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Deep learning‐based assessment of body composition and liver tumour burden for survival modelling in advanced colorectal cancer

BACKGROUND: Personalized therapy planning remains a significant challenge in advanced colorectal cancer care, despite extensive research on prognostic and predictive markers. A strong correlation of sarcopenia or overall body composition and survival has been described. Here, we explore whether auto...

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Autores principales: Keyl, Julius, Hosch, René, Berger, Aaron, Ester, Oliver, Greiner, Tobias, Bogner, Simon, Treckmann, Jürgen, Ting, Saskia, Schumacher, Brigitte, Albers, David, Markus, Peter, Wiesweg, Marcel, Forsting, Michael, Nensa, Felix, Schuler, Martin, Kasper, Stefan, Kleesiek, Jens
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9891942/
https://www.ncbi.nlm.nih.gov/pubmed/36544260
http://dx.doi.org/10.1002/jcsm.13158
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author Keyl, Julius
Hosch, René
Berger, Aaron
Ester, Oliver
Greiner, Tobias
Bogner, Simon
Treckmann, Jürgen
Ting, Saskia
Schumacher, Brigitte
Albers, David
Markus, Peter
Wiesweg, Marcel
Forsting, Michael
Nensa, Felix
Schuler, Martin
Kasper, Stefan
Kleesiek, Jens
author_facet Keyl, Julius
Hosch, René
Berger, Aaron
Ester, Oliver
Greiner, Tobias
Bogner, Simon
Treckmann, Jürgen
Ting, Saskia
Schumacher, Brigitte
Albers, David
Markus, Peter
Wiesweg, Marcel
Forsting, Michael
Nensa, Felix
Schuler, Martin
Kasper, Stefan
Kleesiek, Jens
author_sort Keyl, Julius
collection PubMed
description BACKGROUND: Personalized therapy planning remains a significant challenge in advanced colorectal cancer care, despite extensive research on prognostic and predictive markers. A strong correlation of sarcopenia or overall body composition and survival has been described. Here, we explore whether automated assessment of body composition and liver metastases from standard of care CT images can add to clinical parameters in personalized survival risk prognostication. METHODS: We retrospectively analysed clinical imaging data from 85 patients (50.6% female, mean age 58.9 SD 12.2 years) with colorectal cancer and synchronous liver metastases. Pretrained deep learning models were used to assess body composition and liver metastasis geometry from abdominal CT images before the initiation of systemic treatment. Abdominal muscle‐to‐bone ratio (MBR) was calculated by dividing abdominal muscle volume by abdominal bone volume. MBR was compared with body mass index (BMI), abdominal muscle volume, and abdominal muscle volume divided by height squared. Differences in overall survival based on body composition and liver metastasis parameters were compared using Kaplan–Meier survival curves. Results were correlated with clinical and biomarker data to develop a machine learning model for survival risk prognostication. RESULTS: The MBR, unlike abdominal muscle volume or BMI, was significantly associated with overall survival (HR 0.39, 95% CI: 0.19–0.80, P = 0.009). The MBR (P = 0.022), liver metastasis surface area (P = 0.01) and primary tumour sidedness (P = 0.007) were independently associated with overall survival in multivariate analysis. Body composition parameters did not correlate with KRAS mutational status or primary tumour sidedness. A prediction model based on MBR, liver metastasis surface area and primary tumour sidedness achieved a concordance index of 0.69. CONCLUSIONS: Automated segmentation enables to extract prognostic parameters from routine imaging data for personalized survival modelling in advanced colorectal cancer patients.
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spelling pubmed-98919422023-02-02 Deep learning‐based assessment of body composition and liver tumour burden for survival modelling in advanced colorectal cancer Keyl, Julius Hosch, René Berger, Aaron Ester, Oliver Greiner, Tobias Bogner, Simon Treckmann, Jürgen Ting, Saskia Schumacher, Brigitte Albers, David Markus, Peter Wiesweg, Marcel Forsting, Michael Nensa, Felix Schuler, Martin Kasper, Stefan Kleesiek, Jens J Cachexia Sarcopenia Muscle Original Articles BACKGROUND: Personalized therapy planning remains a significant challenge in advanced colorectal cancer care, despite extensive research on prognostic and predictive markers. A strong correlation of sarcopenia or overall body composition and survival has been described. Here, we explore whether automated assessment of body composition and liver metastases from standard of care CT images can add to clinical parameters in personalized survival risk prognostication. METHODS: We retrospectively analysed clinical imaging data from 85 patients (50.6% female, mean age 58.9 SD 12.2 years) with colorectal cancer and synchronous liver metastases. Pretrained deep learning models were used to assess body composition and liver metastasis geometry from abdominal CT images before the initiation of systemic treatment. Abdominal muscle‐to‐bone ratio (MBR) was calculated by dividing abdominal muscle volume by abdominal bone volume. MBR was compared with body mass index (BMI), abdominal muscle volume, and abdominal muscle volume divided by height squared. Differences in overall survival based on body composition and liver metastasis parameters were compared using Kaplan–Meier survival curves. Results were correlated with clinical and biomarker data to develop a machine learning model for survival risk prognostication. RESULTS: The MBR, unlike abdominal muscle volume or BMI, was significantly associated with overall survival (HR 0.39, 95% CI: 0.19–0.80, P = 0.009). The MBR (P = 0.022), liver metastasis surface area (P = 0.01) and primary tumour sidedness (P = 0.007) were independently associated with overall survival in multivariate analysis. Body composition parameters did not correlate with KRAS mutational status or primary tumour sidedness. A prediction model based on MBR, liver metastasis surface area and primary tumour sidedness achieved a concordance index of 0.69. CONCLUSIONS: Automated segmentation enables to extract prognostic parameters from routine imaging data for personalized survival modelling in advanced colorectal cancer patients. John Wiley and Sons Inc. 2022-12-21 /pmc/articles/PMC9891942/ /pubmed/36544260 http://dx.doi.org/10.1002/jcsm.13158 Text en © 2022 The Authors. Journal of Cachexia, Sarcopenia and Muscle published by John Wiley & Sons Ltd on behalf of Society on Sarcopenia, Cachexia and Wasting Disorders. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Keyl, Julius
Hosch, René
Berger, Aaron
Ester, Oliver
Greiner, Tobias
Bogner, Simon
Treckmann, Jürgen
Ting, Saskia
Schumacher, Brigitte
Albers, David
Markus, Peter
Wiesweg, Marcel
Forsting, Michael
Nensa, Felix
Schuler, Martin
Kasper, Stefan
Kleesiek, Jens
Deep learning‐based assessment of body composition and liver tumour burden for survival modelling in advanced colorectal cancer
title Deep learning‐based assessment of body composition and liver tumour burden for survival modelling in advanced colorectal cancer
title_full Deep learning‐based assessment of body composition and liver tumour burden for survival modelling in advanced colorectal cancer
title_fullStr Deep learning‐based assessment of body composition and liver tumour burden for survival modelling in advanced colorectal cancer
title_full_unstemmed Deep learning‐based assessment of body composition and liver tumour burden for survival modelling in advanced colorectal cancer
title_short Deep learning‐based assessment of body composition and liver tumour burden for survival modelling in advanced colorectal cancer
title_sort deep learning‐based assessment of body composition and liver tumour burden for survival modelling in advanced colorectal cancer
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9891942/
https://www.ncbi.nlm.nih.gov/pubmed/36544260
http://dx.doi.org/10.1002/jcsm.13158
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