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Prospective Evaluation of Hepatocellular Carcinoma Surveillance in At-Risk Patients (Screening HCC)

Prospective Evaluation of Hepatocellular Carcinoma Surveillance in At-Risk Patients Using Semiannual Ultrasound LI-RADS and Alpha-Fetoprotein: A Multicenter Real-World Observational Study

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07764835
Acronym
Screening HCC
Enrollment
300
Registered
2026-08-14
Start date
2026-09-15
Completion date
2029-06-30
Last updated
2026-08-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Advanced Liver Fibrosis, Chronic Hepatitis B, Hepatocellular Carcinoma, Liver Cirrhosis, Metabolic Dysfunction-Associated Steatotic Liver Disease

Keywords

HCC, Hepatocellular Carcinoma, Liver Cancer, HCC Surveillance, US LI-RADS, Ultrasound LI-RADS, Alpha-Fetoprotein, AFP, Liver Cirrhosis, Chronic Hepatitis B, MASLD, Metabolic Dysfunction-Associated Steatotic Liver Disease, Real-World Study, Observational Study, Early Detection, BCLC, Rede D'Or, Brazil

Brief summary

This prospective multicenter observational study evaluates the performance of a structured hepatocellular carcinoma (HCC) surveillance program in patients at increased risk of developing liver cancer. Participants will undergo routine surveillance with semiannual abdominal ultrasound reported using the Ultrasound Liver Imaging Reporting and Data System (US LI-RADS) and serum alpha-fetoprotein (AFP) testing as part of standard clinical care. The study aims to assess HCC detection rates, stage at diagnosis, detection of other hepatic malignancies, and the time intervals between detection, diagnosis, and treatment in a real-world setting. Approximately 300 participants will be enrolled and followed for up to 36 months.

Detailed description

Hepatocellular carcinoma (HCC) is the most common primary liver malignancy and remains a leading cause of cancer-related mortality worldwide. Early detection through surveillance is associated with improved access to curative therapies and better survival outcomes. Despite international guideline recommendations, implementation of surveillance programs remains heterogeneous in routine clinical practice, and limited real-world evidence is available regarding the effectiveness of structured HCC surveillance pathways in Brazil. This prospective multicenter observational study is designed to evaluate the performance of a structured HCC surveillance program implemented within the Rede D'Or healthcare network. The program combines standardized abdominal ultrasound reporting using the Ultrasound Liver Imaging Reporting and Data System (US LI-RADS), regular alpha-fetoprotein (AFP) assessment, dedicated training of healthcare professionals, and predefined referral pathways for diagnostic evaluation and clinical management. The study aims to generate real-world evidence regarding the effectiveness of standardized surveillance strategies in populations at increased risk for HCC. In addition to evaluating HCC detection, the study will assess the clinical characteristics and staging patterns of diagnosed tumors, detection of other malignant liver lesions, and the efficiency of the diagnostic and treatment pathway. Special attention will be given to patients who do not fully meet traditional surveillance criteria but may still present clinically relevant risk for HCC, including individuals with advanced fibrosis and metabolic dysfunction-associated steatotic liver disease (MASLD). No experimental interventions will be administered as part of this protocol. All surveillance procedures, diagnostic investigations, and treatment decisions will be performed according to routine clinical practice and the judgment of treating physicians. Data generated during routine care will be collected prospectively and analyzed to better understand the effectiveness of structured surveillance programs in real-world clinical settings.

Interventions

None listed

Sponsors

D'Or Institute for Research and Education
Lead SponsorOTHER
AstraZeneca
CollaboratorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Written informed consent. * Age 18 years or older. * Liver cirrhosis of any etiology. * Chronic hepatitis B with moderate or high risk of HCC according to PAGE-B criteria. * Non-cirrhotic chronic liver disease with increased risk for HCC, including fibrosis stage 3 or higher or metabolic dysfunction-associated steatotic liver disease (MASLD) with one or more risk factors for HCC. * Followed at hepatology clinics within the Rede D'Or health network. * Eligible for routine HCC surveillance with ultrasound and alpha-fetoprotein according to standard clinical practice.

Exclusion criteria

* Known hepatocellular carcinoma at enrollment. * Previous diagnosis of hepatocellular carcinoma. * Metastatic liver disease. * Other malignant liver tumors present at enrollment. * Clinical condition preventing routine surveillance follow-up. * Inability to provide informed consent.

Design outcomes

Primary

MeasureTime frameDescription
Annual Incidence Rate of Hepatocellular CarcinomaUp to 36 monthsIncidence of newly diagnosed hepatocellular carcinoma among participants enrolled in the structured surveillance program

Secondary

MeasureTime frameDescription
Early-Stage HCC Detection RateUp to 36 monthsProportion of hepatocellular carcinoma cases diagnosed at BCLC stage 0 or A.

Contacts

CONTACTGuilherme C Ambrósio, MSc
guilherme.ambrosio@idor.org+55 11 972763211
CONTACTEscritório O Operações
gestao.ensaiosclinicos@idor.org
PRINCIPAL_INVESTIGATORLeonardo G Fonseca, MD, MSc

D'Or Institute for Research and Education (IDOR)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 15, 2026