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Prognostic Value of Tumor-Infiltrating FoxP3(+) T Cells in Gastrointestinal Cancers: A Meta Analysis

PURPOSE: Tumor-infiltrating FoxP3(+) T cells have been reported in various human tumors, which impaired cell-mediated immunity and promoted disease progression. However, its prognostic value for survival in patients with different gastrointestinal cancers [hepatocellular carcinoma (HCC), colorectal...

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Detalles Bibliográficos
Autores principales: Huang, Yong, Liao, Huaiwei, Zhang, Yong, Yuan, Rongfa, Wang, Fengmei, Gao, Yingtang, Wang, Peng, Du, Zhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4020764/
https://www.ncbi.nlm.nih.gov/pubmed/24827118
http://dx.doi.org/10.1371/journal.pone.0094376
Descripción
Sumario:PURPOSE: Tumor-infiltrating FoxP3(+) T cells have been reported in various human tumors, which impaired cell-mediated immunity and promoted disease progression. However, its prognostic value for survival in patients with different gastrointestinal cancers [hepatocellular carcinoma (HCC), colorectal cancer (CRC), gastric cancer (GC)] remains controversial. METHODS: Relevant literature was searched using PubMed, Embase, Cochrane, Ovid Medline and Chinese wanfang databases. A meta-analysis was conducted to estimate pooled survival and recurrence ratios. The odds ratio (OR) and 95% confidence intervals (CI) were calculated employing fixed- or random-effects models depending on the heterogeneity of the included trials. RESULTS: For HCC and GC, the overall survival at 1, 3 and 5-year of high FoxP3(+) T cells infiltration patients were lower than low FoxP3(+) T cells infiltration patients (P<0.05). The recurrences at 1, 3 and 5-year of high FoxP3(+) T cells infiltration patients were higher than low FoxP3(+) T cells infiltration patients (P<0.001). But for CRC, the overall survival at 1, 3 and 5-year of high FoxP3(+) T cells infiltration patients were higher than low FoxP3(+) T cells infiltration patients (P<0.001). There were no differences in 1, 3 and 5-year recurrences between high and low FoxP3(+) T cells infiltration patients (P>0.05). CONCLUSIONS: Our findings suggested that tumor-infiltrating FoxP3(+) T cells were a factor for a poor prognosis for HCC and GC, but a good prognosis for CRC.