Evidence map›Paper›PMID 38939521›Full record

ArticleHealth care science2023

Predicting venous thromboembolism (VTE) risk in cancer patients using machine learning.

Samir Khan Townsley, Debraj Basu, Jayneel Vora, Ted Wun, Chen-Nee Chuah, Prabhu R V Shankar

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Article in Health care science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

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0cells of the map it votes in
6citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Samir Khan TownsleyDepartment of Electrical and Computer Engineering University of California Davis California USA.
Debraj BasuDepartment of Electrical and Computer Engineering University of California Davis California USA.ORCID 0000-0002-8731-690X
Jayneel VoraDepartment of Computer Science University of California Davis California USA.
Ted WunSchool of Medicine, Davis Health University of California Sacramento California USA.
Chen-Nee ChuahDepartment of Electrical and Computer Engineering University of California Davis California USA.
Prabhu R V ShankarSchool of Medicine, Davis Health University of California Sacramento California USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The association between cancer and venous thromboembolism (VTE) is well-established with cancer patients accounting for approximately 20% of all VTE incidents. In this paper, we have performed a comparison of machine learning (ML) methods to traditional clinical scoring models for predicting the occurrence of VTE in a cancer patient population, identified important features (clinical biomarkers) for ML model predictions, and examined how different approaches to reducing the number of features used in the model impact model performance. Methods: We have developed an ML pipeline including three separate feature selection processes and applied it to routine patient care data from the electronic health records of 1910 cancer patients at the University of California Davis Medical Center. Results: Our ML-based prediction model achieved an area under the receiver operating characteristic curve of 0.778 ± 0.006 (mean ± SD) when trained on a set of 15 features. This result is comparable with the model performance when trained on all features in our feature pool [0.779 ± 0.006 (mean ± SD) with 29 features]. Our result surpasses the most validated clinical scoring system for VTE risk assessment in cancer patients by 16.1%. We additionally found cancer stage information to be a useful predictor after all performed feature selection processes despite not being used in existing score-based approaches. Conclusion: From these findings, we observe that ML can offer new insights and a significant improvement over the most validated clinical VTE risk scoring systems in cancer patients. The results of this study also allowed us to draw insight into our feature pool and identify the features that could have the most utility in the context of developing an efficient ML classifier. While a model trained on our entire feature pool of 29 features significantly outperformed the traditionally used clinical scoring system, we were able to achieve an equivalent performance using a subset of only 15 features through strategic feature selection methods. These results are encouraging for potential applications of ML to predicting cancer-associated VTE in clinical settings such as in bedside decision support systems where feature availability may be limited.

Indexed as

binary classificationcancermachine learning pipelineVTE

Identifiers

PMID38939521
PMCPMC11080820

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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.