CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Intratumoral CD8+ tumor-infiltrating lymphocytes as prognostic predictors in radio-chemoradiotherapy-treated nasopharyngeal carcinoma.
Intratumoral CD8+ tumor-infiltrating lymphocytes as prognostic predictors in radio-chemoradiotherapy-treated nasopharyngeal carcinoma.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
我们的发现表明,瘤内 CD8+ TILs 可作为鼻咽癌可靠的预后生物标志物,其预后价值在局部晚期疾病患者中尤为显著。
TIL(肿瘤浸润淋巴细胞)对鼻咽癌(NPC)的预后价值已获确立,但NPC中CD4⁺和CD8⁺ TIL亚型的预后意义尚不明确。
收集214份经诊断为NPC的组织样本进行免疫组织化学染色。评估肿瘤内(肿瘤细胞巢内)和间质(肿瘤细胞巢周围间质)区域的CD4⁺和CD8⁺ TIL密度,并分析TIL密度与无进展生存期(PFS)和总生存期(OS)的相关性。
肿瘤内CD8⁺ TIL水平较高与疾病进展风险降低(HR 0.382;95% CI 0.178–0.819;P=0.013)及死亡风险降低(HR 0.265;95% CI 0.104–0.675;P=0.005)显著相关。尽管间质CD8⁺ TIL水平较高与更长的PFS和OS相关,但差异未达到统计学显著性(分别为P=0.114和P=0.079)。CD4⁺ TIL与PFS或OS均无显著相关性。多变量分析中,肿瘤内CD8⁺ TIL仍是PFS和OS的独立预后因素。亚组分析显示,在局部晚期患者中,较高的肿瘤内CD8⁺ TIL与PFS改善(HR 0.329;95% CI 0.129–0.843;P=0.021)及OS改善(HR 0.209;95% CI 0.064–0.681;P=0.009)显著相关。相反,在早期患者中,CD8⁺或CD4⁺ TIL均与PFS或OS无显著相关性。
研究结果提示,肿瘤内CD8⁺ TIL是NPC可靠的预后生物标志物,其预后价值在局部晚期患者中尤为明显。
The prognostic value of tumor-infiltrating lymphocytes (TILs) in nasopharyngeal carcinoma (NPC) has been established. However, the prognostic significance of CD4+ and CD8+ TIL subtypes in NPC remains unclear.
We collected 214 tissue samples diagnosed with NPC for immunohistochemical staining. The density of CD4+ and CD8+ TILs was evaluated in intratumoral (within tumor cell nests) and stromal (the surrounding stroma of tumor cell nests) areas. Correlations between TIL density and progression-free survival (PFS) and overall survival (OS) were analyzed.
High levels of intratumoral CD8+ TILs were significantly associated with reduced risk of disease progression (HR 0.382; 95% CI, 0.178-0.819, P = 0.013) and death (HR 0.265; 95% CI, 0.104-0.675, P = 0.005). Although high stromal CD8+ TIL levels were linked to higher PFS and OS, these differences did not reach statistical significance (P = 0.114 and P = 0.079, respectively). CD4+ TILs showed no significant correlation with PFS or OS. In multivariate analysis, intratumoral CD8+ TILs remained an independent prognostic factor for PFS and OS. Subgroup analysis revealed that in patients with locally advanced disease, high intratumoral CD8+ TILs were significantly associated with improved PFS (HR 0.329; 95% CI, 0.129-0.843, P = 0.021) and OS (HR 0.209; 95% CI, 0.064-0.681, P = 0.009). Conversely, in early-stage patients, neither CD8+ nor CD4+ TILs were significantly associated with PFS or OS.
Our findings suggest that intratumoral CD8+ TILs serve as a reliable prognostic biomarker for NPC, with their prognostic value particularly pronounced in patients with locally advanced disease.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
MEMBER ACCOUNT
登录成功会直接打开下一页。