Skip to main content

Advertisement

Log in

Radiomics machine-learning signature for diagnosis of hepatocellular carcinoma in cirrhotic patients with indeterminate liver nodules

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

Abstract

Purpose

To enhance clinician’s decision-making by diagnosing hepatocellular carcinoma (HCC) in cirrhotic patients with indeterminate liver nodules using quantitative imaging features extracted from triphasic CT scans.

Material and methods

We retrospectively analyzed 178 cirrhotic patients from 27 institutions, with biopsy-proven liver nodules classified as indeterminate using the European Association for the Study of the Liver (EASL) guidelines. Patients were randomly assigned to a discovery cohort (142 patients (pts.)) and a validation cohort (36 pts.). Each liver nodule was segmented on each phase of triphasic CT scans, and 13,920 quantitative imaging features (12 sets of 1160 features each reflecting the phenotype at one single phase or its change between two phases) were extracted. Using machine-learning techniques, the signature was trained and calibrated (discovery cohort), and validated (validation cohort) to classify liver nodules as HCC vs. non-HCC. Effects of segmentation and contrast enhancement quality were also evaluated.

Results

Patients were predominantly male (88%) and CHILD A (65%). Biopsy was positive for HCC in 77% of patients. LI-RADS scores were not different between HCC and non-HCC patients. The signature included a single radiomics feature quantifying changes between arterial and portal venous phases: DeltaV-A_DWT1_LL_Variance-2D and reached area under the receiver operating characteristic curve (AUC) of 0.70 (95%CI 0.61–0.80) and 0.66 (95%CI 0.64–0.84) in discovery and validation cohorts, respectively. The signature was influenced neither by segmentation nor by contrast enhancement.

Conclusion

A signature using a single feature was validated in a multicenter retrospective cohort to diagnose HCC in cirrhotic patients with indeterminate liver nodules. Artificial intelligence could enhance clinicians’ decision by identifying a subgroup of patients with high HCC risk.

Key Points

• In cirrhotic patients with visually indeterminate liver nodules, expert visual assessment using current guidelines cannot accurately differentiate HCC from differential diagnoses. Current clinical protocols do not entail biopsy due to procedural risks. Radiomics can be used to non-invasively diagnose HCC in cirrhotic patients with indeterminate liver nodules, which could be leveraged to optimize patient management.

• Radiomics features contributing the most to a better characterization of visually indeterminate liver nodules include changes in nodule phenotype between arterial and portal venous phases: the “washout” pattern appraised visually using EASL and EASL guidelines.

• A clinical decision algorithm using radiomics could be applied to reduce the rate of cirrhotic patients requiring liver biopsy (EASL guidelines) or wait-and-see strategy (AASLD guidelines) and therefore improve their management and outcome.

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

A:

Arterial CT phase

AASLD:

The American Association for the Study of Liver Diseases

AUC:

Area under the receiver operating characteristic curve

CCC:

Concordance correlation coefficient

CT:

Computed tomography

Delta:

Dual phase defined by the change between imaging features extracted from two different CT phases (A-NC, V-A, V-NC)

Delta1A-P:

Dual phase defined by the change between arterial and non-contrast CT phases, using standardized subtraction (delta 1)

Delta1V-A:

Dual phase defined by the change between portal venous and arterial CT phases, using standardized subtraction (delta 1)

Delta1V-NC:

Dual phase defined by the change between portal venous and non-contrast CT phases, using standardized subtraction (delta 1)

Delta2A-NC:

Dual phase defined by the change between arterial and non-contrast CT phases, using direct subtraction (delta 2)

Delta2V-A:

Dual phase defined by the change between portal venous and arterial CT phases, using direct subtraction (delta 2)

Delta2V-NC:

Dual phase defined by the change between portal venous and non-contrast CT phases, using direct subtraction (delta 2)

Delta3A-NC:

Dual phase defined by the change between arterial and non-contrast CT phases, using relative subtraction (delta 3)

Delta3V-A:

Dual phase defined by the change between portal venous and arterial CT phases, using relative subtraction (delta 3)

Delta3V-NC:

Dual phase defined by the change between portal venous and non-contrast CT phases, using relative subtraction (delta 3)

DWF_LL:

Discrete wavelet frame in the low-pass channel radiomics feature

DWT1_LL:

Dual-tree wavelet transform in the low-pass channel radiomics feature

EASL:

The European Association for the Study of the Liver

GLCM:

Gray-level co-occurrence matrix radiomics feature

HCC:

Hepatocellular carcinoma

KNN:

K-Nearest neighbor machine-learning algorithm

LI-RADS:

