TY - JOUR
T1 - Diagnostic performance of LI-RADS version 2018 for evaluation of pediatric hepatocellular carcinoma
AU - Khanna, Geetika
AU - Chavhan, Govind B.
AU - Schooler, Gary R.
AU - Fraum, Tyler J.
AU - Alazraki, Adina L.
AU - Squires, Judy H.
AU - Salter, Amber
AU - Podberesky, Daniel J.
AU - Towbin, Alexander J.
N1 - Funding Information:
Author contributions: Guarantors of integrity of entire study, G.K., G.R.S.; study concepts/study design or data acquisition or data analysis/interpretation, all authors; manuscript drafting or manuscript revision for important intellectual content, all authors; approval of final version of submitted manuscript, all authors; agrees to ensure any questions related to the work are appropriately resolved, all authors; literature research, G.K., G.B.C., T.J.F., J.H.S., D.J.P., A.J.T.; clinical studies, G.K., G.B.C., G.R.S., T.J.F., A.L.A., J.H.S., D.J.P., A.J.T.; experimental studies, A.J.T.; statistical analysis, G.K., A.S.; and manuscript editing, all authors Disclosures of Conflicts of Interest: G.K. disclosed no relevant relationships. G.B.C. Activities related to the present article: disclosed no relevant relationships. Activities not related to the present article: received honorarium from Bayer for serving as moderator during discussion/interview on contrast media. Other relationships: disclosed no relevant relationships. G.R.S. Activities related to the present article: disclosed no relevant relationships. Activities not related to the present article: received grant funding from the Children’s Oncology Group/National Cancer Institute for a project, Radiomics in Hepatoblastoma: Correlation with Outcomes Data from COG (AHEP0731); was an invited speaker at the course “Pediatric Imaging Essentials: Techniques, Pearls and Pitfalls” in 2020. Other relationships: disclosed no relevant relationships. T.J.F. Activities related to the present article: disclosed no relevant relationships. Activities not related to the present article: consulted on AI product development for Arterys; provided research support for oncologic PET/CT project at Siemens. Other relationships: disclosed no relevant relationships. A.L.A. Activities related to the present article: disclosed no relevant relationships. Activities not related to the present article: received compensation for expert testimony; is employed by Children’s Healthcare of Atlanta. Other relationships: disclosed no relevant relation- ships. J.H.S. disclosed no relevant relationships. A.S. Activities related to the present article: disclosed no relevant relationships. Activities not related to the present article: serves as statistical editor for Circulation: Cardiovascular Imaging, a journal of the American Heart Association. Other relationships: disclosed no relevant relationships. D.J.P. Activities related to the present article: disclosed no relevant relationships. Activities not related to the present article: serves as a consultant for Guerbet and various law firms; received payment from Fujifilm and Canon for lectures; receives royalties from Elsevier for chapter authorship; receives travel reimbursements from Philips and Siemens for site visits. Other relationships: disclosed no relevant relationships. A.J.T. Activities related to the present article: disclosed no relevant relationships. Activities not related to the present article: serves as a consultant for Applied Radiology; has received grants/pending grants from Guerbet and the Cystic Fibrosis Foundation; receives royalties from Elsevier for chapter authorship. Other relationships: disclosed no relevant relationships.
