Evidence map›Paper›PMID 37671649›Full record

ArticleAmerican journal of hematology2023

Measurable residual disease monitoring in patients with acute myeloid leukemia treated with lower-intensity therapy: Roadmap from an ELN-DAVID expert panel.

Farhad Ravandi, Jacqueline Cloos, Francesco Buccisano, Richard Dillon, Konstanze Döhner, Sylvie D Freeman, Christopher S Hourigan, Gerrit J Ossenkoppele, Gail J Roboz, Marion Subklewe and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in American journal of hematology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
6.4field-weighted citation impact, top 3% 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

13 citing papers in PubMed, 22 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

17 authors at 14 institutions in 6 countries.

Farhad RavandiDepartment of Leukemia, The University of Texas-MD Anderson Cancer Center, Houston, Texas, USA.ORCID 0000-0002-7621-377X
Jacqueline CloosDepartment of Hematology, Amsterdam University Medical Center (UMC), Cancer Center Amsterdam, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Francesco BuccisanoDepartment of Biomedicine and Prevention, Hematology, University Tor Vergata, Rome, Italy.ORCID 0000-0003-4320-9253
Richard DillonDepartment of Medical and Molecular Genetics, King's College, London, UK.
Konstanze DöhnerDepartment of Internal Medicine III, University Hospital of Ulm, Ulm, Germany.
Sylvie D FreemanInstitute of Immunology and Immunotherapy, University of Birmingham, Birmingham, UK.
Christopher S HouriganLaboratory of Myeloid Malignancy, Hematology Branch, National Heart, Lung, and Blood Institute, Bethesda, Maryland, USA.
Gerrit J OssenkoppeleDepartment of Hematology, Amsterdam University Medical Center (UMC), Cancer Center Amsterdam, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Gail J RobozDivision of Hematology and Oncology, Department of Medicine, Weill Cornell Medicine, New York, New York, USA.
Marion SubkleweDepartment of Medicine III, University Hospital, Ludwig Maximilian University Munich, München, Germany.
Christian ThiedeDepartment of Medicine I, University Hospital Carl Gustav Carus, Dresden, Germany.
Isabell ArnhardtDepartment of Hematology, Hemostasis, Oncology, and Stem Cell Transplantation, Hannover Medical School, Hannover, Germany.
Peter J M ValkDepartment of Hematology, Erasmus MC Cancer Institute, University Medical Center Rotterdam, Rotterdam, The Netherlands.
Adriano VendittiDepartment of Biomedicine and Prevention, Hematology, University Tor Vergata, Rome, Italy.ORCID 0000-0002-0245-0553
Andrew H WeiDepartment of Haematology, Peter MacCallum Cancer Centre, Royal Melbourne Hospital, University of Melbourne and Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.
Roland B WalterTranslational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, Washington, USA.
Michael HeuserDepartment of Hematology, Hemostasis, Oncology, and Stem Cell Transplantation, Hannover Medical School, Hannover, Germany.
Amsterdam Neuroscience · NLMedizinische Hochschule Hannover · DEUniversity of Rome Tor Vergata · ITCornell University · USErasmus MC Cancer Institute · NLFred Hutch Cancer Center · USKing's College London · GBLudwig-Maximilians-Universität München · DENational Heart Lung and Blood Institute · USThe Royal Melbourne Hospital · AUThe University of Texas MD Anderson Cancer Center · USUniversity Hospital Carl Gustav Carus · DEUniversity Hospital Ulm · DEUniversity of Birmingham · GB

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
Cancer Research UK 29806NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

With the availability of effective targeted agents, significant changes have occurred in the management of patients with acute myeloid leukemia (AML) over the past several years, particularly for those considered unfit for intensive chemotherapy. While testing for measurable residual disease (MRD) is now routinely performed in patients treated with intensive chemotherapy to refine prognosis and, possibly, inform treatment decision-making, its value in the context of lower-intensity regimens is unclear. As such regimens have gained in popularity and can be associated with higher response rates, the need to better define the role of MRD assessment and the appropriate time points and assays used for this purpose has increased. This report outlines a roadmap for MRD testing in patients with AML treated with lower-intensity regimens. Experts from the European LeukemiaNet (ELN)-DAVID AML MRD working group reviewed all available data to propose a framework for MRD testing in future trials and clinical practice. A Delphi poll served to optimize consensus. Establishment of uniform standards for MRD assessments in lower-intensity regimens used in treating patients with AML is clinically relevant and important for optimizing testing and, ultimately, improving treatment outcomes of these patients.

Indexed as

Leukemia, Myeloid, AcuteHumansNeoplasm, ResidualPrognosisTreatment Outcome

Identifiers

PMID37671649
PMCPMC10841357
OpenAlexW4386467290

What OpenQuestion holds

Textmetadata
LicenceTDM
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.