Reference : Reproducibility of measurements of potential doubling time of tumour cells in the mul...
Scientific journals : Article
Human health sciences : Oncology
http://hdl.handle.net/2268/122137
Reproducibility of measurements of potential doubling time of tumour cells in the multicentre National Cancer Institute protocol
English
COUCKE, Philippe mailto [Centre Hospitalier Universitaire de Liège - CHU > > Radiothérapie >]
Paschoud, N [> >]
Pavy, J-J [> >]
Weber, P [> >]
Weber, K [> >]
Dubray, B [> >]
Wilson, G-D [> >]
1999
British Journal of Cancer
Nature Publishing Group
T92-0045 (323–332)
Yes (verified by ORBi)
International
0007-0920
1532-1827
London
United Kingdom
[en] proliferation ; flow cytometry ; multicentre ; conventional radiotherapy ; reproducibility
[en] We compared the flow cytometric measurement and analysis of the potential doubling time ( Tpot) between three centres involved in
the National Cancer Institute (NCI) protocol T92-0045. The primary purpose was to understand and minimize the variation within the
measurement. A total of 102 specimens were selected at random from patients entered into the trial. Samples were prepared, stained, run
and analysed in each centre and a single set of data analysed by all three centres. Analysis of the disc data set revealed that the
measurement of labelling index (LI) was robust and reproducible. The estimation of duration of S-phase ( Ts) was subject to errors of profile
interpretation, particularly DNA ploidy status, and analysis. The LI dominated the variation in Tpot such that the level of final agreement, after
removal of outliers and ploidy agreement, reached correlation coefficients of 0.9. The sample data showed poor agreement within each of the
components of the measurement. There was some improvement when ploidy was in agreement, but correlation coefficients failed to exceed
values of 0.5 for Tpot. The data suggest that observer-associated analysis of Ts and tissue processing and tumour heterogeneity were the
major causes of variability in the Tpot measurement. The first two aspects can be standardized and minimized, but heterogeneity will remain a
problem with biopsy techniques.
http://hdl.handle.net/2268/122137

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