CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Association between FOXP3 Expression and Disease-Free Survival in Triple Negative Breast Cancer.
Association between FOXP3 Expression and Disease-Free Survival in Triple Negative Breast Cancer.
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高 FOXP3 表达与三阴性乳腺癌 (TNBC) 患者较低的 DFS 相关。
三阴性乳腺癌(TNBC)是一种侵袭性亚型,缺乏雌激素、孕激素和HER2受体,因复发和转移风险高而常预后不良。FOXP3表达与抗肿瘤免疫受抑相关,可能是TNBC的预后标志物。然而,FOXP3表达与TNBC无病生存期(DFS)的关系仍有争议。本研究旨在探讨TNBC患者FOXP3表达与DFS的关系,以增进对其预后意义的认识。
这项回顾性研究纳入47例TNBC患者。通过免疫组化评估FOXP3表达,并根据最佳截断值将其分为低表达和高表达。采用Cox回归进行单因素和多因素分析,以确定各变量与DFS的关系;生存分析采用Kaplan-Meier法和log-rank检验。
所有患者均为女性,其中多数年龄超过50岁(66%)。多数患者肿瘤直径大于2 cm(87.2%),并有淋巴血管侵犯(LVI,66%)。高级别肿瘤(3级)占多数(93.6%),多数患者TIL(肿瘤浸润淋巴细胞)水平中等(91.5%)。FOXP3表达与年龄(p=0.253)、肿瘤大小(p=0.308)、淋巴结状态(p=0.466)、肿瘤分级(p=0.476)、LVI(p=0.422)、患者分期(p=0.644)及TIL(p=0.783)均无显著相关。然而,FOXP3高表达与较差DFS显著相关(p=0.019);较高分期也与较差DFS相关(p=0.002)。
TNBC患者FOXP3高表达与较低DFS相关。FOXP3表达与年龄、肿瘤大小、淋巴结状态、肿瘤分级、LVI、TIL或癌症分期均无关。
Triple-negative breast cancer (TNBC) is an aggressive subtype lacking estrogen, progesterone, and HER2 receptors, often leading to poor prognosis due to high recurrence and metastasis. FOXP3 expression, associated with suppressed anti-tumor immunity, is a potential prognostic marker in TNBC. However, the association between FOXP3 expression and disease-free survival (DFS) in TNBC remains controversial. This study aims to explore the relationship between FOXP3 expression and DFS in TNBC patients, contributing to the understanding of its prognostic significance.
This retrospective study included 47 TNBC patients. Immunohistochemistry examination assessed FOXP3 expression, which was then categorized into low and high expression based on an optimal cut-off point. Univariate and multivariate analyses were conducted using Cox regression test to determine association between variables and DFS. Survival analysis was assessed using the Kaplan-Meier method and the log-rank test.
All patients were female mostly over 50 years old (66%). The majority had tumors >2 cm (87.2%) and LVI (66%). High-grade tumors (grade 3) were predominant (93.6%). Most patients showed moderate TIL levels (91.5%). No significant associations were found between FOXP3 expression and age (p=0.253), tumor size (p=0.308), lymph node status (p=0.466), tumor grade (p=0.476), LVI (p=0.422), patient's stage (p=0.644), and TILs (p=0.783). However, high FOXP3 expression was significantly associated with worse DFS (p=0.019). Additionally, a higher stage was associated with worse DFS (p=0.002).
High FOXP3 expression is associated with lower DFS in TNBC patients. FOXP3 expression was not associated with age, tumor size, lymph node status, tumor grade, LVI, TILs, or cancer stage.
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