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Utility of Abbreviated Magnetic Resonance Imaging as a Screening Tool for Hepatocellular Carcinoma in Cirrhotic Patients

Utility of Abbreviated Magnetic Resonance Imaging as a Screening Tool for Hepatocellular Carcinoma in Cirrhotic Patients

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05716620
Enrollment
380
Registered
2023-02-08
Start date
2022-02-08
Completion date
2025-02-07
Last updated
2023-02-08

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

Conditions

Hepatocellular Carcinoma

Keywords

HCC, cirrhosis, chronic liver disease, hepatitis B & C

Brief summary

The goal of this study is Utility of abbrevational magnetic resonance imaging as a screening tool for hepatocellular carcinoma in cirrhotic patients. The primary objective of the study is: • HCC detection rate of US vs AMRI in cirrhotic patients The secondary objective of the study are: * False referral rate of US vs AMRI: false referral will be defined as lack of HCC on complete MRI despite a positive US or AMRI. * Positive predictive value of US vs AMRI: The positive predictive value will be defined as the number of patients with true positive results in patients with positive US/AMRI. Participants will be evaluated by two rounds of screening 6 months apart using paired US and non-enhanced AMRI.

Detailed description

Hepatocellular carcinoma (HCC) is the fifth most common cancer and is the second leading cause of cancer related death. The most important risk factor is cirrhosis of any etiology, particularly chronic hepatitis b and hepatitis c virus infection. Curative treatment (resection, transplant, or ablation) can be offered to patients diagnosed with early HCC. As the disease remains asymptomatic, most HCCs are diagnosed at an intermediate to terminal stage. Screening is an effective strategy to diagnose early HCC. The current guidelines recommend bi-annual screening with ultrasound (US) with or without alpha- fetoprotein (AFP). The overall sensitivity for detection of HCC using US screening is 60% while it is only 22% for detection of very early and early HCC. This results in many patients having progression of HCC despite being on screening program. Although computed tomography (CT) is widely available, the cumulative radiation dose from multiple screening CT scans makes CT screening unsuitable. Magnetic resonance imaging (MRI) has a high sensitivity and specificity for diagnosis of HCC owing to its high contrast resolution. A recent study showed significantly better sensitivity of HCC detection during screening using contrast enhanced MRI (CE-MRI) as compared with US. The use of CE-MRI entails high cost and risk of nephrogenic systemic fibrosis and is not well suited for screening from the health economics standpoint. Recently abbreviated MRI (AMRI) has been proposed as an acceptable alternative to US for HCC screening. AMRI involves acquisition of only a few MRI sequences rather than the complete MRI. This results in lesser table time and in turn reduced cost. However, most of the data is from retrospective studies. We propose a prospective study to evaluate the role of AMRI for HCC screening.

Interventions

DIAGNOSTIC_TESTMRI

USG and MRI will be performed on the same day. US will be performed prior to MRI. There will be two rounds of screening 6 months apart using paired US and non-enhanced AMRI.

Sponsors

Indian Council of Medical Research
CollaboratorOTHER_GOV
Post Graduate Institute of Medical Education and Research, Chandigarh
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
40 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

1. Age\>40 years 2. Presence of cirrhosis 3. Annual risk of HCC \>5% 4. No HCC on pre-enrollment imaging not more than 6 months back. 5. Risk factors including diabetes mellitus, metabolic syndrome, family history of HCC.

Exclusion criteria

1. Child C status 2. Diagnosed or follow up case of HCC 3. Other malignancies 4. Pregnancy, lactation 5. Contraindications to MRI (pacemaker, cochlear implant, claustrophobia) 6. Chronic renal disease or contrast allergy precluding administration of intravenous MRI contrast agent (for reference standard)

Design outcomes

Primary

MeasureTime frameDescription
HCC detection rate of US vs AMRI in cirrhotic patientsDay 7 from the time of enrolment till 12 month's scannumber of HCCs detected by US / AMRI divided by the actual number of HCCs based reference standard

Secondary

MeasureTime frameDescription
False referral rateDay 7 from the time of enrolment till 12 month's scannumber of false positive results divided by the sum of true negative and false- positive results
Sensitivity, specificity of US vs AMRIDay 7 from the time of enrolment till 12 month's scanSensitivity, specificity of US vs AMRI
positive predictive value of US vs AMRIDay 7 from the time of enrolment till 12 month's scanpositive predictive value of US vs AMRI
negative predictive value of US vs AMRIDay 7 from the time of enrolment till 12 month's scannegative predictive value of US vs AMRI
Survival of patientsDay 7 from the time of enrolment till 12 month's scanPatients who develop HCC during the 1-year follow up period using Kaplan Meier survival analysis.

Countries

India

Contacts

Primary ContactPANKAJ GUPTA
pankajgupta959@gmail.com8194896927

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 13, 2026