Prognostic assessment of B-cell chronic lymphocytic leukemia (CLL) patients
is generally based on either Rai or Binet clinical staging systems. Howeve
r, new biological parameters which reflect the clinical heterogeneity of di
sease are under investigation. Cellular and molecular features including tu
mor cell proliferation, immunophenotype, adhesion molecules expression and
release, karyotypic abnormalities and biological findings of increased angi
ogenesis have been correlated with tumor mass and survival. It is not clear
, however, whether the newly identified prognostic parameters will eventual
ly replace clinical variables representative of tumor mass. More likely, bi
ological parameters might be incorporated into clinico-prognostic models th
us leading to the formulation of a clinico-biological system for CLL.