Evidence map›Paper›PMID 27862464›Full record

Trial reportJournal of internal medicine2017

Randomized assessment of imatinib in patients with acute ischaemic stroke treated with intravenous thrombolysis.

N Wahlgren, M Thorén, B Höjeberg, T-B Käll, A-C Laska, C Sjöstrand, J Höijer, H Almqvist, S Holmin, A Lilja and 4 more

Open access · hybridAbstract readClinical Trial, Phase IIMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Journal of internal medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 2 pooled it
4.7field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

33 citing papers in PubMed, 2 syntheses or guidelines pooled it, 65 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Review
  5. Article
  6. Article
  7. PA System in the Pathogenesis of Ischemic Stroke.Arteriosclerosis, thrombosis, and vascular biology · 2025
    Review
  8. Imatinib on target in stroke recovery.The Journal of clinical investigation · 2025
    Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Diabetes and the treatment of ischemic stroke.Journal of diabetes and its complications · 2022
    Review
  15. Article
  16. Article
  17. Article
  18. Infection of Brain Pericytes Underlying Neuropathology of COVID-19 Patients.International journal of molecular sciences · 2021
    Article
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 6 institutions in 2 countries.

N WahlgrenDepartment of Neurology, Karolinska University Hospital, Stockholm, Sweden.
M ThorénDepartment of Neurology, Karolinska University Hospital, Stockholm, Sweden.
B HöjebergDepartment of Neurology, Capio St Göran Hospital, Stockholm, Sweden.
T-B KällDepartment of Internal Medicine, Södersjukhuset, Stockholm, Sweden.
A-C LaskaDepartment of Internal Medicine, Danderyd Hospital, Stockholm, Sweden.
C SjöstrandDepartment of Neurology, Karolinska University Hospital, Stockholm, Sweden.
J HöijerUnit of Biostatistics, Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.
H AlmqvistDepartment of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.
S HolminDepartment of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.
A LiljaDepartment of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.
L FredrikssonDepartment of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.
D LawrenceDepartment of Internal Medicine, Division of Cardiovascular Medicine, University of Michigan Medical School, Ann Arbor, MI, USA.
U ErikssonDepartment of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.
N AhmedDepartment of Neurology, Karolinska University Hospital, Stockholm, Sweden.
Karolinska Institutet · SEKarolinska University Hospital · SEDanderyds sjukhus · SESaint Göran Hospital · SEStockholm South General Hospital · SEUniversity of Michigan–Ann Arbor · US

Funding

Unraveling the role of tPA in the neurovascular unitR01HL055374 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI David Antonetti, Daniel A Lawrence · 1995 to 2026
$8.6M
Mechanism of thrombolytic tPA induced intracerebral hemorrhage after strokeR01NS079639 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LAWRENCE, DANIEL A · 2012 to 2016
$1.7M
NHLBI NIH HHS R01 HL055374NINDS NIH HHS R01 NS079639
6 · The paper itself

Abstract

backgroundImatinib, a tyrosine kinase inhibitor, has been shown to restore blood-brain barrier integrity and reduce infarct size, haemorrhagic transformation and cerebral oedema in stroke models treated with tissue plasminogen activator. We evaluated the safety of imatinib, based on clinical and neuroradiological data, and its potential influence on neurological and functional outcomes.

methodsA phase II randomized trial was performed in patients with acute ischaemic stroke treated with intravenous thrombolysis. A total of 60 patients were randomly assigned to four groups [3 (active): 1 (control)]; the active treatment groups received oral imatinib for 6 days at three dose levels (400, 600 and 800 mg). Primary outcome was any adverse event; secondary outcomes were haemorrhagic transformation, cerebral oedema, neurological severity on the National Institutes of Health Stroke Scale (NIHSS) at 7 days and at 3 months and functional outcomes on the modified Rankin scale (mRS).

resultsFour serious adverse events were reported, which resulted in three deaths (one in the control group and two in the 400-mg dose group; one patient in the latter group did not receive active treatment and the other received two doses). Nonserious adverse events were mostly mild, resulting in full recovery. Imatinib ameliorated neurological outcomes with an improvement of 0.6 NIHSS points per 100 mg imatinib (P = 0.02). For the 800-mg group, the mean unadjusted and adjusted NIHSS improvements were 4 (P = 0.037) and 5 points (P = 0.012), respectively, versus controls. Functional independence (mRS 0-2) increased by 18% versus controls (61 vs. 79; P = 0.296).

conclusionThis phase II study showed that imatinib is safe and tolerable and may reduce neurological disability in patients treated with intravenous thrombolysis after ischaemic stroke. A confirmatory randomized trial is currently underway.

Indexed as

Thrombolytic TherapyAdolescentAdultAgedAged, 80 and overBrain IschemiaDrug Administration ScheduleFemaleHumansImatinib MesylateMaleMiddle AgedProspective StudiesProtein-Tyrosine KinasesStrokeTreatment OutcomeImatinib MesylateProtein-Tyrosine Kinasescerebral infarctcerebral oedemaimatinibintracerebral haemorrhagestrokethrombolysis

Identifiers

PMID27862464
PMCPMC5573589
OpenAlexW2550765437

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.