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Prognostic Significance of B-Cells and pSTAT3 in Patients with Ovarian Cancer

BACKGROUND: Several previous studies have identified a strong association between T-cell infiltration and clinical outcome in ovarian cancer. The role of B-cells remains controversial, however. METHODS: Forty-nine paraffin-embedded omental specimens derived from patients with high grade epithelial o...

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Detalles Bibliográficos
Autores principales: Yang, Chunmei, Lee, Heehyoung, Jove, Veronica, Deng, Jiehui, Zhang, Wang, Liu, Xueli, Forman, Stephen, Dellinger, Thanh H., Wakabayashi, Mark, Yu, Hua, Pal, Sumanta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3542323/
https://www.ncbi.nlm.nih.gov/pubmed/23326565
http://dx.doi.org/10.1371/journal.pone.0054029
Descripción
Sumario:BACKGROUND: Several previous studies have identified a strong association between T-cell infiltration and clinical outcome in ovarian cancer. The role of B-cells remains controversial, however. METHODS: Forty-nine paraffin-embedded omental specimens derived from patients with high grade epithelial ovarian cancer were assessed. Immunohistochemical analyses were performed to characterize expression of CD19(+) B-cells and pSTAT3 as high (>50% positively staining cells [PSCs]) or low (<50% PSCs). The Kaplan-Meier method with log-rank test was used to determine the association between clinicopathologic parameters and overall survival (OS). A multi-variate Cox proportional hazards regression analysis including nature of debulking (primary vs secondary), histology, tumor grade, receipt of prior chemotherapy, B-cell infiltration and pSTAT3 expression was performed. RESULTS: Median OS was 160.6 months in those patients with low B-cell expression vs 47.3 months in those with high B-cell expression (P = 0.0015). Similarly, median OS was improved in those patients with low pSTAT3 expression (160.6 vs 47.9 months, P = 0.02). In a multivariate model to predict survival, only the degree of B-cell infiltration and clinical stage were retained. pSTAT3 expression did not enter the final model, possibly be due to a high positive correlation with B-cell infiltration (r = 0.82, P<0.0001). CONCLUSIONS: Increased B-cell infiltration and pSTAT3 expression in omental tissue are associated with poorer survival.