Evidence map›Paper›PMID 28096091›Full record

ReviewBlood2017

Allogeneic hematopoietic stem cell transplantation for MDS and CMML: recommendations from an international expert panel.

Theo de Witte, David Bowen, Marie Robin, Luca Malcovati, Dietger Niederwieser, Ibrahim Yakoub-Agha, Ghulam J Mufti, Pierre Fenaux, Guillermo Sanz, Rodrigo Martino and 20 more

Registry-linked trialOpen access · bronzeAbstract readReview
In one paragraph

Review in Blood, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07539779 (The Efficacy and Safety of Luspatercept in Preventing Poor Erythroid Engraftment After Allo-HSCT for Hematological Malignancies With Moderate to Severe Myelofibrosis), which is not on this map. Cited by 172 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
172citing papers in PubMed, 4 pooled it
24.4field-weighted citation impact, top 1% 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.

NCT07539779 phase2 / phase3not yet recruitingnot on this mapstarted 2026, after this paper: background citation

The Efficacy and Safety of Luspatercept in Preventing Poor Erythroid Engraftment After Allo-HSCT for Hematological Malignancies With Moderate to Severe Myelofibrosis: A Prospective, Multicenter, Randomized Controlled Study

TypeinterventionalSponsorNanfang Hospital, Southern Medical UniversityRan2026 to 2030Enrolled196ConditionsLuspatercept, Poor Erythroid Engraftment, Hematological Malignancies, Myelofibrosis (MF)ArmsLuspatercept, Control
3 · Its place in the literature

Who cites it

172 citing papers in PubMed, 4 syntheses or guidelines pooled it, 370 citations in OpenAlex.

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  9. Donor-Derived Cytokine-Induced Killer Cell Infusion as Consolidation after Nonmyeloablative Allogeneic Transplantation for Myeloid Neoplasms.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2019
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112 more citing papers are in PubMed but not listed here.

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

30 authors at 20 institutions in 12 countries.

Theo de WitteDepartment of Tumor Immunology, Radboud Institute of Molecular Life Sciences, Radboud University Medical Center, Nijmegen, The Netherlands.
David BowenSt. James's Institute of Oncology, Leeds, United Kingdom.
Marie RobinDepartment of Hematology and Bone Marrow Transplantation, Hôpital Saint-Louis/Assistance Publique-Hôpitaux de Paris (AP-HP)/University Paris 7, Paris, France.
Luca MalcovatiPoliclinica San Matteo, University of Pavia, Pavia, Italy.ORCID 0000-0002-1460-1611
Dietger NiederwieserDivision of Hematology, Oncology, and Hemostasiology, University of Leipzig, Leipzig, Germany.
Ibrahim Yakoub-AghaCentre International de Recherche sur l'Inflammation de Lille, INSERM U995/Centre Hospitalier Universitaire/Université Lille 2, Lille, France.
Ghulam J MuftiDepartment of Haematological Medicine, School of Medicine, Guy's, King's College and St. Thomas's Hospitals, London, United Kingdom.
Pierre FenauxService d'Hématologie Seniors, Hôpital Saint-Louis/AP-HP/University Paris 7, Paris, France.
Guillermo SanzHospital Universitario La Fe, Valencia, Spain.
Rodrigo MartinoDivision of Clinical Hematology, Hematology Department, Hospital de la Santa Creu i Sant Pau/Autonomous University of Barcelona, Barcelona, Spain.ORCID 0000-0001-5143-4042
Emilio Paolo AlessandrinoClinica Ematologica, Fondazione Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Policlinico San Matteo, Pavia, Italy.
Francesco OnidaHematology and Bone Marrow Transplantation Center, Fondazione IRCCS Ospedale Maggiore Policlinico/University of Milan, Milan, Italy.
Argiris SymeonidisHematology Division, Department of Internal Medicine, University of Patras Medical School, Patras, Greece.
Jakob PasswegHematology Division, Basel University Hospital, Basel, Switzerland.
Guido KobbeMedical Faculty, University Hospital Düsseldorf/Heinrich Heine University, Düsseldorf, Germany.
Arnold GanserDepartment of Hematology, Hemostasis, Oncology and Stem Cell Transplantation, Hannover Medical School, Hannover, Germany.
Uwe PlatzbeckerMedizinische Klinik und Poliklinik I, Universitätsklinikum Carl Gustav Carus, Dresden, Germany.
Jürgen FinkeDepartment of Medicine, Hematology, and Oncology, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Michel van GelderInternal Medicine, Maastricht University Medical Center, Maastricht, The Netherlands.
Arjan A van de LoosdrechtDepartment of Hematology, Vrije Universiteit (VU) University Medical Center, Amsterdam, The Netherlands.
Per LjungmanKarolinska University Hospital, Huddinge, Sweden.
Reinhard StauderDepartment of Internal Medicine V, Innsbruck Medical University, Innsbruck, Austria.
Liisa VolinComprehensive Cancer Center, Helsinki University Hospital, Helsinki, Finland.
H Joachim DeegFred Hutchinson Cancer Research Center, Seattle, WA.
Corey CutlerDana-Farber Cancer Institute, Boston, MA.
Wael SaberCenter for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, WI.
Richard ChamplinDepartment of Stem Cell Transplant and Cellular Therapy, University of Texas MD Anderson Cancer Center, Houston, TX.
Sergio GiraltAdult Bone Marrow Transplant Service, Memorial Sloan Kettering Cancer Center, New York, NY.
Claudio AnasettiMoffitt Cancer Center, Tampa, FL; and.
Nicolaus KrögerDepartment for Stem Cell Transplantation, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Université Paris Cité · FRDana-Farber Cancer Institute · USDüsseldorf University Hospital · DEHelsinki University Hospital · FIHospital Universitari i Politècnic La Fe · ESInnsbruck Medical University · ATInserm · FRIstituti di Ricovero e Cura a Carattere Scientifico · ITKarolinska University Hospital · SELeipzig University · DEMaastricht University · NLMedical College of Wisconsin · USMedizinische Hochschule Hannover · DEMemorial Sloan Kettering Cancer Center · USMoffitt Cancer Center · USRadboud University Nijmegen · NLSt James's University Hospital · GBSt Thomas' Hospital · GBThe University of Texas MD Anderson Cancer Center · USUniversitat Autònoma de Barcelona · ES

