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Texture and CT-features in differentiation of hypervascular pancreatic neuroendocrine tumors from renal cell carcinoma metastases: diagnostic model

https://doi.org/10.24835/1607-0763-1247

Abstract

Objective: to develop a diagnostic model that includes CT and radiomic features for the differential diagnosis of pancreatic neuroendocrine tumors (PNETs) G1 and G2 and pancreatic renal cell carcinoma (RCC) metastases.

Material and Methods. 78 patients with 79 hypervascular PNETs and 17 patients with 24 pancreatic RCC metastases who underwent pancreatic resection and histological verification were selected in the study. All the patients underwent preoperative contrast enhanced CT (CECT). We assessed tumor attenuation, composition (cystic/solid), homogeneity (homogeneous/heterogeneous), calcification and presence of the main pancreatic duct (MPD) dilation. We calculated lesion-to-parenchyma contrast (LPC), relative tumor enhancement ratio (RTE) and extracted 52 texture features for arterial phase of CECT. Qualitative and texture features were compared between PNETs and pancreatic RCC metastasis. The selection of predictors for the logistic model was carried out in 2 successive stages: 1) selection of predictors based on one-factor logistic models, the selection criterion was p < 0.2; 2) selection of predictors using L2 regularization (LASSO regression after standardization of independent variables). The selected predictors were included in a logistic regression model without interactions, the coefficients of which were estimated using the maximum likelihood method with a penalty of 0.8.

Results. There was no difference in composition, homogeneity (homogeneous/heterogeneous) and presence of the MPD dilation between groups. We did not find calcification in pancreatic RCC metastasis, in contrast to the PNETs (9% contained calcifications). After selection, the LCR, CONVENTIONAL_HUmin, GLCM_Correlation, NGLDM_Coarseness were included in the final diagnostic model, which showed a sensitivity and specificity of 95.8%; 62% in the prediction of pancreatic RCC metastases.

Conclusion. The diagnostic model developed on the basis of texture and CT-features has high sensitivity (95.8%) with moderate specificity (62%), which allows it to be used in complex diagnostic cases to determine the patient's treatment tactics.

About the Authors

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 – postgraduate student, Radiology department

27, Bol'shaya Serpukhovskaia str., Moscow, 117997



G. G. Karmazanovsky
A.V. Vishnevsky National Medical Research Center of Surgery of the Ministry of Healthcare of the Russian Federation
Russian Federation

Grigory G. Kаrmаnovsky – Academician of the Russiаn Асаdemy of Sсienсes, doсt. of med. sсi., Professor of radiology department, Radiology department

27, Bol'shaya Serpukhovskaia str., Moscow, 117997



M. G. Lapteva
N.N. Blokhin National Medical Research Center of Oncology of the Ministry of Healthcare of the Russian Federation
Russian Federation

Mariya G. Lapteva – PhD, radiologist, Radiology Department

23, Kashirskoe shosse, Moscow, 115478



K. A. Zamyatina
A.V. Vishnevsky National Medical Research Center of Surgery of the Ministry of Healthcare of the Russian Federation
Russian Federation

Kseniia A. Zamiatina – postgraduate student, Radiology Department

27, Bol'shaya Serpukhovskaia str., Moscow, 117997



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

Valeriya S. Tikhonova – postgraduate student, Radiology Department

27, Bol'shaya Serpukhovskaia str., Moscow, 117997



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 – PhD, senior researcher, Radiology Department

27, Bol'shaya Serpukhovskaia str., Moscow, 117997



V. Yu. Struchkov
A.V. Vishnevsky National Medical Research Center of Surgery of the Ministry of Healthcare of the Russian Federation
Russian Federation

Vladimir Yu. Struchkov – PhD, junior researcher, Abdominal Surgery Department

27, Bol'shaya Serpukhovskaia str., Moscow, 117997



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

Andrey V. Glotov – PhD, pathologist, Pathological Department

27, Bol'shaya Serpukhovskaia str., Moscow, 117997



I. S. Proskuryakov
N.N. Blokhin National Medical Research Center of Oncology of the Ministry of Healthcare of the Russian Federation
Russian Federation

