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首页> 外文期刊>Transplantation: Official Journal of the Transplantation Society >A multicenter, open-label, pharmacokinetic/pharmacodynamic safety, and tolerability study of basiliximab (Simulect) in pediatric de novo renal transplant recipients.
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A multicenter, open-label, pharmacokinetic/pharmacodynamic safety, and tolerability study of basiliximab (Simulect) in pediatric de novo renal transplant recipients.

机译:巴利昔单抗(Simulect)在小儿新生肾脏移植受者中的多中心,开放性,药代动力学/药效学安全性和耐受性研究。

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BACKGROUND Basiliximab (Simulect) has been shown to be safe and effective in adult renal transplant recipients, when used in combination with cyclosporine (Neoral) and corticosteroids. We report on the safety and preliminary efficacy of basiliximab in pediatric de novo renal transplant recipients.METHODS This was an open-label, 12-month study of basiliximab in 41 patients (2 cohorts: <9 and 9 to <16 years). In phase 1, two intravenous (IV) bolus injections of basiliximab (12 mg/m ) were administered (before and 4 days postsurgery). In phase 2, two injections (<40 kg, 10 mg and >/=40 kg, 20 mg) were administered at the same time points. Most patients (26/41 [63%]) received cadaveric kidneys. Almost half of the patients had three human leukocyte antigen mismatches with the organ donors. Concurrent immunosuppression included Neoral and corticosteroids. Azathioprine was allowed after 28 days.RESULTS All patients completed the 1-year study. The acute tolerability of basiliximab via IV bolus injection was good, without evidence of cytokine-release syndrome or acute local reactions. All patients experienced adverse events, but most (71%) were mild or asymptomatic. No deaths or malignancies occurred. The incidence and types of serious adverse events (59%) and serious infections (44%) were as expected in this patient population, and few were drug-related (7% and 5%, respectively). Thirty-eight patients (93%) had infections, mostly urinary tract infections, as expected for renal transplant patients. Six patients (15%) had drug-related adverse events. Biopsy-confirmed acute rejection episodes occurred in 6/41 (15%) of patients during the first 6 months posttransplantation and in 9/41 (22%) patients during the first 12 months. Five patients (12%) experienced graft loss, none of which were preceded by acute rejection episodes.CONCLUSIONS Basiliximab is safe and well tolerated when administered by IV bolus injection in de novo pediatric renal transplant recipients. These preliminary data suggest that basiliximab, given in combination with cyclosporine and corticosteroids, is an effective immunosuppressive regimen for the prevention of acute rejection in pediatric renal transplantation.
机译:背景技术当与环孢菌素(Neoral)和皮质类固醇联合使用时,Basiliximab(Simulect)已被证明在成人肾移植受者中是安全有效的。我们报告了巴利昔单抗在小儿新生肾脏移植接受者中的安全性和初步疗效。方法这是一项开放性的12个月的巴利昔单抗在41例患者中的研究(2个队列:<9和9至<16岁)。在第1阶段中(手术前和手术后4天)进行了两次静脉注射(IV)的巴西利昔单抗(12 mg / m 2)推注。在阶段2中,在同一时间点两次注射(<40 kg,10 mg和> / = 40 kg,20 mg)。大多数患者(26/41 [63%])接受了尸体肾脏。几乎一半的患者的三个人类白细胞抗原与器官供体不匹配。并发免疫抑制包括神经和皮质类固醇。 28天后允许使用硫唑嘌呤。结果所有患者均完成了为期1年的研究。经静脉推注巴利昔单抗的急性耐受性良好,没有细胞因子释放综合征或急性局部反应的证据。所有患者均发生不良事件,但大多数(71%)为轻度或无症状。没有死亡或恶性肿瘤发生。严重不良事件的发生率和类型(59%)和严重感染(44%)与该患者人群中的预期相符,很少与药物有关(分别为7%和5%)。肾移植患者中有38名患者(93%)感染,主要是尿路感染。六名患者(15%)发生了与药物相关的不良事件。活检证实的急性排斥反应发作发生在移植后的前6个月的患者中,占6/41(15%),而在移植的最初12个月中,患者中占9/41(22%)。 5例患者(占12%)经历了移植物丢失,但均未出现急性排斥反应。结论在新生小儿肾脏移植受者静脉推注时,Basiliximab安全且耐受良好。这些初步数据表明,与环孢素和皮质类固醇合用的巴利昔单抗是预防小儿肾移植急性排斥反应的有效免疫抑制方案。

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