BACKGROUND. Cytologic sampling is performed routinely after radiothera
py for cervical carcinoma. The prognostic significance of postirradiat
ion dysplastic and atypical cells is uncertain because of difficulties
in distinguishing preneoplastic and cancerous changes from benign rad
iation changes. DNA cytometry studies may provide a more objective met
hod of identifying significant lesions. METHODS, Postirradiation cervi
cal carcinoma patients with cervical/vaginal smears containing atypica
l or dysplastic cells were identified prospectively. Papanicolaou smea
rs were destained, restained with a Feulgen stain, and evaluated for D
NA content using image cytometry. Pathologic and clinical records were
monitored on each patient for evidence of recurrence or biopsy-proven
dysplasia. RESULTS, Of 46 patients, 14 had been diagnosed on cytology
as having atypical squamous cells, 4 as having atypical/suspicious ce
lls, 12 with low grade squamous intraepithelial lesions (SIL), 3 with
high grade SIL, and 13 with ungraded SIL. DNA histograms were classifi
ed as follows: 14 diploid, 19 polyploid, and 13 aneuploid. Cytologic d
iagnosis and histogram type were correlated significantly and both cor
related with clinical outcome. The probability of either postirradiati
on dysplasia or recurrence was as follows: SIL, 82%; suspicious, 100%;
polyploid, 79%; and aneuploid, 92%. Patients with atypical squamous c
ells of undetermined significance or diploidy most frequently had nega
tive follow-up (57% each). AU patients with both SIL and aneuploidy de
veloped either dysplasia or recurrence. The stage of disease did not c
orrelate with outcome or histogram pattern. CONCLUSIONS, DNA analysis
of postirradiation cytologic smears demonstrating atypia or dysplasia
may provide useful ancillary information. The presence of aneuploidy u
sually signifies either recurrence or dysplasia. Polyploidy most frequ
ently occurs in dysplastic processes, whereas diploid histograms usual
ly denote a benign disease course. (C) 1998 American Cancer-Society.