Abstract 2777: Automatic contrast phase classification of polyphasic CT scans.

Abstract Contrast phases refer to the different stages of blood vessel, tissue, or organ enhancement following the administration of an intravenous contrast agent during CT scans. Contrast phases help distinguish abnormal lesions from normal tissue, where lesions appear hypo- or hyper-vascular, depending on the disease. Therefore, selecting the appropriate phase based on the specific pathology is crucial for accurate detection, meaningful diagnostic interpretation, clinical workflows, and robust quantitative analysis. However, in many polyphasic CT scans, information about phases is missing from the metadata. This study presents a fully automated pipeline to predict the contrast phase of CT scans, using organ-based image features. Our approach has the following novel contributions: (1) Focuses on a limited set of organs (aorta, portal vein, kidney), reducing reliance on extensive organ coverage. This is useful for scans with varying field-of-view where many organs may be absent. (2) Introduces engineered features derived from first-order PyRadiomic statistics, quantifying inter-organ relationships to capture phase-specific intensity patterns. Our pipeline distinguishes non-contrast scans and all three major contrast phases: arterial, portal venous, delayed. Automated segmentation of the aorta, portal vein/splenic vein, and kidneys is performed using TotalSegmentator, a state-of-the-art deep learning algorithm for CT scan segmentation. For each organ mask, a comprehensive set of first-order statistical features, including mean, median, minimum, maximum, standard deviation, skewness, kurtosis, energy, and entropy, is extracted with PyRadiomics to capture intensity distributions. Engineered features reflecting the mean and maximum intensity differences between organs are created, along with the total mean intensity of all three organs, to better distinguish phases. The model was trained and validated on the TOPAZ-1 phase 3 biliary tract cancer trial dataset. TOPAZ-1 comprised of 1418 CT baseline scans (447 portal venous, 396 arterial, 323 non-contrast, 252 delayed) annotated by a radiologist with eight years of experience. For classification, a random forest classifier was developed. Classification achieved an overall accuracy of 0.97, with weighted average precision, recall, and f1-score all at 0.97. Per-phase precision, recall and f1-score all exceed 0.93. On analysis, the engineered features indicate the arterial phase is characterized by a brighter aorta, the venous phase by a brighter portal vein, the delayed phase by increased renal intensity, and non-contrast scans by lower overall intensity relative to the other scans. These patterns align with radiologist expectations and support the model's interpretability. By focusing on organs and features that are most indicative of phase differences, the pipeline yields a simple and interpretable model that achieves accurate polyphasic CT phase identification. Citation Format: Georgia Hughes, Mayank Patwari, Yi Wei, Michael Parker, James Parkin, Zhenning Zhang, Aleksandr Filippov. Automatic contrast phase classification of polyphasic CT scans [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 2777.

Authors

Institutions

Publication Details

Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-2777
Primary Topic
Radiomics and Machine Learning in Medical Imaging
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Abstract 2777: Automatic contrast phase classification of polyphasic CT scans.

Aleksandr Filippov, Georgia K. Hughes, Michael Parker, Mayank Patwari et al.
Cancer Research
Radiomics and Machine Learning in Medical Imaging
article

Abstract 2777: Automatic contrast phase classification of polyphasic CT scans.

Aleksandr Filippov, Georgia K. Hughes, Michael Parker, Mayank Patwari, James Parkin, Yi Wei, Zhenning Zhang
article en

Abstract

Abstract Contrast phases refer to the different stages of blood vessel, tissue, or organ enhancement following the administration of an intravenous contrast agent during CT scans. Contrast phases help distinguish abnormal lesions from normal tissue, where lesions appear hypo- or hyper-vascular, depending on the disease. Therefore, selecting the appropriate phase based on the specific pathology is crucial for accurate detection, meaningful diagnostic interpretation, clinical workflows, and robust quantitative analysis. However, in many polyphasic CT scans, information about phases is missing from the metadata. This study presents a fully automated pipeline to predict the contrast phase of CT scans, using organ-based image features. Our approach has the following novel contributions: (1) Focuses on a limited set of organs (aorta, portal vein, kidney), reducing reliance on extensive organ coverage. This is useful for scans with varying field-of-view where many organs may be absent. (2) Introduces engineered features derived from first-order PyRadiomic statistics, quantifying inter-organ relationships to capture phase-specific intensity patterns. Our pipeline distinguishes non-contrast scans and all three major contrast phases: arterial, portal venous, delayed. Automated segmentation of the aorta, portal vein/splenic vein, and kidneys is performed using TotalSegmentator, a state-of-the-art deep learning algorithm for CT scan segmentation. For each organ mask, a comprehensive set of first-order statistical features, including mean, median, minimum, maximum, standard deviation, skewness, kurtosis, energy, and entropy, is extracted with PyRadiomics to capture intensity distributions. Engineered features reflecting the mean and maximum intensity differences between organs are created, along with the total mean intensity of all three organs, to better distinguish phases. The model was trained and validated on the TOPAZ-1 phase 3 biliary tract cancer trial dataset. TOPAZ-1 comprised of 1418 CT baseline scans (447 portal venous, 396 arterial, 323 non-contrast, 252 delayed) annotated by a radiologist with eight years of experience. For classification, a random forest classifier was developed. Classification achieved an overall accuracy of 0.97, with weighted average precision, recall, and f1-score all at 0.97. Per-phase precision, recall and f1-score all exceed 0.93. On analysis, the engineered features indicate the arterial phase is characterized by a brighter aorta, the venous phase by a brighter portal vein, the delayed phase by increased renal intensity, and non-contrast scans by lower overall intensity relative to the other scans. These patterns align with radiologist expectations and support the model's interpretability. By focusing on organs and features that are most indicative of phase differences, the pipeline yields a simple and interpretable model that achieves accurate polyphasic CT phase identification. Citation Format: Georgia Hughes, Mayank Patwari, Yi Wei, Michael Parker, James Parkin, Zhenning Zhang, Aleksandr Filippov. Automatic contrast phase classification of polyphasic CT scans [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 2777.

Cancer ResearchVol. 86(7_Supplement)
Norfolk and Norwich University Hospital (GB), Abzena (United Kingdom) (GB), AstraZeneca (Japan) (JP)
Life in Land
Openalex Percentile: Top 4%
Radiomics and Machine Learning in Medical Imaging
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.