Zhou Chenhao, Weng Jialei, Gao Yuan, Liu Chunxiao, Zhu Xiaoqiang, Zhou Qiang, Li Chia-Wei, Sun Jialei, Atyah Manar, Yi Yong, Ye Qinghai, Shi Yi, Dong Qiongzhu, Liu Yingbin, Hung Mien-Chie, Ren Ning
Department of Liver Surgery, Liver Cancer Institute, Zhongshan Hospital, and Key Laboratory of Carcinogenesis and Cancer Invasion (Ministry of Education), Fudan University, Shanghai, China.
Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
J Clin Transl Hepatol. 2022 Oct 28;10(5):925-938. doi: 10.14218/JCTH.2021.00283. Epub 2022 Feb 21.
Hepatocellular carcinoma (HCC) is the most common primary liver cancer and the incidence and mortality rates are increasing. Given the limited treatments of HCC and promising application of immunotherapy for cancer, we aimed to identify an immune-related prognostic signature that can predict overall survival (OS) rates and immunotherapy response in HCC.
The initial signature development was conducted using a training dataset from the Cancer Genome Atlas followed by independent internal and external validations from that resource and the Gene Expression Omnibus. A signature based nomogram was generated using multivariate Cox regression analysis. The associations of signature score with tumor immune phenotype and response to immunotherapy were analyzed using single-sample gene set enrichment analysis and tumor immune dysfunction and exclusion algorithm. A cohort from Zhongshan Hospital was employed to verify the predictive robustness of the signature regarding prognostic risk and immunotherapy response.
The prognostic signature, IGS, consisting of 22 immune-related genes, had independent prognostic ability, with training and validation cohorts. Also, IGS stratified HCC patients with different outcomes in subgroups. The prognostic accuracy of IGS was better than three reported prognostic signatures. The IGS-based nomogram had high accuracy and significant clinical benefits in predicting 3- and 5-year OS. IGS reflected distinct immunosuppressive phenotypes in low- and high-score groups. Patients with low IGS scores were more likely than those with high scores to benefit from immunotherapy.
IGS predicted HCC prognosis and response to immunotherapy, and contributed to individualized clinical management.
肝细胞癌(HCC)是最常见的原发性肝癌,其发病率和死亡率呈上升趋势。鉴于HCC的治疗方法有限且癌症免疫疗法应用前景广阔,我们旨在确定一种免疫相关的预后特征,以预测HCC患者的总生存率(OS)和免疫治疗反应。
首先使用来自癌症基因组图谱(Cancer Genome Atlas)的训练数据集进行初始特征开发,随后从该资源和基因表达综合数据库(Gene Expression Omnibus)进行独立的内部和外部验证。使用多变量Cox回归分析生成基于特征的列线图。使用单样本基因集富集分析以及肿瘤免疫功能障碍和排除算法分析特征评分与肿瘤免疫表型及免疫治疗反应之间的关联。采用来自中山医院的队列来验证该特征在预后风险和免疫治疗反应方面预测的稳健性。
由22个免疫相关基因组成的预后特征IGS在训练和验证队列中具有独立的预后能力。此外,IGS在亚组中对不同预后的HCC患者进行了分层。IGS的预后准确性优于三个已报道的预后特征。基于IGS的列线图在预测3年和5年OS方面具有高准确性和显著的临床益处。IGS在低分和高分群体中反映出不同的免疫抑制表型。IGS评分低的患者比评分高的患者更有可能从免疫治疗中获益。
IGS可预测HCC的预后和对免疫治疗的反应,并有助于个体化临床管理。