Evidence map›Paper›PMID 25365068›Full record

ArticleBone marrow transplantation2015

Pre-transplantation risk factors to develop sclerotic chronic GvHD after allogeneic HSCT: a multicenter retrospective study from the Société Française de Greffe de Moelle et de Thérapie Cellulaire (SFGM-TC).

M Y Detrait, S Morisset, R Peffault de Latour, I Yakoub-Agha, R Crocchiolo, R Tabrizi, J-O Bay, P Chevalier, F Barraco, N Raus and 7 more

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Bone marrow transplantation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact, top 97% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Trial
  2. Article
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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

17 authors at 8 institutions in 1 country.

M Y DetraitHematology Department, Groupement Hospitalier Sud, Hospices Civils de Lyon, Université Claude Bernard Lyon EST, Pierre Bénite, France.
S MorissetBiostatistician, Clinical Research Unit, Department of Hematology, Groupement Hospitalier Sud, Hospices Civils de Lyon, Pierre Bénite, France.
R Peffault de LatourBlood and Marrow Transplantation Unit,Hôpital Saint-Louis, AP-HP, Paris, France.
I Yakoub-AghaService des Maladies du Sang, CHU Lille, Lille, France.
R CrocchioloBlood and marrow transplantation Program, Hematology Department, Institut Paoli-Calmettes, Marseille, France.
R TabriziHematology Department, Hôpital du Haut Levêque, Pessac, France.
J-O BayHematology Department, CHU Clermont-Ferrand, Hôpital Estaing, Clermont-Ferrand, France.
P ChevalierHematology Department, Center Hospitalier Universitaire (CHU) de Nantes, Nantes, France.
F BarracoHematology Department, Groupement Hospitalier Sud, Hospices Civils de Lyon, Université Claude Bernard Lyon EST, Pierre Bénite, France.
N RausData management of SFGM-TC, Centre Hospitalier Lyon Sud, Pierre-Bénite, France.
S VigourouxHematology Department, Hôpital du Haut Levêque, Pessac, France.
L MagroService des Maladies du Sang, CHU Lille, Lille, France.
M MohtyHematology Department, Center Hospitalier Universitaire (CHU) de Nantes, Nantes, France.
N MilpiedHematology Department, Hôpital du Haut Levêque, Pessac, France.
D BlaiseBlood and marrow transplantation Program, Hematology Department, Institut Paoli-Calmettes, Marseille, France.
G SociéBlood and Marrow Transplantation Unit,Hôpital Saint-Louis, AP-HP, Paris, France.
M MichalletHematology Department, Groupement Hospitalier Sud, Hospices Civils de Lyon, Université Claude Bernard Lyon EST, Pierre Bénite, France.
Hôpital Cardiologique du Haut-Lévêque · FRCentre Hospitalier Universitaire de Lille · FRCentre Hospitalier Universitaire de Nantes · FRHôpital Lyon Sud · FRUniversité Claude Bernard Lyon 1 · FRAssistance Publique – Hôpitaux de Paris · FRCentre Hospitalier Universitaire de Clermont-Ferrand · FRHôpital Saint-Louis · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sclerotic chronic GvHD (cGvHD) is one of the most severe complications after allo-hematopoietic stem cell transplantation (HSCT). Risk factors associated with this complication remain not very well defined. With the aim to define a pre-transplantation risk profile, we have conducted a French retrospective analysis in 705 consecutive patients between 2005 and 2010. Analyses to determine pre-transplantation risk factors included as variables: patient and donor age, kind of donor, HLA matching, ABO matching, sex-matching, diagnosis, stem cell source, gender, GvHD prophylaxis and antithymocyte globulin (ATG) in the conditioning regimen. The cumulative incidence of sclerotic cGvHD was 18% (95% CI, 16.6-19.6) 3 years after onset of cGvHD. In univariate analysis, we found a significantly lower number of sclerotic cGvHD form in patients transplanted from cord blood cells (P=0.0021), in patients with a one mismatched donor (P=0.041) and in patients who had received ATG in the conditioning regimen (P=0.002). In multivariate analysis, factors associated with an increased risk of sclerotic cGvHD were young patient age, multiple myeloma and PBSC as the stem cell source. ATG in conditioning regimen and cord blood unit as the stem cell source were associated with a lower risk.

Indexed as

Cord Blood Stem Cell TransplantationHematopoietic Stem Cell TransplantationTransplantation ConditioningAllograftsAntilymphocyte SerumChronic DiseaseFemaleFranceGraft vs Host DiseaseHematologic DiseasesHumansImmunosuppressive AgentsMaleRetrospective StudiesRisk FactorsSclerosisAntilymphocyte SerumImmunosuppressive Agents

Identifiers

PMID25365068
OpenAlexW1526925388

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.