Department of Oncology, 70570Zhujiang Hospital, Southern Medical University, Guang Zhou, China.
Department of Urology, 70570Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Cancer Control. 2020 Jan-Dec;27(1):1073274820976665. doi: 10.1177/1073274820976665.
In recent years, immune checkpoint inhibitors (ICIs) targeting CTLA-4 or PD1/PDL1 have achieved remarkable success in the treatment of bladder cancer (BLCA), but only a few patients have shown durable clinical benefits. The prognostic role of a mutant form of the tumor suppressor gene TP53 (TP53-MT) in predicting the efficacy of ICIs is highly controversial; therefore, in this study, we obtained data for 210 patients from an immunotherapy cohort, 412 patients from The Cancer Genome Atlas (TCGA)-BLCA cohort and 18 BLCA cell lines from Genomics of Drug Sensitivity in Cancer (GDSC), and we performed integrated bioinformatic analysis to explore the relationships between TP53-MT and clinical benefits derived from ICI treatment and the underlying mechanisms. We conclude that TP53-MT is a potential indicator of a relatively good response to ICIs and associated with prolonged overall survival (OS) (log-rank test, hazard ratio (HR) = 0.65 [95% confidence interval (CI), 0.44-0.99], p = 0.041). Through integrated analysis with several platforms, we found that TP53-MT patients were more likely to benefit from ICIs than wild-type P53 (TP53-WT) patients, which may be the result of 2 major mechanisms. First, the patients with TP53-MT showed stronger tumor antigenicity and tumor antigen presentation, as indicated by a higher tumor mutational load, a higher neoantigen load and increased expression of MHC; second, the antitumor immunity preexisting in tumors was stronger in samples with TP53-MT than in those with TP53-WT, including enrichment of interferon-gamma, positive regulation of TNF secretion pathways and increased expression of some immunostimulatory molecules, such as CXCL9 and CXCL10. This study provided some clues for identifying patients who would potentially benefit from ICIs at the somatic genomic level, developing new indications for targeted second-generation sequencing and promoting the development of precision medicine.
近年来,针对 CTLA-4 或 PD1/PDL1 的免疫检查点抑制剂(ICIs)在膀胱癌(BLCA)的治疗中取得了显著的成功,但只有少数患者表现出持久的临床获益。肿瘤抑制基因 TP53 的突变形式(TP53-MT)在预测 ICIs 疗效中的预后作用存在很大争议;因此,在这项研究中,我们从免疫治疗队列中获得了 210 名患者的数据,从癌症基因组图谱(TCGA)-BLCA 队列中获得了 412 名患者的数据,从癌症药物敏感性基因组学(GDSC)中获得了 18 个 BLCA 细胞系的数据,并进行了综合生物信息学分析,以探讨 TP53-MT 与从 ICI 治疗中获得的临床益处之间的关系及其潜在机制。我们得出结论,TP53-MT 是对 ICIs 相对较好反应的潜在指标,并与延长的总生存期(OS)相关(对数秩检验,风险比(HR)=0.65[95%置信区间(CI),0.44-0.99],p=0.041)。通过与多个平台的综合分析,我们发现 TP53-MT 患者比野生型 P53(TP53-WT)患者更有可能从 ICIs 中获益,这可能是两个主要机制的结果。首先,TP53-MT 患者表现出更强的肿瘤抗原性和肿瘤抗原呈递,表现为肿瘤突变负荷更高、新抗原负荷更高和 MHC 表达增加;其次,与 TP53-WT 相比,TP53-MT 样本中存在更强的抗肿瘤免疫,包括干扰素-γ富集、TNF 分泌途径的正调控和某些免疫刺激分子(如 CXCL9 和 CXCL10)表达增加。这项研究为在体细胞基因组水平上识别可能从 ICIs 中获益的患者提供了一些线索,为靶向第二代测序开发新的适应症,并促进精准医学的发展。