National Liver Cancer Screening Trial

Hepatitis B Clinical Trial

— TRACER  

Official title:

National Liver Cancer Screening Trial

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06084234
• Other study ID #: TRACER
• Secondary ID: 2U24CA086368-22
• Status: Recruiting
• Phase: Phase 4
• Start date: December 26, 2023
• Est. completion date: December 31, 2034

Study information

• Verified date: February 2024
• Source: University of Texas Southwestern Medical Center
• Contact: Amit Singal, MD, MS
• Phone: 214.645.6216
• Email: Amit.Singal[@]UTSouthwestern.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The National Liver Cancer Screening Trial is an adaptive randomized phase IV Trial comparing ultrasound-based versus biomarker-based screening in 5500 patients with cirrhosis from any etiology or patients with chronic hepatitis B infection. Eligible patients will be randomized in a 1:1 fashion to Arm A using semi-annual ultrasound and AFP-based screening or Arm B using semi-annual screening using GALAD alone. Randomization will be stratified by sex, enrolling site, Child Pugh class (A vs. B), and HCC etiology (viral vs. non-viral). Patients will be recruited from 15 sites (mix of tertiary care and large community health systems) over a 3-year period, and the primary endpoint of the phase IV trial, reduction in late-stage HCC, will be assessed after 5.5 years.

Description:

The TRACER phase IV biomarker study is a randomized trial comparing ultrasound-based screening versus a biomarker-based strategy in patients with cirrhosis. In brief, 5500 patients with cirrhosis from any etiology would be randomized in a 1:1 fashion to Arm A offering semi-annual ultrasound +/- AFP-based screening or Arm B offering semi-annual biomarker-based screening. Randomization will be stratified by site, Child Pugh class (A vs. B), liver disease etiology (viral, non-viral, and non-cirrhotic HBV infection) and sex. Patients will be recruited from 15 sites (mix of tertiary care and large community health systems) over a 3-year period, and reduction in the proportion of late-stage HCC, will be assessed at the end of Year 5.5. If the results are promising, study team will continue extended follow-up and compare the incidence of late-stage HCC between the two arms at Year 8 and reduction in HCC mortality during long term follow up. Study team will include adult patients, age ≥ 18 years, with Child Pugh class A or B cirrhosis of any etiology or non-cirrhotic chronic hepatitis B virus infection with PAGE-B score >9. Study team will exclude patients post liver transplantation, patients with Child Pugh C cirrhosis, patients with significant comorbidity and limited life expectancy, and those with history of other malignancy, except non-melanoma skin cancer or indolent tumors, within 3 years prior to enrollment given lack of screening recommendations in those patient populations. Study team will also exclude patients with suspicious liver masses at baseline as well as those with a solid lesion ≥1 cm on ultrasound or AFP ≥20 ng/mL without diagnostic evaluation to exclude HCC. Study team will also exclude patients in whom the provider plans to follow the patient with CT or MRI-based surveillance. GALAD is not recommended in patients with pregnancy or active warfarin use given known impact on biomarker performance, so these patients will be excluded. At enrollment, study team will record patient demographics and clinical characteristics using a combination of electronic medical records and patient questionnaires. Patients will then be offered semi-annual surveillance as defined by their study arm: ultrasound and AFP for patients in Arm A and the biomarker, GALAD, for patients in Arm B. Repeat surveillance tests will be offered every six months (per assigned arm) for patients with normal surveillance results. Diagnostic evaluation with multi-phasic CT or contrast-enhanced MRI will be recommended for any patients with abnormal screening results. Patients with normal diagnostic testing (i.e., false positive result) will be recommended to return to their assigned surveillance arm. Standardized criteria from the AASLD and LI-RADS will be used to define incident HCC. Study team will use a set of validated surveys (e.g., Psychological Consequences Questionnaire, Decision Regret scale, FACIT-COST) to measure secondary outcomes of interest including psychological and financial harms.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 5500
• Est. completion date: December 31, 2034
• Est. primary completion date: December 31, 2029
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 85 Years

Eligibility

Inclusion Criteria:

Patient must meet all of the following inclusion criteria:

1. Adult patients ages 18-85 with cirrhosis from any etiology or with chronic hepatitis B with a PAGE-B score greater than 9 within 12 months of enrollment

2. Patient is eligible for HCC surveillance according to treating physician or by the site investigator

3. Able to provide informed consent

4. Life expectancy >6 months (after consent) as determined by the treating provider or site investigator Exclusion Criteria:

Patient will be excluded for any of the following exclusion criteria:

1. Child Pugh C cirrhosis

2. History or clinical symptoms of hepatocellular carcinoma or cholangiocarcinoma

3. History of solid nodule on baseline ultrasound (i.e., lesion 1cm or greater) within 9 months prior to consent without subsequent diagnostic CT/MRI demonstrating benign nature)

