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Carcinoma, HepatocellularPhase 4TRACERNCT06084234

National Liver Cancer Screening Trial

A Phase 4 study testing GALAD and Liver Ultrasound with or without AFP in people with Carcinoma, Hepatocellular and Liver Cancer, run by University of Texas Southwestern Medical Center at 19 sites in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
Search all trials

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. Read more about this study

Who is it for?
Ages 18 to 85 years
What is being tested?
GALAD and Liver Ultrasound with or without AFP
Could I receive a placebo?
No, everyone receives an active treatment
How many people
5,500 participants
Where
19 sitesUnited States
Study dates
26 Dec 2023to 31 Dec 2034
Phase
Phase 4
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 85 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Patient must meet all of the following inclusion criteria:
  • 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
  • Patient is eligible for HCC surveillance according to treating physician or by the site investigator
  • Able to provide informed consent
  • Life expectancy >6 months (after consent) as determined by the treating provider or site investigator

Who cannot join

  • Patient will be excluded for any of the following exclusion criteria:
  • Child Pugh C cirrhosis
  • History or clinical symptoms of hepatocellular carcinoma or cholangiocarcinoma
  • 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)
  • 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
  • Newly diagnosed LR-3 greater than or equal to 1 cm within 6 months prior to consent
Show all 20Show fewer
  • History of LR-4, LR-5, or LR-M on multi-phase CT or contrast-enhanced MRI within 6 months prior to consent
  • 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
  • Patient's provider is planning to use MRI- or CT- based surveillance moving forward
  • History of a transjugular intrahepatic portosystemic shunt (TIPS)
  • History of Fontan associated liver disease or cardiac cirrhosis
  • History of solid organ transplantation
  • Actively listed for liver transplantation
  • Diagnosis of alcohol-associated hepatitis within 3 months prior to consent
  • Documented current or continued signs and symptoms of acute Wilson disease (acute liver failure, acute neurological deficits, hemolysis)
  • In patients with primary sclerosing cholangitis (PSC): Current active cholangitis within 90 days prior to consent
  • 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)
  • In patients living with HIV: CD4+ T cell count less than 100 cells/mm3 within 60 days prior to consent
  • Known pregnancy at consent
  • Active warfarin use

Trial locations and contacts

19 sites in 1 country. Contact the study team or a site near you to ask about taking part.

19 sites in 1 country

United States19 sites, 18 recruiting
  • University of Michigan

    Ann Arbor, Michigan, 48109

    Shay Robison, roshay@med.umich.edu

    Neehar Parikh, MD, MS

    Recruiting
  • Massachusetts General Hospital

    Boston, Massachusetts, 02114

    Megan Michta, MMICHTA@mgh.harvard.edu

    Irun Bhan, MD

    Recruiting
  • University of North Carolina

    Chapel Hill, North Carolina, 27599

    Andrew Moon, MD, 919-843-5936, Andrew.Moon@unchealth.unc.edu

    Bhagyashree Behera, 919-843-5936, BB_Behera@med.unc.edu

    Recruiting
  • Northwestern University

    Chicago, Illinois, 60611

    Laura Kulik, MD, 312-694-1293, laura.kulik@nm.org

    Kimberly Sipich, 312-694-1293, k-sipich@northwestern.edu

    Recruiting
  • Case Western Reserve University

    Cleveland, Ohio, 44106

    Active, not recruiting
  • The Cleveland Clinic

    Cleveland, Ohio, 44195

    Taebin Son, 216-444-9508, Sont16@ccf.org

    Shilpa Junna

    Recruiting
  • UT Southwestern Medical Center and Parkland Hospital

    Dallas, Texas, 75390

    Katharine McCallister, 214-645-1378, TRACER@UTSouthwestern.edu

    Amit Singal, MD, MS

    Recruiting
  • Henry Ford Health System

    Detroit, Michigan, 48202

    Jessica Peruski, jperusk1@hfhs.org

    Reena Salgia, MD

    Recruiting
  • Baylor College of Medicine

    Houston, Texas, 77021

    Emad Sorial, 713-798-7370, Emad.Sorial@bcm.edu

    Sara.Fares@bcm.edu

    Recruiting
  • Indiana University

    Indianapolis, Indiana, 46202

    Sherri Cummins, shcummin@iu.edu

    Naga Chalasani, MD

    Recruiting
  • University of Southern California

    Los Angeles, California, 90089

    Kali Zhou, MD

    Kali Zhou, MD

    Recruiting
  • The Feinstein Institutes, Northwell Health, Inc.

