Skip to main content

Advertisement

Log in

Two nomograms based on radiomics models using triphasic CT for differentiation of adrenal lipid-poor benign lesions and metastases in a cancer population: an exploratory study

  • Imaging Informatics and Artificial Intelligence
  • Published:
European Radiology Aims and scope Submit manuscript

Abstract

Objectives

To investigate the effectiveness of CT-based radiomics nomograms in differentiating adrenal lipid-poor benign lesions and metastases in a cancer population.

Methods

This retrospective study enrolled 178 patients with cancer history from three medical centres categorised as those with adrenal lipid-poor benign lesions or metastases. Patients were divided into training, validation, and external testing cohorts. Radiomics features were extracted from triphasic CT images (unenhanced, arterial, and venous) to establish three single-phase models and one triphasic radiomics model using logistic regression. Unenhanced and triphasic nomograms were established by incorporating significant clinico-radiological factors and radscores. The models were evaluated by the receiver operating characteristic curve, Delong’s test, calibration curve, and decision curve.

Results

Lesion side, diameter, and enhancement ratio resulted as independent factors and were selected into nomograms. The areas under the curves (AUCs) of unenhanced and triphasic radiomics models in validation (0.878, 0.914, p = 0.381) and external testing cohorts (0.900, 0.893, p = 0.882) were similar and higher than arterial and venous models (validation: 0.842, 0.765; testing: 0.814, 0.806). Unenhanced and triphasic nomograms yielded similar AUCs in validation (0.903, 0.906, p = 0.955) and testing cohorts (0.928, 0.946, p = 0.528). The calibration curves showed good agreement and decision curves indicated satisfactory clinical benefits.

Conclusion

Unenhanced and triphasic CT-based radiomics nomograms resulted as a useful tool to differentiate adrenal lipid-poor benign lesions from metastases in a cancer population. They exhibited similar predictive efficacies, indicating that enhanced examinations could be avoided in special populations.

Key Points

• All four radiomics models and two nomograms using triphasic CT images exhibited favourable performances in three cohorts to characterise the cancer population’s adrenal benign lesions and metastases.

• Unenhanced and triphasic radiomics models had similar predictive performances, outperforming arterial and venous models.

• Unenhanced and triphasic nomograms also exhibited similar efficacies and good clinical benefits, indicating that contrast-enhanced examinations could be avoided when identifying adrenal benign lesions and metastases.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6

Similar content being viewed by others

Abbreviations

APW:

Absolute percentage wash-out

AUC :

Area under the curve

ER:

Enhancement ratio

FNAB:

Fine needle aspiration biopsy

ICC:

Inter correlation coefficient

LASSO:

Least Absolute Shrinkage and Selection Operator

PWI:

Percentage wash-in

ROC:

Receiver operating characteristic curve

ROI:

Region of interest

RPW:

Relative percentage wash-out

RQS:

Radiomics quality score

References

  1. Lam KY, Lo CY (2002) Metastatic tumours of the adrenal glands: a 30-year experience in a teaching hospital. Clin Endocrinol (Oxf) 56:95–101

    Article  PubMed  Google Scholar 

  2. Fassnacht M, Arlt W, Bancos I et al (2016) Management of adrenal incidentalomas: European Society of Endocrinology Clinical Practice Guideline in collaboration with the European Network for the Study of Adrenal Tumors. Eur J Endocrinol 175:G1–G34

    Article  CAS  PubMed  Google Scholar 

  3. Spartalis E, Drikos I, Ioannidis A et al (2019) Metastatic carcinomas of the adrenal glands: from diagnosis to treatment. Anticancer Res 39:2699–2710

    Article  CAS  PubMed  Google Scholar 

  4. Albano D, Agnello F, Midiri F et al (2019) Imaging features of adrenal masses. Insights Imaging 10:1

    Article  PubMed  PubMed Central  Google Scholar 

  5. Remer EM, Obuchowski N, Ellis JD, Rice TW, Adelstein DJ, Baker ME (2000) Adrenal mass evaluation in patients with lung carcinoma: a cost-effectiveness analysis. AJR Am J Roentgenol 174:1033–1039

    Article  CAS  PubMed  Google Scholar 

  6. Elsayes KM, Emad-Eldin S, Morani AC, Jensen CT (2018) Practical approach to adrenal imaging. Urol Clin North Am 45:365–387

    Article  PubMed  Google Scholar 

  7. Caoili EM, Korobkin M, Francis IR, Cohan RH, Dunnick NR (2000) Delayed enhanced CT of lipid-poor adrenal adenomas. AJR Am J Roentgenol 175:1411–1415

