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

Cancer Manag Res

State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University Cancer Center, Guangzhou 510060, People's Republic of China.

Published: May 2019

AI Article Synopsis

  • The study investigates how pretreatment serum HBV DNA levels relate to the clinical outcomes of NSCLC patients with chronic hepatitis B.
  • Retrospective data from 188 NSCLC patients were analyzed, focusing on various prognostic factors, including HBV DNA levels, to assess their impact on patient survival.
  • Findings indicate that while HBV DNA is a significant prognostic marker, a nomogram combining several factors provides a more accurate prediction of survival than relying solely on HBV DNA or traditional TNM staging.

Article Abstract

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. 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. 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 (=0.028), treatment (=0.002), HBV DNA (<0.001), and GPS (=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 (=0.48). However, the C-index values of nomogram model were statistically higher both than HBV DNA (0.76 vs 0.67, <0.001), and TNM stage (0.76 vs 0.69, <0.001). Pretreatment serum HBV DNA copy numbers can act as a prognostic marker of survival for NSCLC patients with chronic HBV infection.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6549665PMC
http://dx.doi.org/10.2147/CMAR.S198714DOI Listing

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