Evidence map›Paper›PMID 32483590›Full record

ArticleJournal of the American Medical Informatics Association : JAMIA2020

Unsupervised machine learning and prognostic factors of survival in chronic lymphocytic leukemia.

Caitlin E Coombes, Zachary B Abrams, Suli Li, Lynne V Abruzzo, Kevin R Coombes

Open access · bronzeAbstract read
In one paragraph

Article in Journal of the American Medical Informatics Association : JAMIA, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

17 citing papers in PubMed, 32 citations in OpenAlex.

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  9. SillyPutty: Improved clustering by optimizing the silhouette width.bioRxiv : the preprint server for biology · 2023
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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

5 authors at 2 institutions in 1 country.

Caitlin E CoombesThe Ohio State University College of Medicine, Columbus, Ohio, USA.
Zachary B AbramsDepartment of Biomedical Informatics, The Ohio State University, Columbus, Ohio, USA.
Suli LiDepartment of Statistics and Data Science, Cornell University, Ithaca, New York, USA.
Lynne V AbruzzoDepartment of Pathology, The Ohio State University, Columbus, Ohio, USA.
Kevin R CoombesDepartment of Biomedical Informatics, The Ohio State University, Columbus, Ohio, USA.
The Ohio State University · USCornell University · US

Funding

Secondary Use of Karyotype Data to Predict Outcomes in CLLR03CA235101 · NCI · OHIO STATE UNIVERSITY · PI COOMBES, KEVIN ROBERT · 2019 to 2020
$156k
NCI NIH HHS R03 CA235101
6 · The paper itself

Abstract

objectiveUnsupervised machine learning approaches hold promise for large-scale clinical data. However, the heterogeneity of clinical data raises new methodological challenges in feature selection, choosing a distance metric that captures biological meaning, and visualization. We hypothesized that clustering could discover prognostic groups from patients with chronic lymphocytic leukemia, a disease that provides biological validation through well-understood outcomes.

methodsTo address this challenge, we applied k-medoids clustering with 10 distance metrics to 2 experiments ("A" and "B") with mixed clinical features collapsed to binary vectors and visualized with both multidimensional scaling and t-stochastic neighbor embedding. To assess prognostic utility, we performed survival analysis using a Cox proportional hazard model, log-rank test, and Kaplan-Meier curves.

resultsIn both experiments, survival analysis revealed a statistically significant association between clusters and survival outcomes (A: overall survival, P = .0164; B: time from diagnosis to treatment, P = .0039). Multidimensional scaling separated clusters along a gradient mirroring the order of overall survival. Longer survival was associated with mutated immunoglobulin heavy-chain variable region gene (IGHV) status, absent Zap 70 expression, female sex, and younger age.

conclusionsThis approach to mixed-type data handling and selection of distance metric captured well-understood, binary, prognostic markers in chronic lymphocytic leukemia (sex, IGHV mutation status, ZAP70 expression status) with high fidelity.

Indexed as

MutationUnsupervised Machine LearningAdultAgedAged, 80 and overFemaleHumansImmunoglobulin Heavy ChainsKaplan-Meier EstimateLeukemia, Lymphocytic, Chronic, B-CellMaleMiddle AgedPrognosisProportional Hazards ModelsZAP-70 Protein-Tyrosine KinaseImmunoglobulin Heavy ChainsZAP70 protein, humanZAP-70 Protein-Tyrosine Kinasechronic lymphocytic leukemiaclinical informatics, mixed-type dataclusteringunsupervised machine learning

Identifiers

PMID32483590
PMCPMC7647286
OpenAlexW3032612410

What OpenQuestion holds

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LicenceCC BY-NC
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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.