IMMUNOCYTOCHEMICAL ANALYSIS OF UTERINE PAPILLARY SEROUS CARCINOMAS FOR ESTROGEN AND PROGESTERONE RECEPTORS

Citation
Sa. Umpierre et al., IMMUNOCYTOCHEMICAL ANALYSIS OF UTERINE PAPILLARY SEROUS CARCINOMAS FOR ESTROGEN AND PROGESTERONE RECEPTORS, International journal of gynecological pathology, 13(2), 1994, pp. 127-130
Citations number
15
Categorie Soggetti
Obsetric & Gynecology",Pathology
ISSN journal
02771691
Volume
13
Issue
2
Year of publication
1994
Pages
127 - 130
Database
ISI
SICI code
0277-1691(1994)13:2<127:IAOUPS>2.0.ZU;2-M
Abstract
Uterine papillary serous carcinoma (UPSC), an aggressive histologic va riant of endometrial cancer, is particularly resistant to cytotoxic ch emotherapy. In reviewing a group of patients treated with cisplatin, d oxorubicin. and cyclophosphamide, we were surprised to find that 90% o f specimens tested by biochemical analysis were positive for estrogen receptor (ER), progesterone receptor (PR), or both. To further study r eceptor content and localization, we performed immunocytochemical anal ysis (ICA) on 29 archival UPSC specimens. In ER studies, three specime ns were unevaluable because of inadequate internal controls; of the re maining 26, only two were ER positive, showing weak, focal staining. I n PR studies, 18 samples had adequate controls, and all tumor specimen s were receptor negative. Corresponding biochemical ER data were avail able for 11 cases, of which 10 were ER positive. ICA, however, showed all 10 to be negative. Biochemical PR data were available for seven sa mples: Six were positive. All six biochemically positive PR specimens were PR negative when analyzed by ICA. Biochemical assays for ER and P R may overestimate positivity as a result of contamination with normal tissue or the presence of receptor-positive typical endometrial adeno carcinoma in tumors of mixed histology. ICA may eliminate this problem , but it has technical limitations, especially when used for archival tissue analysis. Because urinary papillary serous carcinoma appears to be a receptor-negative tumor, further evaluation of hormonal therapy is not likely to be beneficial.