    Article  CAS  PubMed  Google Scholar 

  8. Mayo-Smith WW, Song JH, Boland GL et al (2017) Management of incidental adrenal masses: a white paper of the ACR Incidental Findings Committee. J Am Coll Radiol 14:1038–1044

    Article  PubMed  Google Scholar 

  9. Mayo-Smith WW, Boland GW, Noto RB, Lee MJ (2001) State-of-the-art adrenal imaging. Radiographics 21:995–1012

    Article  CAS  PubMed  Google Scholar 

  10. Koo HJ, Choi HJ, Kim HJ, Kim SO, Cho KS (2014) The value of 15-minute delayed contrast-enhanced CT to differentiate hyperattenuating adrenal masses compared with chemical shift MR imaging. Eur Radiol 24:1410–1420

    Article  PubMed  Google Scholar 

  11. Platzek I, Sieron D, Plodeck V, Borkowetz A, Laniado M, Hoffmann RT (2019) Chemical shift imaging for evaluation of adrenal masses: a systematic review and meta-analysis. Eur Radiol 29:806–817

    Article  PubMed  Google Scholar 

  12. Boland GW, Dwamena BA, Jagtiani Sangwaiya M et al (2011) Characterization of adrenal masses by using FDG PET: a systematic review and meta-analysis of diagnostic test performance. Radiology. https://doi.org/10.1148/radiol.11100569/

  13. Porte HL, Ernst OJ, Delebecq T, Métois D, Lemaitre LG, Wurtz AJ (1999) Is computed tomography guided biopsy still necessary for the diagnosis of adrenal masses in patients with resectable non-small-cell lung cancer? Eur J Cardiothorac Surg 15:597–601

    Article  CAS  PubMed  Google Scholar 

  14. Pagani JJ (1984) Non-small cell lung carcinoma adrenal metastases computed tomography and percutaneous needle biopsy in their diagnosis. Cancer 53:1058–1060

    Article  CAS  PubMed  Google Scholar 

  15. Lambin P, Leijenaar RTH, Deist TM et al (2017) Radiomics: the bridge between medical imaging and personalized medicine. Nat Rev Clin Oncol 14:749–762

    Article  PubMed  Google Scholar 

  16. Limkin EJ, Sun R, Dercle L et al (2017) Promises and challenges for the implementation of computational medical imaging (radiomics) in oncology. Ann Oncol 28:1191–1206

    Article  CAS  PubMed  Google Scholar 

  17. Ji GW, Zhang YD, Zhang H et al (2019) Biliary tract cancer at CT: a radiomics-based model to predict lymph node metastasis and survival outcomes. Radiology 290:90–98

    Article  PubMed  Google Scholar 

  18. Kang B, Sun C, Gu H et al (2020) T1 stage clear cell renal cell carcinoma: A CT-based radiomics nomogram to estimate the risk of recurrence and metastasis. Front Oncol 10:579619

    Article  PubMed  PubMed Central  Google Scholar 

  19. Chong H, Gong Y, Pan X et al (2021) Peritumoral dilation radiomics of gadoxetate disodium-enhanced MRI excellently predicts early recurrence of hepatocellular carcinoma without macrovascular invasion after hepatectomy. J Hepatocell Carcinoma 8:545–563

    Article  PubMed  PubMed Central  Google Scholar 

  20. Wu W, Parmar C, Grossmann P et al (2016) Exploratory study to identify radiomics classifiers for lung cancer histology. Front Oncol 6:71

    Article  PubMed  PubMed Central  Google Scholar 

  21. Stanzione A, Galatola R, Cuocolo R, Romeo V, Verde F, Mainenti PP, Brunetti A, Maurea S (2022) Radiomics in cross-sectional adrenal imaging: a systematic review and quality assessment study. Diagnostics (Basel) 12(3):578. https://doi.org/10.3390/diagnostics12030578

  22. Shoemaker K, Hobbs BP, Bharath K, Ng CS, Baladandayuthapani V (2018) Tree-based methods for characterising tumor density heterogeneity. Pac Symp Biocomput 23:216–227

    PubMed  PubMed Central  Google Scholar 

  23. Elmohr MM, Fuentes D, Habra MA et al (2019) Machine learning-based texture analysis for differentiation of large adrenal cortical tumours on CT. Clin Radiol 74:818 e811–818 e817

    Article  Google Scholar 

  24. Shi B, Zhang GM, Xu M, Jin ZY, Sun H (2019) Distinguishing metastases from benign adrenal masses: what can CT texture analysis do? Acta Radiol 60:1553–1561