Publisher Copyright:
© RSNA, 2021
PY - 2021/4
Y1 - 2021/4
N2 - Background: The Liver Imaging Reporting and Data System (LI-RADS) has standardized the evaluation of adult but not pediatric hepatocellular carcinoma (HCC). Purpose: To evaluate the performance of LI-RADS version 2018 for diagnosis of pediatric HCC. Materials and Methods: This multi-institution retrospective study evaluated all available dynamic CT and/or MRI scans of pediatric (18 years) HCC from five institutions between July 2009 and April 2019. The control group included an equal number of other enhancing hepatic lesions. Blinded to final diagnosis, three radiologists independently applied LI-RADS version 2018 criteria. The reference standard was pathologic examination or more than 1 year follow-up. Sensitivity and specificity of LI-RADS were computed using a dichotomous classification of LR-1, LR-2, or LR-3 versus LR-4, LR-5, LR-TIV (tumor in vein), or LR-M (probably or definitely malignant but not HCC-specific) for predicting hepatic malignancy in the entire cohort and in patients at risk for HCC. Results: The cohort consisted of 116 children: 58 with HCC (mean age, 12 years 6 5; 31 girls) and 58 with other enhancing hepatic masses (mean age, 12 years 6 5; 42 girls). Frequencies of major criteria in classic HCC for the three readers were as follows: nonrim arterial phase hyperenhancement, 49%–62% (19–24 of 39 patients); nonperipheral “washout,” 36%–59% (14–23 of 39 patients); and enhancing “capsule,” 28%–38% (11–15 of 39 patients). For the full cohort, the sensitivity of LR-4, LR-5, LR-TIV, or LR-M for malignancy among the three readers ranged from 85% (95% CI: 76, 94) to 88% (95% CI: 80, 96); specificity of LR-1, LR-2, or LR-3 for benignity ranged from 54% (95% CI: 40, 68) to 70% (95% CI: 57, 83). In the at-risk subgroup, sensitivity ranged from 58% (95% CI: 36, 80) to 68% (95% CI: 48, 89); specificity ranged from 56% (95% CI: 37, 74) to 63% (95% CI: 45, 81). All lesions categorized as LR-TIV (n = 10–13) were HCCs. Conclusion: Liver Imaging Reporting and Data System version 2018 had moderate sensitivity but low specificity for the diagnosis of pediatric hepatocellular carcinoma (HCC), which had low frequencies of the major criteria used for adult HCC diagnosis.
AB - Background: The Liver Imaging Reporting and Data System (LI-RADS) has standardized the evaluation of adult but not pediatric hepatocellular carcinoma (HCC). Purpose: To evaluate the performance of LI-RADS version 2018 for diagnosis of pediatric HCC. Materials and Methods: This multi-institution retrospective study evaluated all available dynamic CT and/or MRI scans of pediatric (18 years) HCC from five institutions between July 2009 and April 2019. The control group included an equal number of other enhancing hepatic lesions. Blinded to final diagnosis, three radiologists independently applied LI-RADS version 2018 criteria. The reference standard was pathologic examination or more than 1 year follow-up. Sensitivity and specificity of LI-RADS were computed using a dichotomous classification of LR-1, LR-2, or LR-3 versus LR-4, LR-5, LR-TIV (tumor in vein), or LR-M (probably or definitely malignant but not HCC-specific) for predicting hepatic malignancy in the entire cohort and in patients at risk for HCC. Results: The cohort consisted of 116 children: 58 with HCC (mean age, 12 years 6 5; 31 girls) and 58 with other enhancing hepatic masses (mean age, 12 years 6 5; 42 girls). Frequencies of major criteria in classic HCC for the three readers were as follows: nonrim arterial phase hyperenhancement, 49%–62% (19–24 of 39 patients); nonperipheral “washout,” 36%–59% (14–23 of 39 patients); and enhancing “capsule,” 28%–38% (11–15 of 39 patients). For the full cohort, the sensitivity of LR-4, LR-5, LR-TIV, or LR-M for malignancy among the three readers ranged from 85% (95% CI: 76, 94) to 88% (95% CI: 80, 96); specificity of LR-1, LR-2, or LR-3 for benignity ranged from 54% (95% CI: 40, 68) to 70% (95% CI: 57, 83). In the at-risk subgroup, sensitivity ranged from 58% (95% CI: 36, 80) to 68% (95% CI: 48, 89); specificity ranged from 56% (95% CI: 37, 74) to 63% (95% CI: 45, 81). All lesions categorized as LR-TIV (n = 10–13) were HCCs. Conclusion: Liver Imaging Reporting and Data System version 2018 had moderate sensitivity but low specificity for the diagnosis of pediatric hepatocellular carcinoma (HCC), which had low frequencies of the major criteria used for adult HCC diagnosis.
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U2 - 10.1148/RADIOL.2021203559
DO - 10.1148/RADIOL.2021203559
M3 - Article
C2 - 33620289
AN - SCOPUS:85103473613
SN - 0033-8419
VL - 299
SP - 190
EP - 199
JO - Radiology
JF - Radiology
IS - 1
ER -