CELLULAR KINETICS IN RECTAL-CANCER

Measurements of dynamic tumour cell kinetic parameters, particularly t he potential doubling time (T-pot), may have potential as predictive a ssays for treatment outcome after radiotherapy. This paper details the distributions of T-pot and other kinetic and DNA content parameters m easured in rectal cancers. Biopsies were taken from 119 patients appro ximately 6 h after infusion of 200 mg m(-2) bromodeoxyuridine (BrdUrd) . The samples were analysed by bivariate DNA/BrdUrd flow cytometry. Th e primary purpose of the study was to measure the kinetic parameters o f labelling index (LI), duration of S-phase (T-s) and T-pot. Secondari ly, tumour DNA ploidy (DNA index) and S-phase fractions (SPFs) were al so estimated from the univariate DNA histograms. The 101 evaluable pat ients were classified according to clinical stage as T2 (n = 12), T3 ( n = 53), T4 (n = 28) or recurrent tumours (n = 8). Of the evaluable tu mours, 73 were DNA aneuploid. The median LI, T-s, and T-pot of the ane uploid tumours were 21%, 20 h and 3.3 days respectively. The calculate d LI, T-s, and T-pot of diploid rumours were subject to uncertainties because of the contribution of normal cells. The LI and SPF of all tum ours were, however, significantly (P < 0.001) correlated, having a cor relation coefficient of only 0.76. The wide distributions of values fo r LI (quartiles 13.5%, 26.9%) and T-pot (quartiles 2.4, 5.6 days) that were found are necessary baseline information if these parameters are to be useful in individual treatment selection or as predictors of tr eatment outcome.