LI-RADS Treatment Response Algorithm: Performance and Diagnostic Accuracy With Radiologic-Pathologic Explant Correlation in Patients With SBRT-Treated Hepatocellular Carcinoma
Our purpose was to evaluate the accuracy of LI-RADS Treatment Response Algorithm (LR-TRA) for assessing the viability of hepatocellular carcinoma (HCC) treated with stereotactic body radiation therapy (SBRT), using explant pathology as the gold standard. This retrospective study included patients wh...
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Published in | International journal of radiation oncology, biology, physics Vol. 112; no. 3; pp. 704 - 714 |
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Main Authors | , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
Elsevier Inc
01.03.2022
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Abstract | Our purpose was to evaluate the accuracy of LI-RADS Treatment Response Algorithm (LR-TRA) for assessing the viability of hepatocellular carcinoma (HCC) treated with stereotactic body radiation therapy (SBRT), using explant pathology as the gold standard.
This retrospective study included patients who underwent SBRT for locoregional treatment of HCC between 2008 and 2019 with subsequent liver transplantation. Five radiologists independently assessed all treated lesions by using the LR-TRA. Imaging and posttransplant histopathology were compared. Lesions were categorized as either completely (100%) or incompletely (<100%) necrotic, and performance characteristics and predictive values for the LR-TR viable and nonviable categories were calculated for each reader. Interreader reliability was calculated using the Fleiss kappa test.
A total of 40 treated lesions in 26 patients (median age, 63 years [interquartile range, 59.4-65.5]; 23 men) were included. For lesions treated with SBRT, sensitivity for incomplete tumor necrosis across readers ranged between 71% and 86%, specificity between 85% and 96%, and positive predictive value between 86% and 92%, when the LR-TR equivocal category was treated as nonviable, accounting for subject clustering. When the LR-TR equivocal category was treated as viable, sensitivity of complete tumor necrosis for lesions treated with SBRT ranged from 88% to 96%, specificity from 71% to 93%, and negative predictive value from 85% to 96%. Interreader reliability was fair (k = 0.22; 95% confidence interval, 0.13-0.33). Although a loss of arterial phase hyperenhancement (APHE) was highly correlated with pathologically nonviable tumor on explant, almost half of the patients with APHE had pathologically nonviable tumor on explant.
LR-TRA v2018 performs well for predicting complete and incomplete necrosis in HCC treated with SBRT. In contrast to other locoregional therapies, the presence of APHE after SBRT does not always indicate viable tumor and suggests that observation may be an appropriate strategy for these patients. |
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AbstractList | Our purpose was to evaluate the accuracy of LI-RADS Treatment Response Algorithm (LR-TRA) for assessing the viability of hepatocellular carcinoma (HCC) treated with stereotactic body radiation therapy (SBRT), using explant pathology as the gold standard.PURPOSEOur purpose was to evaluate the accuracy of LI-RADS Treatment Response Algorithm (LR-TRA) for assessing the viability of hepatocellular carcinoma (HCC) treated with stereotactic body radiation therapy (SBRT), using explant pathology as the gold standard.This retrospective study included patients who underwent SBRT for locoregional treatment of HCC between 2008 and 2019 with subsequent liver transplantation. Five radiologists independently assessed all treated lesions by using the LR-TRA. Imaging and posttransplant histopathology were compared. Lesions were categorized as either completely (100%) or incompletely (<100%) necrotic, and performance characteristics and predictive values for the LR-TR viable and nonviable categories were calculated for each reader. Interreader reliability was calculated using the Fleiss kappa test.METHODS AND MATERIALSThis retrospective study included patients who underwent SBRT for locoregional treatment of HCC between 2008 and 2019 with subsequent liver transplantation. Five radiologists independently assessed all treated lesions by using the LR-TRA. Imaging and posttransplant histopathology were compared. Lesions were categorized as either completely (100%) or