Evidence map›Paper›PMID 38936913›Full record

ArticleIn vivo (Athens, Greece)

Molecular and Clinical Insights in the Increasing Detection of

Flávia Melo Cunha DE Pinho Pessoa, Beatriz Maria Dias Nogueira, Caio Bezerra Machado, Igor Valentim Barreto, Anna Karolyna DA Costa Machado, Renan Brito Gadelha, Deivide DE Sousa Oliveira, Rodrigo Monteiro Ribeiro, Fabiana Aguiar Carneiro Silva, Lívia Andrade Gurgel and 8 more

Abstract read
In one paragraph

Article in In vivo (Athens, Greece). 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. Article
  2. Cancer diagnosis & prognosis
    Review
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

18 authors.

Flávia Melo Cunha DE Pinho Pessoa *Department of Medicine, Pharmacogenetics Laboratory, Drug Research and Development Center (NPDM), Federal University of Ceará, Fortaleza, CE, Brazil.
Beatriz Maria Dias Nogueira *Department of Medicine, Pharmacogenetics Laboratory, Drug Research and Development Center (NPDM), Federal University of Ceará, Fortaleza, CE, Brazil.
Caio Bezerra MachadoDepartment of Medicine, Pharmacogenetics Laboratory, Drug Research and Development Center (NPDM), Federal University of Ceará, Fortaleza, CE, Brazil.
Igor Valentim BarretoDepartment of Medicine, Pharmacogenetics Laboratory, Drug Research and Development Center (NPDM), Federal University of Ceará, Fortaleza, CE, Brazil.
Anna Karolyna DA Costa MachadoDepartment of Medicine, Pharmacogenetics Laboratory, Drug Research and Development Center (NPDM), Federal University of Ceará, Fortaleza, CE, Brazil.
Renan Brito GadelhaDepartment of Medicine, Pharmacogenetics Laboratory, Drug Research and Development Center (NPDM), Federal University of Ceará, Fortaleza, CE, Brazil.
Deivide DE Sousa OliveiraDepartment of Medicine, Pharmacogenetics Laboratory, Drug Research and Development Center (NPDM), Federal University of Ceará, Fortaleza, CE, Brazil.
Rodrigo Monteiro RibeiroDepartment of Hematology, Fortaleza General Hospital (HGF), Fortaleza, CE, Brazil.
Fabiana Aguiar Carneiro SilvaDepartment of Hematology, Fortaleza General Hospital (HGF), Fortaleza, CE, Brazil.
Lívia Andrade GurgelDepartment of Hematology, Fortaleza General Hospital (HGF), Fortaleza, CE, Brazil.
Jaira Costa MedeirosDepartment of Hematology, Fortaleza General Hospital (HGF), Fortaleza, CE, Brazil.
Aurélia DA Rocha MacielDepartment of Hematology, Fortaleza General Hospital (HGF), Fortaleza, CE, Brazil.
Germison Silva LopesDepartment of Hematology, César Cals General Hospital, Fortaleza, CE, Brazil.
Ricardo Parente Garcia VieiraDepartment of Hematology, São Vicente de Paulo Maternity Hospital, Barbalha, CE, Brazil.
Manoel Odorico DE Moraes FilhoDepartment of Medicine, Pharmacogenetics Laboratory, Drug Research and Development Center (NPDM), Federal University of Ceará, Fortaleza, CE, Brazil.
Maria Elisabete Amaral DE MoraesDepartment of Medicine, Pharmacogenetics Laboratory, Drug Research and Development Center (NPDM), Federal University of Ceará, Fortaleza, CE, Brazil.
André Salim KhayatDepartment of Biological Sciences, Oncology Research Center, Federal University of Pará, Belém, PA, Brazil.
Caroline Aquino Moreira-NunesDepartment of Medicine, Pharmacogenetics Laboratory, Drug Research and Development Center (NPDM), Federal University of Ceará, Fortaleza, CE, Brazil; carolfam@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimAcute myeloid leukemia (AML) is a myeloproliferative neoplasm marked by abnormal clonal expansion of hematopoietic progenitor cells, displaying karyotypic aberrations and genetic mutations as prognostic indicators. The World Health Organization (WHO) and the European LeukemiaNet guidelines categorize BCR::ABL1 p190+ AML as high risk. This study explored the identification of the increased incidence of BCR::ABL1 p190+ in our AML population. PATIENTS AND

methodsThis study included 96 AML patients stratified according to WHO guidelines. Subsequently, patients were screened for genetic abnormalities, such as BCR::ABL1 p 190+, PML::RARA, RUNX1::RUNX1T1, and CBFB::MYH11 by quantitative reverse transcription polymerase chain reaction (RT-qPCR) analysis.

resultsAmong 96 AML patients, 36 displayed BCR::ABL1 p190+, overcoming the expected global incidence. Age variations (19 to 78 years) showed no significant laboratory differences between BCR::ABL1 p190+ and non-BCR::ABL p190+ cases. The overall survival analysis revealed no statistically significant differences among the patients (p=0.786).

conclusionThe analyzed population presented a higher frequency of BCR::ABL1 p190+ detection in adult AML patients when compared to what is described in the worldwide literature. Therefore, more studies are needed to establish the reason why this incidence is higher and what the best treatment approach should be in these cases.

Indexed as

Fusion Proteins, bcr-ablLeukemia, Myeloid, AcuteAdultAgedFemaleHumansMaleMiddle AgedMutationPrognosisYoung AdultFusion Proteins, bcr-ablAcute myeloid leukemiagene fusionhematologic malignancyoncogene protein p190

Identifiers

PMID38936913
PMCPMC11215616

What OpenQuestion holds

Textmetadata
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.