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Abstract
Highlights
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- Both epithelial ovarian and endometrial cancer demonstrate high expression of FRA (folate receptor alpha) compared to normal ovarian and endometrial tissue
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- FRA expression is not altered by chemotherapy exposure at interval debulking surgery nor at recurrence
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- Immunohistochemical FRA staining at diagnosis can guide the decision whether to use FRA targeted therapy upon recurrence
Objective
Based
on its expression profile, folate receptor alpha (FRA) is an attractive
candidate for targeted diagnostics and therapeutics. However,
applicability of these agents in residual or recurrent disease could be
influenced by chemotherapy. We evaluated whether chemotherapy modified
FRA expression in non-mucinous epithelial ovarian (EOC) and endometrial
carcinoma (EC).
Methods
FRA
staining was evaluated by immunohistochemistry, using MAb 26B3, in 81
patients (41 EOCs, 40 ECs) and 17 control tissues (5 benign ovarian
cysts, 5 normal ovarian, 7 normal endometrial tissues). Chemotherapy
effect was evaluated in 42 patients (30 paired samples at primary and
interval debulking surgery, 12 from primary and recurrent disease). FRA
expression was assessed using a semi-quantitative staining algorithm,
the M-score (range 0-50).
Conclusions
This
study shows no significant difference in FRA expression after
chemotherapy, strengthening the rationale for FRA targeted diagnostics
and therapeutics in FRA expressing tumors, whether newly diagnosed or at
recurrence.
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