Su Hyun Lyu, Andrey Makeev, Dan Li, Andreu Badal, Andrew M Hernandez, John M Boone, Stephen J Glick
{"title":"评估乳腺CT微钙化检出率的混合模拟。","authors":"Su Hyun Lyu, Andrey Makeev, Dan Li, Andreu Badal, Andrew M Hernandez, John M Boone, Stephen J Glick","doi":"10.1117/1.JMI.12.S2.S22015","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>Virtual imaging trials (VITs) are of interest for regulatory evaluation because they enable faster and more cost-effective evaluation of new imaging technologies than patient clinical trials. Our purpose is to develop a hybrid VIT methodology for breast computed tomography (CT) applications and use it to investigate microcalcification detectability.</p><p><strong>Approach: </strong>Ray tracing was used to generate projection images of clusters of five microcalcifications which varied in diameter, chemical composition, and density. These simulated projection images were added to patient projection images acquired with the fourth-generation breast CT scanner from UC Davis (Doheny) and reconstructed using the Feldkamp filtered backprojection algorithm with varying apodization kernels. Volumes of interest and maximum intensity projections were extracted from the reconstructed volumes. Human observers (HOs) and deep learning model observers (DLMOs) were used to detect calcification clusters, and receiver operating characteristic curve analysis was used to analyze detection performance.</p><p><strong>Results: </strong>DLMO detected 0.18-mm type I calcifications with AUC = 0.80 and 0.21 mm calcifications with <math><mrow><mi>AUC</mi> <mo>=</mo> <mn>0.99</mn></mrow> </math> . HO performance was inferior to deep learning model observer performance, but both HO and DLMO detected 0.21-mm type I calcifications with <math><mrow><mi>AUC</mi> <mo>></mo> <mn>0.90</mn></mrow> </math> and 0.24-mm type I calcifications with near-perfect performance. Microcalcification clusters embedded in adipose tissue were more conspicuous than clusters embedded in fibroglandular tissue. There was superior detection performance for clusters located anteriorly within the breast compared with clusters located posteriorly within the breast.</p><p><strong>Conclusions: </strong>A hybrid approach for virtual imaging trials shows promise for the assessment of imaging systems across a broad range of parameters.</p>","PeriodicalId":47707,"journal":{"name":"Journal of Medical Imaging","volume":"12 Suppl 2","pages":"S22015"},"PeriodicalIF":1.7000,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12225739/pdf/","citationCount":"0","resultStr":"{\"title\":\"Hybrid simulation of breast CT for assessing microcalcification detectability.\",\"authors\":\"Su Hyun Lyu, Andrey Makeev, Dan Li, Andreu Badal, Andrew M Hernandez, John M Boone, Stephen J Glick\",\"doi\":\"10.1117/1.JMI.12.S2.S22015\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Purpose: </strong>Virtual imaging trials (VITs) are of interest for regulatory evaluation because they enable faster and more cost-effective evaluation of new imaging technologies than patient clinical trials. Our purpose is to develop a hybrid VIT methodology for breast computed tomography (CT) applications and use it to investigate microcalcification detectability.</p><p><strong>Approach: </strong>Ray tracing was used to generate projection images of clusters of five microcalcifications which varied in diameter, chemical composition, and density. These simulated projection images were added to patient projection images acquired with the fourth-generation breast CT scanner from UC Davis (Doheny) and reconstructed using the Feldkamp filtered backprojection algorithm with varying apodization kernels. Volumes of interest and maximum intensity projections were extracted from the reconstructed volumes. Human observers (HOs) and deep learning model observers (DLMOs) were used to detect calcification clusters, and receiver operating characteristic curve analysis was used to analyze detection performance.</p><p><strong>Results: </strong>DLMO detected 0.18-mm type I calcifications with AUC = 0.80 and 0.21 mm calcifications with <math><mrow><mi>AUC</mi> <mo>=</mo> <mn>0.99</mn></mrow> </math> . HO performance was inferior to deep learning model observer performance, but both HO and DLMO detected 0.21-mm type I calcifications with <math><mrow><mi>AUC</mi> <mo>></mo> <mn>0.90</mn></mrow> </math> and 0.24-mm type I calcifications with near-perfect performance. Microcalcification clusters embedded in adipose tissue were more conspicuous than clusters embedded in fibroglandular tissue. There was superior detection performance for clusters located anteriorly within the breast compared with clusters located posteriorly within the breast.</p><p><strong>Conclusions: </strong>A hybrid approach for virtual imaging trials shows promise for the assessment of imaging systems across a broad range of parameters.</p>\",\"PeriodicalId\":47707,\"journal\":{\"name\":\"Journal of Medical Imaging\",\"volume\":\"12 Suppl 2\",\"pages\":\"S22015\"},\"PeriodicalIF\":1.7000,\"publicationDate\":\"2025-11-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12225739/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Medical Imaging\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1117/1.JMI.12.S2.S22015\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/7/3 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q3\",\"JCRName\":\"RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Medical Imaging","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1117/1.JMI.12.S2.S22015","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/7/3 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING","Score":null,"Total":0}
Hybrid simulation of breast CT for assessing microcalcification detectability.
Purpose: Virtual imaging trials (VITs) are of interest for regulatory evaluation because they enable faster and more cost-effective evaluation of new imaging technologies than patient clinical trials. Our purpose is to develop a hybrid VIT methodology for breast computed tomography (CT) applications and use it to investigate microcalcification detectability.
Approach: Ray tracing was used to generate projection images of clusters of five microcalcifications which varied in diameter, chemical composition, and density. These simulated projection images were added to patient projection images acquired with the fourth-generation breast CT scanner from UC Davis (Doheny) and reconstructed using the Feldkamp filtered backprojection algorithm with varying apodization kernels. Volumes of interest and maximum intensity projections were extracted from the reconstructed volumes. Human observers (HOs) and deep learning model observers (DLMOs) were used to detect calcification clusters, and receiver operating characteristic curve analysis was used to analyze detection performance.
Results: DLMO detected 0.18-mm type I calcifications with AUC = 0.80 and 0.21 mm calcifications with . HO performance was inferior to deep learning model observer performance, but both HO and DLMO detected 0.21-mm type I calcifications with and 0.24-mm type I calcifications with near-perfect performance. Microcalcification clusters embedded in adipose tissue were more conspicuous than clusters embedded in fibroglandular tissue. There was superior detection performance for clusters located anteriorly within the breast compared with clusters located posteriorly within the breast.
Conclusions: A hybrid approach for virtual imaging trials shows promise for the assessment of imaging systems across a broad range of parameters.
期刊介绍:
JMI covers fundamental and translational research, as well as applications, focused on medical imaging, which continue to yield physical and biomedical advancements in the early detection, diagnostics, and therapy of disease as well as in the understanding of normal. The scope of JMI includes: Imaging physics, Tomographic reconstruction algorithms (such as those in CT and MRI), Image processing and deep learning, Computer-aided diagnosis and quantitative image analysis, Visualization and modeling, Picture archiving and communications systems (PACS), Image perception and observer performance, Technology assessment, Ultrasonic imaging, Image-guided procedures, Digital pathology, Biomedical applications of biomedical imaging. JMI allows for the peer-reviewed communication and archiving of scientific developments, translational and clinical applications, reviews, and recommendations for the field.