Prognostic significance of Ki-67 levels and hormone receptor expression in low-grade serous ovarian carcinoma: an investigation of the Tumor Bank Ovarian Cancer Network.

免疫组织化学 浆液性癌 病理 上皮性卵巢癌 卵巢肿瘤 卵巢 癌症 阶段(地层学) 上皮性卵巢癌
作者
Jalid Sehouli,Elena Ioana Braicu,Rolf Richter,Carsten Denkert,Paul Jank,Philipp Jurmeister,Catarina Alisa Kunze,Jan Budczies,Sylvia Darb-Esfahani,Wolfgang D. Schmitt,Alexander Traut,Jacek P. Grabowski,Eliane T Taube,Helmut Plett
出处
期刊:Human Pathology [Elsevier]
卷期号:85: 299-308 被引量:14
标识
DOI:10.1016/j.humpath.2018.10.020
摘要

Summary Low-grade serous ovarian carcinoma (LGSOC) has recently come up as a distinct rare entity of epithelial ovarian cancer. Predictive and prognostic markers are not well studied yet. Because Ki-67 and hormone receptors (HR) have been established as relevant cancer biomarkers in several malignant tumors, we evaluated Ki-67 and HR expression rates by immunohistochemistry in 68 patients with LGSOC. We used a standardized cutoff finder algorithm to analyze prognostic significance for overall survival (OS) and progression-free survival (PFS). Cox regression showed a significant continuous decrease in OS for higher proliferation rates with an HR  of 1.07% (95% confidence interval, 1.01%-3.67%; P = .048) but not in PFS (P = .86). Cutoff finder analysis revealed the best possible cutoff for OS at 6.28% (P = .04) and for PFS at 1.85% proliferative activity (P = .04). Estrogen receptors (ERs) were expressed in most LGSOC patients (n = 61; 89.7%), progesterone receptor (PR) in about half of patients (n = 33; 48.5%). For both ER/PR, a statistically significant cutoff for PFS could be determined, which was at 75% of positive tumor cells for ER (P = .02) and at 15% of positive tumor cells for PR (P = .03). For OS, HR expression showed a tendency toward better OS for HR-positive tumors but did not turn out statistically significant. Our results show that Ki-67 is a valuable prognostic marker in the subgroup of LGSOC. We could also show that most LGSOCs express HRs but that this expression is associated with a better PFS, a finding valuable in times of antihormonal therapy in LGSOC.
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