incompletely (<100%) necrotic, and performance characteristics and predictive values for the LR-TR viable and nonviable categories were calculated for each reader. Interreader reliability was calculated using the Fleiss kappa test.A total of 40 treated lesions in 26 patients (median age, 63 years [interquartile range, 59.4-65.5]; 23 men) were included. For lesions treated with SBRT, sensitivity for incomplete tumor necrosis across readers ranged between 71% and 86%, specificity between 85% and 96%, and positive predictive value between 86% and 92%, when the LR-TR equivocal category was treated as nonviable, accounting for subject clustering. When the LR-TR equivocal category was treated as viable, sensitivity of complete tumor necrosis for lesions treated with SBRT ranged from 88% to 96%, specificity from 71% to 93%, and negative predictive value from 85% to 96%. Interreader reliability was fair (k = 0.22; 95% confidence interval, 0.13-0.33). Although a loss of arterial phase hyperenhancement (APHE) was highly correlated with pathologically nonviable tumor on explant, almost half of the patients with APHE had pathologically nonviable tumor on explant.RESULTSA total of 40 treated lesions in 26 patients (median age, 63 years [interquartile range, 59.4-65.5]; 23 men) were included. For lesions treated with SBRT, sensitivity for incomplete tumor necrosis across readers ranged between 71% and 86%, specificity between 85% and 96%, and positive predictive value between 86% and 92%, when the LR-TR equivocal category was treated as nonviable, accounting for subject clustering. When the LR-TR equivocal category was treated as viable, sensitivity of complete tumor necrosis for lesions treated with SBRT ranged from 88% to 96%, specificity from 71% to 93%, and negative predictive value from 85% to 96%. Interreader reliability was fair (k = 0.22; 95% confidence interval, 0.13-0.33). Although a loss of arterial phase hyperenhancement (APHE) was highly correlated with pathologically nonviable tumor on explant, almost half of the patients with APHE had pathologically nonviable tumor on explant.LR-TRA v2018 performs well for predicting complete and incomplete necrosis in HCC treated with SBRT. In contrast to other locoregional therapies, the presence of APHE after SBRT does not always indicate viable tumor and suggests that observation may be an appropriate strategy for these patients.CONCLUSIONSLR-TRA v2018 performs well for predicting complete and incomplete necrosis in HCC treated with SBRT. In contrast to other locoregional therapies, the presence of APHE after SBRT does not always indicate viable tumor and suggests that observation may be an appropriate strategy for these patients. Our purpose was to evaluate the accuracy of LI-RADS Treatment Response Algorithm (LR-TRA) for assessing the viability of hepatocellular carcinoma (HCC) treated with stereotactic body radiation therapy (SBRT), using explant pathology as the gold standard. Our purpose was to evaluate the accuracy of LI-RADS Treatment Response Algorithm (LR-TRA) for assessing the viability of hepatocellular carcinoma (HCC) treated with stereotactic body radiation therapy (SBRT), using explant pathology as the gold standard. This retrospective study included patients who underwent SBRT for locoregional treatment of HCC between 2008 and 2019 with subsequent liver transplantation. Five radiologists independently assessed all treated lesions by using the LR-TRA. Imaging and posttransplant histopathology were compared. Lesions were categorized as either completely (100%) or incompletely (<100%) necrotic, and performance characteristics and predictive values for the LR-TR viable and nonviable categories were calculated for each reader. Interreader reliability was calculated using the Fleiss kappa test. A total of 40 treated lesions in 26 patients (median age, 63 years [interquartile range, 59.4-65.5]; 23 men) were included. For lesions treated with SBRT, sensitivity for incomplete tumor necrosis across readers ranged between 71% and 86%, specificity between 85% and 96%, and positive predictive value between 86% and 92%, when the LR-TR equivocal category was treated as nonviable, accounting for subject clustering. When the LR-TR equivocal category was treated as viable, sensitivity of complete tumor necrosis for lesions treated with SBRT ranged from 88% to 96%, specificity from 71% to 93%, and negative predictive value from 85% to 96%. Interreader reliability was fair (k = 0.22; 95% confidence interval, 0.13-0.33). Although a loss of arterial phase hyperenhancement (APHE) was highly correlated with pathologically nonviable tumor on explant, almost half of the patients with APHE had pathologically nonviable tumor on explant. LR-TRA v2018 performs well for predicting complete and incomplete necrosis in HCC treated with SBRT. In contrast to other locoregional therapies, the presence of APHE after SBRT does not always indicate viable tumor and suggests that observation may be an appropriate strategy for these patients. |
