Endovascular Acute Stroke Intervention - Tandem OCclusion Trial

Official title

A Multi-centre, Prospective, Randomized, Open-label, Blinded Endpoint (PROBE) Controlled Trial Comparing Cervical Internal Carotid Artery Stenting to no Stenting During Thrombectomy for Tandem Occlusion Stroke

Overview

Patients with tandem occlusion or tandem lesion (TL), that is, stroke with an acute intracranial anterior circulation occlusion and an ipsilateral cervical ICA (c-ICA) high-grade stenosis or occlusion, constitute about 15-20% of patients undergoing endovascular thrombectomy (EVT). However, the optimal treatment of acute stroke patients with TL remains uncertain, as relatively few patients with TL were included in the major randomized controlled trials of EVT and management of the c-ICA was generally not specified by protocol nor analyzed post-hoc. Recent large multi-centre retrospective cases series suggest that acutely stented patients may have more favorable outcomes than patients treated with angioplasty alone or those with no acute ICA intervention, but high quality randomized trial data are lacking. EASI-TOC, a phase 3, academic multi-centre, controlled trial (PROBE design) with embedded pilot phase, will seek to determine if in patients undergoing acute intracranial thrombectomy for anterior circulation stroke with concurrent ipsilateral symptomatic high-grade (≥70%) atherosclerotic stenosis or occlusion of the extracranial ICA, endovascular ICA revascularization with stenting is superior to intracranial thrombectomy alone with regards to functional outcome at 90 days. Patients will be randomized to Acute stenting or No acute stenting (1:1 allocation).

Detailed description

EASI-TOC is a phase III multi-centre, prospective, randomized, open-label, blinded endpoint (PROBE) controlled trial (1:1 allocation).

The trial will seek to determine if in patients undergoing acute intracranial thrombectomy for anterior circulation stroke with concurrent ipsilateral symptomatic high-grade (≥70%) atherosclerotic stenosis or occlusion of the extracranial ICA, endovascular ICA revascularization with stenting is superior to intracranial thrombectomy alone with regards to functional outcome at 90 days (measured using the Modified Rankin Scale).

EASI-TOC will be conducted at 10-12 high-volume comprehensive stroke centres in Canada.

458 male and female adult (aged ≥ 18 years) patients will be enrolled.

Patients will be randomized (1:1) to undergo acute ICA stenting during the thrombectomy procedure (either before or after intracranial thrombectomy, at the discretion of the treating physician) or to intracranial thrombectomy alone without ICA stenting. Deferred ICA intervention is allowed, if indicated. Randomization will be centralized and web-based. Stratification will be performed for use or not of IV alteplase and for enrolling site.

Patients will be treated acutely and followed up to one year.

Our primary hypothesis assumes a greater proportion of patients with 90-day mRS 0-2 in the stenting group versus the no stenting group (55% versus 40%). Assuming a minimal clinically important difference of 15 % between groups experiencing no crossover, a total of 173 patients per group would be sufficient to detect this difference, with a power of 80 % and a significance level of 5 %. Taking into account a cross-over rate of 10% (5% in either direction) and a loss to follow-up of 5 %, the total sample size will increase to 450 patients.

Primary analysis will be by Intention-to-treat. Pre-specified as-treated, sex-specific and subgroup analyses will also be performed.

Informed consent will be obtained from patients or their surrogate. Deferral of consent will be allowed if permitted by local ethics committees.

Interventions

• Device Carotid artery stenting
  The type of stent should be one commonly used for ICA stenting. Balloon angioplasty before and/or after stent placement will be allowed as required. Stenting should be performed after intracranial thrombectomy unless specific technical circumstances suggest that access to the intracranial circulation requires anterograde stenting. Embolic protection devices should not be used routinely during ICA stent placement.
• Drug Antiplatelet Agents
  The following antiplatelet regimen should be used: For patients having received IV thrombolysis, immediate post-procedural oral or intrarectal single antiplatelet agents, (Aspirin 325mg PO or 650mg PR). A second agent (usually Clopidogrel 300mg PO) is added after follow-up brain imaging at 12-24 hours confirms absence of significant ICH. For patients having not been treated with IV thrombolysis, dual antiplatelet therapy (Aspirin 325mg PO or 650mg PR and Clopidogrel 300-600mg PO) is given immedi

