Purpose: To examine whether in vitro measurements of normal and tumour
cell radiosensitivity can be used as prognostic factors in clinical o
ncology. Materials and methods: Stage I-III cervix carcinoma patients
were treated with radical radiotherapy with a minimum of 3 years' foll
ow-up. Lymphocyte and tumour radiosensitivities were assayed using, re
spectively, a limiting dilution and soft agar clonogenic assay to obta
in surviving fraction at 2 Gy (SF2). The results were related, in an a
ctuarial analysis, to late morbidity assessed using the France-Italian
glossary. Results: Patients with radiosensitive lymphocytes had a sig
nificantly increased risk of developing late complications (n=93, p=0.
002). Increasing tumour radiosensitivity was associated with an increa
sed risk of morbidity (n=113, p=0.032). ii significant correlation was
found between fibroblast and tumour cell radiosensitivity (r=0.57, p=
0.03), but a weak inverse association was found between lymphocyte and
tumour cell radiosensitivity (r= -0.32, p=0.03). Patients with radios
ensitive lymphocytes and tumour cells had higher levels of late compli
cations than those whose cells were radioresistant. Conclusion: The wo
rk described highlights the importance of cellular radiosensitivity as
a parameter determining the clinical response to radiotherapy.