Clinicopathological Correlation Of Er, Pr And Her 2 Neu In Epithelial Ovarian Tumors
DOI:
https://doi.org/10.69980/ajpr.v28i5.665Keywords:
Ovarian carcinoma, epithelial ovarian tumors, estrogen receptor, progesterone receptor, HER2/neu, immunohistochemistry, prognostic markersAbstract
Background: Expression of estrogen receptor (ER), progesterone receptor (PR) and human epidermal growth factor receptor‑2 (HER2/neu) may reflect tumor biology and prognostic strata in epithelial ovarian tumors (EOTs). We evaluated their immunohistochemical (IHC) expression and clinicopathological correlations in a North Indian cohort.
Methods: In a five‑year study (2010–2015) at SKIMS, 50 consecutive EOTs were analyzed (benign, borderline and malignant). Routine histopathology and IHC for ER, PR and HER2/neu were performed on formalin‑fixed paraffin‑embedded tissue. Intensity was semi‑quantitatively graded (0/1+/2+/3+). For HER2/neu, 1+ was considered negative. Clinicopathological variables included histotype, grade, FIGO stage, nodal status, lymphovascular invasion (LVI), capsular invasion, metastatic status and pre‑operative CA‑125 where available.
Results: Of 50 EOTs, 8 (16%) were benign, 9 (18%) borderline and 33 (66%) malignant. Among malignant tumors, serous histology predominated (23/33; 69.7%), followed by mucinous (9/33; 27.3%) and clear cell carcinoma (1/33; 3.0%). ER was positive in 30/33 malignant cases, PR in 28/33 and HER2/neu in 5/33; all benign and borderline tumors were HER2/neu‑negative. High‑grade carcinomas more often showed higher ER and PR expression than low‑grade tumors. ER/PR positivity was enriched in cases with adverse features (metastasis, LVI, capsular invasion), while HER2/neu was largely negative across strata. Stage‑3 tumors showed higher ER/PR intensity compared with stage‑1/2. Elevated CA‑125 was more frequent in high‑grade than low‑grade disease.
Conclusions: In this cohort, ER and PR expression was significantly more frequent and stronger in malignant versus benign/borderline EOTs, and associated with higher grade and advanced stage, whereas HER2/neu overexpression was infrequent and restricted to carcinomas. These findings support potential utility of ER/PR profiling for prognostication and selection for endocrine strategies in ovarian carcinoma, while HER2/neu appears to have limited role in this setting.
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