4. AFP >20 ng/mL within 6 months prior to consent, in the absence of a contrast-enhanced CT or MRI within 6 months of AFP (before or after) level demonstrating lack of suspicious liver lesions

5. Newly diagnosed LR-3 greater than or equal to 1 cm within 6 months prior to consent

6. History of LR-4, LR-5, or LR-M on multi-phase CT or contrast-enhanced MRI within 6 months prior to consent

7. Presence of another active cancer besides non-melanomatous skin cancer or indolent cancer under active surveillance (e.g., prostate cancer or renal cell carcinoma) within the 2 years prior to consent

8. Patient's provider is planning to use MRI- or CT- based surveillance moving forward

9. History of a transjugular intrahepatic portosystemic shunt (TIPS)

10. History of Fontan associated liver disease or cardiac cirrhosis

11. History of solid organ transplantation

12. Actively listed for liver transplantation

13. Diagnosis of alcohol-associated hepatitis within 3 months prior to consent

14. Documented current or continued signs and symptoms of acute Wilson disease (acute liver failure, acute neurological deficits, hemolysis)

15. In patients with primary sclerosing cholangitis (PSC): Current active cholangitis within 90 days prior to consent

16. Known or documented habitual non-adherence to previous research studies or medical procedures or unwillingness to adhere to protocol (e.g., unwilling to obtain consent or samples)

17. In patients living with HIV: CD4+ T cell count less than 100 cells/mm3 within 60 days prior to consent

18. Known pregnancy at consent

19. Active warfarin use

Related Conditions & MeSH terms

• Carcinoma, Hepatocellular
• Hepatitis B
• Liver Cancer
• Liver Cirrhosis
• Liver Neoplasms

Intervention

Diagnostic Test:
• GALAD
GALAD is a 3 biomarker panel incorporating AFP, AFP-L3% and DCP (all FDA approved), with patient age and sex.
• Liver Ultrasound with or without AFP
This intervention consists of current standard of care ultrasound based surveillance with or without alpha-fetoprotein measurement.

Locations

Country	Name	City	State
United States	University of Michigan	Ann Arbor	Michigan
United States	Massachusetts General Hospital	Boston	Massachusetts
United States	UT Southwestern Medical Center and Parkland Hospital	Dallas	Texas
United States	Henry Ford Health System	Detroit	Michigan
United States	Baylor College of Medicine	Houston	Texas
United States	Indiana University	Indianapolis	Indiana
United States	University of Southern California	Los Angeles	California
United States	The Feinstein Institutes, Northwell Health, Inc.	Manhasset	New York
United States	University of Pennsylvania	Philadelphia	Pennsylvania
United States	University of California, San Francisco	San Francisco	California

Sponsors (7)

Lead Sponsor	Collaborator
University of Texas Southwestern Medical Center	Baylor College of Medicine, Dana-Farber Cancer Institute, Fred Hutchinson Cancer Center, National Cancer Institute (NCI), University of Michigan, University of Pennsylvania

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Proportion of HCC detected at late stage	Proportion of HCC detected at a late stage, defined as HCC beyond Milan Criteria (one tumor less than or equal to 5 cm or 2-3 tumors each less than or equal to 3 cm, in the absence of vascular invasion or extra-hepatic metastases)	5.5 years
Secondary	HCC Screening utilization	Defined as proportion time covered by screening; each completed screening test (US +/- AFP or GALAD) will provide up to six months of coverage (numerator) divided by the total follow-up for each patient.	5.5 years
Secondary	Proportion of HCC detected at a late-stage (defined based on BCLC stage)	Defined as HCC beyond BCLC stage A (single tumor of any size without vascular invasion or extrahepatic spread; or 2-3 tumors equal to or less than 3 cm each, without vascular invasion or extrahepatic spread)	5.5 years
Secondary	Incidence of late-stage HCC	Defined as incidence of HCC (extended follow-up) beyond Milan Criteria or BCLC stage A	8 years
Secondary	Proportion of HCC cases that receive Curative therapy	Defined as count of participants in receipt of liver transplantation, surgical resection, local ablative therapy, or radiation segmentectomy	5.5 years
Secondary	Number of participants who encountered screening related physical harm	Physical harms will be defined as count of participants in receipt of diagnostic imaging for false positive or indeterminate results.	5.5 years
Secondary	Number of participants who encountered screening related financial harm	Financial harms will be defined by direct costs (charges for all screening and diagnostic testing and co-pays) and indirect costs (e.g., travel and lost wages)	5.5 years
Secondary	Number of participants who encountered screening related Psychological harm	Count of participants who encountered Psychological harms that includes cancer-specific worry and decisional regret.	5.5 years