Prospective external validation of radiomics‐based predictive model of distant metastasis after dynamic tumor tracking stereotactic body radiation therapy in patients with non‐small‐cell lung cancer: A multi‐institutional analysis

Background and purpose This study aims to externally validate a predictive model for distant metastasis (DM) with computed tomography (CT)‐based radiomics features in prospectively enrolled non‐small‐cell lung cancer patients undergoing dynamic tumor‐tracking stereotactic body radiation therapy (DTT...

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Veröffentlicht in:Journal of Applied Clinical Medical Physics 2024-10, Vol.25 (10), p.e14475-n/a
Hauptverfasser: Adachi, Takanori, Nakamura, Mitsuhiro, Matsuo, Yukinori, Karasawa, Katsuyuki, Kokubo, Masaki, Sakamoto, Takashi, Hiraoka, Masahiro, Mizowaki, Takashi
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container_title Journal of Applied Clinical Medical Physics
container_volume 25
creator Adachi, Takanori
Nakamura, Mitsuhiro
Matsuo, Yukinori
Karasawa, Katsuyuki
Kokubo, Masaki
Sakamoto, Takashi
Hiraoka, Masahiro
Mizowaki, Takashi
description Background and purpose This study aims to externally validate a predictive model for distant metastasis (DM) with computed tomography (CT)‐based radiomics features in prospectively enrolled non‐small‐cell lung cancer patients undergoing dynamic tumor‐tracking stereotactic body radiation therapy (DTT‐SBRT). Materials and methods The study collected retrospective data from 567 patients across 11 institutions as the training dataset and prospectively enrolled 42 patients from four institutions as the external test dataset. Four clinical features were collected, and 944 CT‐based radiomic features were extracted from gross tumor volumes. After standardization and feature selection, DM predictive models were developed using fine and gray regression (FG) and random survival forest (RSF), incorporating clinical and radiomic features, and their combinations within the training dataset. Then, the model was applied to the test dataset, dividing patients into high‐ and low‐risk groups based on medians of risk scores. Model performance was assessed using the concordance index (C‐index), and the statistical significance between groups was evaluated using Gray's test. Results In the training dataset, 122 of 567 patients (21.5%) developed DM, compared to 9 of 42 patients (21.4%) in the test dataset. In the test dataset, the C‐indices of the clinical, radiomics, and hybrid models with FG were 0.559, 0.544, and 0.560, respectively, whereas those with RSF were 0.576, 0.604, and 0.627, respectively. The hybrid model with RSF, which exhibited the best predictive performance of all models, identified 7 of 23 patients (30.4%) as high risk and 2 of 19 patients (10.5%) as low risk for DM incidence in the test dataset (p = 0.116). Conclusion Although predictive models for DM lack significance when applied to prospectively enrolled cases undergoing DTT‐lung SBRT, the model with RSF exhibits a consistent capacity to effectively classify patients at a high risk of developing DM.
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Materials and methods The study collected retrospective data from 567 patients across 11 institutions as the training dataset and prospectively enrolled 42 patients from four institutions as the external test dataset. Four clinical features were collected, and 944 CT‐based radiomic features were extracted from gross tumor volumes. After standardization and feature selection, DM predictive models were developed using fine and gray regression (FG) and random survival forest (RSF), incorporating clinical and radiomic features, and their combinations within the training dataset. Then, the model was applied to the test dataset, dividing patients into high‐ and low‐risk groups based on medians of risk scores. Model performance was assessed using the concordance index (C‐index), and the statistical significance between groups was evaluated using Gray's test. Results In the training dataset, 122 of 567 patients (21.5%) developed DM, compared to 9 of 42 patients (21.4%) in the test dataset. In the test dataset, the C‐indices of the clinical, radiomics, and hybrid models with FG were 0.559, 0.544, and 0.560, respectively, whereas those with RSF were 0.576, 0.604, and 0.627, respectively. The hybrid model with RSF, which exhibited the best predictive performance of all models, identified 7 of 23 patients (30.4%) as high risk and 2 of 19 patients (10.5%) as low risk for DM incidence in the test dataset (p = 0.116). Conclusion Although predictive models for DM lack significance when applied to prospectively enrolled cases undergoing DTT‐lung SBRT, the model with RSF exhibits a consistent capacity to effectively classify patients at a high risk of developing DM.