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Supervised learning based on tumor imaging and biopsy transcriptomics predicts response of hepatocellular carcinoma to transarterial chemoembolization
Although transarterial chemoembolization (TACE) is the most widely used treatment for intermediate-stage, unresectable hepatocellular carcinoma (HCC), it is only effective in a subset of patients. In this study, we combine clinical, radiological, and genomics data in supervised machine-learning mode...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8606904/ https://www.ncbi.nlm.nih.gov/pubmed/34841291 http://dx.doi.org/10.1016/j.xcrm.2021.100444 |
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author | Boldanova, Tuyana Fucile, Geoffrey Vosshenrich, Jan Suslov, Aleksei Ercan, Caner Coto-Llerena, Mairene Terracciano, Luigi M. Zech, Christoph J. Boll, Daniel T. Wieland, Stefan Heim, Markus H. |
author_facet | Boldanova, Tuyana Fucile, Geoffrey Vosshenrich, Jan Suslov, Aleksei Ercan, Caner Coto-Llerena, Mairene Terracciano, Luigi M. Zech, Christoph J. Boll, Daniel T. Wieland, Stefan Heim, Markus H. |
author_sort | Boldanova, Tuyana |
collection | PubMed |
description | Although transarterial chemoembolization (TACE) is the most widely used treatment for intermediate-stage, unresectable hepatocellular carcinoma (HCC), it is only effective in a subset of patients. In this study, we combine clinical, radiological, and genomics data in supervised machine-learning models toward the development of a clinically applicable predictive classifier of response to TACE in HCC patients. Our study consists of a discovery cohort of 33 tumors through which we identify predictive biomarkers, which are confirmed in a validation cohort. We find that radiological assessment of tumor area and several transcriptomic signatures, primarily the expression of FAM111B and HPRT1, are most predictive of response to TACE. Logistic regression decision support models consisting of tumor area and RNA-seq gene expression estimates for FAM111B and HPRT1 yield a predictive accuracy of ∼90%. Reverse transcription droplet digital PCR (RT-ddPCR) confirms these genes in combination with tumor area as a predictive classifier for response to TACE. |
format | Online Article Text |
id | pubmed-8606904 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-86069042021-11-26 Supervised learning based on tumor imaging and biopsy transcriptomics predicts response of hepatocellular carcinoma to transarterial chemoembolization Boldanova, Tuyana Fucile, Geoffrey Vosshenrich, Jan Suslov, Aleksei Ercan, Caner Coto-Llerena, Mairene Terracciano, Luigi M. Zech, Christoph J. Boll, Daniel T. Wieland, Stefan Heim, Markus H. Cell Rep Med Report Although transarterial chemoembolization (TACE) is the most widely used treatment for intermediate-stage, unresectable hepatocellular carcinoma (HCC), it is only effective in a subset of patients. In this study, we combine clinical, radiological, and genomics data in supervised machine-learning models toward the development of a clinically applicable predictive classifier of response to TACE in HCC patients. Our study consists of a discovery cohort of 33 tumors through which we identify predictive biomarkers, which are confirmed in a validation cohort. We find that radiological assessment of tumor area and several transcriptomic signatures, primarily the expression of FAM111B and HPRT1, are most predictive of response to TACE. Logistic regression decision support models consisting of tumor area and RNA-seq gene expression estimates for FAM111B and HPRT1 yield a predictive accuracy of ∼90%. Reverse transcription droplet digital PCR (RT-ddPCR) confirms these genes in combination with tumor area as a predictive classifier for response to TACE. Elsevier 2021-11-16 /pmc/articles/PMC8606904/ /pubmed/34841291 http://dx.doi.org/10.1016/j.xcrm.2021.100444 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Report Boldanova, Tuyana Fucile, Geoffrey Vosshenrich, Jan Suslov, Aleksei Ercan, Caner Coto-Llerena, Mairene Terracciano, Luigi M. Zech, Christoph J. Boll, Daniel T. Wieland, Stefan Heim, Markus H. Supervised learning based on tumor imaging and biopsy transcriptomics predicts response of hepatocellular carcinoma to transarterial chemoembolization |
title | Supervised learning based on tumor imaging and biopsy transcriptomics predicts response of hepatocellular carcinoma to transarterial chemoembolization |
title_full | Supervised learning based on tumor imaging and biopsy transcriptomics predicts response of hepatocellular carcinoma to transarterial chemoembolization |
title_fullStr | Supervised learning based on tumor imaging and biopsy transcriptomics predicts response of hepatocellular carcinoma to transarterial chemoembolization |
title_full_unstemmed | Supervised learning based on tumor imaging and biopsy transcriptomics predicts response of hepatocellular carcinoma to transarterial chemoembolization |
title_short | Supervised learning based on tumor imaging and biopsy transcriptomics predicts response of hepatocellular carcinoma to transarterial chemoembolization |
title_sort | supervised learning based on tumor imaging and biopsy transcriptomics predicts response of hepatocellular carcinoma to transarterial chemoembolization |
topic | Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8606904/ https://www.ncbi.nlm.nih.gov/pubmed/34841291 http://dx.doi.org/10.1016/j.xcrm.2021.100444 |
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