Evidence map›Paper›PMID 27965196›Full record

ArticleBlood2017

Sickle cell disease: an international survey of results of HLA-identical sibling hematopoietic stem cell transplantation.

Eliane Gluckman, Barbara Cappelli, Francoise Bernaudin, Myriam Labopin, Fernanda Volt, Jeanette Carreras, Belinda Pinto Simões, Alina Ferster, Sophie Dupont, Josu de la Fuente and 27 more

Abstract readMulticenter Study
In one paragraph

Article in Blood, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 221 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
221citing papers in PubMed, 4 pooled it
–field-weighted citation impact
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

221 citing papers in PubMed, 4 syntheses or guidelines pooled it.

  1. Pooled it
  2. Guideline
  3. Hematopoietic stem cell transplantation for people with sickle cell disease.The Cochrane database of systematic reviews · 2020
    Pooled it
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  13. Post-Transcriptional Genetic Silencing ofThe New England journal of medicine · 2021
    Trial
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  17. Characteristics of Late Fatal Infections after Allogeneic Hematopoietic Cell Transplantation.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2019
    Trial
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  19. Observational
  20. Article

161 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

37 authors.

Eliane GluckmanEurocord, Paris-Diderot University Equipe d'Accueil 3518, Hospital Saint Louis, Paris, France.
Barbara CappelliMonacord, International Observatory on Sickle Cell Disease, Centre Scientifique de Monaco, Monaco.
Francoise BernaudinDepartment of Pediatrics, Referral Center for Sickle Cell Disease, Centre Hospitalier Intercommunal Créteil, Paris XII University, Créteil, France.
Myriam LabopinEuropean Society for Blood and Marrow Transplantation Statistical Unit, Hospital Saint Antoine, Assistance Publique-Hôpitaux de Paris, Paris, France.
Fernanda VoltEurocord, Paris-Diderot University Equipe d'Accueil 3518, Hospital Saint Louis, Paris, France.
Jeanette CarrerasDepartment of Medicine, Center for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, WI.
Belinda Pinto SimõesRibeirão Preto Medical School, University of São Paulo, São Paulo, Brazil.
Alina FersterHemato-Oncology Unit, Hospital Universitaire des Enfants Reine Fabiola, Université Libre de Bruxelles, Brussels, Belgium.
Sophie DupontCliniques Universitaires Saint Luc, Hemato-Oncology Unit, Brussels, Belgium.
Josu de la FuenteCentre for Haematology, Imperial College London, London, United Kingdom.
Jean-Hugues DalleHemato-immunology, Hospital Robert Debré and Paris-Diderot University, Paris, France.
Marco ZeccaPediatric Hematology-Oncology, Fondazione Istituto di Ricovero e Cura a Carattere Scientifico Policlinico San Matteo, Pavia, Italy.
Mark C WaltersUniversity of California San Francisco Benioff Children's Hospital, Oakland, CA.
Lakshmanan KrishnamurtiAflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Atlanta, GA.
Monica BhatiaMorgan Stanley Children's Hospital of New York, New York, NY.
Kathryn LeungBaylor College of Medicine, Houston, TX.
Gregory YanikChildren's Hospital of Michigan, Detroit, MI.
Joanne KurtzbergPediatric Blood and Marrow Transplant Program, Duke University Medical Center, Durham, NC.
Nathalie DhedinAdolescent and Young Adults Hematology Department, Hospital Saint-Louis, Paris, France.
Mathieu KuentzDepartment of Pediatrics, Referral Center for Sickle Cell Disease, Centre Hospitalier Intercommunal Créteil, Paris XII University, Créteil, France.
Gerard MichelDepartment of Pediatric Hematology and Oncology and Research Unit Equipe d'Accueil 3279, Aix-Marseille University and Timone Children's Hospital Marseille, Marseille, France.
Jane ApperleyImperial College London, Hammersmith Hospital, London, United Kingdom.
Patrick LutzService D'hémato Oncologie Pédiatrique, Centre Hospitalier Universitaire de Strasbourg, Strasbourg, France.
Bénédicte NevenPediatric Hematology-Immunology Department, Hospital Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, Paris, France.
Yves BertrandDepartment of Pediatric Hematology and Oncology, University Hospital of Lyon, Lyon, France.
Jean Pierre VannierEquipe d'Accueil 3829, Institut de Recherche et d'Innovation Biomédicale, Faculté de Médecine-Pharmacie, Rouen, France.
Mouhab AyasPaediatric Haematology/Oncology, King Faisal Specialist Hospital & Research Centre, Riyadh, Saudi Arabia.
Marina CavazzanaBiotherapy Department, Necker Children's Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.
Susanne Matthes-MartinStem Cell Transplantation Unit, St. Anna Children's Hospital, Vienna, Austria.
Vanderson RochaEurocord, Paris-Diderot University Equipe d'Accueil 3518, Hospital Saint Louis, Paris, France.
Hanadi ElayoubiEurocord, Paris-Diderot University Equipe d'Accueil 3518, Hospital Saint Louis, Paris, France.
Chantal KenzeyEurocord, Paris-Diderot University Equipe d'Accueil 3518, Hospital Saint Louis, Paris, France.
Peter BaderDepartment for Stem Cell Transplantation and Immunology, Clinic for Children and Adolescents, University Hospital Frankfurt, Goethe University, Frankfurt, Germany.
Franco LocatelliDipartimento di Oncoematologia Pediatrica, Istituto di Ricovero e Cura a Carattere Scientifico, Ospedale Bambino Gesù, Rome, Italy.
Annalisa RuggeriEurocord, Paris-Diderot University Equipe d'Accueil 3518, Hospital Saint Louis, Paris, France.
Mary EapenDepartment of Medicine, Center for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, WI.
Eurocord, the Pediatric Working Party of the European Society for Blood and Marrow Transplantation, and the Center for International Blood and Marrow Transplant Research