    Manhasset, New York, 11030

    Dibnain Nanda, dnanda1@northwell.edu

    Sanjaya Satapathy, MBBS, MS

    Recruiting
  • Hennepin Healthcare

    Minneapolis, Minnesota, 55415

    Jose Debes, MD, 9527379762, debes003@umn.edu

    Daniel Akah, 9527379762, Dakah@bermancenter.org

    Recruiting
  • University of Minnesota

    Minneapolis, Minnesota, 55455

    Elizabeth Aby, MD, 612-625-8999, abyxx002@umn.edu

    Erin Wesley, wesle091@umn.edu

    Recruiting
  • University of Pennsylvania

    Philadelphia, Pennsylvania, 19104

    Grace Kim, gracekim.lee@pennmedicine.upenn.edu

    Jorge Marrero, MD,MS

    Recruiting
  • Stanford University

    Redwood City, California, 94063

    Paul Kwo, MD, 650-723-5135, pkwo@stanford.edu

    Jennifer Smart, 650-721-8517, Jsmart2@stanford.edu

    Recruiting
  • Virginia Commonwealth University

    Richmond, Virginia, 23219

    Hannah Lee, MD, 804-828-4060, Hannah.Lee@vcuhealth.org

    Hannah Cook, 804-628-9312, Hannah.Cook1@vcuhealth.org

    Recruiting
  • Kaiser Permanente

    Roseville, California, 95661

    Sreepriya Balasubramanian, MD, MPH, 916-474-6221, Sreepriya.Balasubramanian@kp.org

    Quyen Chau, 415-833-3468, Quyen.X.Chau@kp.org

    Recruiting
  • University of California, San Francisco

    San Francisco, California, 94117

    Rae Davis, rayshawnda.davis@ucsf.edu

    Neil Mehta, MD

    Recruiting

Other trials in United States

About this study

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.

Read the detailed 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.

Being tested
GALAD, Liver Ultrasound with or without AFP
Keywords
Hepatocellular carcinoma surveillance, GALAD, Alpha Fetoprotein
Medical subject headings
Carcinoma, Hepatocellular, Liver Neoplasms, Liver Cirrhosis, Hepatitis B

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • GALADDiagnostic test

    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 AFPDiagnostic test

    This intervention consists of current standard of care ultrasound based surveillance with or without alpha-fetoprotein measurement.

Study groups in NCT06084234
Study groupRoleWhat they receive
Arm A: Semi-annual surveillance using liver ultrasound +/- alpha-fetoproteinActive comparatorParticipants in this arm will undergo current standard of care surveillance procedures i.e. liver ultrasound with or without alpha fetoprotein (AFP) measurement.
Receives: Diagnostic Test: Liver Ultrasound with or without AFP
Arm B: Semi-annual surveillance using GALADExperimentalFor participants in this arm, study team will order GALAD measurement every 6 months +/- 3 months.
Receives: Diagnostic Test: GALAD

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. 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)

    Measured: 5.5 years

Secondary outcomes (7)
  1. 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.

    Measured: 5.5 years

  2. 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)

    Measured: 5.5 years

  3. Incidence of late-stage HCC

    Defined as incidence of HCC (extended follow-up) beyond Milan Criteria or BCLC stage A

    Measured: 8 years

  4. 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

    Measured: 5.5 years

  5. 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.

    Measured: 5.5 years

  6. 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)

    Measured: 5.5 years

  7. Number of participants who encountered screening related Psychological harm

    Count of participants who encountered Psychological harms that includes cancer-specific worry and decisional regret.

    Measured: 5.5 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted16 Oct 2023
  2. Study start26 Dec 2023
  3. Primary completion31 Dec 2029 (estimated)
  4. Study completion31 Dec 2034 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 4
Primary purpose
Screening
Allocation
Randomised
Intervention model
Parallel groups
Model description
This is a randomized open-label study comparing US ± AFP vs. GALAD-based surveillance every 6 (± 3-month window) months starting at randomization.
Masking
None (open label)
Enrolment
5,500 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06084234
Sponsor's protocol ID
TRACER
Other IDs
2U24CA086368-22
Acronym
TRACER
Status last verified
Sep 2026
First submitted
10 Oct 2023
Last updated
25 Sep 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
Yes
Individual data sharing
No

Publications

  • Singal AG, Parikh ND, Kanwal F, Marrero JA, Deodhar S, Page-Lester S, Lopez C, Feng Z, Tayob N. National Liver Cancer Screening Trial (TRACER) study protocol. Hepatol Commun. 2024 Nov 4;8(11):e0565. doi: 10.1097/HC9.0000000000000565. eCollection 2024 Nov 1.

    PubMed 39495136

Questions about this trial

What is this clinical trial studying?

A Phase 4 study testing GALAD and Liver Ultrasound with or without AFP in people with Carcinoma, Hepatocellular and Liver Cancer, run by University of Texas Southwestern Medical Center at 19 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 20 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 25 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 19 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Amit Singal, MD, MS (214-645-8821, Amit.Singal@UTSouthwestern.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Proportion of HCC detected at late stage (time frame: 5.5 years). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06084234, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 25 Sep 2026.

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