抗相似的暴露水平,<35 kg的儿科患者应接受两次10 mg剂量,> / = 35 kg的儿科患者应接受静脉输注或推注两种20 mg剂量的巴利昔单抗。第一剂在手术前给予,第二剂在移植后第4天给予。

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