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NEJM:晚期常染色体显性多囊肾病采用托伐普坦治疗效果分析!

2017-11-05 xing.T MedSci原创

由此可见,相比于安慰剂,托伐普坦可以减缓晚期ADPKD患者eGFR的下降。

在先前由早期常染色体显性遗传性多囊肾病(ADPKD;估计的肌酐清除率≥60ml/min)患者参与的试验中,血管加压素V2受体拮抗剂托伐普坦可以减缓肾脏总体积和肾小球滤过率(GFR)下降的增长,但也导致了转氨酶和胆红素水平更高。托伐普坦在晚期ADPKD患者的疗效仍是未知的。最近,顶级医学期刊NEJM上针对这一问题发表了一篇研究文章。

研究人员进行了一项3期、随机停药、多中心、安慰剂对照、双盲试验。在一个包含序贯安慰剂和托伐普坦治疗的为期8周的前随机化期,在此期间,研究人员对每个病人的托伐普坦无剂量限制的副作用进行了评估,1370例ADPKD,这些患者为18岁至55岁的eGFR为25-65ml/min/1.73m2或56岁至65岁eGFR为25-44 ml/min/1.73m2的个体,按1:1的比例被随机分配接受托伐普坦或安慰剂治疗12个月。该研究的主要终点是从基线到随访后估计的肾小球滤过率变化,并对每个病人参与的确切时间进行调整,每月进行安全性评估。

在托伐普坦组,估计的肾小球滤过率从基线的变化为-2.34 ml/min/1.73m2(95%可信区间为-2.81至-1.87),相比于安慰剂组的-3.61 ml/min/1.73m2(95%可信区间为-4.08至-3.14)(差异为1.27 ml/min/1.73m2;95% 可信区间为0.86至1.68;P<0.001)。研究人员发现托伐普坦组681例受试者中有38例(5.6%)患者丙氨酸氨基转移酶水平升高(超过正常上限的3倍),而安慰剂组685例受试者中有8例(1.2%)患者丙氨酸氨基转移酶水平升高。停止服用托伐普坦后转氨酶水平升高是可逆的。胆红素水平也未高于正常范围上限的两倍。

由此可见,相比于安慰剂,托伐普坦可以减缓晚期ADPKD患者eGFR的下降。

原始出处:

Vicente E. Torres,.et al. Tolvaptan in Later-Stage Autosomal Dominant Polycystic Kidney Disease.NEJM.2017. http://www.nejm.org/doi/full/10.1056/NEJMoa1710030

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    2017-11-05 131****1460

    学习了受益匪浅

    0

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attachment=null, authenticateStatus=null, createdAvatar=https://wx.qlogo.cn/mmopen/jW482SpianMayicTRbRZ5RzUn81b5CF5ibVPib8jWI92iciaxmqGHlwruOnK4SVZykd4iahqo1hicklIibyZoxm55X7EM8BW9eX1h1hQ2/0, createdBy=8aa81937526, createdName=李东泽, createdTime=Sun Nov 05 10:32:38 CST 2017, time=2017-11-05, status=1, ipAttribution=), GetPortalCommentsPageByObjectIdResponse(id=258829, encodeId=30f925882951, content=谢谢分享.学习了, beContent=null, objectType=article, channel=null, level=null, likeNumber=95, replyNumber=0, topicName=null, topicId=null, topicList=[], attachment=null, authenticateStatus=null, createdAvatar=https://wx.qlogo.cn/mmopen/NUyjXTCJjo6Nx0VGA4QMDzOP8oAgnV4h51EjSfehJ9QxyiaSmw8PB56BhY8KXFSxHCibXrzcy4abrzSibXQPxJ9kzrLcJyhhB8a/0, createdBy=1d3b1672603, createdName=明月清辉, createdTime=Sun Nov 05 09:47:28 CST 2017, time=2017-11-05, status=1, ipAttribution=)]
    2017-11-05 李东泽

    是很好的学习材料.不错.以后会多学习.

    0

  10. 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    2017-11-05 明月清辉

    谢谢分享.学习了

    0

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总之,与安慰剂相比,采用伯舒替尼200毫克/天治疗可以减少ADPKD患者的肾脏肿大。整个胃肠道和肝脏的毒性与之前伯舒替尼的研究一致;并没有发现新的毒性反应。

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