The application of a workflow integrating the variable reproducibility and harmonizability of radiomic features on a phantom dataset
Radiomics–the high throughput extraction of quantitative features from medical images and their correlation with clinical and biological endpoints- is the subject of active and extensive research. Although the field shows promise, the generalizability of radiomic signatures is affected significantly...
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Published in | PloS one Vol. 16; no. 5; p. e0251147 |
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Main Authors | , , , , , , , , |
Format | Journal Article Web Resource |
Language | English |
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United States
Public Library of Science
07.05.2021
Public Library of Science (PLoS) |
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Online Access | Get full text |
ISSN | 1932-6203 1932-6203 |
DOI | 10.1371/journal.pone.0251147 |
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Abstract | Radiomics–the high throughput extraction of quantitative features from medical images and their correlation with clinical and biological endpoints- is the subject of active and extensive research. Although the field shows promise, the generalizability of radiomic signatures is affected significantly by differences in scan acquisition and reconstruction settings. Previous studies reported on the sensitivity of radiomic features (RFs) to test-retest variability, inter-observer segmentation variability, and intra-scanner variability. A framework involving robust radiomics analysis and the application of a post-reconstruction feature harmonization method using ComBat was recently proposed to address these challenges. In this study, we investigated the reproducibility of RFs across different scanners and scanning parameters using this framework. We analysed thirteen scans of a ten-layer phantom that were acquired differently. Each layer was subdivided into sixteen regions of interest (ROIs), and the scans were compared in a pairwise manner, resulting in seventy-eight different scenarios. Ninety-one RFs were extracted from each ROI. As hypothesized, we demonstrate that the reproducibility of a given RF is not a constant but is dependent on the heterogeneity found in the data under analysis. The number (%) of reproducible RFs varied across the pairwise scenarios investigated, having a wide range between 8 (8.8%) and 78 (85.7%) RFs. Furthermore, in contrast to what has been previously reported, and as hypothesized in the robust radiomics analysis framework, our results demonstrate that ComBat cannot be applied to all RFs but rather on a percentage of those–the “ComBatable” RFs–which differed depending on the data being harmonized. The number (%) of reproducible RFs following ComBat harmonization varied across the pairwise scenarios investigated, ranging from 14 (15.4%) to 80 (87.9%) RFs, and was found to depend on the heterogeneity in the data. We conclude that the standardization of image acquisition protocols remains the cornerstone for improving the reproducibility of RFs, and the generalizability of the signatures developed. Our proposed approach helps identify the reproducible RFs across different datasets. |
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AbstractList | Radiomics-the high throughput extraction of quantitative features from medical images and their correlation with clinical and biological endpoints- is the subject of active and extensive research. Although the field shows promise, the generalizability of radiomic signatures is affected significantly by differences in scan acquisition and reconstruction settings. Previous studies reported on the sensitivity of radiomic features (RFs) to test-retest variability, inter-observer segmentation variability, and intra-scanner variability. A framework involving robust radiomics analysis and the application of a post-reconstruction feature harmonization method using ComBat was recently proposed to address these challenges. In this study, we investigated the reproducibility of RFs across different scanners and scanning parameters using this framework. We analysed thirteen scans of a ten-layer phantom that were acquired differently. Each layer was subdivided into sixteen regions of interest (ROIs), and the scans were compared in a pairwise manner, resulting in seventy-eight different scenarios. Ninety-one RFs were extracted from each ROI. As hypothesized, we demonstrate that the reproducibility of a given RF is not a constant but is dependent on the heterogeneity found in the data under analysis. The number (%) of reproducible RFs varied across the pairwise scenarios investigated, having a wide range between 8 (8.8%) and 78 (85.7%) RFs. Furthermore, in contrast to what has been previously