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首页> 外文期刊>European journal of heart failure: journal of the Working Group on Heart Failure of the European Society of Cardiology >Rationale and design of the European multicentre study on Stem Cell therapy in IschEmic Non‐treatable Cardiac diseasE (SCIENCE)
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Rationale and design of the European multicentre study on Stem Cell therapy in IschEmic Non‐treatable Cardiac diseasE (SCIENCE)

机译:缺血性不可治疗心脏病患者干细胞疗法欧洲多长期研究的理由与设计(科学)

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Abstract Aims Ischaemic heart failure (IHF) patients have a poor prognosis even with current guideline‐derived therapy. Intramyocardial injections of autologous or allogeneic mesenchymal stromal cells might improve cardiac function leading to better clinical outcome. Methods The SCIENCE (Stem Cell therapy in IschEmic Non‐treatable Cardiac diseasE) consortium has initiated a Horizon 2020 funded multicentre phase II study in six European countries. It is a double‐blind, placebo‐controlled trial testing the safety and efficacy of allogeneic Cardiology Stem Cell Centre Adipose‐derived Stromal Cells (CSCC_ASC) from healthy donors or placebo in 138 symptomatic IHF patients. Main inclusion criteria are New York Heart Association class II–III, left ventricular ejection fraction ?45% and N‐terminal pro‐B‐type natriuretic peptide levels ?300?pg/mL. Patients are randomized in a 2:1 pattern to receive intramyocardial injections of either CSCC_ASC or placebo. CSCC_ASC and placebo treatments are prepared centralized at Rigshospitalet in 5?mL vials as an off‐the‐shelf product. Vials are distributed to all clinical partners and stored in nitrogen vapour tanks ready to be used directly after thawing. A total of 100?×?10 6 CSCC_ASC or placebo are injected directly into viable myocardium in the infarct border zone using the NOGA XP system (BDS, Cordis, Johnson & Johnson, USA). Primary endpoint is a centralized core‐laboratory assessed change in left ventricular end‐systolic volume at 6‐month follow‐up measured by echocardiography. The trial started in January 2017, 58 patients were included and treated until July 2018. Conclusion The SCIENCE trial will provide clinical data on efficacy and safety of intramyocardial cell therapy of allogeneic adipose‐derived stromal cells from healthy donors in patients with IHF.
机译:摘要目的缺血性心力衰竭(IHF)患者即使目前的指南衍生治疗也具有较差的预后。自体或同种异体间充质基质细胞的肌动内容注射可能改善心脏功能,导致更好的临床结果。方法科学(缺血性不可治疗心脏病的干细胞疗法)联盟已启动六个欧洲国家的地平线2020资助的多元期II研究。它是一种双盲,安慰剂对照试验,测试同种异体心脏病学干细胞中心的安全性和有效性脂肪衍生的基质细胞(CSCC_ASC)在138例症状IHF患者中的健康供体或安慰剂。主要含有标准是纽约心脏关联III级-III,左心室喷射级分,左心室喷射级分,N-末端PRO-B型利钠肽水平& 300〜pg / ml。患者在2:1的模式中随机化,以接受CSCC_ASC或安慰剂的肌动脉内注射。 CSCC_ASC和安慰剂治疗在5?ML小瓶中以5?ml小瓶中的钙培训中的集中制备。小瓶分布到所有临床合作伙伴,并储存在氮气罐中,准备在解冻后直接使用。使用Noga XP系统(BDS,Cordis,Johnson&Amp; Johnson,USA)直接将100个?×10 6 CSCC_ASC或安慰剂直接注射到Infarct边境区域中的可行心肌。主要终点是通过超声心动图测量的6个月随访的6个月随访中的集中核心实验室评估左心室 - 收缩量的变化。审判于2017年1月开始,58名患者被包括并治疗至2018年7月。结论科学试验将提供来自IHF患者健康供体的同种异体脂肪源性基质细胞的肌动态细胞治疗的疗效和安全性。

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