Evidence map›Paper›PMID 24162791›Full record

Trial reportHaematologica2014

Comparison of horse and rabbit antithymocyte globulin in immunosuppressive therapy for refractory cytopenia of childhood.

Ayami Yoshimi, Marry M van den Heuvel-Eibrink, Irith Baumann, Stephan Schwarz, Ingrid Simonitsch-Klupp, Pascale de Paepe, Vit Campr, Gitte Birk Kerndrup, Maureen O'Sullivan, Rita Devito and 17 more

Registry-linked trialOpen access · goldAbstract readClinical Trial
In one paragraph

Trial report in Haematologica, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00662090 (Prospective Non-randomized Multi-center Study for Epidemiology and Characterization of Myelodysplastic Syndromes), which is not on this map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.5field-weighted citation impact, top 10% 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.

NCT00662090 recruitingnot on this map

Prospective Non-randomized Multi-center Study for Epidemiology and Characterization of Myelodysplastic Syndromes (MDS) and Juvenile Myelomonocytic Leucemia (JMML) in Childhood

TypeobservationalSponsorUniversity Hospital FreiburgRan2010 to 2027Enrolled260ConditionsMyelodysplastic Syndromes, Juvenile Myelomonocytic Leukemia
3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 38 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Article
  7. Myelodysplastic and myeloproliferative disorders of childhood.Hematology. American Society of Hematology. Education Program · 2016
    Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

27 authors at 18 institutions in 10 countries.

Ayami Yoshimiayami.yoshimi@uniklinik-freiburg.de.
Marry M van den Heuvel-Eibrink
Irith Baumann
Stephan Schwarz
Ingrid Simonitsch-Klupp
Pascale de Paepe
Vit Campr
Gitte Birk Kerndrup
Maureen O'Sullivan
Rita Devito
Roos Leguit
Miguel Hernandez
Michael Dworzak
Barbara de Moerloose
Jan Stary
Henrik Hasle
Owen P Smith
Marco Zecca
Albert Catala
Markus Schmugge
Franco Locatelli
Monika Führer
Alexandra Fischer
Anne Guderle
Peter Nöllke
Brigitte Strahm
Charlotte M Niemeyer
University of Freiburg · DEGhent University Hospital · BEMedical University of Vienna · ATAarhus University Hospital · DKBambino Gesù Children's Hospital · ITCharles University · CZChildren's Health Ireland at Crumlin · IEErasmus MC - Sophia Children’s Hospital · NLHospital Sant Joan de Déu Barcelona · ESHospital Universitari i Politècnic La Fe · ESLudwig-Maximilians-Universität München · DEOur Lady's Hospital · IEPoliclinico San Matteo Fondazione · ITStichting Kinderoncologie Nederland · NLUniversity Children's Hospital Zurich · CHUniversity Hospital in Motol · CZUniversity of Pavia · ITVejle Sygehus · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Refractory cytopenia of childhood is the most common subtype of myelodysplastic syndrome in children. In this study, we compared the outcome of immunosuppressive therapy using horse antithymocyte globulin (n=46) with that using rabbit antithymocyte globulin (n=49) in 95 patients with refractory cytopenia of childhood and hypocellular bone marrow. The response rate at 6 months was 74% for horse antithymocyte globulin and 53% for rabbit antithymocyte globulin (P=0.04). The inferior response in the rabbit antithymocyte globulin group resulted in lower 4-year transplantation-free (69% versus 46%; P=0.003) and failure-free (58% versus 48%; P=0.04) survival rates in this group compared with those in the horse antithymocyte globulin group. However, because of successful second-line hematopoietic stem cell transplantation, overall survival was comparable between groups (91% versus 85%; P=ns). The cumulative incidence of relapse (15% versus 9%; P=ns) and clonal evolution (12% versus 4%; P=ns) at 4 years was comparable between groups. Our results suggest that the outcome of immunosuppressive therapy with rabbit antithymocyte globulin is inferior to that of horse antithymocyte globulin. Although immunosuppressive therapy is an effective therapy in selected patients with refractory cytopenia of childhood, the long-term risk of relapse or clonal evolution remains. (ClinicalTrial.gov identifiers: NCT00662090).

Indexed as

Immunosuppression TherapyAdolescentAnimalsAntilymphocyte SerumChildChild, PreschoolFemaleHorsesHumansImmunosuppressive AgentsInfantMalePancytopeniaRabbitsRecurrenceRisk FactorsAntilymphocyte SerumImmunosuppressive Agents

Identifiers

PMID24162791
PMCPMC3971075
OpenAlexW2168079441

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.