HCC Risk and Monitoring in Patients With Type 2 Diabetes

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorNational Taiwan University Hospital

About this trial

Liver cancer is a significant malignancy in Taiwan. With the widespread implementation of antiviral therapies, hepatitis B and C-related liver cancer has gradually declined; however, metabolic dysfunction-associated liver cancer continues to increase, particularly among patients with type 2 diabetes mellitus (T2DM) who also present with significant liver fibrosis. Current clinical guidelines lack standardized recommendations for liver cancer screening in this specific population, and data from prospective randomized controlled trials remain scarce.This study is a prospective randomized controlled trial enrolling patients aged 18 years, diagnosed with T2DM, and with a FIB-4 \> 2.67. Participants will be randomly assigned to either the surveillance group or the standard-care group. The surveillance group will undergo blood tests every 6 months to monitor liver function, AFP, and PIVKA-II, alongside the calculation of the GAAD score. The standard-care group will receive liver function tests every 6 months according to routine clinical practice. Abdominal ultrasound or computed tomography (CT) scans will be arranged by clinicians when clinically indicated. All participants will undergo abdominal ultrasound at baseline and at the end of the third year, with blood samples and clinical data collected periodically. The primary endpoint of this study is the tumor size at the time of liver cancer diagnosis. Secondary endpoints include liver cancer staging, number of liver cancer tumors, liver cancer incidence, the proportion of patients receiving curative treatment, and the degree of liver fibrosis as reflected by changes in FIB-4. This study expects to clarify the clinical benefits of a GAAD score-based surveillance strategy compared to standard care in T2DM patients with high FIB-4 scores, thereby providing evidence-based support for future liver cancer screening strategies and clinical guidelines.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age 18 years or older.

Diagnosed with type 2 diabetes mellitus and clinically followed with regular outpatient visits.

FIB-4 index greater than 2.67 (calculated based on AST, ALT, and platelet count within the past 6 months).

Willing and able to provide written informed consent.

Disqualifiers

HBsAg positive.

Anti-HCV positive and HCV RNA positive (patients with anti-HCV positive but negative HCV RNA are still eligible).

Prior history of hepatobiliary malignancies.

Undergoing regular abdominal ultrasound screening more than once per year.

Trial design

Design model

Parallel

Treatments tested in this trial

  • GAAD score

    Diagnostic test

    GAAD score (Gender, age, AFP, DC) will be measured every 6 months in the GAAD Surveillance Group.

Treatment groups

2,400 Participants
are divided into 2 treatment groups
Group A: Standard Care GroupNo intervention 0 interventions
Group B: GAAD Surveillance GroupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Maximum tumor diameter of hepatocellular carcinoma (cm).

The maximal tumor diameter of all HCC tumors, measured in centimeters

Time frame
From the date of enrollment up to 3 years.

Secondary outcomes

1

Stage of hepatocellular carcinoma.

The stage of HCC, using the BCLC staging and the AJCC TNM staging

Time frame
From the date of enrollment up to 3 years.
2

Number of hepatocellular carcinoma tumors

The number of HCC tumors evaluated by abdominal CT or MRI exams

Time frame
From the date of enrollment up to 3 years
3

Incidence of hepatocellular carcinoma

The rate of new HCC developed during the study

Time frame
From the date of enrollment up to 3 years
4

Proportion of hepatocellular carcinoma cases receiving curative treatment.

Proportion of hepatocellular carcinoma cases receiving curative treatment (including liver transplantation, surgical resection, local ablation, proton therapy, and etc.)

Time frame
From the date of enrollment up to 3 years.

Other outcomes

Sponsors and contacts

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