4.7 Article

The impact of plasma epstein-barr virus DNA and fibrinogen on nasopharyngeal carcinoma prognosis: an observational study

Journal

BRITISH JOURNAL OF CANCER
Volume 111, Issue 6, Pages 1102-1111

Publisher

SPRINGERNATURE
DOI: 10.1038/bjc.2014.393

Keywords

nasopharyngeal carcinoma; EBV DNA; fibrinogen; survival

Categories

Funding

  1. Ministry of Science and Technology of China [2011CB504300]
  2. National Natural Science Foundation of China [81025014, 81230045, 91019015, 81071932, 30600755, 81072226]
  3. 863 Project [2012AA02A501]
  4. National Key Basic Research Program of China [2013CB910304]
  5. Sci-Tech Project Foundation of Guangdong Province [2011B080701034]
  6. Sci-Tech Project Foundation of Guangzhou City [2011J4300100]
  7. Sun Yatsen University Clinical Research 5010 Program
  8. Fundamental Research Funds for the Central Universities

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Background: The impact of combining plasma fibrinogen levels with Epstein-Barr Virus DNA (EBV DNA) levels on the prognosis for patients with nasopharyngeal carcinoma (NPC) was evaluated. Methods: In this observational study, 2563 patients with non-metastatic NPC were evaluated for the effects of circulating plasma fibrinogen and EBV DNA levels on disease-free survival (DFS), distant metastasis-free survival (DMFS), and overall survival (OS). Results: Compared with the bottom biomarker tertiles, TNM stage-adjusted hazard ratios (HR, 95% confidence intervals (CIs)) for predicting DFS in fibrinogen tertiles 2 to 3 were 1.26 (1.00 to 1.60) and 1.81 (1.45 to 2.26), respectively; HR for EBV DNA tertiles 2 to 3 were 1.49 (1.12 to 1.98) and 4.24 (3.27 to 5.49), respectively. After additional adjustment for established risk factors, both biomarkers were still associated (P for trend <0.001) with reduced DFS (HR: 1.79, 95% CI, 1.43 to 2.25 for top fibrinogen tertiles; HR: 4.04, 95% CI: 3.10 to 5.27 for top EBV DNA tertiles compared with the bottom tertiles). For patients with advanced-stage disease, those with high fibrinogen levels (>= 3.34 gl(-1)) presented with worse DFS, regardless of EBV DNA >= 4000 or <4000 copies ml(-1) subgroup. Similar findings were observed for DMFS and OS. Conclusions: Circulating fibrinogen and EBV DNA significantly correlate with NPC patients survival. Combined fibrinogen and EBV DNA data lead to improved prognostic prediction in advanced-stage disease.

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