    Article  PubMed  Google Scholar 

  25. Lee HY, Oh YL, Park SY (2021) Hyperattenuating adrenal lesions in lung cancer: biphasic CT with unenhanced and 1-min enhanced images reliably predicts benign lesions. Eur Radiol 31:5948–5958

    Article  CAS  PubMed  Google Scholar 

  26. Koo TK, Li MY (2016) A guideline of selecting and reporting intraclass correlation coefficients for reliability research. J Chiropr Med 15:155–163

    Article  PubMed  PubMed Central  Google Scholar 

  27. Mazzella A, Loi M, Mansuet-Lupo A et al (2019) Clinical characteristics, molecular phenotyping, and management of isolated adrenal metastases from lung cancer. Clin Lung Cancer 20:405–411

    Article  PubMed  Google Scholar 

  28. Moreno P, de la Quintana BA, Musholt TJ et al (2013) Adrenalectomy for solid tumor metastases: results of a multicenter European study. Surgery 154:1215–1222 discussion 1222-1213

    Article  PubMed  Google Scholar 

  29. Andersen MB, Bodtger U, Andersen IR, Thorup KS, Ganeshan B, Rasmussen F (2021) Metastases or benign adrenal lesions in patients with histopathological verification of lung cancer: Can CT texture analysis distinguish? Eur J Radiol 138:109664

    Article  PubMed  Google Scholar 

  30. Moawad AW, Ahmed A, Fuentes DT, Hazle JD, Habra MA, Elsayes KM (2021) Machine learning-based texture analysis for differentiation of radiologically indeterminate small adrenal tumors on adrenal protocol CT scans. Abdom Radiol (NY) 46:4853–4863

    Article  PubMed  Google Scholar 

  31. Ho LM, Samei E, Mazurowski MA et al (2019) Can texture analysis be used to distinguish benign from malignant adrenal nodules on unenhanced CT, contrast-enhanced CT, or In-phase and opposed-phase MRI? AJR Am J Roentgenol 212:554–561

    Article  PubMed  Google Scholar 

  32. Nagayama Y, Inoue T, Oda S et al (2020) Adrenal adenomas versus metastases: diagnostic performance of dual-energy spectral CT virtual noncontrast imaging and iodine maps. Radiology 296:324–332

    Article  PubMed  Google Scholar 

  33. Seo JM, Park BK, Park SY, Kim CK (2014) Characterization of lipid-poor adrenal adenoma: chemical-shift MRI and washout CT. AJR Am J Roentgenol 202:1043–1050

    Article  PubMed  Google Scholar 

  34. Marty M, Gaye D, Perez P et al (2018) Diagnostic accuracy of computed tomography to identify adenomas among adrenal incidentalomas in an endocrinological population. Eur J Endocrinol 178:439–446

    Article  CAS  PubMed  Google Scholar 

  35. Sasaguri K, Takahashi N, Takeuchi M, Carter RE, Leibovich BC, Kawashima A (2016) Differentiation of benign from metastatic adrenal masses in patients with renal cell carcinoma on contrast-enhanced CT. AJR Am J Roentgenol 207:1031–1038

    Article  PubMed  Google Scholar 

Download references

Acknowledgements

We sincerely thank Jingjing Cui and Kui Sun for their assistance with radiomics analysis. We also thank Xinya Zhao for his assistance with the article revision.

Funding

This study was supported by the National Natural Science Foundation of China (81871354, 81571672) and the Academic Promotion Program of Shandong First Medical University (2019QL023).

Author information

Authors and Affiliations

Authors

Corresponding authors

Correspondence to Congshan Ji or Ximing Wang.

Ethics declarations

Guarantor

The scientific guarantor of this publication is Ximing Wang.

Conflict of interest

Author Jingjing Cui declares relationships with the following companies: United Imaging Intelligence (Beijing) Co., Ltd. The remaining authors of this manuscript declare no relationships with any companies, whose products or services may be related to the subject matter of the article.

Statistics and biometry

Jingjing Cui (one of the authors) and Kui Sun (not included in the authors) have significant statistical expertise.

Informed consent

The need for informed consent was waived by the Institutional Review Board.

Ethical approval

Institutional Review Board approval was obtained.

Methodology

• retrospective

• diagnostic or prognostic study

• multicenter study

Additional information

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary information

ESM 1

(DOCX 2454 kb)

Rights and permissions

Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Wang, G., Kang, B., Cui, J. et al. Two nomograms based on radiomics models using triphasic CT for differentiation of adrenal lipid-poor benign lesions and metastases in a cancer population: an exploratory study. Eur Radiol 33, 1873–1883 (2023). https://doi.org/10.1007/s00330-022-09182-8

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00330-022-09182-8

Keywords

Navigation