Surface CD14 positivity in B-cell chronic lymphocytic leukaemia is relatedto clinical outcome

Citation
V. Callea et al., Surface CD14 positivity in B-cell chronic lymphocytic leukaemia is relatedto clinical outcome, BR J HAEM, 107(2), 1999, pp. 347-352
Citations number
30
Categorie Soggetti
Hematology,"Cardiovascular & Hematology Research
Journal title
BRITISH JOURNAL OF HAEMATOLOGY
ISSN journal
00071048 → ACNP
Volume
107
Issue
2
Year of publication
1999
Pages
347 - 352
Database
ISI
SICI code
0007-1048(199911)107:2<347:SCPIBC>2.0.ZU;2-G
Abstract
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.