Vv. Khien et al., Clinical evaluation of lentil lectin-reactive alpha-fetoprotein-L3 in histology-proven hepatocellular carcinoma, INT J B MAR, 16(2), 2001, pp. 105-111
Introduction: Serum alpha-fetoprotein (AFP) is a useful marker of hepatocel
lular carcinoma (HCC), although the serum AFP concentration is also increas
ed in patients with chronic liver diseases (CLD). The analysis of AFP glyco
-forms has been known to be of diagnostic value. We applied the lectin-affi
nity electrophoresis and antibody-affinity blotting techniques to HCC patie
nts in Vietnam in order to better understand the role of lentil lectin-affi
nity AFP-L3 in the diagnosis and differential diagnosis of HCC, and its rel
ationship with the biological characteristics of HCC.
Methods: Lens culinaris agglutinin-reactive AFP (AFP-L3) was measured in 65
patients with histologically proven HCC and 25 patients with CLD. All pati
ents had serum AFP levels above 54 ng/mL. AFP-LS levels were determined by
lectin affinity electrophoresis coupled with antibody-affinity blotting. Th
e diagnosis of HCC was confirmed histologically by ultrasound-guided biopsy
.
Results: The mean value of AFP-L3 in the HCC patients was 49.6 +/- 21.6%, w
hich was significantly higher (p <0.001) than that in the 25 CLD patients (
10.7 +/- 4.3%). When the cutoff level for AFP-L3 was set at 15% (mean +/- S
D), the sensitivity was 96.9%, the specificity 92.0% and the accuracy 95.5%
in the 65 HCC patients. There was no clear correlation between serum AFP l
evel and AFP-L3 percentage (r=0.16). There was no correlation between AFP-L
3 and the maximum diameter of HCC nodules (r=0.05). However, the mean AFP-L
3 value was higher in moderately or poorly differentiated HCC than in well
differentiated tumors (p <0.001).
Conclusions: AFP-L3 is potentially a clinically useful marker for the diffe
rentiation of increased AFP levels in hepatocellular carcinoma and chronic
liver diseases. The AFP-L3 percentage is closely related to HCC differentia
tion. We consider the analysis of AFP-L3 a useful adjunct in the diagnosis
of HCC.