Jl. Dhautcourt et al., QUALITY-CONTROL STUDY BY THE FRENCH CYTOMETRY ASSOCIATION ON FLOW CYTOMETRIC DNA CONTENT AND S-PHASE FRACTION (S-PERCENT), Cytometry, 26(1), 1996, pp. 32-39
Clinical use of flow cytometric (FCM) DNA analysis requires effective
quality controls, Thirty-two laboratories with various degrees of FCM
experience participated in the first phase of a quality control progra
m organized by the Association Francaise de Cytometrie. All received d
iskettes containing ten list-mode files and ten histogram files that w
ere derived from FCM analysis of various unfixed tumor specimens, A to
tal of 610 responses on DNA ploidy and cell cycle were obtained with t
hree different DNA analysis softwares: CellFit used by (44% of respons
es), MultiCycle (44%), and ModFit (12%), After statistical analysis, 3
1% of the responses were excluded from the final analysis for precise
reasons, The groups were too small to carry out a valid analysis of th
e slight differences in the percentage of cells in the DNA synthesis p
hase (S%) between CellFit and MultiCycle. To estimate the influence of
gating on the final cell-cycle results, five of the histogram files w
ere derived from corresponding list-mode files, but the participating
laboratories were unaware of this, A good correlation (r = 0.98) was o
btained for S% values in the five paired files, The fact that 31% of t
he responses had to be excluded clearly reflects inadequate training i
n the use of these analysis softwares and, in some cases, a failure to
grasp the biological meaning of the results, in contrast, the laborat
ories fulfilling consensus recommendations obtained remarkably homogen
eous results, showing that standardization is feasible. (C) 1996 Wiley
-Liss, Inc.