Preview

Medical Visualization

Advanced search

Potential to use textural features extracted from CT images to predict the grade of clear cell renal cell cancer

https://doi.org/10.24835/1607-0763-1645

Abstract

In order to select the most appropriate and effective treatment tactics for patients with clear cell renal cancer (ccRC), a multi-phase computed tomography (CT) with intravenous contrast is performed during the preoperative stage. It is possible that textural analysis data obtained from segmentation of CT data can be used to predict the likelihood of high-grade ccRC, which could potentially adjust treatment tactics.

Purpose: to perform a textural analysis of the preoperative multiphase CT data in patients with verified ссRC, to identify texture features that allow predicting ccRC grade

Material and methods: Retrospective analysis of data from 189 pre-operative CT studies was performed on 164 patients who underwent renal resection or nephrectomy, and the ccRC was morphologicaly verified using the WHO/ISUP grade classification system. CcRC grade 1–2 was verified in 130 cases, ccRC grade 3–4 was verified in 59 cases. For the performance of textural analysis, data from the corticomedullar, nephrographic and excretory CT phases were used, segmentation was carried out with 2D and 3D methods. The study was conducted retrospectively.

Results. The most informative in ccRC grade predicting were the textural features obtained from 3D tumor segmentation in the corticomedullar and excretory CT phases.

The largest number of textural features linearly associated with the ccRC grade 3–4 odds logarithm was obtained from a textural analysis of 3D tumor segmentation data in the corticomedullar and nephrographic CT phases.

The smallest number of textural features statistically significantly associated with the ccRC grade was obtained from a textural analysis of 2D segmentation data in the excretory phase of CT.

In conducting a multi-factor analysis of texture features as predictors of the ccRC grade, the most effective way to obtain texture features was to analyze the results of 3D segmentation into the excretory phase using the first 6 main components as predictors, explaining the 80% and more dispersion of the values of textural features.

The highest values of Nagelkerke pseudo-R2 (0.49) and AUC (0.87) were found in a multi-factor logistic regression model, which included SHAPE_Sphericity and SHAPE_Compacity as precursors to 3D segmentation in the excretory phase when using the Reflect filter.

The model with one textural indicator included – DISCRETIZED_TLG – in 2D segmentation into the excretory phase using a Reflect filter was characterized by slightly lower Nagelkerke pseudo-R2 (0.44) and AUC (0.85).

Based on the data obtained, we have developed two multi-factor models for predicting the probability of a grade 3–4 ccRC, based on 3D and 2D methods of tumor segmentation in CT images. The model using 3D segmentation data was characterized by predictive accuracy, sensitivity and specificity of 80%, 79.7% and 80.2%, respectively. Discriminative characteristics of the model using 3D segmentation data have surpassed those of the model using 2D segmentation data.

Conclusion. In the course of our work, we proved that it is possible to use textural features obtained from the analysis of CT data with contrast enhancement to predict the ccRC grade and developed a high-precision diagnostic model for predicting ccRC grade.

About the Authors

N. A. Karelskaya
A.V. Vishnevsky National Medical Research Center of Surgery of the Ministry of Healthcare of the Russian Federation
Russian Federation

Natalya A. Karelskaya – Cand. of Sci. (Med.), senior researcher, Radiology Department, A.V. Vishnevsky National Medical Research Center of Surgery, Moscow
https://orcid.org/0000-0001-8723-8916
E-mail: karelskaya.n@yandex.ru



S. V. Khromova
A.V. Vishnevsky National Medical Research Center of Surgery of the Ministry of Healthcare of the Russian Federation
Russian Federation

Stanislava V. Khromova – Graduate Student, Radiology Department, A.V. Vishnevsky National Medical Research Center of Surgery, Moscow
https://orcid.org/0000-0002-8083-4843



I. S. Gruzdev
A.V. Vishnevsky National Medical Research Center of Surgery of the Ministry of Healthcare of the Russian Federation
Russian Federation

Ivan S. Gruzdev – Cand. of Sci. (Med.),  senior researcher, Radiology Department, A.V. Vishnevsky National Medical Research Center of Surgery, Moscow
https://orcid.org/0000-0003-0781-9898



E. V. Kondratyev
A.V. Vishnevsky National Medical Research Center of Surgery of the Ministry of Healthcare of the Russian Federation
Russian Federation

Evgeny V. Kondratyev – Cand. of Sci. (Med.), head of Radiology Department, A.V. Vishnevsky National Medical Research Center of Surgery, Moscow
https://orcid.org/0000-0001-7070-3391



References

1. Global Cancer Observatory: Cancer Today; WHO International Agency for Research on Cancer: Lyon, France, 2022; Available online: https://gco.iarc.fr/today (accessed on 2 March 2026).

