A risk score for the prognosis prediction of the muscle-invasive bladder cancer patients who received gemcitabine plus cisplatin chemotherapy

被引:0
作者
Guo, Yupeng [1 ]
Dong, Jing [1 ]
Ji, Tao [1 ]
Li, Xiaoxia [1 ]
Rong, Shengzhong [1 ]
Guan, Hongjun [1 ]
机构
[1] Mudanjiang Med Univ, Dept Epidemiol & Stat, Sch Publ Hlth, Mudanjiang 157011, Heilongjiang, Peoples R China
来源
AGING-US | 2022年 / 14卷 / 23期
基金
中国国家自然科学基金;
关键词
bladder cancer; chemotherapy; gemcitabine; cisplatin; prognosis; NEOADJUVANT CHEMOTHERAPY; METHOTREXATE; VINBLASTINE; DOXORUBICIN; CYSTECTOMY; SIGNATURE; TRIAL;
D O I
暂无
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
To develop an individualized gene-based risk score to predict the prognosis of muscle-invasive bladder cancer (MIBC) patients who received GC regimens. We downloaded transcriptome profiling data and clinical information from the Cancer Genome Atlas (TCGA) database. We identified 1854 survival-associated genes and then constructed the risk score based on six special genes selected from the survival-associated genes. We divided patients into high-risk and low-risk groups according to the median risk score. High-risk patients have significantly poorer overall survival than low-risk patients (log-rank test chi-square = 38.08, p = 7e-10, C-index = 0.785, se = 0.032). The risk score was evaluated by Kaplan-Meier survival curve, time-dependent ROC curves, and C-index. Multivariate Cox regression and nomogram suggested that the risk score was an independent prognostic indicator. Gene set enrichment analysis indicated that the survival-associated genes were significantly enriched in immune-related terms. Among six special genes, CHPF2, TRAV26-2, and BTF3P12 were found to be immune-related genes. In conclusion, our risk score provided an indicator to predict the prognosis of MIBC patients who received GC regimens and potential immunotherapeutic targets for MIBC.
引用
收藏
页码:9715 / 9729
页数:15
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