Evidence map›Paper›PMID 31763792›Full record

ArticleCurrent protocols in cytometry2019

Immunophenotypic Detection of Measurable Residual (Stem Cell) Disease Using LAIP Approach in Acute Myeloid Leukemia.

Wendelien Zeijlemaker, Angele Kelder, Jacqueline Cloos, Gerrit Jan Schuurhuis

Abstract read
In one paragraph

Article in Current protocols in cytometry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing 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

38 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Acute Myeloid Leukemia-Use of Measurable Residual Disease to Improve Outcomes.Advances in experimental medicine and biology · 2025
    Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Minimal Residual Disease in Acute Myeloid Leukemia: Old and New Concepts.International journal of molecular sciences · 2024
    Review
  18. Article
  19. Article
  20. MRD-directed and risk-adapted individualized stratified treatment of AML.Chinese journal of cancer research = Chung-kuo yen cheng yen chiu · 2023
    Article
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

4 authors.

Wendelien ZeijlemakerDepartment of Hematology, Amsterdam University Medical Center, Cancer Center VU University Medical Center, Amsterdam, The Netherlands.
Angele KelderDepartment of Hematology, Amsterdam University Medical Center, Cancer Center VU University Medical Center, Amsterdam, The Netherlands.
Jacqueline CloosDepartment of Hematology, Amsterdam University Medical Center, Cancer Center VU University Medical Center, Amsterdam, The Netherlands.
Gerrit Jan SchuurhuisDepartment of Hematology, Amsterdam University Medical Center, Cancer Center VU University Medical Center, Amsterdam, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Half of the patients with acute myeloid leukemia (AML), who achieve complete remission after chemotherapy treatment, will ultimately experience a relapse. Measurable residual disease (MRD) is an important post-treatment risk factor in AML, because it gives additional information about the depth of the remission. Within MRD, the small population of leukemic stem cells (LSCs) is thought to be at the base of the actual relapse. In this protocol, the flow cytometric detection of MRD and LSCs herein is outlined. We give a detailed overview of the sampling procedures for optimal multiparameter flow cytometry assessment of both MRD and LSC, using leukemia associated immunophenotypes (LAIPs) and LSC markers. Moreover, an overview of the gating strategies to detect LAIPs and LSC markers is provided. This protocol serves as guidance for flow cytometric detection of measurable residual (stem cell) disease necessary for proper therapeutic decision making in AML patients. © 2019 The Authors. Basic Protocol 1: Immunophenotypic LAIP detection for measurable residual disease monitoring Basic Protocol 2: Immunophenotypic detection of CD34+CD38- leukemic stem cells.

Indexed as

ADP-ribosyl Cyclase 1Antigens, CD34Biomarkers, TumorBone Marrow CellsCell CountCells, CulturedFlow CytometryHumansImmunophenotypingLeukemia, Myeloid, AcuteMonitoring, PhysiologicNeoplasm, ResidualNeoplastic Stem CellsRecurrenceADP-ribosyl Cyclase 1Antigens, CD34Biomarkers, Tumoracute myeloid leukemia (AML)leukemia associated immunophenotypes (LAIPs)leukemic stem cells (LSCs)measurable residual disease (MRD)multiparameter flow cytometry (MFC)

Identifiers

PMID31763792
PMCPMC6856793

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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.