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- Publisher Website: 10.1111/apt.16272
- Scopus: eid_2-s2.0-85099766722
- PMID: 33486805
- WOS: WOS:000611844500001
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Article: Applications of Machine Learning Models in the Prediction of Gastric Cancer risk in patients after Helicobacter pylori eradication
Title | Applications of Machine Learning Models in the Prediction of Gastric Cancer risk in patients after Helicobacter pylori eradication |
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Authors | |
Issue Date | 2021 |
Publisher | Wiley-Blackwell. The Journal's web site is located at http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-2036 |
Citation | Alimentary Pharmacology and Therapeutics, 2021, v. 53 n. 8, p. 864-872 How to Cite? |
Abstract | Background:
The risk of gastric cancer after Helicobacter pylori (H. pylori) eradication remains unknown.
Aim:
To evaluate the performances of seven different machine learning models in predicting gastric cancer risk after H. pylori eradication.
Methods:
We identified H. pylori-infected patients who had received clarithromycin-based triple therapy between 2003 and 2014 in Hong Kong. Patients were divided into training (n = 64 238) and validation sets (n = 25 330), according to period of eradication therapy. The data were used to construct seven machine learning models to predict risk of gastric cancer development within 5 years after H. pylori eradication. A total of 26 clinical variables were input into these models. The performances were measured by the area under receiver operating characteristic curve (AUC) analysis.
Results:
During a mean follow-up of 4.7 years, 0.21% of H. pylori-eradicated patients developed gastric cancer. Of the seven machine learning models, extreme gradient boosting (XGBoost) had the best performance in predicting cancer development (AUC 0.97, 95%CI 0.96-0.98), and was superior to conventional logistic regression (AUC 0.90, 95% CI 0.84-0.92). With the XGBoost model, the number of patients considered at high risk of gastric cancer was 6.6%, with miss rate of 1.9%. Patient age, presence of intestinal metaplasia, and gastric ulcer were the heavily weighted factors used by the XGBoost.
Conclusion:
Based on simple baseline patient information, machine learning model can accurately predict the risk of post-eradication gastric cancer. This model could substantially reduce the number of patients who require endoscopic surveillance. |
Persistent Identifier | http://hdl.handle.net/10722/300692 |
ISSN | 2023 Impact Factor: 6.6 2023 SCImago Journal Rankings: 2.794 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Leung, WK | - |
dc.contributor.author | Cheung, KS | - |
dc.contributor.author | LI, B | - |
dc.contributor.author | Law, SYK | - |
dc.contributor.author | Lui, TKL | - |
dc.date.accessioned | 2021-06-18T14:55:38Z | - |
dc.date.available | 2021-06-18T14:55:38Z | - |
dc.date.issued | 2021 | - |
dc.identifier.citation | Alimentary Pharmacology and Therapeutics, 2021, v. 53 n. 8, p. 864-872 | - |
dc.identifier.issn | 0269-2813 | - |
dc.identifier.uri | http://hdl.handle.net/10722/300692 | - |
dc.description.abstract | Background: The risk of gastric cancer after Helicobacter pylori (H. pylori) eradication remains unknown. Aim: To evaluate the performances of seven different machine learning models in predicting gastric cancer risk after H. pylori eradication. Methods: We identified H. pylori-infected patients who had received clarithromycin-based triple therapy between 2003 and 2014 in Hong Kong. Patients were divided into training (n = 64 238) and validation sets (n = 25 330), according to period of eradication therapy. The data were used to construct seven machine learning models to predict risk of gastric cancer development within 5 years after H. pylori eradication. A total of 26 clinical variables were input into these models. The performances were measured by the area under receiver operating characteristic curve (AUC) analysis. Results: During a mean follow-up of 4.7 years, 0.21% of H. pylori-eradicated patients developed gastric cancer. Of the seven machine learning models, extreme gradient boosting (XGBoost) had the best performance in predicting cancer development (AUC 0.97, 95%CI 0.96-0.98), and was superior to conventional logistic regression (AUC 0.90, 95% CI 0.84-0.92). With the XGBoost model, the number of patients considered at high risk of gastric cancer was 6.6%, with miss rate of 1.9%. Patient age, presence of intestinal metaplasia, and gastric ulcer were the heavily weighted factors used by the XGBoost. Conclusion: Based on simple baseline patient information, machine learning model can accurately predict the risk of post-eradication gastric cancer. This model could substantially reduce the number of patients who require endoscopic surveillance. | - |
dc.language | eng | - |
dc.publisher | Wiley-Blackwell. The Journal's web site is located at http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-2036 | - |
dc.relation.ispartof | Alimentary Pharmacology and Therapeutics | - |
dc.rights | Submitted (preprint) Version This is the pre-peer reviewed version of the following article: [FULL CITE], which has been published in final form at [Link to final article using the DOI]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. Accepted (peer-reviewed) Version This is the peer reviewed version of the following article: [FULL CITE], which has been published in final form at [Link to final article using the DOI]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. | - |
dc.title | Applications of Machine Learning Models in the Prediction of Gastric Cancer risk in patients after Helicobacter pylori eradication | - |
dc.type | Article | - |
dc.identifier.email | Leung, WK: waikleung@hku.hk | - |
dc.identifier.email | Cheung, KS: cks634@hku.hk | - |
dc.identifier.email | Law, SYK: slaw@hku.hk | - |
dc.identifier.email | Lui, TKL: lkl484@hku.hk | - |
dc.identifier.authority | Leung, WK=rp01479 | - |
dc.identifier.authority | Cheung, KS=rp02532 | - |
dc.identifier.authority | Law, SYK=rp00437 | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1111/apt.16272 | - |
dc.identifier.pmid | 33486805 | - |
dc.identifier.scopus | eid_2-s2.0-85099766722 | - |
dc.identifier.hkuros | 322908 | - |
dc.identifier.volume | 53 | - |
dc.identifier.issue | 8 | - |
dc.identifier.spage | 864 | - |
dc.identifier.epage | 872 | - |
dc.identifier.isi | WOS:000611844500001 | - |
dc.publisher.place | United Kingdom | - |