Effect of baseline Alberta Stroke Program Early CT Score on safety and efficacy of intra-arterial treatment: a subgroup analysis of a randomised phase 3 trial (MR CLEAN)

Albert J. Yoo*, Olvert A. Berkhemer, Puck S. S. Fransen, Lucie A. van den Berg, Debbie Beumer, Hester F. Lingsma, Wouter J. Schonewille, Marieke E. S. Sprengers, Rene van den Berg, Marianne A. A. van Walderveen, Ludo F. M. Beenen, Marieke J. H. Wermer, Geert J. Lycklama a Nijeholt, Jelis Boiten, Sjoerd F. M. Jenniskens, Joseph C. J. Bot, Anna M. M. Boers, Henk A. Marquering, Yvo B. W. E. M. Roos, Robert J. van OostenbruggeDiederik W. J. Dippel, Aad van der Lugt, Wim H. van Zwam, Charles B. L. M. Majoie

*Corresponding author for this work

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Background Whether infarct size modifies intra-arterial treatment effect is not certain, particularly in patients with large infarcts. We examined the effect of the baseline Alberta Stroke Program Early CT Score (ASPECTS) on the safety and efficacy of intra-arterial treatment in a subgroup analysis of the Multicenter Randomized Clinical Trial of Endovascular Treatment for Acute Ischemic Stroke in the Netherlands (MR CLEAN). Methods MR CLEAN was a randomised, controlled, open-label, phase 3 trial of intra-arterial treatment in patients (aged >= 18 years from the Netherlands) with proximal arterial occlusion of the anterior circulation, given intraarterial treatment within 6 h of stroke onset. The primary outcome was 90 day modified Rankin Scale (mRS) score. We estimated the intra-arterial treatment effect for all patients in MR CLEAN who had ASPECTS graded by using multivariable ordinal logistic regression analysis (a proportional odds model) to calculate the adjusted common odds ratio for a shift towards a better functional outcome according to the mRS for intra-arterial treatment and usual care than for usual care alone. We entered an interaction term into the model to test for interaction with prespecified ASPECTS subgroups: 0-4 (large infarct) versus 5-7 (moderate infarct) versus 8-10 (small infarct). MR CLEAN is registered with the Netherlands Trial Registry, number NTR1804, and the ISRCTN Registry, number ISRCTN10888758. Findings 496 patients-232 (47%) in the intra-arterial treatment and usual care group and 264 (53%) in the usual care alone group were included in the analysis. We noted no significant difference in intra-arterial treatment effect between the ASPECTS subgroups according to 90 day ordinal mRS (adjusted common odds ratio interaction term relative to ASPECTS 8-10: ASPECTS 0-4: 0.79 [95% CI 0.20-3-19], p=0.740; and ASPECTS 5-7: 1.02 [0.44-2.35], p=0.966). Intra-arterial treatment did not cause a significant increase in the proportion of patients with at least one serious adverse event in any of the ASPECTS subgroups (ASPECTS 0-4: eight [73%] of 11 patients in treatment and usual care group vs 11 [58%] of 19 in usual care alone group, p=0.42; ASPECTS 5-7: 32 [59%] of 54 vs 19 [49%] of 39, p=0.31; ASPECTS 8-10: 70 [42%] of 167 vs 82 [40%] of 206; p=0.68). For death within 7 days or within 30 days and hemicraniectomy, the differences between the intra-arterial treatment and usual care versus usual care alone groups were not significant by ASPECTS subgroups. A significantly higher proportion of patients had recurrent ischaemic stroke in the intra-arterial treatment plus usual care group than in the usual care alone group in the ASPECTS 8-10 subgroup (eight [5%] vs one [
Original languageEnglish
Pages (from-to)685-694
JournalLancet Neurology
Issue number7
Publication statusPublished - Jun 2016

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