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在一项多中心、开放标签、随机试验中,转换为依维莫司并减少钙调神经磷酸酶抑制剂后胸段移植受者的长期结局。

Long-term outcomes of thoracic transplant recipients following conversion to everolimus with reduced calcineurin inhibitor in a multicenter, open-label, randomized trial.

作者信息

Gullestad Lars, Eiskjaer Hans, Gustafsson Finn, Riise Gerdt C, Karason Kristjan, Dellgren Göran, Rådegran Göran, Hansson Lennart, Gude Einar, Bjørtuft Øystein, Jansson Kjell, Schultz Hans Henrik, Solbu Dag, Iversen Martin

机构信息

Department of Cardiology, Oslo University Hospital Rikshospitalet, Oslo, Norway.

Faculty of Medicine, K.G. Jebsen Cardiac Research Centre and Center for Heart Failure Research, University of Oslo, Oslo, Norway.

出版信息

Transpl Int. 2016 Jul;29(7):819-29. doi: 10.1111/tri.12783. Epub 2016 May 30.

Abstract

The NOCTET study randomized 282 patients ≥1 year after heart or lung transplantation to continue conventional calcineurin inhibitor (CNI) therapy or to start everolimus with reduced-exposure CNI. Last follow-up, at ≥5 years postrandomization (mean: 5.6 years) was attended by 72/140 everolimus patients (51.4%) and 91/142 controls (64.1%). Mean measured GFR remained stable in the everolimus group from randomization (51.3 ml/min) to last visit (51.4 ml/min) but decreased in controls (from 50.5 ml/min to 45.3 ml/min) and was significantly higher with everolimus at last follow-up (P = 0.004). The least squares mean (SE) change from randomization was -1.5 (1.7)ml/min with everolimus versus -7.2 (1.7)ml/min for controls (difference: 5.7 [95% CI 1.7; 9.6]ml/min; P = 0.006). The difference was accounted for by heart transplant patients (difference: 6.9 [95% 2.3; 11.5]ml/min; P = 0.004). Lung transplant patients showed no between-group difference at last follow-up. Rates of rejection, death, and major cardiac events were similar between groups, as was graft function. Pneumonia was more frequent with everolimus (18.3% vs. 6.4%). In conclusion, introducing everolimus in maintenance heart transplant patients, with reduced CNI, achieves a significant improvement in renal function which is maintained for at least 5 years, but an early renal benefit in lung transplant patients was lost. Long-term immunosuppressive efficacy was maintained.

摘要

NOCTET研究将282例心脏或肺移植术后≥1年的患者随机分组,分别继续接受传统钙调神经磷酸酶抑制剂(CNI)治疗或开始使用低暴露量CNI联合依维莫司治疗。在随机分组≥5年(平均5.6年)时进行末次随访,140例依维莫司组患者中有72例(51.4%)参与,142例对照组患者中有91例(64.1%)参与。依维莫司组从随机分组时(51.3 ml/min)至末次随访时平均实测肾小球滤过率(GFR)保持稳定(51.4 ml/min),而对照组则下降(从50.5 ml/min降至45.3 ml/min),且在末次随访时依维莫司组的GFR显著更高(P = 0.004)。依维莫司组自随机分组起的最小二乘均值(SE)变化为-1.5(1.7)ml/min,对照组为-7.2(1.7)ml/min(差值:5.7 [95%CI 1.7;9.6]ml/min;P = 0.006)。这种差异在心脏移植患者中更为明显(差值:6.9 [95% 2.3;11.5]ml/min;P = 0.004)。肺移植患者在末次随访时组间差异不明显。两组间的排斥反应、死亡和主要心脏事件发生率以及移植物功能相似。依维莫司组肺炎更为常见(18.3%对6.4%)。总之,在心脏移植维持治疗患者中引入依维莫司并减少CNI用量可显著改善肾功能,且至少维持5年,但肺移植患者早期的肾脏获益消失。长期免疫抑制疗效得以维持。

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