A multiomics approach-based prediction of radiation pneumonia in lung cancer patients: impact on survival outcome

Purpose To predict the risk of radiation pneumonitis (RP), a multiomics model was built to stratify lung cancer patients. Our study also investigated the impact of RP on survival. Methods This study retrospectively collected 100 RP and 99 matched non-RP lung cancer patients treated with radiotherapy...

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Veröffentlicht in:Journal of cancer research and clinical oncology 2023-09, Vol.149 (11), p.8923-8934
Hauptverfasser: Niu, Lishui, Chu, Xianjing, Yang, Xianghui, Zhao, Hongxiang, Chen, Liu, Deng, Fuxing, Liang, Zhan, Jing, Di, Zhou, Rongrong
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container_end_page 8934
container_issue 11
container_start_page 8923
container_title Journal of cancer research and clinical oncology
container_volume 149
creator Niu, Lishui
Chu, Xianjing
Yang, Xianghui
Zhao, Hongxiang
Chen, Liu
Deng, Fuxing
Liang, Zhan
Jing, Di
Zhou, Rongrong
description Purpose To predict the risk of radiation pneumonitis (RP), a multiomics model was built to stratify lung cancer patients. Our study also investigated the impact of RP on survival. Methods This study retrospectively collected 100 RP and 99 matched non-RP lung cancer patients treated with radiotherapy from two independent centres. They were divided into training (n = 175) and validation cohorts (n = 24). The radiomics, dosiomics and clinical features were extracted from planning CT and electronic medical records and were analysed by LASSO Cox regression. A multiomics prediction model was developed by the optimal algorithm. Overall survival (OS) between the RP, non-RP, mild RP, and severe RP groups was analysed by the Kaplan‒Meier method. Results Sixteen radiomics features, two dosiomics features, and one clinical feature were selected to build the best multiomics model. The optimal performance for predicting RP was the area under the receiver operating characteristic curve (AUC) of the testing set (0.94) and validation set (0.92). The RP patients were divided into mild (≤ 2 grade) and severe (> 2 grade) RP groups. The median OS was 31 months for the non-RP group compared with 49 months for the RP group (HR = 0.53, p = 0.0022). Among the RP subgroup, the median OS was 57 months for the mild RP group and 25 months for the severe RP group (HR = 3.72, p 
doi_str_mv 10.1007/s00432-023-04827-7
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Our study also investigated the impact of RP on survival. Methods This study retrospectively collected 100 RP and 99 matched non-RP lung cancer patients treated with radiotherapy from two independent centres. They were divided into training (n = 175) and validation cohorts (n = 24). The radiomics, dosiomics and clinical features were extracted from planning CT and electronic medical records and were analysed by LASSO Cox regression. A multiomics prediction model was developed by the optimal algorithm. Overall survival (OS) between the RP, non-RP, mild RP, and severe RP groups was analysed by the Kaplan‒Meier method. Results Sixteen radiomics features, two dosiomics features, and one clinical feature were selected to build the best multiomics model. The optimal performance for predicting RP was the area under the receiver operating characteristic curve (AUC) of the testing set (0.94) and validation set (0.92). The RP patients were divided into mild (≤ 2 grade) and severe (&gt; 2 grade) RP groups. The median OS was 31 months for the non-RP group compared with 49 months for the RP group (HR = 0.53, p = 0.0022). Among the RP subgroup, the median OS was 57 months for the mild RP group and 25 months for the severe RP group (HR = 3.72, p &lt; 0.0001). Conclusions The multiomics model contributed to improving the accuracy of RP prediction. Compared with the non-RP patients, the RP patients displayed longer OS, especially the mild RP patients.