The development of
hepatocellular carcinoma (HCC) is often associated with chronic
inflammation, suggesting a strong relationship between
inflammation and
carcinogenesis. This study evaluated the prognostic values of inflammatory and T-helper (Th)
cytokines in the clinical outcome and survival of HCC. The study included 110 patients with HCC undergoing loco-regional
therapy and 24 healthy controls. Five Th1/Th2
cytokines and
C-reactive protein (CRP) were quantified before and after loco-regional treatment, using
enzyme-linked
immunosorbent assays. Levels of CRP,
interleukin (IL)-4, and
IL-6 were higher in patients with HCC than those in healthy subjects.
Tumor characteristics, Child-Pugh class, and CRP,
IL-6, and
IL-10 levels were associated with HCC survival (all P<0.05). With multivariate analysis, higher
IL-6 levels were identified as the independent
cytokine for shorter survival (P=0.010). Higher CRP and
IL-6 levels correlated well with larger
tumor size, poor Child-Pugh function, and shorter survival, with a significant inter-correlation (r=0.667). On serial measurements, the association of CRP with
tumor response was stronger than that of α-
fetoprotein or other
cytokines.
IL-6 and CRP are strong inflammatory indicators predictive of outcome in patients with HCC receiving loco-regional
therapy. This study suggests that inflammatory activation of the IL-6/CRP network may be a potential therapeutic target and
biomarker for HCC.