Evidence map›Paper›PMID 37393163›Full record

ArticleHematology, transfusion and cell therapy

Prognostic implications of the ID1 expression in acute myeloid leukemia patients treated in a resource-constrained setting.

Aleide S Lima, Matheus F Bezerra, Amanda Moreira-Aguiar, Isabel Weinhäuser, Bianca L Santos, Raul M Falcão, Maria L Salustiano-Bandeira, Pedro L Franca-Neto, Marinus M Lima, Felipe Saldanha-Araujo and 4 more

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Article in Hematology, transfusion and cell therapy. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

14 authors.

Aleide S LimaUniversidade Federal de Pernambuco (UFPE), Recife, PE, Brazil.
Matheus F BezerraInstituto Aggeu Magalhães, Fiocruz, Recife, Pernambuco, PE, Brazil.
Amanda Moreira-AguiarUniversidade Federal de Pernambuco (UFPE), Recife, PE, Brazil.
Isabel WeinhäuserCancer Research Centre Groningen, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
Bianca L SantosUniversidade Federal de Pernambuco (UFPE), Recife, PE, Brazil.
Raul M FalcãoBioinformatics Multidisciplinary Environment (BioME), Metrópole Digital Institute, Universidade Federal do Rio Grande do Norte (UFRN), Natal, RN, Brazil.
Maria L Salustiano-BandeiraUniversidade Federal de Pernambuco (UFPE), Recife, PE, Brazil.
Pedro L Franca-NetoUniversidade Federal de Pernambuco (UFPE), Recife, PE, Brazil.
Marinus M LimaUniversidade Federal de Pernambuco (UFPE), Recife, PE, Brazil.
Felipe Saldanha-AraujoLaboratório de Hematologia e Células-Tronco, Universidade de Brasília (UnB) Brasília, DF, Brazil.
Juan L Coelho-SilvaHematology Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD, USA.
Diego A Pereira-MartinsCancer Research Centre Groningen, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
Marcos A BezerraUniversidade Federal de Pernambuco (UFPE), Recife, PE, Brazil.
Antonio R Lucena-AraujoUniversidade Federal de Pernambuco (UFPE), Recife, PE, Brazil. Electronic address: antonio.araujo@ufpe.br.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe aberrant expression of the inhibitor of DNA binding (ID1) gene has been frequently associated with the leukemogenesis and prognostication acute myeloid leukemia (AML), although its clinical importance has never been investigated in patients treated outside well-controlled clinical trials.

methodsUsing quantitative real-time polymerase chain reaction, we investigated the role of the ID1 expression in the clinical outcomes of non-selected patients with acute myeloid leukemia treated in a real-life setting.

resultsOverall, 128 patients were enrolled. Patients with high ID1 expression had a lower 3-year overall survival (OS) rate of 9%, with the 95% confidence interval (95%CI) at 3 to 20%, compared to patients with a low ID1 expression (22%, 95%CI: 11 - 34%) (p = 0.037), although these findings did not retain significance after adjustment (hazard ratio (HR): 1.5, 95%CI: 0.98 - 2.28; p = 0.057). The ID1 expression had no impact on post-induction outcomes (disease-free survival, p = 0.648; cumulative incidence of relapse, p = 0.584).

conclusionsAlthough we are aware thar our data are confronted with many variables that cannot be fully controlled, including drug unavailability, risk-adapted treatment, comorbidities and the time from diagnosis to treatment initiation, we are firm believers that such an initiative can provide more realistic data on understudied populations, in particular those from low- and middle-income countries.

Indexed as

ID1Low- and middle-income countriesPrognostication

Identifiers

PMID37393163
PMCPMC11221249

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LicenceCC BY-NC-ND
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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.