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.
Hum Pathol
; 85: 299-308, 2019 03.
Article
em En
| MEDLINE
| ID: mdl-30428389
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 â¯ofâ¯1.07% (95% confidence interval, 1.01%-3.67%; Pâ¯=â¯.048) but not in PFS (Pâ¯=â¯.86). Cutoff finder analysis revealed the best possible cutoff for OS at 6.28% (Pâ¯=â¯.04) and for PFS at 1.85% proliferative activity (Pâ¯=â¯.04). Estrogen receptors (ERs) were expressed in most LGSOC patients (nâ¯=â¯61; 89.7%), progesterone receptor (PR) in about half of patients (nâ¯=â¯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 (Pâ¯=â¯.02) and at 15% of positive tumor cells for PR (Pâ¯=â¯.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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Base de dados:
MEDLINE
Assunto principal:
Neoplasias Ovarianas
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Receptores de Progesterona
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Receptores de Estrogênio
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Cistadenocarcinoma Seroso
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Antígeno Ki-67
Tipo de estudo:
Observational_studies
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Prognostic_studies
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Risk_factors_studies
Limite:
Adult
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Aged
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Aged80
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Female
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Humans
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Middle aged
Idioma:
En
Ano de publicação:
2019
Tipo de documento:
Article