Evidence map›Paper›PMID 29330391›Full record

ArticleBone marrow transplantation2018

Impact of antithymocyte globulin doses in reduced intensity conditioning before allogeneic transplantation from matched sibling donor for patients with acute myeloid leukemia: a report from the acute leukemia working party of European group of Bone Marrow Transplantation.

Raynier Devillier, Myriam Labopin, Patrice Chevallier, Marie-Pierre Ledoux, Gérard Socié, Anne Huynh, Jean-Henri Bourhis, Jean-Yves Cahn, Gabrielle Roth-Guepin, Ghulam Mufti and 8 more

Registry-linked trialOpen access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Bone marrow transplantation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03818334 (Use of Post Transplant Cyclophosphamide as Graft Versus Host Disease Prophylaxis in Matched Unrelated Donor Stem Cell Transplantation for Hematological Malignancies, a Prospective Randomized Controlled Trial), which is not on this map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing 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.

NCT03818334 phase2 / phase3recruitingnot on this map

Use of Post Transplant Cyclophosphamide as Graft Versus Host Disease Prophylaxis in Matched Unrelated Donor Stem Cell Transplantation for Hematological Malignancies, a Prospective Randomized Controlled Trial

TypeinterventionalSponsorHospital Israelita Albert EinsteinRan2018 to 2026Enrolled50ConditionsBone Marrow Transplant Complications, Graft Versus Host Disease, Infection Viral, Engraft FailureArmsCyclophosphamide, ATG
3 · Its place in the literature

Who cites it

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

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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 14 institutions in 4 countries.

Raynier DevillierDepartment of Hematology, Institut Paoli Calmettes, Marseille, France.
Myriam LabopinDepartment of Hematology, University Hospital Saint Antoine, APHP, Paris, France.
Patrice ChevallierDepartment of Hematology, University Hospital Nantes, Nantes, France.
Marie-Pierre LedouxDepartment of Hematology, University Hospital Hautepierre, Strasbourg, France.
Gérard SociéDepartment of Hematology, University Hopital St Louis, APHP, Paris, France.
Anne HuynhDepartment of Hematology, University Insitute of cancer of Toulouse-Oncopole, Toulouse, France.
Jean-Henri BourhisDepartment of Hematology, Institut Gustave Roussy, Villejuif, France.
Jean-Yves CahnDepartment of Hematology, University Hospital A. Michallon, Grenoble, France.
Gabrielle Roth-GuepinDepartment of Hematology, University Hospital Nancy, Vandoeuvre-lès-Nancy, France.
Ghulam MuftiDepartment of Hematology, King's College Hospital, London, UK.
Déborah DesmierDepartment of Hematology, University Hospital La Miletrie, Poitiers, France.
Mauricette MichalletDepartment of Hematology, University Hospital Lyon Sud, Lyon, France.
Nathalie FegueuxDepartment of Hematology, University Hospital Montpellier, Montpellier, France.
Fabio CiceriDepartment of Hematology, San Raffaele Hospital, Milano, Italy.
Fréderic BaronDepartment of Hematology, University of Liège, Liège, Belgium.
Didier BlaiseDepartment of Hematology, Institut Paoli Calmettes, Marseille, France.ORCID http://orcid.org/0000-0002-5684-9447
Arnon NaglerEBMT ALWP Office, Pierre and Marie Curie University, Paris, France.
Mohamad MohtyDepartment of Hematology, University Hospital Saint Antoine, APHP, Paris, France. mohamad.mohty@inserm.fr.
Aix-Marseille Université · FRSorbonne Université · FRAssistance Publique – Hôpitaux de Paris · FRCentre Hospitalier Régional et Universitaire de Nancy · FRCentre Hospitalier Universitaire de Montpellier · FRHôpital Albert Michallon · FRHôpital d'Hautepierre · FRHôpital Lyon Sud · FRInstitut Gustave Roussy · FRInstitut universitaire du cancer de Toulouse Oncopole · FRKing's College Hospital · GBLaboratoire de Génétique Cellulaire · FRSheba Medical Center · ILUniversity of Liège · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antithymocyte globulin (ATG) is commonly used for graft-vs.-host disease (GVHD) prophylaxis in unrelated donor allogeneic transplantation (Allo-HSCT). However, its use is still controversial in matched sibling donor (MSD) Allo-HSCT, notably after reduced intensity conditioning (RIC). ATG dose may influence the outcome, explaining in part the discordant conclusions in MSD Allo-HSCT. We, therefore, analyzed the impact of ATG doses in patients with acute myeloid leukemia in first complete remission undergoing RIC Allo-HSCT from a MSD. We analyzed 234 patients from the EBMT registry and compared outcome according to given ATG dose (high dose: ≥ 6 mg/kg, n = 39 or low dose: < 6 mg/kg, n = 195). No difference was found in the cumulative incidence of acute (grade 2-4: high dose vs. low dose: 21% vs. 13%, p = 0.334; adjusted hazard ratio (HR): 1.20, p = 0.712) and chronic GVHD (extensive: high dose vs. low dose: 19% vs. 18%, p = 0.897; adjusted HR: 1.01, p = 0.980). In contrast, high dose of ATG significantly increased the incidence of relapse (52% vs. 26%, p = 0.011; adjusted HR: 1.31, p = 0.001) leading to impaired outcome (HR progression-free survival (PFS): 1.23, p = 0.002; HR overall survival (OS): 1.17, p = 0.029; HR GVHD and relapse-free survival (GRFS): 1.20, p = 0.005). We conclude that an ATG dose <6 mg/kg is sufficient for GVHD prophylaxis, while higher doses impair disease control and outcome.

Indexed as

Tissue DonorsAdultAgedAntilymphocyte SerumDose-Response Relationship, DrugFemaleGraft vs Host DiseaseHematopoietic Stem Cell TransplantationHumansLeukemia, Myeloid, AcuteMaleMiddle AgedRecurrenceRetrospective StudiesSiblingsSurvival AnalysisAntilymphocyte Serum

Identifiers

PMID29330391
OpenAlexW2783119073

What OpenQuestion holds

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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.