Author | Aslam, Anum Maturen, Katherine E. Westerhoff, Maria Mendiratta-Lala, Mishal Stein, Erica B. Sun, Yilun Masch, William Lawrence, Theodore S. Owen, Dawn Kaza, Ravi K. Maurino, Chris Shampain, Kimberly L. Do, Richard Kinh Gian Cuneo, Kyle Parikh, Neehar D. Sonnenday, Christopher J. |
Author_xml | – sequence: 1 givenname: Mishal surname: Mendiratta-Lala fullname: Mendiratta-Lala, Mishal email: mmendira@med.umich.edu organization: Department of Radiology, University of Michigan Health System, Ann Arbor, Michigan – sequence: 2 givenname: Anum surname: Aslam fullname: Aslam, Anum organization: Department of Radiology, University of Michigan Health System, Ann Arbor, Michigan – sequence: 3 givenname: Katherine E. surname: Maturen fullname: Maturen, Katherine E. organization: Department of Radiology, University of Michigan Health System, Ann Arbor, Michigan – sequence: 4 givenname: Maria surname: Westerhoff fullname: Westerhoff, Maria organization: Department of Pathology, University of Michigan Health System, Ann Arbor, Michigan – sequence: 5 givenname: Chris surname: Maurino fullname: Maurino, Chris organization: Department of Radiology, University of Michigan Health System, Ann Arbor, Michigan – sequence: 6 givenname: Neehar D. surname: Parikh fullname: Parikh, Neehar D. organization: Department of Radiology, University of Michigan Health System, Ann Arbor, Michigan – sequence: 7 givenname: Yilun surname: Sun fullname: Sun, Yilun organization: Radiation Oncology, University of Michigan Health System, Ann Arbor, MI – sequence: 8 givenname: Christopher J. surname: Sonnenday fullname: Sonnenday, Christopher J. organization: Department of Surgery, University of Michigan Health System, Ann Arbor, Michigan – sequence: 9 givenname: Erica B. surname: Stein fullname: Stein, Erica B. organization: Department of Radiology, University of Michigan Health System, Ann Arbor, Michigan – sequence: 10 givenname: Kimberly L. surname: Shampain fullname: Shampain, Kimberly L. organization: Department of Radiology, University of Michigan Health System, Ann Arbor, Michigan – sequence: 11 givenname: Ravi K. surname: Kaza fullname: Kaza, Ravi K. organization: Department of Radiology, University of Michigan Health System, Ann Arbor, Michigan – sequence: 12 givenname: Kyle surname: Cuneo fullname: Cuneo, Kyle organization: Radiation Oncology, University of Michigan Health System, Ann Arbor, MI – sequence: 13 givenname: William surname: Masch fullname: Masch, William organization: Department of Radiology, University of Michigan Health System, Ann Arbor, Michigan – sequence: 14 givenname: Richard Kinh Gian surname: Do fullname: Do, Richard Kinh Gian organization: Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, New York – sequence: 15 givenname: Theodore S. surname: Lawrence fullname: Lawrence, Theodore S. organization: Radiation Oncology, University of Michigan Health System, Ann Arbor, MI – sequence: 16 givenname: Dawn surname: Owen fullname: Owen, Dawn organization: Radiation Oncology, Mayo Clinic Rochester, Rochester, Minnesota |
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SubjectTerms | ACCURACY ALGORITHMS Carcinoma, Hepatocellular - diagnostic imaging Carcinoma, Hepatocellular - pathology Carcinoma, Hepatocellular - radiotherapy Contrast Media CORRELATIONS DIAGNOSIS HEPATOMAS Humans Liver Neoplasms - diagnostic imaging Liver Neoplasms - pathology Liver Neoplasms - radiotherapy Magnetic Resonance Imaging - methods Male Middle Aged PATHOLOGY PATIENTS RADIOLOGY AND NUCLEAR MEDICINE Radiosurgery RADIOTHERAPY Reproducibility of Results Retrospective Studies Sensitivity and Specificity VIABILITY |
Title | LI-RADS Treatment Response Algorithm: Performance and Diagnostic Accuracy With Radiologic-Pathologic Explant Correlation in Patients With SBRT-Treated Hepatocellular Carcinoma |
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