Li Linhai, Ouyang Yiming, Wang Wenrong, Hou Dezhi, Zhu Yu
Department of General Surgery, the First People's Hospital of Yunnan Province, the Affiliated Hospital of Kunming University of Science and Technology, Kunming, China.
PeerJ. 2019 Dec 10;7:e7993. doi: 10.7717/peerj.7993. eCollection 2019.
Gastric cancer (GC) is the fourth most frequently diagnosed malignancy and the second leading cause of cancer-associated mortality worldwide. The tumor microenvironment, especially tumor-infiltrating immune cells (TIICs), exhibits crucial roles both in promoting and inhibiting cancer growth. The aim of the present study was to evaluate the landscape of TIICs and develop a prognostic nomogram in GC.
A gene expression profile obtained from a dataset from The Cancer Genome Atlas (TCGA) was used to quantify the proportion of 22 TIICs in GC by the CIBERSORT algorithm. LASSO regression analysis and multivariate Cox regression were applied to select the best survival-related TIICs and develop an immunoscore formula. Based on the immunoscore and clinical information, a prognostic nomogram was built, and the predictive accuracy of it was evaluated by the area under the curve (AUC) of the receiver operating characteristic curve (ROC) and the calibration plot. Furthermore, the nomogram was validated by data from the International Cancer Genome Consortium (ICGC) dataset.
In the GC samples, macrophages (25.3%), resting memory CD4 T cells (16.2%) and CD8 T cells (9.7%) were the most abundant among 22 TIICs. Seven TIICs were filtered out and used to develop an immunoscore formula. The AUC of the prognostic nomogram in the TCGA set was 0.772, similar to that in the ICGC set (0.730) and whole set (0.748), and significantly superior to that of TNM staging alone (0.591). The calibration plot demonstrated an outstanding consistency between the prediction and actual observation. Survival analysis revealed that patients with GC in the high-immunoscore group exhibited a poor clinical outcome. The result of multivariate analysis revealed that the immunoscore was an independent prognostic factor.
The immunoscore could be used to reinforce the clinical outcome prediction ability of the TNM staging system and provide a convenient tool for risk assessment and treatment selection for patients with GC.
胃癌(GC)是全球第四大最常被诊断出的恶性肿瘤,也是癌症相关死亡的第二大主要原因。肿瘤微环境,尤其是肿瘤浸润免疫细胞(TIICs),在促进和抑制癌症生长方面都发挥着关键作用。本研究的目的是评估TIICs的格局,并建立一个胃癌的预后列线图。
使用从癌症基因组图谱(TCGA)数据集中获得的基因表达谱,通过CIBERSORT算法量化胃癌中22种TIICs的比例。应用LASSO回归分析和多变量Cox回归来选择与生存最相关的TIICs,并建立一个免疫评分公式。基于免疫评分和临床信息,构建了一个预后列线图,并通过受试者操作特征曲线(ROC)的曲线下面积(AUC)和校准图来评估其预测准确性。此外,该列线图通过国际癌症基因组联盟(ICGC)数据集的数据进行了验证。
在胃癌样本中,巨噬细胞(25.3%)、静息记忆CD4 T细胞(16.2%)和CD8 T细胞(9.7%)是22种TIICs中含量最丰富的。筛选出7种TIICs用于建立免疫评分公式。TCGA组中预后列线图的AUC为0.772,与ICGC组(0.730)和整体组(0.748)相似,且显著优于单独的TNM分期(0.591)。校准图显示预测与实际观察之间具有出色的一致性。生存分析表明,高免疫评分组的胃癌患者临床结局较差。多变量分析结果显示,免疫评分是一个独立的预后因素。
免疫评分可用于增强TNM分期系统对临床结局的预测能力,并为胃癌患者的风险评估和治疗选择提供一个便捷的工具。