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基于数字病理的免疫评分对鼻咽癌的预后价值。

Prognostic value of immune score in nasopharyngeal carcinoma using digital pathology.

机构信息

State Key Laboratory of Oncology in South China, Collaborative Innovation Center of Cancer Medicine, Guangdong Key Laboratory of Nasopharyngeal Carcinoma Diagnosis andTherapy, Sun Yat-sen University Cancer Center, GuangZhou, China.

Department of Radiation Oncology, Guilin Medical University Affiliated Hospital, Guilin, China.

出版信息

J Immunother Cancer. 2020 Jul;8(2). doi: 10.1136/jitc-2019-000334.

Abstract

BACKGROUND

Tumor-infiltrating lymphocytes have been reported as prognostic markers in tumors. We aimed to assess the prognostic value of total T cell (CD3) density, cytotoxic T cell (CD8) density and memory T cell (CD45RO) density in patients with nasopharyngeal carcinoma (NPC).

METHODS

The expression of CD3, CD8 and CD45RO was detected by immunohistochemistry in the training (n=221) and validation cohorts (n=115). The densities of these three markers were quantified by digital pathology both in the tumor and stroma. Then, we developed the immune score based on the density of these three markers and further analyzed its prognostic value.

RESULTS

The high density of CD3, CD8 and CD45RO T cells both in the tumor and/or stroma were significantly associated with the decrease in mortality in the training cohort, respectively. High immune score predicted a prolonged overall survival (OS) (HR 0.34, 95% CI 0.18 to 0.64, p=0.001, disease-free survival (DFS) (HR 0.44, 95% CI 0.25 to 0.78, p=0.005) and distant metastasis-free survival (DMFS) (HR 0.43, 95% CI 0.21 to 0.87, p=0.018) in NPC patients. The findings were confirmed in the validation cohort. Multivariate analysis revealed that immune score remained an independent prognostic indicator for OS, DFS and DMFS. In addition, we established a nomogram with the integration of all independent variables to predict individual risk of death.

CONCLUSIONS

We established an immune score model, which provides a reliable estimate of the risk of death, disease progress and distant metastasis in NPC patients.

摘要

背景

肿瘤浸润淋巴细胞已被报道为肿瘤的预后标志物。我们旨在评估总 T 细胞(CD3)密度、细胞毒性 T 细胞(CD8)密度和记忆 T 细胞(CD45RO)密度在鼻咽癌(NPC)患者中的预后价值。

方法

在训练队列(n=221)和验证队列(n=115)中,通过免疫组织化学检测 CD3、CD8 和 CD45RO 的表达。通过数字病理学对这三种标志物在肿瘤和基质中的密度进行定量。然后,我们基于这三种标志物的密度建立了免疫评分,并进一步分析了其预后价值。

结果

肿瘤和/或基质中高 CD3、CD8 和 CD45RO T 细胞的高密度均与训练队列中死亡率的降低显著相关。高免疫评分预测总生存期(OS)(HR 0.34,95%CI 0.18 至 0.64,p=0.001)、无病生存期(DFS)(HR 0.44,95%CI 0.25 至 0.78,p=0.005)和无远处转移生存期(DMFS)(HR 0.43,95%CI 0.21 至 0.87,p=0.018)延长。这些发现在验证队列中得到了证实。多变量分析显示,免疫评分仍然是 OS、DFS 和 DMFS 的独立预后指标。此外,我们建立了一个列线图,整合了所有独立变量,以预测个体死亡风险。

结论

我们建立了一个免疫评分模型,为 NPC 患者的死亡、疾病进展和远处转移风险提供了可靠的估计。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd3f/7371227/ec44fab489e7/jitc-2019-000334f01.jpg

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