Cardiac cell-repair therapy: clinical issues.

Bernard J Gersh, Robert D Simari
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引用次数: 13

Abstract

The possibility that cardiac cell-repair therapy might become a clinical reality is a challenge worthy of the current state of technological and scientific expertise at the start of the 21(st) century. The success of preclinical and early clinical studies is a strong inducement to move ahead with larger clinical trials, but caution is warranted given our lack of understanding of the potential mechanisms by which cell-repair therapy exerts a benefit on ventricular function, perfusion, and infarct size, irrespective of the type of cell, method, site, and disease entity. There are multiple clinical, mechanistic, and safety questions requiring answers, and these will be forthcoming only if the design of clinical trials is carefully tailored to answer specific questions. These questions, in turn, will require the use of different and multiple end points, depending on the specific issue and study. Accordingly, this review addresses the limitations of current clinical studies, the design of future trials, and the concept of a hierarchical series of end points that might provide answers to a host of different questions. Clinical and basic scientists need to approach the next generation of trials in partnership.

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心脏细胞修复疗法:临床问题。
心脏细胞修复疗法可能成为临床现实的可能性是值得在21世纪初的技术和科学专业知识的当前状态的挑战。临床前和早期临床研究的成功是推进更大规模临床试验的有力诱因,但鉴于我们缺乏对细胞修复疗法在心室功能、灌注和梗死面积方面发挥益处的潜在机制的理解,无论细胞类型、方法、部位和疾病实体如何,都有必要谨慎。有许多临床、机制和安全性的问题需要回答,这些问题只有在临床试验的设计被仔细地剪裁以回答特定的问题时才会出现。这些问题,反过来,将需要使用不同的和多个终点,取决于具体的问题和研究。因此,本文综述了当前临床研究的局限性,未来试验的设计,以及可能为许多不同问题提供答案的分层终点系列的概念。临床和基础科学家需要合作开展下一代试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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