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Localization and density of tertiary lymphoid structures associate with molecular subtype and clinical outcome in colorectal cancer liver metastases

结直肠癌 医学 免疫组织化学 克拉斯 免疫系统 内科学 癌症 转录组 总体生存率 肿瘤科 癌症研究 病理 基因 基因表达 免疫学 生物 遗传学
作者
Chong Zhang,Xiangyu Wang,Jie‐Liang Zuo,Xuefu Wang,Xiaowen Feng,Bo Zhang,Yi-Tong Li,Chenhe Yi,Peng Zhang,Xiaochen Ma,Zhenmei Chen,Wei Wang,Jiahao Han,Baorui Tao,Rui Zhang,Tianqi Wang,Li Tong,Zhong Sheng Tong,Siyu Wang,Xiaofei Zheng,Wen-Kang Yuan,Zi-Jie Kan,Jie Fan,Xiangyang Hu,Jun Li,Chao Zhang,Jinhong Chen
出处
期刊:Journal for ImmunoTherapy of Cancer [BMJ]
卷期号:11 (2): e006425-e006425 被引量:25
标识
DOI:10.1136/jitc-2022-006425
摘要

Tertiary lymphoid structures (TLSs) have been proposed to assess the prognosis of patients with cancer. Here, we investigated the prognostic value and relevant mechanisms of TLSs in colorectal cancer liver metastases (CRCLM).603 patients with CRCLM treated by surgical resection from three cancer centers were included. The TLSs were categorized according to their anatomic subregions and quantified, and a TLS scoring system was established for intratumor region (T score) and peritumor region (P score). Differences in relapse-free survival (RFS) and overall survival (OS) between groups were determined. Multiplex immunohistochemical staining (mIHC) was used to determine the cellular composition of TLSs in 40 CRCLM patients.T score positively correlated with superior prognosis, while P score negatively associated with poor survival (all p<0.05). Meanwhile, T score was positively associated with specific mutation subtype of KRAS. Furthermore, TLSs enrichment gene expression was significantly associated with survival and transcriptomic subtypes of CRCLM. Subsequently, mIHC showed that the densities of Treg cells, M2 macrophages and Tfh cells were significantly higher in intratumor TLSs than in peritumor TLSs (p=0.029, p=0.047 and p=0.041, respectively), and the frequencies of Treg cells and M2 macrophages were positively correlated with P score, while the frequencies of Tfh cells were positively associated with T scores in intratumor TLSs (all p<0.05). Next, based on the distribution and abundance of TLSs, an Immune Score combining T score and P score was established which categorized CRCLM patients into four immune classes with different prognosis (all p<0.05). Among them, patients with higher immune class have more favorable prognoses. The C-index of Immune Class for RFS and OS was higher than Clinical Risk Score statistically. These results were also confirmed by the other two validation cohorts.The distribution and abundance of TLSs is significantly associated with RFS and OS of CRCLM patients, and a novel immune class was proposed for predicting the prognosis of CRCLM patients.

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