Classification of adrenocortical carcinoma, pheochromocytoma, and adrenal adenomas using contrast-enhanced computed tomography with machine learning and texture features: a cross-sectional study
- Authors: Manaev A.V.1,2, Tarbaeva N.V.1, Buryakina S.A.1, Kovalevich L.D.1, Khairieva A.V.1, Urusova L.S.1, Pachuashvili N.V.1, Mel'nichenko G.A.1, Mokrysheva N.G.1, Sinitsyn V.E.3,4
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Affiliations:
- Endocrinology Research Centre
- National Research Nuclear University “MEPhI”
- Lomonosov Moscow State University
- Research and Practical Clinical Center for Diagnostics and Telemedicine Technologies
- Issue: Vol 6, No 4 (2025)
- Pages: 541-557
- Section: Original Study Articles
- URL: https://ogarev-online.ru/DD/article/view/373795
- DOI: https://doi.org/10.17816/DD659812
- EDN: https://elibrary.ru/KHKZTQ
- ID: 373795
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Abstract
BACKGROUND: Differential diagnosis of adrenocortical carcinoma, pheochromocytoma, and adrenal adenomas based on contrast-enhanced computed tomography remains challenging because of substantial overlap in their radiologic characteristics. Existing classification approaches based on conventional morphological criteria demonstrate limited accuracy, which may result in misdiagnosis and inappropriate treatment strategies.
AIM: This study aimed to develop a machine learning model for multiclass classification of adrenal lesions (adenomas, adrenocortical carcinoma, and pheochromocytoma) using contrast-enhanced computed tomography data with texture features.
METHODS: This was a single-center, cross-sectional study with retrospective computed tomography data acquisition and prospective re-analysis of imaging results. Contrast-enhanced computed tomography images were processed using PyRadiomics to extract texture features for each computed tomography phase. Data standardization was performed to reduce the impact of variability in scanning parameters. LightGBM, XGBoost, and CatBoost gradient boosting models were trained using stratified five-fold cross-validation. Diagnostic performance was assessed using recall, precision, F1-score, macro-averaged F1-score, specificity, balanced accuracy, and area under the receiver operating characteristic curve (AUC) for each diagnostic category.
RESULTS: The study included data from 425 patients with histologically verified adrenal tumors: 42 cases of adrenocortical carcinoma, 204 pheochromocytomas, and 179 adrenal adenomas. The developed machine learning models demonstrated high classification performance by cross-validation for adrenal adenomas (F1-score up to 0.916 for the XGBoost model) and pheochromocytomas (F1-score up to 0.855 for the XGBoost model), but substantially lower performance for adrenocortical carcinoma (F1-score up to 0.521 for the CatBoost model). The highest AUC values reached 0.971 for adenomas (LightGBM), 0.924 for pheochromocytomas (LightGBM), and 0.879 for adrenocortical carcinoma (CatBoost). Balanced accuracy reached up to 0.773, and the macro-averaged F1-score reached 0.747 (CatBoost model). Analysis of the most informative features showed that parameters reflecting texture homogeneity and intensity across different contrast-enhancement phases were most relevant for classification.
CONCLUSION: Radiomics and machine learning methods provide high diagnostic accuracy for multiclass classification of adrenal lesions on contrast-enhanced computed tomography for adrenal adenomas and pheochromocytomas. However, diagnostic performance for adrenocortical carcinoma remains limited, which may be related to tumor heterogeneity and the relatively small number of cases.
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##article.viewOnOriginalSite##About the authors
Almaz V. Manaev
Endocrinology Research Centre; National Research Nuclear University “MEPhI”
Email: a.manaew2016@yandex.ru
ORCID iD: 0009-0003-8035-676X
SPIN-code: 2902-9767
Russian Federation, Moscow; Moscow
Natalia V. Tarbaeva
Endocrinology Research Centre
Email: ntarbaeva@inbox.ru
ORCID iD: 0000-0001-7965-9454
SPIN-code: 5808-8065
MD, Cand. Sci. (Medicine)
Russian Federation, MoscowSvetlana A. Buryakina
Endocrinology Research Centre
Email: sburyakina@yandex.ru
ORCID iD: 0000-0001-9065-7791
SPIN-code: 5675-0651
MD, Cand. Sci. (Medicine)
Russian Federation, MoscowLiliya D. Kovalevich
Endocrinology Research Centre
Email: liliyakovalevich@gmail.com
ORCID iD: 0000-0001-8958-8223
SPIN-code: 1642-5694
Russian Federation, Moscow
Angelina V. Khairieva
Endocrinology Research Centre
Email: komarito@mail.ru
ORCID iD: 0000-0002-6758-5918
SPIN-code: 4516-8297
Russian Federation, Moscow
Liliya S. Urusova
Endocrinology Research Centre
Email: liselivanova89@yandex.ru
ORCID iD: 0000-0001-6891-0009
SPIN-code: 5151-3675
MD, Dr. Sci. (Medicine)
Russian Federation, MoscowNano V. Pachuashvili
Endocrinology Research Centre
Email: npachuashvili@bk.ru
ORCID iD: 0000-0002-8136-0117
SPIN-code: 3477-8994
MD, Cand. Sci. (Medicine)
Russian Federation, MoscowGalina A. Mel'nichenko
Endocrinology Research Centre
Author for correspondence.
Email: Melnichenko.Galina@endocrincentr.ru
ORCID iD: 0000-0002-5634-7877
SPIN-code: 8615-0038
MD, Dr. Sci. (Medicine), Professor
Russian Federation, MoscowNatalia G. Mokrysheva
Endocrinology Research Centre
Email: mokrisheva.natalia@endocrincentr.ru
ORCID iD: 0000-0002-9717-9742
SPIN-code: 5624-3875
MD, Dr. Sci. (Medicine), Professor
Russian Federation, MoscowValentin E. Sinitsyn
Lomonosov Moscow State University; Research and Practical Clinical Center for Diagnostics and Telemedicine Technologies
Email: vsini@mail.ru
ORCID iD: 0000-0002-5649-2193
SPIN-code: 8449-6590
MD, Dr. Sci. (Medicine), Professor
Russian Federation, Moscow; MoscowReferences
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