Ilya S. Proskuryakov – PhD, oncologist, Department of Interventional Radiology

23, Kashirskoe shosse, Moscow, 115478



D. V. Podluzhny
N.N. Blokhin National Medical Research Center of Oncology of the Ministry of Healthcare of the Russian Federation
Russian Federation

Danil V. Podluzhnyi – PhD, Head of the Oncology Department of Surgical Treatment Methods (Hepato-pancreatobiliary Tumors)

23, Kashirskoe shosse, Moscow, 115478



A. Sh. Revishvili
A.V. Vishnevsky National Medical Research Center of Surgery of the Ministry of Healthcare of the Russian Federation
Russian Federation

Amiran Sh. Revishvili – Academician of the Russiаn Асаdemy of Sсienсes, Doсt. of Sсi. (Med.), Professor, Director

27, Bol'shaya Serpukhovskaia str., Moscow, 117997



References

1. Ouzaid I., Capitanio U., Staehler M. et al. Surgical Metastasectomy in Renal Cell Carcinoma: A Systematic Review. Eur. Urol. Oncol. 2019; 2 (2): 141–149. https://doi.org/10.1016/J.EUO.2018.08.028

2. Padala S.A., Barsouk A., Thandra K.C. et al. Epidemiology of Renal Cell Carcinoma. Wld J. Oncol. 2020; 11 (3): 79–87. https://doi.org/10.14740/WJON1279

3. Shah M.H., Goldner W.S., Benson A.B. et al. Neuroendocrine and Adrenal Tumors, Version 2.2021, NCCN Clinical Practice Guidelines in Oncology. J. Natl. Compr. Canc. Netw. 2021; 19 (7): 839–867. https://doi.org/10.6004/JNCCN.2021.0032

4. Campbell S.C., Uzzo R.G., Karam J.A. et al. Renal Mass and Localized Renal Cancer: Evaluation, Management, and Follow-up: AUA Guideline: Part II. J. Urol. 2021; 206 (2): 209–218. https://doi.org/10.1097/JU.0000000000001912

5. Almeida R.R., Lo G.C., Patino M. et al. Advances in Pancreatic CT Imaging. Am. J. Roentgenol. 2018; 211 (1): 52–66. https://doi.org/10.2214/AJR.17.18665

6. Lee N.J., Hruban R.H., Fishman E.K. Pancreatic neuroendocrine tumor: review of heterogeneous spectrum of CT appearance. Abdom. Radiol. 2018; 43 (11): 3025–3034. https://doi.org/10.1007/s00261-018-1574-4

7. Sellner F. Observations on Solitary Versus Multiple Isolated Pancreatic Metastases of Renal Cell Carcinoma: Another Indication of a Seed and Soil Mechanism? Cancers. 2019; 11 (9): 1379. https://doi.org/10.3390/CANCERS11091379

8. Nogueira M., Dias S.C., Silva A.C. et al. Solitary pancreatic renal cell carcinoma metastasis. Autopsy. Case Reports. 2018; 8 (2): e2018023. https://doi.org/10.4322/ACR.2018.023

9. Akirov A., Larouche V., Alshehri S. et al. Treatment Options for Pancreatic Neuroendocrine Tumors. Cancers. 2019; 11 (6): 828. https://doi.org/10.3390/CANCERS11060828

10. Barthet M., Giovannini M., Lesavre N. et al. Endoscopic ultrasound-guided radiofrequency ablation for pancreatic neuroendocrine tumors and pancreatic cystic neoplasms: A prospective multicenter study. Endoscopy. 2019; 51 (9): 836–842. https://doi.org/10.1055/A-0824-7067/ID/JR17031-18

11. Fazio N., Kulke M., Rosbrook B. et al. Updated Efficacy and Safety Outcomes for Patients with Well-Differentiated Pancreatic Neuroendocrine Tumors Treated with Sunitinib. Target. Oncol. 2021; 16 (1): 27–35. https://doi.org/10.1007/S11523-020-00784-0/FIGURES/4

