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Serum hepatitis B viral (HBV) DNA is a predictive biomarker for survival in non-small cell lung cancer patients with chronic HBV infection

机译:血清乙型肝炎病毒(HBV)DNA是具有慢性HBV感染的非小细胞肺癌患者生存的预测生物标志物

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摘要

>Purpose: To study the association between pretreatment serum hepatitis B viral (HBV) DNA copy numbers and clinical outcome of non-small cell lung cancer (NSCLC) patients with chronic HBV infection.>Patients and methods: We retrospectively evaluated the medical records of NSCLC HBV (+) patients between January 2008 and December 2010. The HBV DNA copy numbers and other prognostic factors including albumin (ALB), C-reactive protein (CRP), platelet, neutrophil–lymphocyte ratio (NLR), platelet–lymphocyte ratio (PLR), and Glasgow Prognostic Score (GPS) were obtained before any antitumor treatment. Kaplan–Meier curves and the log-rank test were used to calculate prognostic significance. A multivariable Cox proportional hazard regression was modeled to analyze the independent prognostic factors for NSCLC HBV (+) patients. All independent prognostic factors in the Cox multivariable analysis were used to build a nomogram. The predictive accuracy of HBV DNA, TNM stage and nomogram was evaluated with the concordance index (C-index) and time-dependent receiver operating characteristics (ROC) curves, and simultaneously compared with traditional TNM staging system respectively.>Results: A total of 188 patients were recruited in this study; the median age was 56 years, and the median overall survival (OS) was 34 months. Cox multivariate analysis results showed independent factors for OS including TNM stage (P=0.028), treatment (P=0.002), HBV DNA (P<0.001), and GPS (P=0.026). The nomogram model for survival was built based on four prognostic factors. The C-index for HBV DNA was 0.67, 0.69 for TNM stage, and 0.76 for the nomogram model. There was no statistical difference between HBV DNA and TNM stage (P=0.48). However, the C-index values of nomogram model were statistically higher both than HBV DNA (0.76 vs 0.67, P<0.001), and TNM stage (0.76 vs 0.69, P<0.001).>Conclusion: Pretreatment serum HBV DNA copy numbers can act as a prognostic marker of survival for NSCLC patients with chronic HBV infection.
机译:>目的:研究治疗前血清乙型肝炎病毒(HBV)DNA拷贝数与非小细胞肺癌(NSCLC)慢性HBV感染患者临床结局之间的关系。>患者和方法::我们回顾性评估了2008年1月至2010年12月期间NSCLC HBV(+)患者的病历。HBVDNA拷贝数和其他预后因素包括白蛋白(ALB),C反应蛋白(CRP),血小板,在进行任何抗肿瘤治疗之前,均获得了中性粒细胞-淋巴细胞比(NLR),血小板-淋巴细胞比(PLR)和格拉斯哥预后评分(GPS)。 Kaplan–Meier曲线和对数秩检验用于计算预后意义。对多变量Cox比例风险回归进行建模,以分析NSCLC HBV(+)患者的独立预后因素。 Cox多变量分析中所有独立的预后因素均用于构建诺模图。通过一致性指数(C-index)和时间依赖性接收者操作特征(ROC)曲线评估了HBV DNA,TNM分期和列线图的预测准确性,并分别与传统TNM分期系统进行了比较。>结果:< / strong>这项研究共招募了188名患者;中位年龄为56岁,中位总生存(OS)为34个月。 Cox多变量分析结果显示OS的独立因素包括TNM分期(P = 0.028),治疗(P = 0.002),HBV DNA(P <0.001)和GPS(P = 0.026)。基于四个预后因素建立了生存的列线图模型。 HBV DNA的C指数为0.67,TNM阶段的C指数为0.69,列线图模型的C指数为0.76。 HBV DNA与TNM分期之间无统计学差异(P = 0.48)。然而,列线图模型的C-指数值在统计学上均高于HBV DNA(0.76 vs 0.67,P <0.001)和TNM分期(0.76 vs 0.69,P <0.001)。>结论:血清HBV DNA拷贝数可以作为慢性HBV感染的NSCLC患者生存的预后标志。

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