Evidence map›Paper›PMID 29321824›Full record

ArticleWorld journal of stem cells2017

High frequency of CD34+CD38-/low immature leukemia cells is correlated with unfavorable prognosis in acute myeloid leukemia.

Adriana Plesa, Charles Dumontet, Eve Mattei, Ines Tagoug, Sandrine Hayette, Pierre Sujobert, Isabelle Tigaud, Marie Pierre Pages, Youcef Chelghoum, Fiorenza Baracco and 12 more

Open access · hybridAbstract read
In one paragraph

Article in World journal of stem cells, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 12% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

  1. Pooled it
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  10. Can CD34Frontiers in pediatrics · 2023
    Review
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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 at 4 institutions in 1 country.

Adriana PlesaLaboratory of Hematology, Lyon-Sud Hospital, Hospices Civils de Lyon, Pierre - Bénite Cedex 69495, France.
Charles DumontetLaboratory of Hematology, Lyon-Sud Hospital, Hospices Civils de Lyon, Pierre - Bénite Cedex 69495, France.
Eve MatteiLaboratory of Hematology, Lyon-Sud Hospital, Hospices Civils de Lyon, Pierre - Bénite Cedex 69495, France.
Ines TagougCRCL, INSERM 1052/CNRS 5286, Lyon FR-69008, France.
Sandrine HayetteLaboratory of Hematology, Lyon-Sud Hospital, Hospices Civils de Lyon, Pierre - Bénite Cedex 69495, France.
Pierre SujobertLaboratory of Hematology, Lyon-Sud Hospital, Hospices Civils de Lyon, Pierre - Bénite Cedex 69495, France.
Isabelle TigaudLaboratory of Hematology, Lyon-Sud Hospital, Hospices Civils de Lyon, Pierre - Bénite Cedex 69495, France.
Marie Pierre PagesLaboratory of Hematology, Lyon-Sud Hospital, Hospices Civils de Lyon, Pierre - Bénite Cedex 69495, France.
Youcef ChelghoumDepartment of Hematology, Hospices Civils de Lyon, Pierre - Bénite Cedex 69495, France.
Fiorenza BaraccoDepartment of Hematology, Hospices Civils de Lyon, Pierre - Bénite Cedex 69495, France.
Helene LabussierreDepartment of Hematology, Hospices Civils de Lyon, Pierre - Bénite Cedex 69495, France.
Sophie DucastelleDepartment of Hematology, Hospices Civils de Lyon, Pierre - Bénite Cedex 69495, France.
Etienne PaubelleDepartment of Hematology, Hospices Civils de Lyon, Pierre - Bénite Cedex 69495, France.
Franck Emmanuel NicoliniDepartment of Hematology, Hospices Civils de Lyon, Pierre - Bénite Cedex 69495, France.
Mohamed ElhamriDepartment of Hematology, Hospices Civils de Lyon, Pierre - Bénite Cedex 69495, France.
Lydia CamposLaboratory of Hematology, Nord Hospital, Saint Etienne 42055, France.
Claudiu PlesaDepartment of Hematology, Hospices Civils de Lyon, Pierre - Bénite Cedex 69495, France.
Stéphane MorissetStatistical and Clinical Research, Lyon-Sud Hospital, Hospices Civils de Lyon, Pierre - Bénite Cedex 69495, France.
Gilles SallesDepartment of Hematology, Hospices Civils de Lyon, Pierre - Bénite Cedex 69495, France.
Yves BertrandDepartment of Pediatric Hematology and BMT, IHOP Lyon, Lyon 69001, France.
Mauricette MichalletDepartment of Hematology, Hospices Civils de Lyon, Pierre - Bénite Cedex 69495, France.
Xavier ThomasDepartment of Hematology, Hospices Civils de Lyon, Pierre - Bénite Cedex 69495, France.
Hospices Civils de Lyon · FRCentre National de la Recherche Scientifique · FRHôpital Nord · FRInstitut d’Hématologie et d’Oncologie Pédiatrique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo evaluate the importance of the CD34+CD38- cell population when compared to the CD34+CD38+/low and CD34+CD38+/high leukemic cell sub-populations and to determine its correlations with leukemia characteristics and known prognostic factors, as well as with response to therapy and survival.

methodsTwo hundred bone marrow samples were obtained at diagnosis from 200 consecutive patients with newly diagnosed acute myeloid leukemia (AML) were studied between September 2008 and December 2010 at our Institution (Hematology Department, Lyon, France). The CD34/CD38 cell profile was analyzed by multiparameter flowcytometry approach using 8C panels and FACS CANTO and Diva software (BD Bioscience).

resultsWe analyzed CD34 and CD38 expression in bone marrow samples of 200 AML patients at diagnosis, and investigated the prognostic value of the most immature CD34+CD38- population. Using a cut-off value of 1% of CD34+CD38- from total "bulk leukemic cells" we found that a high (> 1%) level of CD34+CD38- blasts at diagnosis was correlated with advanced age, adverse cytogenetics as well as with a lower rate of complete response after induction and shorter disease-free survival. In a multivariate analysis considering age, leukocytosis, the % of CD34+ blasts cells and the standardized cytogenetic and molecular risk subgroups, a percentage of CD34+CD38- leukemic cells > 1% was an independent predictor of DFS [HR = 2.8 (1.02-7.73),

conclusionTaken together, these results show that a CD34/CD38 "backbone" for leukemic cell analysis by multicolour flowcytometry at diagnosis provides useful prognostic information.

Indexed as

Acute myeloid leukemiaCD34+CD38-/lowImmunophenotypingLeukemic stem cellsPrognosis

Identifiers

PMID29321824
PMCPMC5746643
OpenAlexW2776539879

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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.