Evidence map›Paper›PMID 22383228›Full record

ArticleMultiple sclerosis (Houndmills, Basingstoke, England)2012

A prospective, randomized, controlled trial of autologous haematopoietic stem cell transplantation for aggressive multiple sclerosis: a position paper.

R Saccardi, M S Freedman, M P Sormani, H Atkins, D Farge, L M Griffith, G Kraft, G L Mancardi, R Nash, M Pasquini and 5 more

Open access · hybridAbstract read
In one paragraph

Article in Multiple sclerosis (Houndmills, Basingstoke, England), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
7.5field-weighted citation impact, top 2% 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

43 citing papers in PubMed, 106 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Review
  5. Article
  6. Article
  7. Review
  8. The EBMT-ADWP and the CIBMTR.Handbook of clinical neurology · 2024
    Review
  9. Review
  10. Predictive MRI Biomarkers in MS-A Critical Review.Medicina (Kaunas, Lithuania) · 2022
    Review
  11. Article
  12. Review
  13. Aggressive multiple sclerosis (1): Towards a definition of the phenotype.Multiple sclerosis (Houndmills, Basingstoke, England) · 2020
    Article
  14. Review
  15. Review
  16. Review
  17. Review
  18. Genetically modified hematopoietic stem/progenitor cells that produce IL-10-secreting regulatory T cells.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  19. Review
  20. Cell-based therapeutic strategies for multiple sclerosis.Brain : a journal of neurology · 2017
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 11 institutions in 6 countries.

R SaccardiHematology Department, Careggi University Hospital, Florence, Italy. riccardo.saccardi@aouc.unifi.it
M S Freedman
M P Sormani
H Atkins
D Farge
L M Griffith
G Kraft
G L Mancardi
R Nash
M Pasquini
R Martin
P A Muraro
European Blood and Marrow Transplantation Group
Center for International Blood and Marrow Research
HSCT in MS International Study Group
University of Genoa · ITAzienda Ospedaliero-Universitaria Careggi · ITFred Hutch Cancer Center · USHôpital Saint-Louis · FRImperial College London · GBMedical College of Wisconsin · USNational Institute of Allergy and Infectious Diseases · USOttawa Hospital · CAOttawa Hospital Research InstituteUniversity Hospital of Zurich · CHUniversity of Washington · US

Funding

Medical Research Council G0800679
6 · The paper itself

Abstract

backgroundHaematopoietic stem cell transplantation (HSCT) has been tried in the last 15 years as a therapeutic option in patients with poor-prognosis autoimmune disease who do not respond to conventional treatments. Worldwide, more than 600 patients with multiple sclerosis (MS) have been treated with HSCT, most of them having been recruited in small, single-centre, phase 1-2 uncontrolled trials. Clinical and magnetic resonance imaging outcomes from case series reports or Registry-based analyses suggest that a major response is achieved in most patients; quality and duration of response are better in patients transplanted during the relapsing-remitting phase than in those in the secondary progressive stage.

objectivesAn interdisciplinary group of neurologists and haematologists has been formed, following two international meetings supported by the European and American Blood and Marrow Transplantation Societies, for the purpose of discussing a controlled clinical trial, to be designed within the new scenarios of evolving MS treatments.

conclusionsObjectives of the trial, patient selection, transplant technology and outcome assessment were extensively discussed. The outcome of this process is summarized in the present paper, with the goal of establishing the background and advancing the development of a prospective, randomized, controlled multicentre trial to assess the clinical efficacy of HSCT for the treatment of highly active MS.

Indexed as

Hematopoietic Stem Cell TransplantationResearch DesignAdolescentAdultClinical Trials, Phase III as TopicCooperative BehaviorDisability EvaluationEuropeHumansInternational CooperationMiddle AgedMulticenter Studies as TopicMultiple Sclerosis, Relapsing-RemittingProspective StudiesRandomized Controlled Trials as TopicSeverity of Illness Index

Identifiers

PMID22383228
PMCPMC3389500
OpenAlexW2017412635

What OpenQuestion holds

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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.