Evidence map›Paper›PMID 35048553›Full record

ArticleCancer medicine2022

Measurable residual disease, FLT3-ITD mutation, and disease status have independent prognostic influence on outcome of allogeneic stem cell transplantation in NPM1-mutated acute myeloid leukemia.

Rama Al Hamed, Myriam Labopin, Etienne Daguindau, Riitta Niittyvuopio, Anne Huynh, Gerard Socié, Micha Srour, Jean Henri Bourhis, Nicolaus Kröger, Eleni Tholouli and 11 more

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

7 citing papers in PubMed, 6 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

21 authors at 20 institutions in 10 countries.

Rama Al HamedDepartment of Internal Medicine, Jacobi Medical Center/Albert Einstein College of Medicine, Bronx, New York, USA.ORCID 0000-0002-1095-0224
Myriam LabopinDepartment of Hematology, EBMT Paris Office, CEREST-TC, Saint Antoine Hospital, Paris, France.
Etienne DaguindauHôpital Jean Minjoz, Service d`Hématologie, Besançon, France.
Riitta NiittyvuopioHUCH Comprehensive Cancer Center, Stem Cell Transplantation Unit, Helsinki, Finland.
Anne HuynhCHU - Institut Universitaire du Cancer Toulouse, Oncopole, Toulouse, France.
Gerard SociéDepartment of Hematology - BMT, Hôpital St. Louis, Paris, France.
Micha SrourCHU de Lille, Université de Lille, Lille, France.
Jean Henri BourhisDepartment of Hematology, Gustave Roussy Cancer Campus, BMT Service, Villejuif, France.
Nicolaus KrögerUniversity Hospital Eppendorf, Bone Marrow Transplantation Centre, Hamburg, Germany.
Eleni TholouliClinica Haematology Department, Manchester Royal Infirmary, Manchester, UK.
Goda ChoiDepartment of Hematology, University Medical Center Groningen (UMCG), University of Groningen, Groningen, The Netherlands.
Xavier PoiréDepartment of Haematology, Cliniques Universitaires St. Luc, Brussels, Belgium.
Hans MartinGoethe-Universitaet, Medizinische Klinik II, Hämatologie, Medizinische Onkologie, Frankfurt, Germany.
Marie-Thérèse RubioCHRU BRABOIS, Service Hématologie, Vandoeuvre-lès-Nancy, France.
Pavel JindraDepartment of Hematology/Oncology, Charles University Hospital, Pilsen, Czech Republic.
Didier BlaiseProgramme de Transplantation & Therapie Cellulaire, Centre de Recherche en Cancérologie de Marseille, Marseille, France.
Dietrich BeelenDepartment of Bone Marrow Transplantation, University Hospital, Essen, Germany.
Hélène Labussière-WalletCentre Hospitalier Lyon Sud, Service Hématologie, Lyon, France.
Arnon NaglerHematology Division, Chaim Sheba Medical Center, Tel Hashomer, Israel.
Ali BazarbachiDepartment of Internal Medicine, American University of Beirut, Beirut, Lebanon.
Mohamad MohtyDepartment of Hematology, EBMT Paris Office, CEREST-TC, Saint Antoine Hospital, Paris, France.
Sorbonne Université · FRAmerican University of Beirut · LBCancer Society of Finland · FICentre de Recherche en Cancérologie de Marseille · FRCentre Hospitalier Régional et Universitaire de Nancy · FRCharles University · CZCliniques Universitaires Saint-Luc · BEEssen University Hospital · DEGoethe University Frankfurt · DEHôpital Lyon Sud · FRHôpital Privé Jean Mermo · FRHôpital Saint-Louis · FRInstitut Gustave Roussy · FRInstitut universitaire du cancer de Toulouse Oncopole · FRJacobi Medical Center · USManchester Royal Infirmary · GBSheba Medical Center · ILUniversität Hamburg · DEUniversité de Lille · FRUniversity Medical Center Groningen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nucleophosmin-1 (NPM1) mutations in acute myeloid leukemia (AML) confer a survival advantage in the absence of FLT3-internal tandem duplication (FLT3-ITD). Here, we investigated the main predictors of outcome after allogeneic hematopoietic stem cell transplantation (allo-HCT). We identified 1572 adult (age ≥ 18 year) patients with NPM1-mutated AML in first complete remission (CR1:78%) or second complete remission (CR2:22%) who were transplanted from matched sibling donors (30.8%) or unrelated donors (57.4%) between 2007 and 2019 at EBMT participating centers. Median follow-up for survivors was 23.7 months. FLT3-ITD was present in 69.3% of patients and 39.2% had detectable minimal/measurable residual disease (MRD) at transplant. In multivariate analysis, relapse incidence (RI) and leukemia-free survival (LFS) were negatively affected by concomitant FLT3-ITD mutation (HR 1.66 p = 0.0001, and HR 1.53, p < 0.0001, respectively), MRD positivity at transplant (HR 2.18, p < 10

Indexed as

Hematopoietic Stem Cell TransplantationLeukemia, Myeloid, AcuteAdultfms-Like Tyrosine Kinase 3HumansMutationNucleophosminPrognosisRecurrenceRetrospective StudiesFLT3 protein, humanfms-Like Tyrosine Kinase 3Nucleophosminacute myeloid leukemiaFLT3-ITDminimal residual diseaseNPM-1 mutation

Identifiers

PMID35048553
PMCPMC8855908
OpenAlexW4206469781

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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.