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基于肿瘤芽生和免疫评分的肝细胞癌患者分类

A classification based on tumor budding and immune score for patients with hepatocellular carcinoma.

作者信息

Wei Li, Delin Zhang, Kefei Yuan, Hong Wu, Jiwei Huang, Yange Zhang

机构信息

Department of Liver Surgery & Liver Transplantation, State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University and Collaborative Innovation Center of Biotherapy, Chengdu, China.

Department of Plastic and Burns Surgery, West China Hospital, Sichuan University, Chengdu, China.

出版信息

Oncoimmunology. 2019 Nov 7;9(1):1672495. doi: 10.1080/2162402X.2019.1672495. eCollection 2020.

Abstract

: The role of immune profiling and tumor budding in hepatocellular carcinoma (HCC) remains largely unknown. This study evaluated the association between tumor budding and lymphocytic infiltration in HCC. Meanwhile, HCC patients were stratified based on tumor budding grade and immune score. : A total of 423 HCC patients were divided into training (n = 212) and validation (n = 211) cohort. Tumor slides from resected HCC samples were used for tumor budding assessment. A prognosis-relevant immune score was developed based on five types of immune cells out of eleven immune markers. A classification based on tumor budding grade and immune type was established (IS-TB type). To explore the association of IS-TB type and molecular alterations of HCC, 100 HCC samples and adjacent non-tumor tissues from 100 patients were investigated by whole-exome sequencing. : Tumor budding was an independent adverse prognostic factor for OS and DFS in both of the training and validation cohorts (all values <.05). The rate of high-grade tumor budding was significantly higher in HCC with immature stroma ( < .001), strong α-SMA expression ( = .005), non-steatotic tumors and non-fibrolamellar-HCC ( < .001). Additionally, tumor budding was related to both anti- and pro-tumor immune responses. Patients were classified into immune type A and immune type B according to the immune score. Based on tumor budding grade and immunotype, patients were classified into four subgroups: IS-TB (type I), IS-TB (type II), IS-TB (type III) and IS-TB (type IV). Patients with type III tumor had the best OS and DFS, whereas OS and DFS were the worst for cases with type II tumor. TP53 mutation was more frequent in IS-TB type I (ISTB) patients, while IS-TB type IV (ISTB) harbored high number of CTNNB1 mutation. : Tumor-immune cell interactions in HCC is heterogeneous. HCC classification based on tumor budding and immune score correlates with patient survival and molecular alterations. The defined subtypes may have significance for utilizing individualized treatment in patients with HCC.

摘要

免疫谱分析和肿瘤芽生在肝细胞癌(HCC)中的作用在很大程度上仍不清楚。本研究评估了HCC中肿瘤芽生与淋巴细胞浸润之间的关联。同时,根据肿瘤芽生分级和免疫评分对HCC患者进行分层。

共有423例HCC患者被分为训练队列(n = 212)和验证队列(n = 211)。来自切除的HCC样本的肿瘤切片用于肿瘤芽生评估。基于11种免疫标志物中的5种免疫细胞建立了与预后相关的免疫评分。建立了基于肿瘤芽生分级和免疫类型的分类(IS-TB类型)。为了探究IS-TB类型与HCC分子改变之间的关联,对100例患者的100份HCC样本及相邻非肿瘤组织进行了全外显子测序。

在训练队列和验证队列中,肿瘤芽生都是总生存期(OS)和无病生存期(DFS)的独立不良预后因素(所有P值<.05)。在具有未成熟基质的HCC中(P <.001)、α-SMA强表达(P = .005)、非脂肪变性肿瘤和非纤维板层型HCC中(P <.001),高级别肿瘤芽生的发生率显著更高。此外,肿瘤芽生还与抗肿瘤和促肿瘤免疫反应均相关。根据免疫评分将患者分为免疫A型和免疫B型。基于肿瘤芽生分级和免疫类型,将患者分为四个亚组:IS-TB(I型)、IS-TB(II型)、IS-TB(III型)和IS-TB(IV型)。III型肿瘤患者的OS和DFS最佳,而II型肿瘤患者的OS和DFS最差。TP53突变在IS-TB I型(ISTB)患者中更常见,而IS-TB IV型(ISTB)携带大量CTNNB1突变。

HCC中的肿瘤-免疫细胞相互作用是异质性的。基于肿瘤芽生和免疫评分的HCC分类与患者生存及分子改变相关。所定义的亚型可能对HCC患者个体化治疗的应用具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2684/6959452/6a4154805359/koni-09-01-1672495-g001.jpg

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