Liver Imaging Reporting and Data System

LR-1 to 5 and M:

LI-RADS categories, according to LI-RADS criteria version 2017

MRI:

Magnetic resonance imaging

NASH:

Non-alcoholic steatohepatitis

NC:

Non-contrast CT phase

RF:

Random forest machine-learning algorithm

SMOTE:

Synthetic Minority Over-sampling Technique

SVM:

Support vector machine machine-learning algorithm

V:

Portal venous CT phase

References

  1. European Association for the Study of the Liver (2018) EASL clinical practice guidelines: management of hepatocellular carcinoma. J Hepatol https://doi.org/10.1016/j.jhep.2018.03.019

  2. El-Serag HB, Rudolph KL (2007) Hepatocellular carcinoma: epidemiology and molecular carcinogenesis. Gastroenterology 132:2557–2576

    Article  CAS  Google Scholar 

  3. Tsukuma H, Hiyama T, Tanaka S et al (1993) Risk factors for hepatocellular carcinoma among patients with chronic liver disease. N Engl J Med 328:1797–1801

    Article  CAS  Google Scholar 

  4. Sangiovanni A, Prati GM, Fasani P et al (2006) The natural history of compensated cirrhosis due to hepatitis C virus: a 17-year cohort study of 214 patients. Hepatology 43:1303–1310

    Article  Google Scholar 

  5. Llovet JM, Brú C, Bruix J (1999) Prognosis of hepatocellular carcinoma: the BCLC staging classification. Semin Liver Dis 19:329–338

  6. Di Martino M, De Filippis G, De Santis A et al (2013) Hepatocellular carcinoma in cirrhotic patients: prospective comparison of US, CT and MR imaging. Eur Radiol 23:887–896

    Article  Google Scholar 

  7. Ronot M, Fouque O, Esvan M, Lebigot J, Aubé C, Vilgrain V (2017) Comparison of the accuracy of AASLD and LI-RADS criteria for the non-invasive diagnosis of HCC smaller than 3cm. J Hepatol. https://doi.org/10.1016/j.jhep.2017.12.014

  8. Sersté T, Barrau V, Ozenne V et al (2012) Accuracy and disagreement of computed tomography and magnetic resonance imaging for the diagnosis of small hepatocellular carcinoma and dysplastic nodules: role of biopsy. Hepatology 55:800–806

  9. Forner A, Vilana R, Ayuso C et al (2008) Diagnosis of hepatic nodules 20 mm or smaller in cirrhosis: prospective validation of the noninvasive diagnostic criteria for hepatocellular carcinoma. Hepatology 47:97–104

    Article  Google Scholar 

  10. Heimbach JK, Kulik LM, Finn RS et al (2018) AASLD guidelines for the treatment of hepatocellular carcinoma. Hepatology 67:358–380

    Article  Google Scholar 

  11. Freeman Richard B, Mithoefer A, Ruthazer R et al (2006) Optimizing staging for hepatocellular carcinoma before liver transplantation: a retrospective analysis of the UNOS/OPTN database. Liver Transpl 12:1504–1511

    Article  CAS  Google Scholar 

  12. Yang H, Schwartz LH, Zhao B (2016) A response assessment platform for development and validation of imaging biomarkers in oncology. Tomography 2:406–410

    Article  Google Scholar 

  13. Lin LI (1989) A concordance correlation coefficient to evaluate reproducibility. Biometrics 45:255–268

  14. Berenguer R, Pastor-Juan MR, Canales-Vázquez J et al (2018) Radiomics of CT features may be nonreproducible and redundant: influence of CT acquisition parameters. Radiology 288:407–415 %@ 0033-8419

    Article  Google Scholar 

  15. Dercle L, Lu L, Lichtenstein P et al (2017) Impact of variability in portal venous phase acquisition timing in tumor density measurement and treatment response assessment: metastatic colorectal cancer as a paradigm. JCO Clin Cancer Inform (1):1–8

  16. Dercle L, Billey C, Cognet T et al (2018) Spleno-hepatic index to predict portal hypertension by equilibrium radionuclide ventriculography. Nucl Med Commun 39:1138–1142

    Article  Google Scholar 

  17. Aerts HJ, Velazquez ER, Leijenaar RT et al (2014) Decoding tumour phenotype by noninvasive imaging using a quantitative radiomics approach. Nat Commun 5:4006

    Article  CAS  Google Scholar 

  18. Hatt M, Tixier F, Pierce L, Kinahan PE, Le Rest CC, Visvikis D (2017) Characterization of PET/CT images using texture analysis: the past, the present… any future? Eur J Nucl Med Mol Imaging 44:151–165

