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A predictive model for pain response following radiotherapy for treatment of spinal metastases

To establish a predictive model for pain response following radiotherapy using a combination of radiomic and clinical features of spinal metastasis. This retrospective study enrolled patients with painful spine metastases who received palliative radiation therapy from 2018 to 2019. Pain response was...

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Autores principales: Wakabayashi, Kohei, Koide, Yutaro, Aoyama, Takahiro, Shimizu, Hidetoshi, Miyauchi, Risei, Tanaka, Hiroshi, Tachibana, Hiroyuki, Nakamura, Katsumasa, Kodaira, Takeshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8213735/
https://www.ncbi.nlm.nih.gov/pubmed/34145367
http://dx.doi.org/10.1038/s41598-021-92363-0
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author Wakabayashi, Kohei
Koide, Yutaro
Aoyama, Takahiro
Shimizu, Hidetoshi
Miyauchi, Risei
Tanaka, Hiroshi
Tachibana, Hiroyuki
Nakamura, Katsumasa
Kodaira, Takeshi
author_facet Wakabayashi, Kohei
Koide, Yutaro
Aoyama, Takahiro
Shimizu, Hidetoshi
Miyauchi, Risei
Tanaka, Hiroshi
Tachibana, Hiroyuki
Nakamura, Katsumasa
Kodaira, Takeshi
author_sort Wakabayashi, Kohei
collection PubMed
description To establish a predictive model for pain response following radiotherapy using a combination of radiomic and clinical features of spinal metastasis. This retrospective study enrolled patients with painful spine metastases who received palliative radiation therapy from 2018 to 2019. Pain response was defined using the International Consensus Criteria. The clinical and radiomic features were extracted from medical records and pre-treatment CT images. Feature selection was performed and a random forests ensemble learning method was used to build a predictive model. Area under the curve (AUC) was used as a predictive performance metric. 69 patients were enrolled with 48 patients showing a response. Random forest models built on the radiomic, clinical, and ‘combined’ features achieved an AUC of 0.824, 0.702, 0.848, respectively. The sensitivity and specificity of the combined features model were 85.4% and 76.2%, at the best diagnostic decision point. We built a pain response model in patients with spinal metastases using a combination of clinical and radiomic features. To the best of our knowledge, we are the first to examine pain response using pre-treatment CT radiomic features. Our model showed the potential to predict patients who respond to radiation therapy.
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spelling pubmed-82137352021-06-21 A predictive model for pain response following radiotherapy for treatment of spinal metastases Wakabayashi, Kohei Koide, Yutaro Aoyama, Takahiro Shimizu, Hidetoshi Miyauchi, Risei Tanaka, Hiroshi Tachibana, Hiroyuki Nakamura, Katsumasa Kodaira, Takeshi Sci Rep Article To establish a predictive model for pain response following radiotherapy using a combination of radiomic and clinical features of spinal metastasis. This retrospective study enrolled patients with painful spine metastases who received palliative radiation therapy from 2018 to 2019. Pain response was defined using the International Consensus Criteria. The clinical and radiomic features were extracted from medical records and pre-treatment CT images. Feature selection was performed and a random forests ensemble learning method was used to build a predictive model. Area under the curve (AUC) was used as a predictive performance metric. 69 patients were enrolled with 48 patients showing a response. Random forest models built on the radiomic, clinical, and ‘combined’ features achieved an AUC of 0.824, 0.702, 0.848, respectively. The sensitivity and specificity of the combined features model were 85.4% and 76.2%, at the best diagnostic decision point. We built a pain response model in patients with spinal metastases using a combination of clinical and radiomic features. To the best of our knowledge, we are the first to examine pain response using pre-treatment CT radiomic features. Our model showed the potential to predict patients who respond to radiation therapy. Nature Publishing Group UK 2021-06-18 /pmc/articles/PMC8213735/ /pubmed/34145367 http://dx.doi.org/10.1038/s41598-021-92363-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) .
spellingShingle Article
Wakabayashi, Kohei
Koide, Yutaro
Aoyama, Takahiro
Shimizu, Hidetoshi
Miyauchi, Risei
Tanaka, Hiroshi
Tachibana, Hiroyuki
Nakamura, Katsumasa
Kodaira, Takeshi
A predictive model for pain response following radiotherapy for treatment of spinal metastases
title A predictive model for pain response following radiotherapy for treatment of spinal metastases
title_full A predictive model for pain response following radiotherapy for treatment of spinal metastases
title_fullStr A predictive model for pain response following radiotherapy for treatment of spinal metastases
title_full_unstemmed A predictive model for pain response following radiotherapy for treatment of spinal metastases
title_short A predictive model for pain response following radiotherapy for treatment of spinal metastases
title_sort predictive model for pain response following radiotherapy for treatment of spinal metastases
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8213735/
https://www.ncbi.nlm.nih.gov/pubmed/34145367
http://dx.doi.org/10.1038/s41598-021-92363-0
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