The aberrant expression of the myelomonocytic antigen CD14 was investigated
in 128 untreated patients diagnosed with B-cell chronic lymphocytic leukae
mia (B-CLL). A cut-off value of 5 x 10(9)/l CD14-positive cells was chosen
for statistical analysis because it showed the best discriminating power am
ong patients with different clinical features. 56 cases had a CD14(+) cell
count >5 x 10(9)/l. A significant correlation was found between Rai and Bin
et stages and total tumour mass (TTM) score on one hand, and the absolute C
D14(+) cell cut-off, on the other. This relationship was more evident in Ra
i 0-II and Binet A-B stages, where a CD14(+) cell count >5x10(9)/l was pref
erentially distributed among patients with a higher tumoral mass. In univar
iate analysis the survival probability at 5 and 10 years showed a significa
nt correlation with Rai and Binet stages, TTM score, CD14+ absolute cell co
unt and median age. The median overall survival (OS) was 63 months for pati
ents with a CD14(+) cell count >5 x 10(9)/l and 136 months for those with a
CD14(+) cell count <5 x 10(9)/l. In the multivariate Cox regression model,
Rai stage, age and CD14(+) cell count were independent significant factors
for the prediction of OS. Finally when the same analysis was restricted to
Rai stages 0-II, CD14(+) cell count was the only significant independent p
arameter influencing OS, with a relative death risk of 3.8. In conclusion,
these data reveal that CD14(+) represents an important marker for predictin
g OS in B-CLL patients and, therefore, we suggest that it should be include
d in the immunological characterization of B-CLL.