</description><identifier>ISSN: 1526-9914</identifier><identifier>EISSN: 1526-9914</identifier><identifier>DOI: 10.1002/acm2.14475</identifier><identifier>PMID: 39178139</identifier><language>eng</language><publisher>United States: John Wiley &amp; Sons, Inc</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Analysis ; Cancer therapies ; Carcinoma, Non-Small-Cell Lung - diagnostic imaging ; Carcinoma, Non-Small-Cell Lung - pathology ; Carcinoma, Non-Small-Cell Lung - radiotherapy ; Care and treatment ; Clinical trials ; CT imaging ; Datasets ; Digital television ; distant metastasis ; dynamic tumor tracking ; Female ; Humans ; Image Processing, Computer-Assisted - methods ; Imaging Physics ; Lung cancer ; Lung cancer, Non-small cell ; Lung cancer, Small cell ; Lung Neoplasms - diagnostic imaging ; Lung Neoplasms - pathology ; Lung Neoplasms - radiotherapy ; lung SBRT ; Male ; Medical prognosis ; Medical research ; Medicine, Experimental ; Metastasis ; Middle Aged ; multi‐institutional study ; Neoplasm Metastasis ; Nomograms ; Patients ; Prognosis ; prognostic prediction ; prospective external validation ; Prospective Studies ; Radiation ; Radiation therapy ; Radiomics ; Radiosurgery - methods ; Radiotherapy ; Radiotherapy Dosage ; Radiotherapy Planning, Computer-Assisted - methods ; Radiotherapy, Intensity-Modulated - methods ; Retrospective Studies ; Software ; Tomography, X-Ray Computed - methods ; Tumors</subject><ispartof>Journal of Applied Clinical Medical Physics, 2024-10, Vol.25 (10), p.e14475-n/a</ispartof><rights>2024 The Author(s). is published by Wiley Periodicals, Inc. on behalf of The American Association of Physicists in Medicine.</rights><rights>2024 The Author(s). Journal of Applied Clinical Medical Physics is published by Wiley Periodicals, Inc. on behalf of The American Association of Physicists in Medicine.</rights><rights>COPYRIGHT 2024 John Wiley &amp; Sons, Inc.</rights><rights>2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the "License"). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c4055-655c413fcaa48dbd783d6b6df4743c659cc00c449584117402d7d08c8855a41e3</cites><orcidid>0000-0002-4372-8259 ; 0000-0003-1356-5118 ; 0000-0002-8135-8746</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11466494/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11466494/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,861,882,1413,11544,27906,27907,45556,45557,46034,46458,53773,53775</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39178139$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Adachi, Takanori</creatorcontrib><creatorcontrib>Nakamura, Mitsuhiro</creatorcontrib><creatorcontrib>Matsuo, Yukinori</creatorcontrib><creatorcontrib>Karasawa, Katsuyuki</creatorcontrib><creatorcontrib>Kokubo, Masaki</creatorcontrib><creatorcontrib>Sakamoto, Takashi</creatorcontrib><creatorcontrib>Hiraoka, Masahiro</creatorcontrib><creatorcontrib>Mizowaki, Takashi</creatorcontrib><title>Prospective external validation of radiomics‐based predictive model of distant metastasis after dynamic tumor tracking stereotactic body radiation therapy in patients with non‐small‐cell lung cancer: A multi‐institutional analysis</title><title>Journal of Applied Clinical Medical Physics</title><addtitle>J Appl Clin Med Phys</addtitle><description>Background and purpose This study aims to externally validate a predictive model for distant metastasis (DM) with computed tomography (CT)‐based radiomics features in prospectively enrolled non‐small‐cell lung cancer patients undergoing dynamic tumor‐tracking stereotactic body radiation therapy (DTT‐SBRT). Materials and methods The study collected retrospective data from 567 patients across 11 institutions as the training dataset and prospectively enrolled 42 patients from four institutions as the external test dataset. Four clinical features were collected, and 944 CT‐based radiomic features were extracted from gross tumor volumes. After standardization and feature selection, DM predictive models were developed using fine and gray regression (FG) and random survival forest (RSF), incorporating clinical and radiomic features, and their combinations within the training dataset. Then, the model was applied to the test dataset, dividing patients into high‐ and low‐risk groups based on medians of risk scores. Model performance was assessed using the concordance index (C‐index), and the statistical significance between groups was evaluated using Gray's test. Results In the training dataset, 122 of 567 patients (21.5%) developed DM, compared to 9 of 42 patients (21.4%) in the test dataset. In the test dataset, the C‐indices of the clinical, radiomics, and hybrid models with FG were 0.559, 0.544, and 0.560, respectively, whereas those with RSF were 0.576, 0.604, and 0.627, respectively. The hybrid model with RSF, which exhibited the best predictive performance of all models, identified 7 of 23 patients (30.4%) as high risk and 2 of 19 patients (10.5%) as low risk for DM incidence in the test dataset (p = 0.116). 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Nakamura, Mitsuhiro ; Matsuo, Yukinori ; Karasawa, Katsuyuki ; Kokubo, Masaki ; Sakamoto, Takashi ; Hiraoka, Masahiro ; Mizowaki, Takashi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4055-655c413fcaa48dbd783d6b6df4743c659cc00c449584117402d7d08c8855a41e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Analysis</topic><topic>Cancer therapies</topic><topic>Carcinoma, Non-Small-Cell Lung - diagnostic imaging</topic><topic>Carcinoma, Non-Small-Cell Lung - pathology</topic><topic>Carcinoma, Non-Small-Cell Lung - radiotherapy</topic><topic>Care and treatment</topic><topic>Clinical trials</topic><topic>CT imaging</topic><topic>Datasets</topic><topic>Digital television</topic><topic>distant metastasis</topic><topic>dynamic tumor