Evidence map›Paper›PMID 36300090›Full record

ArticleFrontiers in oncology2022

Concordance in measurable residual disease result after first and second induction cycle in acute myeloid leukemia: An outcome- and cost-analysis.

Jesse M Tettero, Waleed K W Al-Badri, Lok Lam Ngai, Costa Bachas, Dimitri A Breems, Catharina H M J van Elssen, Thomas Fischer, Bjorn T Gjertsen, Gwendolyn N Y van Gorkom, Patrycja Gradowska and 12 more

Abstract read
In one paragraph

Article in Frontiers in oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

22 authors.

Jesse M TetteroDepartment of Hematology, Amsterdam Univerisity Medical Centers location Vrije Universiteit Amsterdam, Amsterdam, Netherlands.
Waleed K W Al-BadriDepartment of Hematology, Amsterdam Univerisity Medical Centers location Vrije Universiteit Amsterdam, Amsterdam, Netherlands.
Lok Lam NgaiDepartment of Hematology, Amsterdam Univerisity Medical Centers location Vrije Universiteit Amsterdam, Amsterdam, Netherlands.
Costa BachasDepartment of Hematology, Amsterdam Univerisity Medical Centers location Vrije Universiteit Amsterdam, Amsterdam, Netherlands.
Dimitri A BreemsDepartment of Hematology, Ziekenhuis Netwerk Antwerpen, Antwerp, Belgium.
Catharina H M J van ElssenDepartment of Internal Medicine, Division of Hematology, GROW-School for Oncology and Developmental Biology, Maastricht University Medical Center, Maastricht, Netherlands.
Thomas FischerDepartment of Hematology and Oncology, Otto von Guericke University Hospital Magdeburg, Magdeburg, Germany.
Bjorn T GjertsenDepartment of Medicine, Hematology Section, Haukeland University Hospital, Bergen, Norway.
Gwendolyn N Y van GorkomDepartment of Internal Medicine, Division of Hematology, GROW-School for Oncology and Developmental Biology, Maastricht University Medical Center, Maastricht, Netherlands.
Patrycja GradowskaThe Dutch-Belgian Hemato-Oncology Cooperative Group (HOVON) Data Center, Department of Hematology, Erasmus Medical Center (MC) Cancer Institute, Rotterdam, Netherlands.
Marjolein J E GreuterDepartment of Epidemiology and Data Science, Amsterdam Univerisity Medical Centers, location Vrije Universiteit Amsterdam, Amsterdam, Netherlands.
Laimonas GriskeviciusHematology, Oncology, Transfusion Medicine Center, Vilnius University Hospital Santaros Klinikos and Vilnius University, Vilnius, Lithuania.
Gunnar JuliussonDepartment of Hematology, Skanes University Hospital, Lund, Sweden.
Johan MaertensDepartment of Hematology, University Hospital Gasthuisberg, Leuven, Belgium.
Markus G ManzDepartment of Medical Oncology and Hematology, University Hospital, Zurich, Switzerland.
Thomas PabstSwiss Group for Clinical Cancer Research (SAKK), Bern, Switzerland.
Jakob PasswegSwiss Group for Clinical Cancer Research (SAKK), Bern, Switzerland.
Kimmo PorkkaDepartment of Hematology, Helsinki University Hospital Cancer Center, Helsinki, Finland.
Bob LöwenbergDepartment of Hematology, Erasmus University Medical Center (MC) and Erasmus MC Cancer Institute, Rotterdam, Netherlands.
Gert J OssenkoppeleDepartment of Hematology, Amsterdam Univerisity Medical Centers location Vrije Universiteit Amsterdam, Amsterdam, Netherlands.
Jeroen J W M JanssenDepartment of Hematology, Amsterdam Univerisity Medical Centers location Vrije Universiteit Amsterdam, Amsterdam, Netherlands.
Jacqueline CloosDepartment of Hematology, Amsterdam Univerisity Medical Centers location Vrije Universiteit Amsterdam, Amsterdam, Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Measurable residual disease (MRD) measured using multiparameter flow-cytometry (MFC) has proven to be an important prognostic biomarker in acute myeloid leukemia (AML). In addition, MRD is increasingly used to guide consolidation treatment towards a non-allogenic stem cell transplantation treatment for MRD-negative patients in the ELN-2017 intermediate risk group. Currently, measurement of MFC-MRD in bone marrow is used for clinical decision making after 2 cycles of induction chemotherapy. However, measurement after 1 cycle has also been shown to have prognostic value, so the optimal time point remains a question of debate. We assessed the independent prognostic value of MRD results at either time point and concordance between these for 273 AML patients treated within and according to the HOVON-SAKK 92, 102, 103 and 132 trials. Cumulative incidence of relapse, event free survival and overall survival were significantly better for MRD-negative (<0.1%) patients compared to MRD-positive patients after cycle 1 and cycle 2 (

Indexed as

acute myeloid leukemiaearlier detectionguided therapymeasurable residual disease (MRD)multiparameter flow cytometry (MFC)prognostic value

Identifiers

PMID36300090
PMCPMC9589259

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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.