Skip to main content
Clinical Trials/NCT05716620
NCT05716620
Recruiting
Not Applicable

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

Post Graduate Institute of Medical Education and Research, Chandigarh1 site in 1 country380 target enrollmentFebruary 8, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hepatocellular Carcinoma
Sponsor
Post Graduate Institute of Medical Education and Research, Chandigarh
Enrollment
380
Locations
1
Primary Endpoint
HCC detection rate of US vs AMRI in cirrhotic patients
Status
Recruiting
Last Updated
3 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
February 8, 2022
End Date
February 7, 2025
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Post Graduate Institute of Medical Education and Research, Chandigarh
Responsible Party
Principal Investigator
Principal Investigator

Pankaj Gupta

Associate Professor

Post Graduate Institute of Medical Education and Research, Chandigarh

Eligibility Criteria

Inclusion Criteria

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

Exclusion Criteria

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

Outcomes

Primary Outcomes

HCC detection rate of US vs AMRI in cirrhotic patients

Time Frame: Day 7 from the time of enrolment till 12 month's scan

number of HCCs detected by US / AMRI divided by the actual number of HCCs based reference standard

Secondary Outcomes

  • False referral rate(Day 7 from the time of enrolment till 12 month's scan)
  • Sensitivity, specificity of US vs AMRI(Day 7 from the time of enrolment till 12 month's scan)
  • positive predictive value of US vs AMRI(Day 7 from the time of enrolment till 12 month's scan)
  • negative predictive value of US vs AMRI(Day 7 from the time of enrolment till 12 month's scan)
  • Survival of patients(Day 7 from the time of enrolment till 12 month's scan)

Study Sites (1)

Loading locations...

Similar Trials