Suppr超能文献

在维持性肾移植患者中转换为贝利尤单抗:一项回顾性多中心欧洲研究。

Conversion to Belatacept in Maintenance Kidney Transplant Patients: A Retrospective Multicenter European Study.

机构信息

Department of Nephrology and Organ Transplantation, CHU Rangueil, Toulouse, France.

Service de Néphrologie-Transplantation, Hôpital Necker, AP-HP, Paris et Université Paris Descartes, Paris.

出版信息

Transplantation. 2018 Sep;102(9):1545-1552. doi: 10.1097/TP.0000000000002192.

Abstract

BACKGROUND

The use of belatacept is not yet approved for maintenance in kidney transplant patients. This retrospective multicenter European study aimed to assess the efficacy and safety of conversion to belatacept in a large cohort of patients in a real-life setting and to identify the predictive factors for improved kidney function after the switch.

METHODS

Two hundred nineteen maintenance kidney transplant patients from 5 European kidney transplant centers were converted to belatacept at 21.2 months (0.1-337.1 months) posttransplantation, mainly because of impaired kidney function. Thirty-two patients were converted to belatacept within the first 3 months posttransplantation. The mean duration of follow-up was 21.9 ± 20.2 months.

RESULTS

The actuarial rate of patients still on belatacept-based therapy was 77.6%. Mean estimated glomerular filtration rate increased from 32 ± 16.4 at baseline to 38 ± 20 mL/min per 1.73 m (P < 0.0001) at last follow-up. Conversion to belatacept before 3 months posttransplantation was the main predictive factor for a significant increase in estimated glomerular filtration rate (of 5 and 10 mL/min per 1.73 m at 3 and 12 months after the switch, respectively). Eighteen patients (8.2%) presented with an acute rejection episode after conversion; 3 developed a donor-specific antibody. Overall efficacy and safety were good, including for the 35 patients that had a donor-specific antibody at conversion.

CONCLUSIONS

The conversion to belatacept was effective, especially when performed early after transplantation.

摘要

背景

贝那普利塞在肾移植患者的维持治疗中尚未得到批准。本回顾性多中心欧洲研究旨在评估在真实环境中,大量患者转换为贝那普利塞的疗效和安全性,并确定转换后肾功能改善的预测因素。

方法

来自 5 个欧洲肾移植中心的 219 例维持性肾移植患者在移植后 21.2 个月(0.1-337.1 个月)转换为贝那普利塞,主要是因为肾功能受损。32 例患者在移植后 3 个月内转换为贝那普利塞。平均随访时间为 21.9±20.2 个月。

结果

仍在接受贝那普利塞治疗的患者的累积生存率为 77.6%。估计肾小球滤过率的平均值从基线时的 32±16.4 增加到最后一次随访时的 38±20 mL/min/1.73 m(P<0.0001)。移植后 3 个月内转换为贝那普利塞是估计肾小球滤过率显著增加的主要预测因素(分别在转换后 3 个月和 12 个月时增加 5 和 10 mL/min/1.73 m)。18 例患者(8.2%)在转换后出现急性排斥反应;3 例患者出现了供体特异性抗体。总体疗效和安全性良好,包括在转换时就已经存在供体特异性抗体的 35 例患者。

结论

转换为贝那普利塞是有效的,尤其是在移植后早期进行时。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验