DNA flow cytometry (FCM) has become a routine method in breast cancer
diagnosis for evaluation of ploidy and proliferation kinetics (cell cy
cle analysis). Image cytometry is less practicable and provides less i
nformation than flow cytometry. An optimized technique with a low coef
ficient of variation is required for optimal results in flow cytometry
. The S-phase fraction and the proliferation index (sum of S-phase fra
ction and G(2)M fraction) provide prognostic and therapeutically relev
ant information. A profound knowledge of the technique and its limitat
ions is indispensable for the interpretation of FCM results. It remain
s to be established whether immunohistological evaluation of cell prol
iferation has the same prognostic value. Future developments are to be
expected from multipara metric analysis and the improvement of mathem
atical analysis of FCM measurements.