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Center for Clinical and Translational Sciences (CCTS)UL1TR000371 · NCATS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MCPHERSON, DAVID D · 2012 to 2016
$13.4M
NCATS NIH HHS UL1 TR000371NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

An international expert panel, active within the European Society for Blood and Marrow Transplantation, European LeukemiaNet, Blood and Marrow Transplant Clinical Trial Group, and the International Myelodysplastic Syndromes Foundation developed recommendations for allogeneic hematopoietic stem cell transplantation (HSCT) in myelodysplastic syndromes (MDS) and chronic myelomonocytic leukemia (CMML). Disease risks scored according to the revised International Prognostic Scoring System (IPSS-R) and presence of comorbidity graded according to the HCT Comorbidity Index (HCT-CI) were recognized as relevant clinical variables for HSCT eligibility. Fit patients with higher-risk IPSS-R and those with lower-risk IPSS-R with poor-risk genetic features, profound cytopenias, and high transfusion burden are candidates for HSCT. Patients with a very high MDS transplantation risk score, based on combination of advanced age, high HCT-CI, very poor-risk cytogenetic and molecular features, and high IPSS-R score have a low chance of cure with standard HSCT and consideration should be given to treating these patients in investigational studies. Cytoreductive therapy prior to HSCT is advised for patients with ≥10% bone marrow myeloblasts. Evidence from prospective randomized clinical trials does not provide support for specific recommendations on the optimal high intensity conditioning regimen. For patients with contraindications to high-intensity preparative regimens, reduced intensity conditioning should be considered. Optimal timing of HSCT requires careful evaluation of the available effective nontransplant strategies. Prophylactic donor lymphocyte infusion (DLI) strategies are recommended in patients at high risk of relapse after HSCT. Immune modulation by DLI strategies or second HSCT is advised if relapse occurs beyond 6 months after HSCT.

Indexed as

Practice Guidelines as TopicHematopoietic Stem Cell TransplantationHumansLeukemia, Myelomonocytic, ChronicMyelodysplastic SyndromesRisk FactorsTransplantation ConditioningTransplantation, Homologous

Identifiers

PMID28096091
PMCPMC5524528
OpenAlexW2575545223

What OpenQuestion holds

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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.