Individual and multicenter efforts have facilitated the recognition of
different parameters with prognostic value at presentation of chronic
myeloid leukemia (CML). Interest is currently focused on the prognost
ic evaluation of features obtained from molecular analysis, and isolat
ion of data with evalutive predictive value. The site of breakpoint wi
thin the M-BCR has been suggested as a prognostic factor in some studi
es. A recent analysis from our group failed to demonstrate differences
in either duration of chronic phase or survival between patients with
5' and 3' breakpoints. We have confirmed in a sequential study that a
decrease in the expression of some myeloid differentiation antigens o
f the blood granulocytes can be a prognostic indicator along CML evolu
tion. Our more recent study, separating blast crises on immunological
and molecular grounds, confirms lymphoid cases as a distinct subgroup
and shows a trend for an association between megakaryoblastic blast cr
isis and 3' location of the breakpoint.