reported, and as hypothesized in the robust radiomics analysis framework, our results demonstrate that ComBat cannot be applied to all RFs but rather on a percentage of those-the "ComBatable" RFs-which differed depending on the data being harmonized. The number (%) of reproducible RFs following ComBat harmonization varied across the pairwise scenarios investigated, ranging from 14 (15.4%) to 80 (87.9%) RFs, and was found to depend on the heterogeneity in the data. We conclude that the standardization of image acquisition protocols remains the cornerstone for improving the reproducibility of RFs, and the generalizability of the signatures developed. Our proposed approach helps identify the reproducible RFs across different datasets. Radiomics-the high throughput extraction of quantitative features from medical images and their correlation with clinical and biological endpoints- is the subject of active and extensive research. Although the field shows promise, the generalizability of radiomic signatures is affected significantly by differences in scan acquisition and reconstruction settings. Previous studies reported on the sensitivity of radiomic features (RFs) to test-retest variability, inter-observer segmentation variability, and intra-scanner variability. A framework involving robust radiomics analysis and the application of a post-reconstruction feature harmonization method using ComBat was recently proposed to address these challenges. In this study, we investigated the reproducibility of RFs across different scanners and scanning parameters using this framework. We analysed thirteen scans of a ten-layer phantom that were acquired differently. Each layer was subdivided into sixteen regions of interest (ROIs), and the scans were compared in a pairwise manner, resulting in seventy-eight different scenarios. Ninety-one RFs were extracted from each ROI. As hypothesized, we demonstrate that the reproducibility of a given RF is not a constant but is dependent on the heterogeneity found in the data under analysis. The number (%) of reproducible RFs varied across the pairwise scenarios investigated, having a wide range between 8 (8.8%) and 78 (85.7%) RFs. Furthermore, in contrast to what has been previously reported, and as hypothesized in the robust radiomics analysis framework, our results demonstrate that ComBat cannot be applied to all RFs but rather on a percentage of those-the "ComBatable" RFs-which differed depending on the data being harmonized. The number (%) of reproducible RFs following ComBat harmonization varied across the pairwise scenarios investigated, ranging from 14 (15.4%) to 80 (87.9%) RFs, and was found to depend on the heterogeneity in the data. We conclude that the standardization of image acquisition protocols remains the cornerstone for improving the reproducibility of RFs, and the generalizability of the signatures developed. Our proposed approach helps identify the reproducible RFs across different datasets.Radiomics-the high throughput extraction of quantitative features from medical images and their correlation with clinical and biological endpoints- is the subject of active and extensive research. Although the field shows promise, the generalizability of radiomic signatures is affected significantly by differences in scan acquisition and reconstruction settings. Previous studies reported on the sensitivity of radiomic features (RFs) to test-retest variability, inter-observer segmentation variability, and intra-scanner variability. A framework involving robust radiomics analysis and the application of a post-reconstruction feature harmonization method using ComBat was recently proposed to address these challenges. In this study, we investigated the reproducibility of RFs across different scanners and scanning parameters using this framework. We analysed thirteen scans of a ten-layer phantom that were acquired differently. Each layer was subdivided into sixteen regions of interest (ROIs), and the scans were compared in a pairwise manner, resulting in seventy-eight different scenarios. Ninety-one RFs were extracted from each ROI. As hypothesized, we demonstrate that the reproducibility of a given RF is not a constant but is dependent on the heterogeneity found in the data under analysis. The number (%) of reproducible RFs varied across the pairwise scenarios investigated, having a wide range between 8 (8.8%) and 78 (85.7%) RFs. Furthermore, in contrast to what has been previously reported, and as hypothesized in the robust radiomics analysis framework, our results demonstrate that ComBat cannot be applied to all RFs but rather on a percentage of those-the "ComBatable" RFs-which differed depending on the data being harmonized. The number (%) of reproducible RFs following ComBat harmonization varied across the pairwise scenarios investigated, ranging from 14 (15.4%) to 80 (87.9%) RFs, and was found to depend on the heterogeneity in the data. We conclude that the standardization of image acquisition protocols remains the cornerstone for improving the reproducibility of RFs, and the generalizability of the signatures developed. Our proposed approach helps identify the reproducible RFs across different datasets. |
