Evidence map›Paper›PMID 36900222›Full record

ArticleCancers2023

Evolving Risk Classifications in AML in a Real-Life Scenario: After Changes upon Changes, Is It More and More Adverse?

Clara Aparicio-Pérez, Esther Prados de la Torre, Joaquin Sanchez-Garcia, Carmen Martín-Calvo, Carmen Martínez-Losada, Javier Casaño-Sanchez, Juana Serrano-López, Josefina Serrano

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Article in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Cancers · 2025
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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

8 authors.

Clara Aparicio-PérezHematology Department, Hospital Universitario Reina Sofía, 14004 Córdoba, Spain.
Esther Prados de la TorreInstituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), 14004 Córdoba, Spain.ORCID 0000-0002-3991-4964
Joaquin Sanchez-GarciaHematology Department, Hospital Universitario Reina Sofía, 14004 Córdoba, Spain.
Carmen Martín-CalvoHematology Department, Hospital Universitario Reina Sofía, 14004 Córdoba, Spain.
Carmen Martínez-LosadaHematology Department, Hospital Universitario Reina Sofía, 14004 Córdoba, Spain.
Javier Casaño-SanchezHematology Department, Hospital Universitario Reina Sofía, 14004 Córdoba, Spain.
Juana Serrano-LópezExperimental Hematology, Fundación Jiménez-Diaz, UAM, 28040 Madrid, Spain.
Josefina SerranoHematology Department, Hospital Universitario Reina Sofía, 14004 Córdoba, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute myeloid leukemia (AML) is a heterogeneous disease classified into three risk categories (favorable, intermediate and adverse) with significant differences in outcomes. Definitions of risk categories evolve overtime, incorporating advances in molecular knowledge of AML. In this study, we analyzed the impacts of evolving risk classifications in 130 consecutive AML patients in a single-center real-life experience. Complete cytogenetic and molecular data were collected using conventional qPCR and targeted Next Generation Sequencing (NGS). Five-year OS probabilities were consistent among all classification models (roughly 50-72%, 26-32% and 16-20% for favorable, intermediate and adverse risk groups, respectively). In the same way, the medians of survival months and prediction power were similar in all models. In each update, around 20% of patients were re-classified. The adverse category consistently increased over time (31% in MRC, 34% in ELN2010, 50% in ELN2017), reaching up to 56% in the recent ELN2022. Noteworthily, in multivariate models, only age and the presence of

Indexed as

acute myeloid leukemiaEuropean Leukemia Netrisk classificationsTP53 mutations

Identifiers

PMID36900222
PMCPMC10001051

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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.