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贝拉西普:用于成年肾移植受者。

Belatacept: in adult kidney transplant recipients.

机构信息

Adis, Auckland, New Zealand.

出版信息

BioDrugs. 2012 Dec 1;26(6):413-24. doi: 10.2165/11208900-000000000-00000.

Abstract

Belatacept is a second-generation cytotoxic T-lymphocyte-associated antigen-4-Ig fusion protein, which down-regulates T-cell response, and is used in the prophylaxis of organ rejection in adults receiving a kidney transplant. This article reviews the pharmacologic properties of belatacept and its clinical efficacy and tolerability in kidney transplant recipients. In the well designed, phase III trials BENEFIT and BENEFIT-EXT (in patients receiving kidneys from living/standard-criteria or extended-criteria donors, respectively), a belatacept-based treatment regimen was noninferior to a cyclosporine (ciclosporin)-based regimen with regard to patient and graft survival and acute graft rejection rate, and was significantly superior to the cyclosporine-based regimen with regard to the rate of renal impairment (in BENEFIT only), at 12 months. Belatacept-based treatment showed long-term efficacy and remained effective after 2, 3, and 4 years with regard to these endpoints. Belatacept was generally well tolerated in patients with kidney transplants from living, standard-criteria, or extended-criteria donors. The most serious adverse events that have been reported with belatacept treatment are post-transplant lymphoproliferative disorder, other malignancies, and serious infections. At month 12, the incidence of new-onset diabetes mellitus after transplant was significantly lower with belatacept than with cyclosporine, and belatacept recipients had significantly lower blood pressure and a significantly smaller increase in certain lipid levels than cyclosporine recipients.

摘要

贝拉西普是一种第二代细胞毒性 T 淋巴细胞相关抗原 4-Ig 融合蛋白,可下调 T 细胞反应,用于预防成人接受肾移植后的器官排斥反应。本文综述了贝拉西普的药理学特性及其在肾移植受者中的临床疗效和耐受性。在设计良好的 III 期 BENEFIT 和 BENEFIT-EXT 试验(分别在接受活体/标准或扩展标准供者肾移植的患者中进行)中,与基于环孢素(环孢菌素)的治疗方案相比,基于贝拉西普的治疗方案在患者和移植物存活率以及急性移植物排斥率方面非劣效,并且在肾损害发生率方面(仅在 BENEFIT 中)显著优于基于环孢素的治疗方案。在 12 个月时,基于贝拉西普的治疗显示出长期疗效,并且在 2、3 和 4 年时这些终点仍有效。基于贝拉西普的治疗在接受活体、标准或扩展标准供者肾移植的患者中总体耐受性良好。与贝拉西普治疗相关的最严重不良事件是移植后淋巴增殖性疾病、其他恶性肿瘤和严重感染。在移植后 12 个月时,与环孢素相比,新发糖尿病的发生率显著降低,且贝拉西普组的血压明显低于环孢素组,某些血脂水平的升高幅度明显小于环孢素组。

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