Primary outcome measures

• Clinical efficacy outcome: proportion of patients achieving a favorable modified Rankin scale score (mRS 0-2) [Time frame: 90 days ± 14 days]

Secondary outcome measures (11)

• Clinical efficacy outcome: Proportion of patients achieving a favorable modified Rankin scale score (mRS 0-2) at 90 days (dichotomized) according to sex [Time frame: 90 days ± 14 days]
• Clinical efficacy outcome: Ordinal logistic regression for functional improvement on the Modified Rankin Scale (mRS) score (shift analysis) [Time frame: 90 days ± 14 days]
• Clinical efficacy outcome: Median National Institutes of Health Stroke Scale (NIHSS) score [Time frame: 24 hours ± 8 hours]
• Clinical efficacy outcome: Median National Institutes of Health Stroke Scale (NIHSS) score [Time frame: 90 days ± 14 days]
• Clinical efficacy outcome: Median Modified Rankin Scale (mRS) score [Time frame: 90 days ± 14 days]
• Clinical efficacy outcome: Rate of clinically confirmed recurrent ipsilateral stroke or retinal ischemia [Time frame: 90 days ± 14 days]
• Radiological efficacy outcome: Proportion of patients with complete or near-complete recanalization [Time frame: End of endovascular procedure]
• Radiological efficacy outcome: Proportion of patients with ICA thrombosis (with or without stent) [Time frame: 90 days ± 14 days]
• Clinical efficacy outcome: Median Montreal Cognitive Assessment (MoCA) score [Time frame: 90 days ± 14 days]
• Clinical efficacy outcome: Rate of any recurrent stroke or retinal ischemia [Time frame: 1 year ± 60 days]
• Clinical efficacy outcome: Proportion of patients achieving a favorable modified Rankin scale (mRS) score [Time frame: 1 year ± 60 days]

Eligibility criteria

Inclusion criteria

• Acute ischemic anterior circulation stroke eligible for endovascular therapy according to local guidelines, with or without prior intravenous thrombolysis:

• Occlusion of the carotid terminus, M1 or M2 segments of the middle cerebral artery (MCA)
• A neurological deficit judged to be disabling by the patient and/or treating physician
• Any acute imaging judged by the treating physician to demonstrate salvageable brain tissue possibly amenable to EVT
• Groin puncture within 24-hours of onset or last known normal
• Tandem ipsilateral high-grade (≥70%) cervical internal carotid artery (ICA) stenosis or occlusion of presumed atherosclerotic etiology on initial non-invasive vascular imaging
• Informed consent from patient or surrogate or deferral of consent, according to local ethics policies

Exclusion criteria

• Pre-existing neurological impairment (modified Rankin score ≥3)
• Any underlying disease or condition making protocol adherence and/or 3-month follow-up unlikely
• Any known contra-indication to EVT, angioplasty/stenting, or antiplatelet therapy
• Tandem ipsilateral high-grade (≥70%) cervical internal carotid artery (ICA) stenosis or occlusion NOT confirmed on conventional angiography
• Ipsilateral ICA stenosis or occlusion attributable to clinically or radiologically confirmed arterial dissection
• Isolated cervical carotid occlusion without intracranial occlusion
• Pregnancy

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation

Randomized

Model

Parallel assignment

Masking

Single blind

Primary purpose

Treatment

Study locations

Canada · 1 center

• Centre Hospitalier de l'Université de Montréal — Montreal

Publications

• Mendes GN, Jacquin G, Iancu D, Roy D, Yu M, Bodson-Clermont P, Fahmi I, Ahmed SU, Almekhlafi M, Buck B, Camden MC, Catanese L, Diestro D, Fahed R, Field TS, Guest W, Hawkes C, Hill MD, Kelly ME, Kim CN, Legault C, Milot G, Moreau F, Muccilli A, Rempel J, Shamy M, Singh RJ, Van Adel BA, Volders D, Shankar J, Singh N, Stapf C, Poppe AY. Endovascular Acute Stroke Intervention-Tandem Occlusion (EASI-T PMID 42024493

Identifiers

NCT: NCT04261478 · MP-02-2020-8614

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