Evidence map›Paper›PMID 27036034›Full record

ArticleOncotarget2016

High CD3+ and CD34+ peripheral blood stem cell grafts content is associated with increased risk of graft-versus-host disease without beneficial effect on disease control after reduced-intensity conditioning allogeneic transplantation from matched unrelated donors for acute myeloid leukemia - an analysis from the Acute Leukemia Working Party of the European Society for Blood and Marrow Transplantation.

Tomasz Czerw, Myriam Labopin, Christoph Schmid, Jan J Cornelissen, Patrice Chevallier, Didier Blaise, Jürgen Kuball, Stephane Vigouroux, Frédéric Garban, Bruno Lioure and 8 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
5.5field-weighted citation impact, top 4% 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

33 citing papers in PubMed, 67 citations in OpenAlex.

  1. Impact of T Cell Dose on Outcome of T Cell-Replete HLA-Matched Allogeneic Peripheral Blood Stem Cell Transplantation.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2019
    Trial
  2. Article
  3. Significance of CD34Transplantation and cellular therapy · 2026
    Article
  4. Article
  5. Donor selection, graft engineering, and dosing oh my!Hematology. American Society of Hematology. Education Program · 2025
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. The Impact of Graft CD3Journal of hematology · 2023
    Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. 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

18 authors at 17 institutions in 7 countries.

Tomasz CzerwDepartment of Bone Marrow Transplantation and Oncohematology, Maria Sklodowska-Curie Memorial Cancer Centre and Institute of Oncology, Gliwice Branch, Gliwice, Poland.
Myriam LabopinClinical Hematology and Cellular Therapy Department, The Acute Leukemia Working Party of the EBMT Office, Hopital Saint-Antoine APHP Paris, France.
Christoph SchmidKlinikum Augsburg, University of Munich, Munich, Germany.
Jan J CornelissenDepartment of Hematology, Erasmus University medical center Cancer Institute, Rotterdam, The Netherlands.
Patrice ChevallierCHU Nantes, Department D`Hematologie, Nantes, France.
Didier BlaiseUnité de Transplantation et de Thérapie Cellulaire, Institut Paoli Calmettes, Marseille, France.
Jürgen KuballUniversity Medical Centre, Department of Haematology, Utrecht, The Netherlands.
Stephane VigourouxCHU Bordeaux, Hôpital Haut-leveque, Pessac, France.
Frédéric GarbanHopital A. Michallon, Hématologie Clinique, Pole Cancérologie, Grenoble, France.
Bruno LioureNouvel Hopital Civil, Strasbourg, France.
Nathalie FegueuxCHU Lapeyronie, Département d`Hématologie Clinique, Montpellier, France.
Laurence ClementHôpital de Brabois, Centre Hospitalier Universitaire (CHU) de Nancy, Vandoeuvres les Nancy, France.
Anna SandstedtUniversity Hospital, Department of Hematology, Linköping, Sweden.
Johan MaertensUniversity Hospital Gasthuisberg, Department of Hematology, Leuven, Belgium.
Gaëlle GuillermCHU Morvan, Brest, France.
Dominique BordessouleCHRU Limoges, Service d`Hématologie Clinique, Limoges, France.
Mohamad MohtyClinical Hematology and Cellular Therapy Department, The Acute Leukemia Working Party of the EBMT Office, Hopital Saint-Antoine APHP Paris, France.
Arnon NaglerHematology and Bone Marrow Transplantation, Chaim Sheba Medical Center, Tel Hashomer, Israel.
Inserm · FRCentre Hospitalier Régional et Universitaire de Nancy · FRCentre Hospitalier Régional Universitaire de Brest · FRCentre Hospitalier Universitaire de Limoges · FRCentre Hospitalier Universitaire de Nantes · FRErasmus MC Cancer Institute · NLHôpital Albert Michallon · FRHôpital Cardiologique du Haut-Lévêque · FRHôpital Civil, Strasbourg · FRHôpital Lapeyronie · FRInstitut Paoli-Calmettes · FRLinköping University Hospital · SESheba Medical Center · ILThe Maria Sklodowska-Curie National Research Institute of Oncology · PLUniversitair Ziekenhuis Leuven · BEUniversity Hospital Augsburg · DEUniversity Medical Center Utrecht · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inconsistent results have been reported regarding the influence of graft composition on the incidence of graft versus host disease (GVHD), disease control and survival after reduced-intensity conditioning (RIC) allogeneic peripheral blood stem cell transplantation (allo-PBSCT). These discrepancies may be at least in part explained by the differences in disease categories, disease status at transplant, donor type and conditioning. The current retrospective EBMT registry study aimed to analyze the impact of CD3+ and CD34+ cells dose on the outcome of RIC allo-PBSCT in patients with acute myelogenous leukemia (AML) in first complete remission, allografted from HLA-matched unrelated donors (10 of 10 match). We included 203 adults. In univariate analysis, patients transplanted with the highest CD3+ and CD34+ doses (above the third quartile cut-off point values, >347 x 10^6/kg and >8.25 x 10^6 /kg, respectively) had an increased incidence of grade III-IV acute (a) GVHD (20% vs. 6%, P = .003 and 18% vs. 7%, P = .02, respectively). There was no association between cellular composition of grafts and transplant-related mortality, AML relapse, incidence of chronic GVHD and survival. Neither engraftment itself nor the kinetics of engraftment were affected by the cell dose. In multivariate analysis, CD3+ and CD34+ doses were the only adverse predicting factors for grade III-IV aGVHD (HR = 3.6; 95%CI: 1.45-9.96, P = .006 and 2.65 (1.07-6.57), P = .04, respectively). These results suggest that careful assessing the CD3+ and CD34+ graft content and tailoring the cell dose infused may help in reducing severe acute GVHD risk without negative impact on the other transplantation outcomes.

Indexed as

Unrelated DonorsAcute DiseaseAdultAgedAntigens, CD34CD3 ComplexFemaleGraft vs Host DiseaseHumansLeukemia, MyeloidMaleMiddle AgedMultivariate AnalysisPeripheral Blood Stem Cell TransplantationRemission InductionRetrospective StudiesAntigens, CD34CD3 Complexacute myeloid leukemia (AML)allogenic transplantationcell dosereduced-intensity conditioningstem cell transplantation

Identifiers

PMID27036034
PMCPMC5053647
OpenAlexW2330024675

What OpenQuestion holds

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LicenceCC BY
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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.