Dm. Gershenson et al., MOLECULAR PROFILE OF ADVANCED-STAGE TRANSITIONAL-CELL CARCINOMA OF THE OVARY, American journal of obstetrics and gynecology, 177(1), 1997, pp. 120-125
OBJECTIVES: Our purpose was to determine the molecular profile of adva
nced-stage transitional cell carcinoma in terms of immunostaining for
p53, epidermal growth factor receptor and HER-2/neu, deoxyribonucleic
acid index, and S-phase fraction and to analyze the prognostic signifi
cance of these markers. STUDY DESIGN: Archival paraffin-embedded tissu
e blocks from 29 advanced stage transitional cell carcinomas were obta
ined. Selected sections of the primary tumors were immunostained for p
53, epidermal growth factor receptor, and HER-2/neu; deoxyribonucleic
acid ploidy and S-phase fraction were determined with use of flow cyto
metry. Clinical information was abstracted from the medical records. S
urvival times were analyzed according to the life-table methods of Kap
lan and Meier, and the statistical significance of the Various factors
was tested with the log-rank test. The proportional hazards model of
Cox was used to identify prognostic factors. RESULTS: Positive immunos
taining was observed for p53 in 13 cases (45%), for epidermal growth f
actor receptor in 14 cases (50%), and for HER-2/neu in 19 cases (65%).
Tumors were diploid in 16 cases (55%) and aneuploid in 13 (45%). The
S-phase fraction was less than or equal to 15% (mean) in 13 cases (45%
) and >15% in 16 cases (55%). The median survival for the entire group
was 52 months. None of the above variables had a significant effect o
n survival time. CONCLUSION: Neither immunostaining for p53, epidermal
growth factor receptor, and HER-2/neu nor deoxyribonucleic acid ploid
y nor S-phase fraction allowed us to distinguish transitional cell car
cinoma from other more common epithelial ovarian cancers. In addition,
no prognostic significance was associated with these biomarkers. A st
udy of larger numbers of cases may be more elucidative.