Evidence map›Paper›PMID 32150667›Full record

ArticleJournal of cellular and molecular medicine2020

Development and validation of a 10-gene prognostic signature for acute myeloid leukaemia.

Zuyi Yang, Jun Shang, Ning Li, Liang Zhang, Tingting Tang, Guoyan Tian, Xiaohui Chen

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.1field-weighted citation impact, top 11% 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

16 citing papers in PubMed, 23 citations in OpenAlex.

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  11. m6A-Related Genes Contribute to Poor Prognosis of Hepatocellular Carcinoma.Computational and mathematical methods in medicine · 2022
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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

7 authors at 2 institutions in 1 country.

Zuyi YangDepartment of Hematology and Oncology, The Affiliated Hospital of Hangzhou Normal University, Hangzhou, China.
Jun ShangSchool of Life Sciences, Fudan University, Shanghai, China.ORCID 0000-0002-5767-1492
Ning LiDepartment of Hematology and Oncology, The Affiliated Hospital of Hangzhou Normal University, Hangzhou, China.
Liang ZhangDepartment of Hematology and Oncology, The Affiliated Hospital of Hangzhou Normal University, Hangzhou, China.
Tingting TangDepartment of Hematology and Oncology, The Affiliated Hospital of Hangzhou Normal University, Hangzhou, China.
Guoyan TianDepartment of Hematology and Oncology, The Affiliated Hospital of Hangzhou Normal University, Hangzhou, China.
Xiaohui ChenDepartment of Hematology and Oncology, The Affiliated Hospital of Hangzhou Normal University, Hangzhou, China.
Affiliated Hospital of Hangzhou Normal University · CNFudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute myeloid leukaemia (AML) is the most common type of adult acute leukaemia and has a poor prognosis. Thus, optimal risk stratification is of greatest importance for reasonable choice of treatment and prognostic evaluation. For our study, a total of 1707 samples of AML patients from three public databases were divided into meta-training, meta-testing and validation sets. The meta-training set was used to build risk prediction model, and the other four data sets were employed for validation. By log-rank test and univariate COX regression analysis as well as LASSO-COX, AML patients were divided into high-risk and low-risk groups based on AML risk score (AMLRS) which was constituted by 10 survival-related genes. In meta-training, meta-testing and validation sets, the patient in the low-risk group all had a significantly longer OS (overall survival) than those in the high-risk group (P < .001), and the area under ROC curve (AUC) by time-dependent ROC was 0.5854-0.7905 for 1 year, 0.6652-0.8066 for 3 years and 0.6622-0.8034 for 5 years. Multivariate COX regression analysis indicated that AMLRS was an independent prognostic factor in four data sets. Nomogram combining the AMLRS and two clinical parameters performed well in predicting 1-year, 3-year and 5-year OS. Finally, we created a web-based prognostic model to predict the prognosis of AML patients (https://tcgi.shinyapps.io/amlrs_nomogram/).

Indexed as

Biomarkers, TumorDisease-Free SurvivalFemaleGene Expression Regulation, NeoplasticHumansKaplan-Meier EstimateLeukemia, Myeloid, AcuteMaleMiddle AgedNeoplasm ProteinsNomogramsPrognosisProportional Hazards ModelsTranscriptomeBiomarkers, TumorNeoplasm Proteinsacute myeloid leukaemiagene expression profilingnomogramprognosissignature

Identifiers

PMID32150667
PMCPMC7176885
OpenAlexW3009623227

What OpenQuestion holds

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LicenceCC BY
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.