Evidence map›Paper›PMID 40116978›Full record

ArticleClinical and experimental medicine2025

Evaluation of leukemic stem cell (CD26 +) in chronic myeloid leukemia patients with different molecular responses and in treatment-free remission.

María Fernanda Camacho, Margot Peña, María Jazmín Toloza, Beatriz Moiraghi, Alicia Enrico, Romina Mariano, Florencia Negri, Carolina Pavlovsky, Verónica Ventriglia, María Josefina Freitas and 3 more

Abstract read
In one paragraph

Article in Clinical and experimental medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

13 authors.

María Fernanda CamachoLaboratorio de Genética Hematológica, IMEX-CONICET/Academia Nacional de Medicina, Ciudad Autónoma de Buenos Aires, Argentina.ORCID http://orcid.org/0009-0006-6148-7563
Margot PeñaDepartamento de Patología Diagnóstica, División Citometría de Flujo, Instituto de Investigaciones Hematológicas "Mariano R. Castex", Academia Nacional de Medicina, Ciudad Autónoma de Buenos Aires, Argentina.
María Jazmín TolozaLaboratorio de Genética Hematológica, IMEX-CONICET/Academia Nacional de Medicina, Ciudad Autónoma de Buenos Aires, Argentina.ORCID http://orcid.org/0000-0002-8391-6764
Beatriz MoiraghiDepartamento de Hematología, Hospital General de Agudos José María Ramos Mejía, Ciudad Autónoma de Buenos Aires, Argentina.
Alicia EnricoDepartamento de Hematología, Hospital Italiano de la Plata, La Plata, Buenos Aires, Argentina.ORCID http://orcid.org/0000-0002-1983-6145
Romina MarianoDepartamento de Hematología, Hospital San Martín, Paraná, Entre Ríos, Argentina.ORCID http://orcid.org/0009-0009-3545-0427
Florencia NegriDepartamento de Hematología, Instituto Privado de Hematología y Hemoterapia, Paraná, Entre Ríos, Argentina.
Carolina PavlovskyDepartamento de Hematología, Fundaleu, Ciudad Autónoma de Buenos Aires, Argentina.
Verónica VentrigliaDepartamento de Hematología, Hospital Nacional Profesor Alejandro Posadas, El Palomar, Buenos Aires, Argentina.
María Josefina FreitasDepartamento de Hematología, Hospital Nacional Profesor Alejandro Posadas, El Palomar, Buenos Aires, Argentina.
Inés EngelbergerDivisión de Clínica Hematológica, Instituto de Investigaciones Hematológicas "Mariano R. Castex"- Academia Nacional de Medicina, Ciudad Autónoma de Buenos Aires, Argentina.
Raquel BengióDivisión de Clínica Hematológica, Instituto de Investigaciones Hematológicas "Mariano R. Castex"- Academia Nacional de Medicina, Ciudad Autónoma de Buenos Aires, Argentina.
Irene LarripaLaboratorio de Genética Hematológica, IMEX-CONICET/Academia Nacional de Medicina, Ciudad Autónoma de Buenos Aires, Argentina. irenelarripa@gmail.com.ORCID http://orcid.org/0000-0001-6602-4265

Funding

Consejo Nacional de Investigaciones Científicas y Técnicas PUE 2018-574Fundación Florencio Fiorini 2023- SI109Novartis Argentina 2022 3005351158GR
6 · The paper itself

Abstract

CD26 + leukemic stem cells (LSC) are a specific marker for chronic myeloid leukemia (CML), absent in healthy individuals and other myeloid neoplasms. These cells can contribute to disease resistance, as they are believed to sustain the leukemic clone despite effective tyrosine kinase inhibitor (TKI) therapy. This study analyzed CD26 + LSC and BCR::ABL1 transcript levels simultaneously using multiparametric flow cytometry and RT-qPCR in 210 chronic-phase patients undergoing TKI therapy and 31 patients in treatment-free remission (TFR). A significant decrease in LSC levels was observed as patients achieved deep molecular response (DMR, BCR::ABL1

Indexed as

Dipeptidyl Peptidase 4Leukemia, Myelogenous, Chronic, BCR-ABL PositiveNeoplastic Stem CellsAdultAgedAged, 80 and overFemaleFlow CytometryFusion Proteins, bcr-ablHumansMaleMiddle AgedProtein Kinase InhibitorsRemission InductionYoung AdultDipeptidyl Peptidase 4DPP4 protein, humanFusion Proteins, bcr-ablProtein Kinase InhibitorsCD26 + leukemic stem cellChronic myeloid leukemiaDeep molecular responseTreatment-free remissionTyrosine kinase inhibitor

Identifiers

PMID40116978
PMCPMC11928407

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.