2. Ferlay J., Colombet M., Soerjomataram I. et al. Cancer incidence and mortality patterns in Europe: Estimates for 40 countries and 25 major cancers in 2018. Eur. J. Cancer. 2018; 103: 356–387. https://doi.org/10.1016/j.ejca.2018.07.005

3. Vartolomei L., Cotruș A., Stanciu C. et al. Quality of Life and Psychological Distress among Patients with Small Renal Masses. J. Clin. Med. 2022; 11 (14): 3944. https://doi.org/10.3390/jcm11143944

4. Hollingsworth J.M., Miller D.C., Daignault S., Hollenbeck B.K. Rising incidence of small renal masses: a need to reassess treatment effect. J. Natl. Cancer Inst. 2006; 98 (18): 1331–1334. https://doi.org/10.1093/jnci/djj362

5. Coy H., Hsieh K., Wu W. et al. Deep learning and radiomics: the utility of Google TensorFlow™ Inception in classifying clear cell renal cell carcinoma and oncocytoma on multiphasic CT. Abdom. Radiol. (NY). 2019; 44 (6): 2009–2020. https://doi.org/10.1007/s00261-019-01929-0

6. Patel H.D., Johnson M.H., Pierorazio P.M. et al. Diagnostic Accuracy and Risks of Biopsy in the Diagnosis of a Renal Mass Suspicious for Localized Renal Cell Carcinoma: Systematic Review of the Literature. J. Urol. 2016; 195 (5): 1340–1347. https://doi.org/10.1016/j.juro.2015.11.029

7. Di Lascio G., Sciarra A., Del Giudice F. et al. Which factors can influence post-operative renal function preservation after nephron-sparing surgery for kidney cancer: a critical review. Cent. European J. Urol. 2022; 75 (1): 14–27. https://doi.org/10.5173/ceju.2021.0256

8. Sohlberg E.M., Metzner T.J., Leppert J.T. The Harms of Overdiagnosis and Overtreatment in Patients with Small Renal Masses: A Mini-review. Eur. Urol. Focus. 2019; 5(6):943–945. https://doi.org/10.1016/j.euf.2019.03.006

9. Hindman N., Ngo L., Genega E.M. et al. Angiomyolipoma with minimal fat: can it be differentiated from clear cell renal cell carcinoma by using standard MR techniques? Radiology. 2012; 265 (2): 468–477. https://doi.org/10.1148/radiol.12112087

10. Sevcenco S., Heinz-Peer G., Ponhold L. et al. Utility and limitations of 3-Tesla diffusion-weighted magnetic resonance imaging for differentiation of renal tumors. Eur. J. Radiol. 2014; 83 (6): 909–913. https://doi.org/10.1016/j.ejrad.2014.02.026

11. Roussel E., Capitanio U., Kutikov A. et al. Novel Imaging Methods for Renal Mass Characterization: A Collaborative Review. Eur. Urol. 2022; 81 (5): 476–488. https://doi.org/10.1016/j.eururo.2022.01.040

12. Ball M.W., Bezerra S.M., Gorin M.A. et al. Grade heterogeneity in small renal masses: potential implications for renal mass biopsy. J. Urol. 2015; 193 (1): 36–40. https://doi.org/10.1016/j.juro.2014.06.067

13. Marconi L., Dabestani S., Lam T.B. et al. Systematic Review and Meta-analysis of Diagnostic Accuracy of Percutaneous Renal Tumour Biopsy. Eur. Urol. 2016; 69 (4): 660–673. https://doi.org/10.1016/j.eururo.2016.04.027

14. Kumar V., Gu Y., Basu S. et al. Radiomics: the process and the challenges. Magn. Reson. Imaging. 2012; 30 (9): 1234–1248. https://doi.org/10.1016/j.mri.2012.06.010

15. Lambin P., Rios-Velazquez E., Leijenaar R. et al. Radiomics: extracting more information from medical images using advanced feature analysis. Eur. J. Cancer. 2012; 48 (4): 441–446. https://doi.org/10.1016/j.ejca.2011.11.036

