Real-world Elecsys® GAAD Implementation and Validation to Improve Surveillance and Early Detection of HCC

NARecruitingINTERVENTIONAL
Enrollment

600

Participants

Timeline

Start Date

January 8, 2024

Primary Completion Date

July 31, 2030

Study Completion Date

July 31, 2030

Conditions
Liver CirrhosisHepatocellular Carcinoma
Interventions
DIAGNOSTIC_TEST

Elecsys® GAAD

Elecsys® GAAD is a CE marked in vitro diagnostic (IVD) multivariate index assay, intended as an aid in the diagnosis of early-stage HCC. It provides a semi quantitative result by combining in an algorithm the quantitative measurements of Elecsys® AFP (alpha-fetoprotein) and Elecsys® PIVKA-II (protein induced by vitamin K absence II) levels in serum and plasma, with gender and age. Clinical evidence showed that Elecsys® GAAD had high performance in detecting HCC (sensitivity 86.5%), particularly early stage (sensitivity 78.9%), with 91.4% specificity for both early and all stages, out-performing current standard of care (Chan et al. 2021). Elecsys® GAAD may be integrated into current surveillance practice to increase early-stage HCC detection rate, reduce unnecessary onward investigations and patient anxiety.

Trial Locations (1)

M13 9WL

RECRUITING

Manchester University NHS Foundation Trust, Manchester

All Listed Sponsors
collaborator

University of Manchester

OTHER

collaborator

Roche Pharma AG

INDUSTRY

collaborator

Unity Insights

UNKNOWN

collaborator

Imperial College London

OTHER

lead

Manchester University NHS Foundation Trust

OTHER_GOV