tracking</topic><topic>Female</topic><topic>Humans</topic><topic>Image Processing, Computer-Assisted - methods</topic><topic>Imaging Physics</topic><topic>Lung cancer</topic><topic>Lung cancer, Non-small cell</topic><topic>Lung cancer, Small cell</topic><topic>Lung Neoplasms - diagnostic imaging</topic><topic>Lung Neoplasms - pathology</topic><topic>Lung Neoplasms - radiotherapy</topic><topic>lung SBRT</topic><topic>Male</topic><topic>Medical prognosis</topic><topic>Medical research</topic><topic>Medicine, Experimental</topic><topic>Metastasis</topic><topic>Middle Aged</topic><topic>multi‐institutional study</topic><topic>Neoplasm Metastasis</topic><topic>Nomograms</topic><topic>Patients</topic><topic>Prognosis</topic><topic>prognostic prediction</topic><topic>prospective external validation</topic><topic>Prospective Studies</topic><topic>Radiation</topic><topic>Radiation therapy</topic><topic>Radiomics</topic><topic>Radiosurgery - methods</topic><topic>Radiotherapy</topic><topic>Radiotherapy Dosage</topic><topic>Radiotherapy Planning, Computer-Assisted - methods</topic><topic>Radiotherapy, Intensity-Modulated - methods</topic><topic>Retrospective Studies</topic><topic>Software</topic><topic>Tomography, X-Ray Computed - methods</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Adachi, Takanori</creatorcontrib><creatorcontrib>Nakamura, Mitsuhiro</creatorcontrib><creatorcontrib>Matsuo, Yukinori</creatorcontrib><creatorcontrib>Karasawa, Katsuyuki</creatorcontrib><creatorcontrib>Kokubo, Masaki</creatorcontrib><creatorcontrib>Sakamoto, Takashi</creatorcontrib><creatorcontrib>Hiraoka, Masahiro</creatorcontrib><creatorcontrib>Mizowaki, Takashi</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Wiley Online Library Free Content</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale Academic OneFile</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; 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Materials and methods The study collected retrospective data from 567 patients across 11 institutions as the training dataset and prospectively enrolled 42 patients from four institutions as the external test dataset. Four clinical features were collected, and 944 CT‐based radiomic features were extracted from gross tumor volumes. After standardization and feature selection, DM predictive models were developed using fine and gray regression (FG) and random survival forest (RSF), incorporating clinical and radiomic features, and their combinations within the training dataset. Then, the model was applied to the test dataset, dividing patients into high‐ and low‐risk groups based on medians of risk scores. Model performance was assessed using the concordance index (C‐index), and the statistical significance between groups was evaluated using Gray's test. Results In the training dataset, 122 of 567 patients (21.5%) developed DM, compared to 9 of 42 patients (21.4%) in the test dataset. In the test dataset, the C‐indices of the clinical, radiomics, and hybrid models with FG were 0.559, 0.544, and 0.560, respectively, whereas those with RSF were 0.576, 0.604, and 0.627, respectively. The hybrid model with RSF, which exhibited the best predictive performance of all models, identified 7 of 23 patients (30.4%) as high risk and 2 of 19 patients (10.5%) as low risk for DM incidence in the test dataset (p = 0.116). Conclusion Although predictive models for DM lack significance when applied to prospectively enrolled cases undergoing DTT‐lung SBRT, the model with RSF exhibits a consistent capacity to effectively classify patients at a high risk of developing DM.</abstract><cop>United States</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>39178139</pmid><doi>10.1002/acm2.14475</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-4372-8259</orcidid><orcidid>https://orcid.org/0000-0003-1356-5118</orcidid><orcidid>https://orcid.org/0000-0002-8135-8746</orcidid><oa>free_for_read</oa></addata></record>
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subjects Adult
Aged
Aged, 80 and over
Analysis
Cancer therapies
Carcinoma, Non-Small-Cell Lung - diagnostic imaging
Carcinoma, Non-Small-Cell Lung - pathology
Carcinoma, Non-Small-Cell Lung - radiotherapy
Care and treatment
Clinical trials
CT imaging
Datasets
Digital television
distant metastasis
dynamic tumor tracking
Female
Humans
Image Processing, Computer-Assisted - methods
Imaging Physics
Lung cancer
Lung cancer, Non-small cell
Lung cancer, Small cell
Lung Neoplasms - diagnostic imaging
Lung Neoplasms - pathology
Lung Neoplasms - radiotherapy
lung SBRT
Male
Medical prognosis
Medical research
Medicine, Experimental
Metastasis
Middle Aged
multi‐institutional study
Neoplasm Metastasis
Nomograms
Patients
Prognosis
prognostic prediction
prospective external validation
Prospective Studies
Radiation
Radiation therapy
Radiomics
Radiosurgery - methods
Radiotherapy
Radiotherapy Dosage
Radiotherapy Planning, Computer-Assisted - methods
Radiotherapy, Intensity-Modulated - methods
Retrospective Studies
Software
Tomography, X-Ray Computed - methods
Tumors
title Prospective external validation of radiomics‐based predictive model of distant metastasis after dynamic tumor tracking stereotactic body radiation therapy in patients with non‐small‐cell lung cancer: A multi‐institutional analysis
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