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依维莫司预防心脏移植受者急性排斥反应和移植血管病变:一项24个月的分析

Prevention of acute rejection and allograft vasculopathy by everolimus in cardiac transplants recipients: a 24-month analysis.

作者信息

Viganò Mario, Tuzcu Murat, Benza Raymond, Boissonnat Pascale, Haverich Axel, Hill James, Laufer Guenther, Love Robert, Parameshwar Jayan, Pulpón Luis Alonso, Renlund Dale, Abeywickrama Kamal, Cretin Nathalie, Starling Randall C, Eisen Howard J

机构信息

Department of Cardiac Surgery, San Matteo Hospital, Pavia, Italy.

出版信息

J Heart Lung Transplant. 2007 Jun;26(6):584-92. doi: 10.1016/j.healun.2007.03.005. Epub 2007 Apr 27.

Abstract

BACKGROUND

Everolimus is an immunosuppressive agent that reduces cardiac allograft vasculopathy. This report presents the 24-month results of a multicenter trial of everolimus vs azathioprine in heart transplantation.

METHODS

A total of 634 patients were randomized to receive 1.5 mg everolimus, 3 mg everolimus or azathioprine, with cyclosporine and steroids. A 12-month, double-blind, double-dummy period was followed by a 12-month open-label period.

RESULTS

At 24 months, the percentage of patients reaching the composite efficacy end-points was significantly lower with everolimus (1.5 mg: 45.9%, p = 0.016; 3 mg: 36.0%, p < 0.001) than with azathioprine (57.5%). The change in maximal intimal thickness from baseline to 24 months was significantly smaller with everolimus 1.5 mg (0.07 mm, p = 0.014) and 3 mg (0.06 mm, p = 0.004) compared with azathioprine (0.15 mm). The 24-month incidence of vasculopathy was 33.3% with everolimus 1.5 mg, 45.5% with everolimus 3 mg and 58.3% with azathioprine (p = 0.017 vs everolimus 1.5 mg). Incidence of cytomegalovirus infection was 3-fold lower in patients receiving everolimus compared with azathioprine (7.2% and 7.1% in the 1.5-mg and 3-mg everolimus cohorts, respectively, and 21% in the azathioprine group; p < 0.0001). Median serum creatinine levels at 24 months were higher with everolimus than with azathioprine, but decreased when cyclosporine exposure was reduced (everolimus 1.5 mg: baseline 167 micromol, after 6 months 157.5 micromol; everolimus 3 mg: baseline 185.6 micromol, after 6 months 160 micromol; azathioprine: baseline 123.3 micromol, after 6 months 127 micromol).

CONCLUSIONS

Everolimus significantly reduced acute rejection and limited the progression of allograft vasculopathy at 24 months compared with azathioprine. Although graft and patient survival was comparable at 24 months, everolimus therapy may improve longer-term outcomes after heart transplantation.

摘要

背景

依维莫司是一种可减轻心脏移植血管病变的免疫抑制剂。本报告展示了依维莫司与硫唑嘌呤在心脏移植中的多中心试验的24个月结果。

方法

总共634例患者被随机分配接受1.5毫克依维莫司、3毫克依维莫司或硫唑嘌呤,并联合环孢素和类固醇。在12个月的双盲、双模拟期之后是12个月的开放标签期。

结果

在24个月时,依维莫司组(1.5毫克:45.9%,p = 0.016;3毫克:36.0%,p < 0.001)达到复合疗效终点的患者百分比显著低于硫唑嘌呤组(57.5%)。与硫唑嘌呤组(0.15毫米)相比,1.5毫克依维莫司组(0.07毫米,p = 0.014)和3毫克依维莫司组(0.06毫米,p = 0.004)从基线到24个月的最大内膜厚度变化显著更小。1.5毫克依维莫司组血管病变的24个月发生率为33.3%,3毫克依维莫司组为45.5%,硫唑嘌呤组为58.3%(与1.5毫克依维莫司组相比,p = 0.017)。接受依维莫司治疗的患者巨细胞病毒感染发生率比接受硫唑嘌呤治疗的患者低3倍(1.5毫克依维莫司组和3毫克依维莫司组分别为7.2%和7.1%,硫唑嘌呤组为21%;p < 0.0001)。24个月时依维莫司组的血清肌酐中位数水平高于硫唑嘌呤组,但当环孢素暴露减少时有所下降(1.5毫克依维莫司组:基线167微摩尔,6个月后157.5微摩尔;3毫克依维莫司组:基线185.6微摩尔,6个月后160微摩尔;硫唑嘌呤组:基线123.3微摩尔,6个月后127微摩尔)。

结论

与硫唑嘌呤相比,依维莫司在24个月时显著降低了急性排斥反应并限制了移植血管病变的进展。尽管24个月时移植物和患者生存率相当,但依维莫司治疗可能会改善心脏移植后的长期结局。

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