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Machine Learning Improves the Prediction of Responses to Immune Checkpoint Inhibitors in Metastatic Melanoma
SIMPLE SUMMARY: Lactate dehydrogenase (LDH) levels prior to treatment are a known biomarker to predict advanced melanoma’s response to immune checkpoint inhibitors (ICI). In this study, we evaluated the ability of machine learning-based models to predict responses to ICI and complement LDH for in pr...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10216156/ https://www.ncbi.nlm.nih.gov/pubmed/37345037 http://dx.doi.org/10.3390/cancers15102700 |
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author | Tabari, Azadeh Cox, Meredith D’Amore, Brian Mansur, Arian Dabbara, Harika Boland, Genevieve Gee, Michael S. Daye, Dania |
author_facet | Tabari, Azadeh Cox, Meredith D’Amore, Brian Mansur, Arian Dabbara, Harika Boland, Genevieve Gee, Michael S. Daye, Dania |
author_sort | Tabari, Azadeh |
collection | PubMed |
description | SIMPLE SUMMARY: Lactate dehydrogenase (LDH) levels prior to treatment are a known biomarker to predict advanced melanoma’s response to immune checkpoint inhibitors (ICI). In this study, we evaluated the ability of machine learning-based models to predict responses to ICI and complement LDH for in predicting the outcomes of metastatic melanoma. A machine learning algorithm was developed using radiomics, and further analysis helped select the most important predictive features and variables. The machine learning model that combined both features extracted from images (radiomics) and pretreatment LDH levels resulted in better predictions of cancer response to ICI than models that only use radiomics features or LDH levels alone. ABSTRACT: Pretreatment LDH is a standard prognostic biomarker for advanced melanoma and is associated with response to ICI. We assessed the role of machine learning-based radiomics in predicting responses to ICI and in complementing LDH for prognostication of metastatic melanoma. From 2008–2022, 79 patients with 168 metastatic hepatic lesions were identified. All patients had arterial phase CT images 1-month prior to initiation of ICI. Response to ICI was assessed on follow-up CT at 3 months using RECIST criteria. A machine learning algorithm was developed using radiomics. Maximum relevance minimum redundancy (mRMR) was used to select features. ROC analysis and logistic regression analyses evaluated performance. Shapley additive explanations were used to identify the variables that are the most important in predicting a response. mRMR selection revealed 15 features that are associated with a response to ICI. The machine learning model combining both radiomics features and pretreatment LDH resulted in better performance for response prediction compared to models that included radiomics or LDH alone (AUC of 0.89 (95% CI: [0.76–0.99]) vs. 0.81 (95% CI: [0.65–0.94]) and 0.81 (95% CI: [0.72–0.91]), respectively). Using SHAP analysis, LDH and two GLSZM were the most predictive of the outcome. Pre-treatment CT radiomic features performed equally well to serum LDH in predicting treatment response. |
format | Online Article Text |
id | pubmed-10216156 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-102161562023-05-27 Machine Learning Improves the Prediction of Responses to Immune Checkpoint Inhibitors in Metastatic Melanoma Tabari, Azadeh Cox, Meredith D’Amore, Brian Mansur, Arian Dabbara, Harika Boland, Genevieve Gee, Michael S. Daye, Dania Cancers (Basel) Article SIMPLE SUMMARY: Lactate dehydrogenase (LDH) levels prior to treatment are a known biomarker to predict advanced melanoma’s response to immune checkpoint inhibitors (ICI). In this study, we evaluated the ability of machine learning-based models to predict responses to ICI and complement LDH for in predicting the outcomes of metastatic melanoma. A machine learning algorithm was developed using radiomics, and further analysis helped select the most important predictive features and variables. The machine learning model that combined both features extracted from images (radiomics) and pretreatment LDH levels resulted in better predictions of cancer response to ICI than models that only use radiomics features or LDH levels alone. ABSTRACT: Pretreatment LDH is a standard prognostic biomarker for advanced melanoma and is associated with response to ICI. We assessed the role of machine learning-based radiomics in predicting responses to ICI and in complementing LDH for prognostication of metastatic melanoma. From 2008–2022, 79 patients with 168 metastatic hepatic lesions were identified. All patients had arterial phase CT images 1-month prior to initiation of ICI. Response to ICI was assessed on follow-up CT at 3 months using RECIST criteria. A machine learning algorithm was developed using radiomics. Maximum relevance minimum redundancy (mRMR) was used to select features. ROC analysis and logistic regression analyses evaluated performance. Shapley additive explanations were used to identify the variables that are the most important in predicting a response. mRMR selection revealed 15 features that are associated with a response to ICI. The machine learning model combining both radiomics features and pretreatment LDH resulted in better performance for response prediction compared to models that included radiomics or LDH alone (AUC of 0.89 (95% CI: [0.76–0.99]) vs. 0.81 (95% CI: [0.65–0.94]) and 0.81 (95% CI: [0.72–0.91]), respectively). Using SHAP analysis, LDH and two GLSZM were the most predictive of the outcome. Pre-treatment CT radiomic features performed equally well to serum LDH in predicting treatment response. MDPI 2023-05-10 /pmc/articles/PMC10216156/ /pubmed/37345037 http://dx.doi.org/10.3390/cancers15102700 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Tabari, Azadeh Cox, Meredith D’Amore, Brian Mansur, Arian Dabbara, Harika Boland, Genevieve Gee, Michael S. Daye, Dania Machine Learning Improves the Prediction of Responses to Immune Checkpoint Inhibitors in Metastatic Melanoma |
title | Machine Learning Improves the Prediction of Responses to Immune Checkpoint Inhibitors in Metastatic Melanoma |
title_full | Machine Learning Improves the Prediction of Responses to Immune Checkpoint Inhibitors in Metastatic Melanoma |
title_fullStr | Machine Learning Improves the Prediction of Responses to Immune Checkpoint Inhibitors in Metastatic Melanoma |
title_full_unstemmed | Machine Learning Improves the Prediction of Responses to Immune Checkpoint Inhibitors in Metastatic Melanoma |
title_short | Machine Learning Improves the Prediction of Responses to Immune Checkpoint Inhibitors in Metastatic Melanoma |
title_sort | machine learning improves the prediction of responses to immune checkpoint inhibitors in metastatic melanoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10216156/ https://www.ncbi.nlm.nih.gov/pubmed/37345037 http://dx.doi.org/10.3390/cancers15102700 |
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