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Clinical Trials in the USA / NCT03878550
Active, not recruiting

Case-Control Study of the Glycotest™ HCC Panel vs AFP for the Detection of Early-stage Hepatocellular Carcinoma

NCT03878550 · tracked via the Priya Life Science USA tracker
Sponsor
Glycotest, Inc.
Phase
Started
2019-05-22
Last updated
2026-09-11

Condition(s) studied

Carcinoma, HepatocellularCirrhosis, Liver

Study summary

Clinical guidelines (AASLD) recommend the use of abdominal ultrasound (US) for surveillance testing for the early detection of Hepatocellular Carcinoma (HCC). The serum protein biomarker alpha-fetoprotein (AFP) is commonly used to augment US but its use alone is not recommended by clinical guidelines. Despite evidence that HCC surveillance improves early detection and reduces mortality from HCC, current HCC surveillance tests lack sensitivity, leaving a significant proportion of patients to present with late-stage disease. The Glycotest HCC Panel has shown better sensitivity than AFP, which is ineffective for the detection of early-stage HCC. This clinical study seeks to validate the Glycotest HCC Panel using a large multicenter cohort of cases and controls that includes patients diagnosed with early-stage HCC against a background of cirrhosis and cirrhotic patients without HCC (at risk) undergoing an established surveillance protocol.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: Cases 1. Males and females ages 18 years or older. 2. Treatment-naïve HCC as defined by LI-RADS (Liver Imaging Reporting and Data System) LR-5 or OPTN (Organ Procurement and Transplantation Network) 5 CT or MRI criteria (all lesions must exhibit arterial phase hyper-enhancement), or histologic evidence. 3. Early-stage HCC defined by single lesion ≤ 5 cm or ≤ 3 lesions ≤ 3 cm determined at enrollment or within 100 days prior without vascular invasion. 4. Cirrhosis based on serum biomarkers (FibroSure®/FibroTest \> 0.74, APRI (AST to Platelet Ratio Index) \> 2, or FIB-4 (Fibrosis-4) \> 3.25), histology, imaging, elastography, or clinical evidence of portal hypertension in the setting of known chronic liver disease. 5. Child-Pugh score A-B8. 6. Subject must be able to understand and provide informed consent. Controls 1. Males and females ages 18 or older. 2. Cirrhosis based on serum biomarkers (FibroSure®/FibroTest \> 0.74, APRI \> 2, or FIB-4 \> 3.25), histology, imaging, elastography, or clinical evidence of portal hypertension in the setting of known chronic liver disease. 3. Evidence of the absence of a solid hepatic mass, suspicious for HCC, at enrollment or within 100 days prior based on one of the following: 1. Negative multiphase CT scan or MRI with contrast at screening/baseline visit, OR 2. Negative abdominal US at both screening/baseline visit AND 6-month follow-up visit, OR 3. Negative abdominal US at screening/baseline visit AND negative multiphase CT scan or MRI with contrast at 6-month or earlier follow-up visit. 4. Child-Pugh score A-B8. 5. Subject must be able to understand and provide informed consent. Exclusion Criteria: Cases 1. Uncontrolled ascites. 2. Uncontrolled encephalopathy. 3. History of liver transplant. 4. Diagnosis of active malignancy or history of active malignancy within 5 years prior to enrollment, including mixed HCC-CCA (cholangiocarcinoma). If previously diagnosed with malignancy, subject must be in remission for at least 5 years prior to enrollment. Prior history of HCC, including resection of HCC at any time, is excluded. 5. Prior treatment of tumor. 6. Any significant non-liver-related medical condition in which expected survival is less than 1 year. Controls 1. Imaging evidence of solid hepatic mass, suspicious for HCC, including lesions meeting LI-RADS LR-3 or LR-4, OPTN-3 or OPTN-4, or LI-RADS LR-M criteria. 2. Uncontrolled ascites. 3. History of liver transplantation. 4. Uncontrolled encephalopathy. 5. Diagnosis of active malignancy or history of active malignancy within 5 years prior to enrollment (if previously diagnosed with malignancy, subject must be in remission for at least 5 years prior to enrollment). History of HCC including resection of HCC at any time, is excluded. 6. Any significant non-liver-related medical condition in which expected survival is less than 1 year.

Primary outcome measure(s)

Trial sites (20)

FacilityCityRegionStatus
Cedars- Sinai Medical Center Los Angeles California
University of California Los Angeles Los Angeles California
Kaiser Permanente Northern California San Francisco California
University of California- San Francisco San Francisco California
Stanford University School of Medicine Stanford California
University of Florida Gainesville Florida
Miami VA Healthcare System Miami Florida
Northwestern University Chicago Illinois
University of Maryland, Baltimore Baltimore Maryland
University of Michigan Ann Arbor Michigan
Henry Ford Health System Detroit Michigan
Mayo Clinic Rochester Minnesota
NYU Langone Health New York New York
Icahn School of Medicine at Mount Sinai New York New York
Montefiore Medical Center The Bronx New York
Hospital of the University of Pennsylvania (HUP) Philadelphia Pennsylvania
Baylor Scott & White Research Institute Dallas Texas
The University of Texas Southwestern Medical Center Dallas Texas
Baylor College of Medicine Houston Texas
Hebrew University- Hadassah Medical Center Jerusalem Israel
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03878550 on ClinicalTrials.gov ↗ ← All trials in the USA