National Liver Cancer Screening Trial (TRACER) study protocol

被引:2
|
作者
Singal, Amit G. [1 ]
Parikh, Neehar D. [2 ]
Kanwal, Fasiha [3 ]
Marrero, Jorge A. [4 ]
Deodhar, Sneha [1 ]
Page-Lester, Stephanie [5 ]
Lopez, Camden [5 ]
Feng, Ziding [5 ]
Tayob, Nabihah [6 ]
机构
[1] UT Southwestern Med Ctr, Dept Internal Med, Dallas, TX USA
[2] Univ Michigan, Dept Internal Med, Ann Arbor, MI USA
[3] Baylor Coll Med, Dept Med, Houston, TX USA
[4] Univ Penn, Dept Internal Med, Philadelphia, PA USA
[5] Fred Hutchinson Canc Res Ctr, Biostat Program, Publ Hlth Sci Div, Seattle, WA USA
[6] Dana Farber Canc Inst, Dept Data Sci, Boston, MA USA
关键词
biomarker; GALAD; liver cancer; screening; ultrasound; HEPATOCELLULAR-CARCINOMA SURVEILLANCE; ILCA WHITE PAPER; BIOMARKER DEVELOPMENT; CLINICAL-PRACTICE; HCC SURVEILLANCE; ASSOCIATION; GALAD; VALIDATION; DIAGNOSIS; COHORT;
D O I
10.1097/HC9.0000000000000565
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background:Professional guidelines recommend HCC screening in at-risk patients using semi-annual ultrasound with or without alpha-fetoprotein (AFP); however, this strategy has limited effectiveness due to low adherence and sensitivity. Increasing data support the potential role of blood-based biomarker panels, which could improve both aspects. The biomarker panel GALAD, comprised of sex, age, and 3 blood biomarkers (AFP, AFP-L3, and des-carboxy prothrombin des-carboxy prothrombin), has shown high sensitivity and specificity in biomarker phase II (case-control) and phase III (retrospective cohort) validation studies. However, prospective validation in a large phase IV biomarker clinical utility trial is necessary before its adoption in practice.Methods:The National Liver Cancer Screening Trial is an adaptive pragmatic randomized phase IV trial, which began enrollment in January 2024, comparing ultrasound-based versus biomarker-based screening in 5500 patients with chronic hepatitis B infection or cirrhosis from any etiology. Eligible patients are randomly assigned in a 1:1 ratio to semi-annual screening with ultrasound +/- alpha-fetoprotein (arm A) or semi-annual screening with GALAD (arm B). Randomization is stratified by enrollment site, liver disease severity (per Child-Pugh class), liver disease etiology (viral, nonviral, and noncirrhotic HBV), and sex. Patients are being recruited from 15 sites (a mix of tertiary care academic referral centers, safety-net health systems, and large community health systems) over a 3-year period, and the primary endpoint, reduction in late-stage HCC, will be assessed at the end of year 5.5.Discussion:The results of this trial will inform the best strategy for HCC screening and early-stage detection in patients with chronic liver diseases. If GALAD shows superiority, HCC screening would primarily shift from an ultrasound-based strategy to the adoption of the biomarker panel.Trial Registration:NCT06084234.Trial Status:The TRACER Study is actively enrolling.
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页数:15
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