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神经保护性卒中治疗的观点

Perspectives on neuroprotective stroke therapy.

作者信息

Schäbitz W-R, Fisher M

机构信息

Department of Neurology, University of Münster, Albert-Schweitzer-Strasse 33, 48129 Münster, Germany.

出版信息

Biochem Soc Trans. 2006 Dec;34(Pt 6):1271-6. doi: 10.1042/BST0341271.

Abstract

After years of setbacks, the perspective of neuroprotective stroke therapy has revived in light of recent study results. We outline in this review how a neuroprotective candidate drug should be developed, beginning with a thorough preclinical evaluation according to the STAIR (Stroke Therapy Academic Industry Roundtable) criteria. Assessing the safety of the candidate drug in the relatively straightforward Phase IIA would be the first step into clinical development. While advancing into Phase IIB, the implementation of a responder analysis, the use of a surrogate biomarker as well as the use of Bayesian methodology should be considered to increase the likelihood of seeing any therapeutic sign. Clinical development in Phase III should consider that previously used dichotomized endpoints appropriate for evaluation of thrombolytic drugs are likely to be insufficient for assessing efficacy of neuroprotective drugs. Detection of a clinically relevant shift in the outcome measure appears to be a more relevant approach for the type of drug that achieves a reduction and not a reverse of the ischaemic lesion.

摘要

历经数年挫折,鉴于近期的研究结果,神经保护性卒中治疗的前景再度燃起。在本综述中,我们概述了神经保护候选药物应如何研发,首先要依据卒中治疗学术产业圆桌会议(STAIR)标准进行全面的临床前评估。在相对简单的IIA期评估候选药物的安全性将是进入临床开发的第一步。在推进到IIB期时,应考虑进行反应者分析、使用替代生物标志物以及采用贝叶斯方法,以增加出现任何治疗迹象的可能性。III期临床开发应考虑到,先前用于评估溶栓药物的二分终点可能不足以评估神经保护药物的疗效。对于旨在减少而非逆转缺血性损伤的药物类型,检测结局指标中具有临床相关性的变化似乎是一种更合适的方法。

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