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Machine learning-based normal tissue complication probability model for predicting albumin-bilirubin (ALBI) grade increase in hepatocellular carcinoma patients

PURPOSE: The aim of this study was to develop a normal tissue complication probability model using a machine learning approach (ML-based NTCP) to predict the risk of radiation-induced liver disease in hepatocellular carcinoma (HCC) patients. MATERIALS AND METHODS: The study population included 201 H...

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Autores principales: Prayongrat, Anussara, Srimaneekarn, Natchalee, Thonglert, Kanokporn, Khorprasert, Chonlakiet, Amornwichet, Napapat, Alisanant, Petch, Shirato, Hiroki, Kobashi, Keiji, Sriswasdi, Sira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9730671/
https://www.ncbi.nlm.nih.gov/pubmed/36476512
http://dx.doi.org/10.1186/s13014-022-02138-8
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author Prayongrat, Anussara
Srimaneekarn, Natchalee
Thonglert, Kanokporn
Khorprasert, Chonlakiet
Amornwichet, Napapat
Alisanant, Petch
Shirato, Hiroki
Kobashi, Keiji
Sriswasdi, Sira
author_facet Prayongrat, Anussara
Srimaneekarn, Natchalee
Thonglert, Kanokporn
Khorprasert, Chonlakiet
Amornwichet, Napapat
Alisanant, Petch
Shirato, Hiroki
Kobashi, Keiji
Sriswasdi, Sira
author_sort Prayongrat, Anussara
collection PubMed
description PURPOSE: The aim of this study was to develop a normal tissue complication probability model using a machine learning approach (ML-based NTCP) to predict the risk of radiation-induced liver disease in hepatocellular carcinoma (HCC) patients. MATERIALS AND METHODS: The study population included 201 HCC patients treated with radiotherapy. The patients’ medical records were retrospectively reviewed to obtain the clinical and radiotherapy data. Toxicity was defined by albumin-bilirubin (ALBI) grade increase. The normal liver dose-volume histogram was reduced to mean liver dose (MLD) based on the fraction size-adjusted equivalent uniform dose (2 Gy/fraction and α/β = 2). Three types of ML-based classification models were used, a penalized logistic regression (PLR), random forest (RF), and gradient-boosted tree (GBT) model. Model performance was compared using the area under the receiver operating characteristic curve (AUROC). Internal validation was performed by 5-fold cross validation and external validation was done in 44 new patients. RESULTS: Liver toxicity occurred in 87 patients (43.1%). The best individual model was the GBT model using baseline liver function, liver volume, and MLD as inputs and the best overall model was an ensemble of the PLR and GBT models. An AUROC of 0.82 with a standard deviation of 0.06 was achieved for the internal validation. An AUROC of 0.78 with a standard deviation of 0.03 was achieved for the external validation. The behaviors of the best GBT model were also in good agreement with the domain knowledge on NTCP. CONCLUSION: We propose the methodology to develop an ML-based NTCP model to estimate the risk of ALBI grade increase. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13014-022-02138-8.
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spelling pubmed-97306712022-12-09 Machine learning-based normal tissue complication probability model for predicting albumin-bilirubin (ALBI) grade increase in hepatocellular carcinoma patients Prayongrat, Anussara Srimaneekarn, Natchalee Thonglert, Kanokporn Khorprasert, Chonlakiet Amornwichet, Napapat Alisanant, Petch Shirato, Hiroki Kobashi, Keiji Sriswasdi, Sira Radiat Oncol Research PURPOSE: The aim of this study was to develop a normal tissue complication probability model using a machine learning approach (ML-based NTCP) to predict the risk of radiation-induced liver disease in hepatocellular carcinoma (HCC) patients. MATERIALS AND METHODS: The study population included 201 HCC patients treated with radiotherapy. The patients’ medical records were retrospectively reviewed to obtain the clinical and radiotherapy data. Toxicity was defined by albumin-bilirubin (ALBI) grade increase. The normal liver dose-volume histogram was reduced to mean liver dose (MLD) based on the fraction size-adjusted equivalent uniform dose (2 Gy/fraction and α/β = 2). Three types of ML-based classification models were used, a penalized logistic regression (PLR), random forest (RF), and gradient-boosted tree (GBT) model. Model performance was compared using the area under the receiver operating characteristic curve (AUROC). Internal validation was performed by 5-fold cross validation and external validation was done in 44 new patients. RESULTS: Liver toxicity occurred in 87 patients (43.1%). The best individual model was the GBT model using baseline liver function, liver volume, and MLD as inputs and the best overall model was an ensemble of the PLR and GBT models. An AUROC of 0.82 with a standard deviation of 0.06 was achieved for the internal validation. An AUROC of 0.78 with a standard deviation of 0.03 was achieved for the external validation. The behaviors of the best GBT model were also in good agreement with the domain knowledge on NTCP. CONCLUSION: We propose the methodology to develop an ML-based NTCP model to estimate the risk of ALBI grade increase. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13014-022-02138-8. BioMed Central 2022-12-07 /pmc/articles/PMC9730671/ /pubmed/36476512 http://dx.doi.org/10.1186/s13014-022-02138-8 Text en © The Author(s) 2022, corrected publication 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Prayongrat, Anussara
Srimaneekarn, Natchalee
Thonglert, Kanokporn
Khorprasert, Chonlakiet
Amornwichet, Napapat
Alisanant, Petch
Shirato, Hiroki
Kobashi, Keiji
Sriswasdi, Sira
Machine learning-based normal tissue complication probability model for predicting albumin-bilirubin (ALBI) grade increase in hepatocellular carcinoma patients
title Machine learning-based normal tissue complication probability model for predicting albumin-bilirubin (ALBI) grade increase in hepatocellular carcinoma patients
title_full Machine learning-based normal tissue complication probability model for predicting albumin-bilirubin (ALBI) grade increase in hepatocellular carcinoma patients
title_fullStr Machine learning-based normal tissue complication probability model for predicting albumin-bilirubin (ALBI) grade increase in hepatocellular carcinoma patients
title_full_unstemmed Machine learning-based normal tissue complication probability model for predicting albumin-bilirubin (ALBI) grade increase in hepatocellular carcinoma patients
title_short Machine learning-based normal tissue complication probability model for predicting albumin-bilirubin (ALBI) grade increase in hepatocellular carcinoma patients
title_sort machine learning-based normal tissue complication probability model for predicting albumin-bilirubin (albi) grade increase in hepatocellular carcinoma patients
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9730671/
https://www.ncbi.nlm.nih.gov/pubmed/36476512
http://dx.doi.org/10.1186/s13014-022-02138-8
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