Evidence map›Paper›PMID 40209178›Full record

ArticleJMIR formative research2025

Web-Based Explainable Machine Learning-Based Drug Surveillance for Predicting Sunitinib- and Sorafenib-Associated Thyroid Dysfunction: Model Development and Validation Study.

Fan-Ying Chan, Yi-En Ku, Wen-Nung Lie, Hsiang-Yin Chen

Abstract readValidation Study
In one paragraph

Article in JMIR formative research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Review
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

4 authors.

Fan-Ying ChanDepartment of Clinical Pharmacy, College of Pharmacy, Taipei Medical University, 250 Wuxing St, Xinyi Dist, Taipei, 11031, Taiwan, 886 2-2736-1661.ORCID 0009-0007-5525-6651
Yi-En KuDepartment of Clinical Pharmacy, College of Pharmacy, Taipei Medical University, 250 Wuxing St, Xinyi Dist, Taipei, 11031, Taiwan, 886 2-2736-1661.ORCID 0009-0001-7387-1136
Wen-Nung LieDepartment of Electrical Engineering, National Chung Cheng University, Chiayi, Taiwan.ORCID 0000-0002-8166-2844
Hsiang-Yin ChenDepartment of Clinical Pharmacy, College of Pharmacy, Taipei Medical University, 250 Wuxing St, Xinyi Dist, Taipei, 11031, Taiwan, 886 2-2736-1661.ORCID 0000-0001-5535-7152

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Unlike one-snap data collection methods that only identify high-risk patients, machine learning models using time-series data can predict adverse events and aid in the timely management of cancer. Objective: This study aimed to develop and validate machine learning models for sunitinib- and sorafenib-associated thyroid dysfunction using a time-series data collection approach. Methods: Time series data of patients first prescribed sunitinib or sorafenib were collected from a deidentified clinical research database. Logistic regression, random forest, adaptive Boosting, Light Gradient-Boosting Machine, and Gradient Boosting Decision Tree were used to develop the models. Prediction performances were compared using the accuracy, precision, recall, F1-score, area under the receiver operating characteristic curve, and area under the precision-recall curve. The optimal threshold for the best-performing model was selected based on the maximum F1-score. SHapley Additive exPlanations analysis was conducted to assess feature importance and contributions at both the cohort and patient levels. Results: The training cohort included 609 patients, while the temporal validation cohort had 198 patients. The Gradient Boosting Decision Tree model without resampling outperformed other models, with area under the precision-recall curve of 0.600, area under the receiver operating characteristic curve of 0.876, and F1-score of 0.583 after adjusting the threshold. The SHapley Additive exPlanations analysis identified higher cholesterol levels, longer summed days of medication use, and clear cell adenocarcinoma histology as the most important features. The final model was further integrated into a web-based application. Conclusions: This model can serve as an explainable adverse drug reaction surveillance system for predicting sunitinib- and sorafenib-associated thyroid dysfunction.

Indexed as

Antineoplastic AgentsDrug MonitoringMachine LearningSorafenibSunitinibThyroid DiseasesAdultAgedFemaleHumansInternetMaleMiddle AgedAntineoplastic AgentsSorafenibSunitinibcancermachine learningsorafenibsunitinibthyroid dysfunctionTKItyrosine kinase inhibitor

Identifiers

PMID40209178
PMCPMC12005597

What Socratic holds

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LicenceCC BY
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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 Socratic graph.