Tenecteplase versus alteplase for stroke thrombolysis evaluation (TASTE): A multicentre, prospective, randomized, open-label, blinded-endpoint, controlled phase III non-inferiority trial protocol

被引:4
作者
Bivard, Andrew [1 ]
Garcia-Esperon, Carlos [2 ]
Churilov, Leonid [1 ]
Spratt, Neil [2 ]
Russell, Michelle [2 ]
Campbell, Bruce C., V [1 ]
Choi, Philip [3 ]
Kleinig, Timothy [4 ]
Ma, Henry [5 ]
Markus, Hugh [6 ]
Molina, Carlos [7 ]
Hsu, Chung [8 ,9 ,10 ]
Tsai, Chon-Haw [8 ,9 ,10 ]
Meretoja, Atte [1 ,11 ]
Strbian, Daniel [11 ]
Butcher, Kenneth [12 ]
Wu, Teddy [13 ]
Davis, Stephen [1 ]
Donnan, Geoffrey [1 ]
Levi, Christopher [2 ]
Parsons, Mark [14 ]
机构
[1] Univ Melbourne, Royal Melbourne Hosp, Melbourne Brain Ctr, Dept Med & Neurol, Parkville, Vic, Australia
[2] Univ Newcastle, John Hunter Hosp, Dept Neurol, Lookout Rd,, Newcastle, NSW, Australia
[3] Box Hill Hosp, Melbourne, Vic, Australia
[4] Royal Adelaide Hosp, Adelaide, SA, Australia
[5] Monash Univ, Sch Clin Sci, Dept Med, Monash Hlth, Clayton, Vic, Australia
[6] Univ Cambridge, Dept Clin Neurosci, Stroke Res Grp, Cambridge, England
[7] Vall dHebron Stroke Ctr, Barcelona, Spain
[8] China Med Univ, Grad Inst Biomed Sci, Taichung, Taiwan
[9] China Med Univ Healthcare Syst, Neurosci & Brain Dis Ctr, Taichung, Taiwan
[10] China Med Univ Hosp, Dept Neurol, Dept Neurol, Lookout Rd, Taichung 2305, Taiwan
[11] Helsinki Univ Hosp, Dept Neurol, Helsinki, Finland
[12] Univ New South Wales, Prince Wales Clin Sch, Sydney, NSW, Australia
[13] Christchurch Hosp, Dept Neurol, Christchurch, New Zealand
[14] Univ New South Wales, Liverpool Hosp, Ingham Inst Appl Med Res, South Western Sydney Clin Sch,Dept Neurol, Liverpool, NSW, Australia
关键词
Clinical trial; stroke; thrombolysis; TASTE; perfusion; tenecteplase; alteplase; ACUTE ISCHEMIC-STROKE; MANAGEMENT;
D O I
10.1177/17474930231154390
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Rationale: Alteplase is the only approved thrombolytic agent for acute stroke. An alternative plasminogen activator, tenecteplase, has been previously shown to increase early biological effectiveness (reperfusion) resulting in early clinical recovery in acute stroke patients with target mismatch on perfusion imaging; however, phase III data are lacking. Aim and hypothesis: In this study, we assess the efficacy and safety of tenecteplase compared to alteplase in acute stroke patients with target mismatch on perfusion imaging. Methods and Design: Tenecteplase (0.25 mg/kg) versus alteplase (0.9 mg/kg) for Stroke Thrombolysis Evaluation (TASTE) is a multicentre, prospective, randomized, open-label, blinded-endpoint (PROBE), controlled phase III non-inferiority trial (2 arms with 1:1 randomization) with an adaptive sample size re-estimation in patients with acute ischemic stroke meeting target mismatch criteria on perfusion imaging. Sample size estimates: Recruiting 728 patients (1:1 tenecteplase vs alteplase) would yield 90% power (two-sided alpha 0.05) to detect a treatment effect of 8% (26% modified Rankin scale (mRS) 0-1 in alteplase arm and 34% mRS 0-1 in tenecteplase arm), with an absolute non-inferiority margin of 3%. Following the pre-planned "promising zone" adaptive sample size re-estimation, the final sample size was set at 832 patients. Study outcomes: The primary outcome measure is the proportion of patients with an mRS score of 0-1 at 3 months. Secondary outcomes include the categorical shift in mRS at 3 months; the proportion of patients with: mRS 0-2, 5-6, and 6; reduction of the National Institutes of Health Stroke Scale (NIHSS) by 8 or more points or reaching 0-1 at 24 h; symptomatic intracerebral hemorrhage within 36 h; and death. Discussion: This pivotal trial will provide important data on the role of tenecteplase in acute ischemic stroke, and the use of imaging-based treatment decision-making for stroke thrombolysis.
引用
收藏
页码:751 / 756
页数:6
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