12. Quhal F., Mori K., Bruchbacher A. et al. First-line Immunotherapy-based Combinations for Metastatic Renal Cell Carcinoma: A Systematic Review and Network Meta-analysis. Eur. Urol. Oncol. 2021; 4 (5): 755–765. https://doi.org/10.1016/J.EUO.2021.03.001

13. Powles T., Albiges L., Bex A. et al. ESMO Clinical Practice Guideline update on the use of immunotherapy in early stage and advanced renal cell carcinoma. Ann. Oncol. 2021; 32 (12): 1511–1519. https://doi.org/10.1016/J.ANNONC.2021.09.014

14. Gu D., Hu Y., Ding H. et al. CT radiomics may predict the grade of pancreatic neuroendocrine tumors: a multicenter study. Eur. Radiol. 2019; 29 (12): 6880–6890. https://doi.org/10.1007/s00330-019-06176-x

15. Lin X., Xu L., Wu A. et al. Differentiation of intrapancreatic accessory spleen from small hypervascular neuroendocrine tumor of the pancreas: textural analysis on contrast-enhanced computed tomography. Acta Radiol. 60 (2019) 553–560. https://doi.org/10.1177/0284185118788895

16. Karmazanovsky G., Gruzdev I., Tikhonova V. et al. Computed tomography-based radiomics approach in pancreatic tumors characterization. Radiol. Medica. 2021; 126: 1388–1395. https://doi.org/10.1007/S11547-021-01405-0/FIGURES/1

17. van der Pol C.B., Lee S., Tsai S. et al. Differentiation of pancreatic neuroendocrine tumors from pancreas renal cell carcinoma metastases on CT using qualitative and quantitative features. Abdom. Radiol. 2019; 44(3): 992–999. https://doi.org/10.1007/s00261-018-01889-x

18. 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. Cancer Res. 2018; 78 (16): 4786–4789. https://doi.org/10.1158/0008-5472.CAN-18-0125

19. Gruzdev I.S., Zamyatina K.A., Tikhonova V.S. et al. Reproducibility of CT texture features of pancreatic neuroendocrine neoplasms. Eur. J. Radiol. 2020; 133: 109371. https://doi.org/10.1016/j.ejrad.2020.109371

20. Kang T.W., Kim S.H., Lee J. et al. Differentiation between pancreatic metastases from renal cell carcinoma and hypervascular neuroendocrine tumour: Use of relative percentage washout value and its clinical implication. Eur. J. Radiol. 2015; 84 (11): 2089–2096. https://doi.org/10.1016/J.EJRAD.2015.08.007

21. Lyu H.-L., Cao J.-X., Wang H.-Y. et al. Differentiation between pancreatic metastases from clear cell renal cell carcinoma and pancreatic neuroendocrine tumor using double-echo chemical shift imaging. Abdom. Radiol. 2018; 43 (10): 2712–2720. https://doi.org/10.1007/s00261-018-1539-7

22. Ambrosetti M.C., Zamboni G.A., Fighera A., Mansueto G. Pancreatic metastases from renal neoplasms and neuroendocrine pancreatic tumours: is a differential diagnosis possible with CT? Hell. J. of Radiol. 2019; 4 (3). 17–21. https://doi.org/10.36162/HJR.V4I3.295


Review

For citations:


Gruzdev I.S., Karmazanovsky G.G., Lapteva M.G., Zamyatina K.A., Tikhonova V.S., Kondratyev E.V., Struchkov V.Yu., Glotov A.V., Proskuryakov I.S., Podluzhny D.V., Revishvili A.Sh. Texture and CT-features in differentiation of hypervascular pancreatic neuroendocrine tumors from renal cell carcinoma metastases: diagnostic model. Medical Visualization. 2022;26(4):102-109. https://doi.org/10.24835/1607-0763-1247

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