Trafermin for stroke recovery: is it time for another randomized clinical trial?

被引:27
作者
Paciaroni, Maurizio [1 ,2 ]
Bogousslavsky, Julien [3 ]
机构
[1] Univ Perugia, Santa Maria della Misericordia Hosp, Stroke Unit, I-06126 Perugia, Italy
[2] Univ Perugia, Santa Maria della Misericordia Hosp, Div Cardiovasc Med, I-06126 Perugia, Italy
[3] Swiss Med Network, Dept Neurol & Neurorehabil, Valmont Genolier, Glion Sur Montr, Switzerland
关键词
basic fibroblast growth factor; neuroprotection; stroke therapy; trafermin; FIBROBLAST-GROWTH-FACTOR; FOCAL CEREBRAL-ISCHEMIA; REDUCES INFARCT SIZE; PROGENITOR-CELL PROLIFERATION; BLOOD-FLOW; RAT-BRAIN; NEUROPROTECTION; NEURONS; MODEL; IMMUNOREACTIVITY;
D O I
10.1517/14712598.2011.616888
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
Introduction: Basic fibroblast growth factor (bFGF) has been shown to reduce volume in acute ischemic stroke models, and to promote functional recovery as well as new synapse formation when given to animals with completed cerebral infarction. A recombinant native form of human bFGF, trafermin, has been tested in Phase III clinical trials in patients with stroke. Areas covered: The role of trafermin in stroke. Data were identified by searching PubMed for single or combined terms including: trafermin, basic fibroblast growth factors, neuroprotection, neuroprotective drugs, stroke therapy, stroke rehabilitation and acute stroke. Original research papers, clinical series and reviews are included. Our research covered all relevant data up until 1 April 2011. Expert opinion: To date, all Phase III trials have failed to demonstrate the superiority of trafermin over placebo when given within 6 h from stroke onset because trafermin causes a dose-dependent hypotension and an increased mortality rate in treated patients. However, a 24-h intravenous infusion seems to be safe for stroke patients and may result in an improved outcome when given 5 - 6 h after infarct. This finding may open renewed interest in restorative treatment for stroke, which could enhance recovery mechanisms rather than immediate neuroprotection. Studies suggest that growth factors can produce improvement in animal models of stroke, even when administered at postischemic intervals from many hours to days, when conventional neuroprotective approaches are typically ineffective. Because of the number of side effects and increased mortality reported in the first clinical studies with high dose of FGF, further experimental studies are necessary to asses whether it is possible to achieve a pharmacologically significant therapeutic level in the brain, by minimizing peripheral side effects. Another randomized clinical trial is needed to test trafermin in stroke patients but to enhance functional recovery.
引用
收藏
页码:1533 / 1541
页数:9
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