16. Ursprung S., Beer L., Bruining A. et al. Radiomics of computed tomography and magnetic resonance imaging in renal cell carcinoma-a systematic review and meta-analysis. Eur. Radiol. 2020; 30 (6): 3558–3566. https://doi.org/10.1007/s00330-020-06666-3

17. Suarez-Ibarrola R., Basulto-Martinez M., Heinze A. et al. Radiomics Applications in Renal Tumor Assessment: A Comprehensive Review of the Literature. Cancers (Basel). 2020; 12 (6): 1387. https://doi.org/10.3390/cancers12061387

18. Campi R., Stewart G.D., Staehler M. et al. Novel Liquid Biomarkers and Innovative Imaging for Kidney Cancer Diagnosis: What Can Be Implemented in Our Practice Today? A Systematic Review of the Literature. Eur. Urol. Oncol. 2021; 4 (1): 22–41. https://doi.org/10.1016/j.euo.2020.12.011

19. Rallis K.S., Kleeman S.O., Grant M. et al. Radiomics for Renal Cell Carcinoma: Predicting Outcomes from Immunotherapy and Targeted Therapies-A Narrative Review. Eur. Urol. Focus. 2021; 7 (4): 717–721. https://doi.org/10.1016/j.euf.2021.04.024

20. Gritskevich A.A., P'yanikin S.S., Adyrkhaev Z.A. et al. Ex vivo kidney resection in pharmacological cold ischemia followed by orthotopic autotransplantation. Transplantologiya. 2016; 3: 27–36. (In Russian)

21. Moch H., Cubilla A.L., Humphrey P.A. et al. The 2016 WHO Classification of Tumours of the Urinary System and Male Genital Organs-Part A: Renal, Penile, and Testicular Tumours. Eur. Urol. 2016; 70 (1): 93–105. https://doi.org/10.1016/j.eururo.2016.02.029

22. Gruzdev I.S., Tikhonova V.S., Zamyatina K.A. et al. Computed tomography in prediction of hypervascular pancreatic neuroendocrine tumors grade: texture analysis and contrast enhancement features. Russian Electronic Journal of Radiology (REJR). 2021; 11 (4): 105–14. (In Russian)

23. Nioche C., Orlhac F., Boughdad S. et al. LIFEx: a freeware for radiomic feature calculation in multimodality imaging to accelerate advances in the characterization of tumor heterogeneity (RRID: SCR_025284). Cancer Research. 2018; 78 (16): 4786–4789. https://doi.org/10.1158/0008-5472.can-18-0125

24. Khromova S.V., Karmazanovsky G.G., Karelskaya N.A., Gruzdev I.S. The texture analysis of computed tomography studies in clear cell renal cell carcinoma: reproducibility of 2D and 3D segmentation. Almanakh klinicheskoy medicini = Almanac of Clinical Medicine. 2024; 52 (1): 25–34. (In Russian)

25. Wu K., Wu P., Yang K. et al. A comprehensive texture feature analysis framework of renal cell carcinoma: pathological, prognostic, and genomic evaluation based on CT images. Eur. Radiol. 2022; 32 (4): 2255–2265. https://doi.org/10.1007/s00330-021-08353-3

26. Yu W., Liang G., Zeng L. et al. Accuracy of CT texture analysis for differentiating low-grade and high-grade renal cell carcinoma: systematic review and meta-analysis. BMJ Open. 2021; 11 (12): e051470. https://doi.org/10.1136/bmjopen-2021-051470

27. Alhussaini A.J., Steele J.D., Jawli A., Nabi G. Radiomics Machine Learning Analysis of Clear Cell Renal Cell Carcinoma for Tumour Grade Prediction Based on Intra-Tumoural Sub-Region Heterogeneity. Cancers (Basel). 2024; 16 (8): 1454. https://doi.org/10.3390/cancers16081454


Review

For citations:


Karelskaya N.A., Khromova S.V., Gruzdev I.S., Kondratyev E.V. Potential to use textural features extracted from CT images to predict the grade of clear cell renal cell cancer. Medical Visualization. (In Russ.) https://doi.org/10.24835/1607-0763-1645

Views: 43

JATS XML


Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.


ISSN 1607-0763 (Print)
ISSN 2408-9516 (Online)