首页> 外文期刊>The Journal of heart and lung transplantation: the official publication of the International Society for Heart Transplantation >Prevention of acute rejection and allograft vasculopathy by everolimus in cardiac transplants recipients: a 24-month analysis.
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Prevention of acute rejection and allograft vasculopathy by everolimus in cardiac transplants recipients: a 24-month analysis.

机译:依维莫司预防心脏移植受者的急性排斥反应和同种异体血管病变:24个月分析。

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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 vseverolimus 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.
机译:背景:依维莫司是一种减少心脏同种异体血管病变的免疫抑制剂。本报告介绍了依维莫司与硫唑嘌呤在心脏移植中进行的多中心试验的24个月结果。方法:总共634例患者被随机分配接受1.5 mg依维莫司,3 mg依维莫司或硫唑嘌呤,环孢素和类固醇治疗。 12个月的双盲双假期之后是12个月的开放标签期。结果:在24个月时,依维莫司(1.5 mg:45.9%,p = 0.016; 3 mg:36.0%,p <0.001)达到复合功效终点的患者百分比显着低于硫唑嘌呤(57.5%) 。与硫唑嘌呤(0.15 mm)相比,依维莫司1.5 mg(0.07 mm,p = 0.014)和3 mg(0.06 mm,p = 0.004)从基线到24个月的最大内膜厚度变化明显较小。依维莫司1.5毫克的24个月血管病变发生率为33.3%,依维莫司3毫克为45.5%,硫唑嘌呤为58.3%(p = 0.017 vs依维莫司1.5毫克)。接受依维莫司的患者巨细胞病毒感染的发生率比硫唑嘌呤低3倍(1.5毫克和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)。依维莫司24个月时血清肌酐水平高于硫唑嘌呤,但当环孢素暴露减少时降低(依维莫司1.5 mg:基线167微摩尔,六个月后为157.5微摩尔;依维莫司3 mg:基线185.6微摩尔,六个月后为160微摩尔;硫唑嘌呤:基线为123.3微摩尔,6个月后为127微摩尔)。结论:与硫唑嘌呤相比,依维莫司在24个月时显着降低了急性排斥反应并限制了同种异体移植血管病的进展。尽管在24个月时移植物和患者的存活率相当,但依维莫司治疗可改善心脏移植后的长期预后。

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