Audience | Academic |
Author | Woodruff, Henry C. Primakov, Sergey Mottaghy, Felix M. Hustinx, Roland Leijenaar, Ralph T. H. Lambin, Philippe Refaee, Turkey Maidment, Andrew D. A. Ibrahim, Abdalla |
AuthorAffiliation | 3 Division of Nuclear Medicine and Oncological Imaging, Department of Medical Physics, University Hospital of Liège and GIGA CRC-in vivo imaging, University of Liège, Liege, Belgium 7 Department of Radiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States of America 4 Department of Nuclear Medicine and Comprehensive Diagnostic Centre Aachen (CDCA), University Hospital RWTH Aachen University, Aachen, Germany 5 Faculty of Applied Medical Sciences, Department of Diagnostic Radiology, Jazan University, Jazan, Saudi Arabia 6 Oncoradiomics SA, Liege, Belgium 1 The D-Lab, Department of Precision Medicine, GROW- School for Oncology, Maastricht University, Maastricht, The Netherlands 2 Department of Radiology and Nuclear Medicine, Maastricht University Medical Centre+, Maastricht, The Netherlands Washington University in St. Louis, UNITED STATES |
AuthorAffiliation_xml | – name: 1 The D-Lab, Department of Precision Medicine, GROW- School for Oncology, Maastricht University, Maastricht, The Netherlands – name: 2 Department of Radiology and Nuclear Medicine, Maastricht University Medical Centre+, Maastricht, The Netherlands – name: 5 Faculty of Applied Medical Sciences, Department of Diagnostic Radiology, Jazan University, Jazan, Saudi Arabia – name: 3 Division of Nuclear Medicine and Oncological Imaging, Department of Medical Physics, University Hospital of Liège and GIGA CRC-in vivo imaging, University of Liège, Liege, Belgium – name: 7 Department of Radiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States of America – name: Washington University in St. Louis, UNITED STATES – name: 4 Department of Nuclear Medicine and Comprehensive Diagnostic Centre Aachen (CDCA), University Hospital RWTH Aachen University, Aachen, Germany – name: 6 Oncoradiomics SA, Liege, Belgium |
Author_xml | – sequence: 1 givenname: Abdalla orcidid: 0000-0003-4138-5755 surname: Ibrahim fullname: Ibrahim, Abdalla – sequence: 2 givenname: Turkey surname: Refaee fullname: Refaee, Turkey – sequence: 3 givenname: Ralph T. H. surname: Leijenaar fullname: Leijenaar, Ralph T. H. – sequence: 4 givenname: Sergey surname: Primakov fullname: Primakov, Sergey – sequence: 5 givenname: Roland surname: Hustinx fullname: Hustinx, Roland – sequence: 6 givenname: Felix M. surname: Mottaghy fullname: Mottaghy, Felix M. – sequence: 7 givenname: Henry C. surname: Woodruff fullname: Woodruff, Henry C. – sequence: 8 givenname: Andrew D. A. surname: Maidment fullname: Maidment, Andrew D. A. – sequence: 9 givenname: Philippe surname: Lambin fullname: Lambin, Philippe |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/33961646$$D View this record in MEDLINE/PubMed |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 scopus-id:2-s2.0-85105526896 Competing Interests: Dr. Philippe Lambin reports, within and outside the submitted work, grants/sponsored research agreements from Varian medical, Oncoradiomics, ptTheragnostic and Health Innovation Ventures. He received an advisor/presenter fee and/or reimbursement of travel costs/external grant writing fee and/or in kind manpower contribution from Oncoradiomics, BHV, Merck, Varian, Elekta and Convert pharmaceuticals. Dr. Lambin has (minority) shares in the company Oncoradiomics, MedC2, LivingMed Biotech and Convert pharmaceuticals and is co-inventor of two issued patents with royalties on radiomics (PCT/NL2014/050248, PCT/NL2014/050728) licensed to Oncoradiomics and one issue patent on mtDNA (PCT/EP2014/059089) licensed to ptTheragnostic/DNAmito, three nonpatentable invention (softwares) licensed to ptTheragnostic/DNAmito, Oncoradiomics and Health Innovation Ventures. Dr. Woodruff, and Dr. Leijenaar have (minority) shares in the company Oncoradiomics. Dr. Mottaghy received an advisor fee and reimbursement of travel costs from Oncoradiomics. He reports institutional grants from GE and Nanomab outside the submitted work. The rest of authors declare no competing interest. This does not alter our adherence to PLOS ONE policies on sharing data and materials. |
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Title | The application of a workflow integrating the variable reproducibility and harmonizability of radiomic features on a phantom dataset |
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