Evidence map›Paper›PMID 25676424›Full record

ArticleLeukemia2015

HLA-matched allogeneic stem cell transplantation improves outcome of higher risk myelodysplastic syndrome A prospective study on behalf of SFGM-TC and GFM.

M Robin, R Porcher, L Adès, E Raffoux, M Michallet, S François, J-Y Cahn, A Delmer, E Wattel, S Vigouroux and 13 more

Registry-linked trialAbstract read
PubMed Publisher
In one paragraph

Article in Leukemia, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05617625 (A Phase II Trial of CD34+ Enriched Transplants From HLA-Compatible Related or Unrelated Donors for Treatment of Patients With Myelodysplastic Syndrome), which is not on this map. Cited by 41 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 1 pooled it
3.6field-weighted citation impact, top 7% 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.

NCT05617625 phase2suspendednot on this mapstarted 2026, after this paper: background citation

A Phase II Trial of CD34+ Enriched Transplants From HLA-Compatible Related or Unrelated Donors for Treatment of Patients With Myelodysplastic Syndrome

TypeinterventionalSponsorGuenther KoehneRan2026 to 2033Enrolled50ConditionsMyelodysplastic Syndromes, Graft Vs Host Disease, Graft-versus-host-diseaseArmsBusulfan, Melphalan, Fludarabine, CliniMACS CD34+ enriched, T-cell depleted peripheral blood stem cell (PBSC)
3 · Its place in the literature

Who cites it

41 citing papers in PubMed, 1 synthesis or guideline pooled it, 84 citations in OpenAlex.

  1. Guideline
  2. Trial
  3. Trial
  4. Article
  5. Therapy of high-risk myelodysplastic syndromes.Bone marrow transplantation · 2026
    Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Is There (Still) a Place for Sequential Conditioning?Current oncology (Toronto, Ont.) · 2025
    Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Observational
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

23 authors at 15 institutions in 1 country.

M Robin1] Hematologie - Transplantation; Assistance Publique Hôpitaux de paris (AP-HP), Hôpital Saint Louis, Paris, France [2] University Paris VII, Denis Diderot, Paris, France [3] Inserm U 1160, Paris, France.
R Porcher1] Team METHODS, Epidemiology and Statistics Sorbonne Paris Cité Research Centre UMR 1153, Inserm, Paris Descartes University, Paris, France [2] AP-HP, Hôpital Hôtel-Dieu, Centre d'Épidémiologie Clinique, Paris, France.
L AdèsHématologie sénior, Assistance Publique Hôpitaux de paris (AP-HP), Hôpital Saint Louis and Hôpital Avicenne, Paris, France.
E RaffouxHématologie adulte, Assistance Publique Hôpitaux de paris (AP-HP), Hôpital Saint Louis, Paris, France.
M MichalletHématologie, CHU, Lyon, France.
S FrançoisHématologie, CHU, Angers, France.
J-Y CahnHématologie, CHU,UMR 5525 CNRS-UJF, Grenoble, France.
A DelmerHématologie, CHU, Reims, France.
E WattelHématologie, CHU, Lyon, France.ORCID 0000000342541692
S VigourouxHématologie, CHU, Bordeaux, France.
J-O BayHématologie, CHU, Clermont-Ferrand, France.
J CornillonHématologie, Institut de Cancérologie de la Loire, Saint-Etienne, France.
A HuynhHématologie, CHU, Toulouse, France.
S NguyenHématologie, hôpital de La Pitié Salpétrière Assistance Publique Hôpitaux de paris (AP-HP), Hôpital Saint Louis, Paris, France.
M-T RubioHématologie, hôpital Saint-Antoine, Assistance Publique Hôpitaux de paris (AP-HP), Hôpital Saint Louis, Paris, France.
L VincentHématologie, CHU, Montpellier, France.
N MaillardHématologie, CHU, Poitiers, France.
A CharbonnierHématologie CHU, Amiens, France.
R P de Latour1] Hematologie - Transplantation; Assistance Publique Hôpitaux de paris (AP-HP), Hôpital Saint Louis, Paris, France [2] University Paris VII, Denis Diderot, Paris, France [3] Inserm U 1160, Paris, France.
O RemanHématologie CHU, Caen, France.
H Dombret1] University Paris VII, Denis Diderot, Paris, France [2] Hématologie sénior, Assistance Publique Hôpitaux de paris (AP-HP), Hôpital Saint Louis and Hôpital Avicenne, Paris, France.
P Fenaux1] University Paris VII, Denis Diderot, Paris, France [2] Hématologie sénior, Assistance Publique Hôpitaux de paris (AP-HP), Hôpital Saint Louis and Hôpital Avicenne, Paris, France.
G Socié1] Hematologie - Transplantation; Assistance Publique Hôpitaux de paris (AP-HP), Hôpital Saint Louis, Paris, France [2] University Paris VII, Denis Diderot, Paris, France [3] Inserm U 1160, Paris, France.
Assistance Publique – Hôpitaux de Paris · FRInserm · FRDélégation Paris 7 · FRInstitut d’Hématologie et d’Oncologie Pédiatrique · FRCentre Hospitalier Universitaire Amiens-Picardie · FRCentre Hospitalier Universitaire d'Angers · FRCentre Hospitalier Universitaire de Bordeaux · FRCentre Hospitalier Universitaire de Caen Normandie · FRCentre Hospitalier Universitaire de Clermont-Ferrand · FRCentre Hospitalier Universitaire de Montpellier · FRCentre Hospitalier Universitaire de Poitiers · FRCentre Hospitalier Universitaire de Reims · FRCentre National de la Recherche Scientifique · FRDélégation Paris 5 · FRSorbonne Université · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Allogeneic hematopoietic stem cell transplantation (HSCT) is considered the only a curative treatment in patients with higher risk myelodysplastic syndrome (MDS), although demethylating agents (DMA) have been reported to improve survival. The advantage of HSCT over other treatment comes from retrospective studies and the aim of the current study was to prospectively test this hypothesis, analyzing in particular patients from the pre-transplant period to avoid the selection bias of performing transplantation. This study was conducted to compare overall survival in MDS patients candidates to transplantation according to donor availability. The majority of patients (76%) received a treatment with DMA after registration, 69% had a human leukocyte antigen (HLA)-identical donor, 70% of whom were transplanted. Baseline patient and disease characteristics were similar according to donor availability. Four-year overall survival was significantly better in patients with an HLA matched donor (37%) compared to patients without donor (15%). There was also evidence that this overall survival advantage was because of transplantation. Mortality risk was decreased after transplantation but it became significant only after the second year post transplant, because of early transplant-related mortality. Our results appear to justify, in higher risk MDS, a transplantation approach in all potential candidates who have an HLA identical donor.

Indexed as

Stem Cell TransplantationAgedAntineoplastic Combined Chemotherapy ProtocolsCombined Modality TherapyFemaleFollow-Up StudiesHistocompatibility TestingHLA AntigensHumansMaleMiddle AgedMyelodysplastic SyndromesNeoplasm StagingPrognosisProspective StudiesRetrospective StudiesHLA Antigens

Identifiers

PMID25676424
OpenAlexW1978195896

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.