10th. International African Conference on Contemporary Scientific Research, Nairobi, Kenya, 19 Ocak - 21 Şubat 2026, ss.125-126, (Özet Bildiri)
Introduction and Purpose: Alpha-fetoprotein (AFP) is a widely used
biomarker in hepatocellular carcinoma (HCC), particularly in AFP-positive cases
where it often reflects tumor burden and biological aggressiveness. However,
AFP levels alone are insufficient for comprehensive prognostic assessment. This
study aims to evaluate the relationships among demographic, clinical, imaging,
and laboratory parameters in AFP-positive HCC patients, and to identify
independent prognostic indicators such as tumor size, portal vein thrombosis
(PVT), liver function, and inflammatory/metabolic markers.
Materials and Methods: This prospective, single-center study included
patients diagnosed with HCC who were AFP-positive at baseline. Evaluated
variables included age, sex, etiology, Child–Turcotte–Pugh (CTP) score,
ascites, varices, cirrhosis, steatosis on ultrasonography, tumor localization
and segment involvement, largest tumor diameter, and presence of PVT.
Laboratory parameters comprised AFP, complete blood count (WBC, HGB, HCT, PLT),
liver function tests (albumin, bilirubin, AST, ALT, GGT, LDH), renal markers
(BUN, creatinine), metabolic indicators (glucose, Na, K, Ca), inflammatory
markers (CRP, ESR), iron metabolism (ferritin), thyroid hormones (TSH, T4),
lipid profile (cholesterol, triglycerides, LDL, HDL), and autoantibodies (ANA,
SMA, AMA). Statistical analyses included descriptive statistics, intergroup
comparisons, and multivariate regression to identify independent prognostic
factors.
Results: A total of 11 AFP-positive HCC patients were analyzed. The majority were
male (63,6%), with a mean age of 65 ± 9.42 years. HBV was the most common etiology
(45,5%), followed by Cryptogenic (27,3%) and MASLD (9,1%). Patients with
advanced CTP class exhibited higher rates of cirrhosis (72,7%), ascites (45,5%),
hypoalbuminemia (3,45±0,75), and thrombocytopenia (196±136). Larger tumor
diameter was significantly associated with PVT (5,36 cm). Elevated AFP levels
correlated with increased tumor burden and advanced BCLC stage. Inflammatory
markers (CRP, LDH) and ferritin showed positive associations with tumor size
and progression. Metabolic abnormalities and steatosis were more frequent in
MASLD-related cases. Multivariate analysis identified tumor size >5 cm,
presence of PVT, and hypoalbuminemia as independent predictors of poor
prognosis.
Discussion and Conclusion: In AFP-positive HCC patients, tumor
burden, vascular invasion, and liver function parameters are critical for
prognostic evaluation. AFP levels should be interpreted alongside imaging and
biochemical markers to guide clinical decision-making. The presence of PVT and
hypoalbuminemia are strong indicators of adverse outcomes, while inflammatory
and metabolic profiles provide complementary insights into disease progression
and etiology. These findings support a multiparametric approach for risk
stratification and therapeutic planning in AFP-positive HCC.