</description><identifier>ISSN: 0171-5216</identifier><identifier>ISSN: 1432-1335</identifier><identifier>EISSN: 1432-1335</identifier><identifier>DOI: 10.1007/s00432-023-04827-7</identifier><identifier>PMID: 37154927</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Biological analysis ; Cancer Research ; Electronic medical records ; Hematology ; Humans ; Internal Medicine ; Lung cancer ; Lung Neoplasms - radiotherapy ; Medicine ; Medicine &amp; Public Health ; Multiomics ; Oncology ; Patients ; Pneumonitis ; Prediction models ; Radiation ; Radiation Pneumonitis - diagnosis ; Radiation Pneumonitis - etiology ; Radiation therapy ; Radiomics ; Retrospective Studies ; Risk Factors ; Survival</subject><ispartof>Journal of cancer research and clinical oncology, 2023-09, Vol.149 (11), p.8923-8934</ispartof><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>2023. 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Our study also investigated the impact of RP on survival. Methods This study retrospectively collected 100 RP and 99 matched non-RP lung cancer patients treated with radiotherapy from two independent centres. They were divided into training (n = 175) and validation cohorts (n = 24). The radiomics, dosiomics and clinical features were extracted from planning CT and electronic medical records and were analysed by LASSO Cox regression. A multiomics prediction model was developed by the optimal algorithm. Overall survival (OS) between the RP, non-RP, mild RP, and severe RP groups was analysed by the Kaplan‒Meier method. Results Sixteen radiomics features, two dosiomics features, and one clinical feature were selected to build the best multiomics model. The optimal performance for predicting RP was the area under the receiver operating characteristic curve (AUC) of the testing set (0.94) and validation set (0.92). The RP patients were divided into mild (≤ 2 grade) and severe (&gt; 2 grade) RP groups. The median OS was 31 months for the non-RP group compared with 49 months for the RP group (HR = 0.53, p = 0.0022). Among the RP subgroup, the median OS was 57 months for the mild RP group and 25 months for the severe RP group (HR = 3.72, p &lt; 0.0001). Conclusions The multiomics model contributed to improving the accuracy of RP prediction. 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Our study also investigated the impact of RP on survival. Methods This study retrospectively collected 100 RP and 99 matched non-RP lung cancer patients treated with radiotherapy from two independent centres. They were divided into training (n = 175) and validation cohorts (n = 24). The radiomics, dosiomics and clinical features were extracted from planning CT and electronic medical records and were analysed by LASSO Cox regression. A multiomics prediction model was developed by the optimal algorithm. Overall survival (OS) between the RP, non-RP, mild RP, and severe RP groups was analysed by the Kaplan‒Meier method. Results Sixteen radiomics features, two dosiomics features, and one clinical feature were selected to build the best multiomics model. The optimal performance for predicting RP was the area under the receiver operating characteristic curve (AUC) of the testing set (0.94) and validation set (0.92). The RP patients were divided into mild (≤ 2 grade) and severe (&gt; 2 grade) RP groups. The median OS was 31 months for the non-RP group compared with 49 months for the RP group (HR = 0.53, p = 0.0022). Among the RP subgroup, the median OS was 57 months for the mild RP group and 25 months for the severe RP group (HR = 3.72, p &lt; 0.0001). Conclusions The multiomics model contributed to improving the accuracy of RP prediction. Compared with the non-RP patients, the RP patients displayed longer OS, especially the mild RP patients.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>37154927</pmid><doi>10.1007/s00432-023-04827-7</doi><tpages>12</tpages></addata></record>
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subjects Biological analysis
Cancer Research
Electronic medical records
Hematology
Humans
Internal Medicine
Lung cancer
Lung Neoplasms - radiotherapy
Medicine
Medicine & Public Health
Multiomics
Oncology
Patients
Pneumonitis
Prediction models
Radiation
Radiation Pneumonitis - diagnosis
Radiation Pneumonitis - etiology
Radiation therapy
Radiomics
Retrospective Studies
Risk Factors
Survival
title A multiomics approach-based prediction of radiation pneumonia in lung cancer patients: impact on survival outcome
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