Funding

Data Resource for Analyzing Blood &Marrow TransplantsU24CA076518 · NCI · MEDICAL COLLEGE OF WISCONSIN · PI Amy M Moskop, Bronwen Shaw · 1998 to 2026
$105.2M
NCI NIH HHS U24 CA076518
6 · The paper itself

Abstract

Despite advances in supportive therapy to prevent complications of sickle cell disease (SCD), access to care is not universal. Hematopoietic cell transplantation is, to date, the only curative therapy for SCD, but its application is limited by availability of a suitable HLA-matched donor and lack of awareness of the benefits of transplant. Included in this study are 1000 recipients of HLA-identical sibling transplants performed between 1986 and 2013 and reported to the European Society for Blood and Marrow Transplantation, Eurocord, and the Center for International Blood and Marrow Transplant Research. The primary endpoint was event-free survival, defined as being alive without graft failure; risk factors were studied using a Cox regression models. The median age at transplantation was 9 years, and the median follow-up was longer than 5 years. Most patients received a myeloablative conditioning regimen (n = 873; 87%); the remainder received reduced-intensity conditioning regimens (n = 125; 13%). Bone marrow was the predominant stem cell source (n = 839; 84%); peripheral blood and cord blood progenitors were used in 73 (7%) and 88 (9%) patients, respectively. The 5-year event-free survival and overall survival were 91.4% (95% confidence interval, 89.6%-93.3%) and 92.9% (95% confidence interval, 91.1%-94.6%), respectively. Event-free survival was lower with increasing age at transplantation (hazard ratio [HR], 1.09;

Indexed as

AdolescentAnemia, Sickle CellChildChild, PreschoolDisease-Free SurvivalFemaleGraft SurvivalHematopoietic Stem Cell TransplantationHistocompatibilityHLA AntigensHumansInfantMaleSiblingsSurveys and QuestionnairesSurvival RateHLA Antigens

Identifiers

PMID27965196
PMCPMC5356458

What OpenQuestion holds

Textmetadata
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.