    Article  Google Scholar 

  19. Banerjee S, Wang DS, Kim HJ et al (2015) A computed tomography radiogenomic biomarker predicts microvascular invasion and clinical outcomes in hepatocellular carcinoma. Hepatology 62:792–800

    Article  Google Scholar 

  20. Bakr SH, Echegaray S, Shah RP et al (2017) Noninvasive radiomics signature based on quantitative analysis of computed tomography images as a surrogate for microvascular invasion in hepatocellular carcinoma: a pilot study. J Med Imaging (Bellingham) 4:041303

  21. Renzulli M, Brocchi S, Cucchetti A et al (2015) Can current preoperative imaging be used to detect microvascular invasion of hepatocellular carcinoma? Radiology 279:432–442

    Article  Google Scholar 

  22. Yasaka K, Akai H, Abe O, Kiryu S (2018) Deep learning with convolutional neural network for differentiation of liver masses at dynamic contrast-enhanced CT: a preliminary study. Radiology 286:887–896

    Article  Google Scholar 

  23. Cerny M, Bergeron C, Billiard JS et al (2018) LI-RADS for MR imaging diagnosis of hepatocellular carcinoma: performance of major and ancillary features. Radiology 171678. https://doi.org/10.1148/radiol.2018171678

  24. Darnell A, Forner A, Rimola J et al (2015) Liver imaging reporting and data system with MR imaging: evaluation in nodules 20 mm or smaller detected in cirrhosis at screening US. Radiology 275:698–707

    Article  Google Scholar 

  25. Tanabe M, Kanki A, Wolfson T et al (2016) Imaging outcomes of liver imaging reporting and data system version 2014 category 2, 3, and 4 observations detected at CT and MR imaging. Radiology 281:129–139

    Article  Google Scholar 

  26. Aubé C, Oberti F, Lonjon J et al (2017) EASL and AASLD recommendations for the diagnosis of HCC to the test of daily practice. Liver Int 37:1515–1525

  27. Kim DW, Jang HY, Kim KW, Shin Y, Park SH (2019) Design characteristics of studies reporting the performance of artificial intelligence algorithms for diagnostic analysis of medical images: results from recently published papers. Korean J Radiol 20:405–410 %@ 1229-6929

    Article  Google Scholar 

  28. Dercle L, Ammari S, Bateson M et al (2017) Limits of radiomic-based entropy as a surrogate of tumor heterogeneity: ROI-area, acquisition protocol and tissue site exert substantial influence. Sci Rep 7:7952

    Article  Google Scholar 

  29. Dercle L, Hartl D, Rozenblum-Beddok L et al (2018) Diagnostic and prognostic value of 18F-FDG PET, CT, and MRI in perineural spread of head and neck malignancies. Eur Radiol 28:1761–1770

    Article  Google Scholar 

  30. Limkin E, 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  Google Scholar 

  31. Sun R, Limkin EJ, Vakalopoulou M et al (2018) A radiomics approach to assess tumour-infiltrating CD8 cells and response to anti-PD-1 or anti-PD-L1 immunotherapy: an imaging biomarker, retrospective multicohort study. Lancet Oncol 19:1180–1191

    Article  CAS  Google Scholar 

Download references

Acknowledgments

This manuscript was revised by Qian Min, statistician. Sincere appreciation is expressed to Tavis Allison and Ronan Trépos for their assistance in the preparation of this manuscript.

Funding

This study was supported through research grants from Alain Rahmouni French Society of Radiology-CERF 2018 (FZM), Fondation Philanthropia (LD), and Fondation Nuovo-Soldati (LD).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Fatima-Zohra Mokrane.

Ethics declarations

Guarantor

The scientific guarantor of this publication is Fatima-Zohra Mokrane.

Conflict of interest

The 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

Qian Min, PhD, and Ronan Trépos, PhD, kindly provided statistical advice for this manuscript.

Informed consent

Written informed consent was waived by the Institutional Review Board.

Ethical approval

Institutional Review Board approval was obtained (IRB form: AAAR9377).

Methodology

• retrospective

• diagnostic

• multicenter study

Additional information

Publisher’s note

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

Electronic supplementary material

ESM 1

(DOCX 23794 kb)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Mokrane, FZ., Lu, L., Vavasseur, A. et al. Radiomics machine-learning signature for diagnosis of hepatocellular carcinoma in cirrhotic patients with indeterminate liver nodules. Eur Radiol 30, 558–570 (2020). https://doi.org/10.1007/s00330-019-06347-w

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00330-019-06347-w

Keywords

Navigation