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Prognostic impact of CD4+ and CD8+ tumor-infiltrating lymphocytes in patients with colorectal cancer.
Tao, Yong; Xie, Ya.
Afiliação
  • Tao Y; Colorectal Surgery, Ningbo City First Hospital, Ningbo, China.
  • Xie Y; Colorectal Surgery, Henan Provincial People's Hospital, Zhengzhou, China.
Acta Chir Belg ; 124(1): 35-40, 2024 Feb.
Article em En | MEDLINE | ID: mdl-36780176
ABSTRACT

OBJECTIVE:

Tumor immune response has been suggested as an important indicator of cancer prognosis. This study was initiated to investigate the association between T lymphocytes and the prognosis of patients with colorectal cancer (CRC).

METHODS:

Included in this study were 129 CRC patients who received surgical treatment in Henan Provincial People's Hospital from January 2003 to January 2014. The level of CD4+ and CD8+ T lymphocytes in tissues was detected by immunohistochemistry (IHC). Survival analysis was conducted by the Kaplan-Meier method and Cox proportional hazards model.

RESULTS:

IHC staining showed that CD8+ T lymphocyte infiltration was high in 88 cases and low in 41 cases, while CD4+ T lymphocyte infiltration was high in 66 cases and low in 63 cases. The level of CD4+ and CD8+ T lymphocytes in CRC tissue was closely related to TNM stage and tumor invasion (p < 0.05). Follow-up analysis showed that both disease-free survival (DFS) and overall survival (OS) were better in patients with a high level of CD8+ and CD4 + CD8+ than those in patients with a low level (p < 0.05). Multivariate analysis showed that TNM stage, lymph node, CD8+ and CD4+ CD8+ were independent risk factors for DFS and OS (p < 0.05).

CONCLUSION:

High level of CD8+ and CD4+ CD8+ may prove to be a potential predictor of better prognosis of CRC patients.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Linfócitos do Interstício Tumoral Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Linfócitos do Interstício Tumoral Idioma: En Ano de publicação: 2024 Tipo de documento: Article