TY - JOUR
T1 - Frequency and Outcomes of Abnormal Imaging in Patients With Cirrhosis Enrolled in a Hepatocellular Carcinoma Surveillance Program
AU - Konerman, Monica A.
AU - Verma, Aashesh
AU - Zhao, Betty
AU - Singal, Amit G.
AU - Lok, Anna S.
AU - Parikh, Neehar D.
N1 - Funding Information:
All adult patients (age ≥18 years) with cirrhosis followed in outpatient hepatology clinics at the University of Michigan between January 2010 and December 2015 were prospectively enrolled in a chronic disease management program. Enrollment in this program was previously shown to increase 1-time screening after implementation. The diagnosis of cirrhosis for entry into the chronic disease management program was based clinically on histology, transient elastography, or imaging showing a nodular liver with or without associated signs of portal hypertension. The chronic disease management program included serial tracking of all laboratory and imaging results, including HCC surveillance, with a capacity to generate reminders at designated intervals. Clinic nurses contacted patients to complete any necessary surveillance testing at recommended intervals. According to the American Association for the Study of Liver Diseases (AASLD) guideline recommendations during the study period, abdominal imaging was required for completion of HCC surveillance, whereas AFP testing was optional and its measurement was provider dependent, although 94% of patients in the cohort had at least 1 AFP measurement. The program captured outside imaging if results were scanned into the electronic medical record and patients were logged into the reminder system.
Funding Information:
Amit G. Singal is on the advisory board for Exact Sciences, Bayer, Eisai, BMS, Exclixia, Gilead, and Abbvie; is a consultant for Glycotest, Roche, Bayer, Eisai, Rocke, Exclixia, Grail, Glycokal, and Target Pharmasolutions; and received research support from Exact Sciences, Glycotest, Wako Diagnostics, Gilead, Abbvie, and Target Pharmasolutions. Anna S. Lok received research funding from Target Pharmasolutions. Neehar D. Parikh consults for Bristol-Myers Squibb and Exelixis; is on the advisory board for Bayer, Eisai, and Exelixis; and received research funding from Bayer, Exact Sciences, and Target Pharmasolutions.
Funding Information:
This study was funded in part by the National Institutes of Health T32DK062708 training grant (Monica A. Konerman), National Cancer Institute RO1CA212008 and RO1CA222900 (Amit G. Singal), and the American Association for the Study of Liver Diseases Advanced/Transplant Hepatology Fellowship (Monica A. Konerman).
Publisher Copyright:
Copyright © 2018 by the American Association for the Study of Liver Diseases.
PY - 2019/3
Y1 - 2019/3
N2 - There are limited data on the downstream effects of hepatocellular carcinoma (HCC) surveillance, including the frequency of false-positive results. We aimed to quantify the incidence of indeterminate nodules (INs) and the follow-up testing needed to resolve these findings among patients enrolled in a structured HCC surveillance program. We retrospectively analyzed adult patients with cirrhosis enrolled in a structured HCC surveillance program in a large tertiary care center. Outcomes included surveillance benefits, defined as early HCC detection, and harm, defined as INs prompting additional diagnostic evaluation. Among 999 patients followed for a median of 2.2 years, HCC surveillance imaging was consistently completed every 6, 9, and 12 months in 46%, 51%, and 68% of patients, respectively. Of 256 (25.6%) patients with abnormal imaging, 69 (27.0%) were diagnosed with HCC and 187 (73.0%) with INs. Most HCC (n = 54, 78.3%) were found within Milan criteria. Among those with an IN, 78.1% returned to ultrasound surveillance after a median of 2 (interquartile range [IQR], 1-3) negative computed tomography (CT)/magnetic resonance imaging (MRI) scans, and 21.9% continued CT/MRI imaging (median, 1; IQR, 1-2). Eleven patients underwent diagnostic liver biopsy. Hypoalbuminemia, thrombocytopenia, and larger nodule size were independently associated with HCC diagnosis. In conclusion, 1 in 4 patients enrolled in an HCC surveillance program had abnormal surveillance imaging, but three-fourths of the lesions were INs, resulting in downstream harm. Improved risk-stratification tools are needed to identify nodules that are benign to reduce follow-up diagnostic evaluation.
AB - There are limited data on the downstream effects of hepatocellular carcinoma (HCC) surveillance, including the frequency of false-positive results. We aimed to quantify the incidence of indeterminate nodules (INs) and the follow-up testing needed to resolve these findings among patients enrolled in a structured HCC surveillance program. We retrospectively analyzed adult patients with cirrhosis enrolled in a structured HCC surveillance program in a large tertiary care center. Outcomes included surveillance benefits, defined as early HCC detection, and harm, defined as INs prompting additional diagnostic evaluation. Among 999 patients followed for a median of 2.2 years, HCC surveillance imaging was consistently completed every 6, 9, and 12 months in 46%, 51%, and 68% of patients, respectively. Of 256 (25.6%) patients with abnormal imaging, 69 (27.0%) were diagnosed with HCC and 187 (73.0%) with INs. Most HCC (n = 54, 78.3%) were found within Milan criteria. Among those with an IN, 78.1% returned to ultrasound surveillance after a median of 2 (interquartile range [IQR], 1-3) negative computed tomography (CT)/magnetic resonance imaging (MRI) scans, and 21.9% continued CT/MRI imaging (median, 1; IQR, 1-2). Eleven patients underwent diagnostic liver biopsy. Hypoalbuminemia, thrombocytopenia, and larger nodule size were independently associated with HCC diagnosis. In conclusion, 1 in 4 patients enrolled in an HCC surveillance program had abnormal surveillance imaging, but three-fourths of the lesions were INs, resulting in downstream harm. Improved risk-stratification tools are needed to identify nodules that are benign to reduce follow-up diagnostic evaluation.
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U2 - 10.1002/lt.25398
DO - 10.1002/lt.25398
M3 - Article
C2 - 30582779
AN - SCOPUS:85062207159
SN - 1527-6465
VL - 25
SP - 369
EP - 379
JO - Liver Transplantation
JF - Liver Transplantation
IS - 3
ER -