Abstract

BackgroundEpstein-Barr virus (EBV)-associated nasopharyngeal carcinoma (NPC) in endemic regions may have undetectable plasma EBV DNA.MethodsWe prospectively recruited 518 patients with non-metastatic NPC and measured their pre-treatment plasma EBV DNA. The stage distribution and prognosis between pre-treatment plasma EBV DNA-negative (0–20 copies/ml) and EBV DNA-positive (>20 copies/ml) patients following radical treatment were compared.ResultsSeventy-eight patients (15.1%) were plasma EBV DNA-negative, and 62 in this subset (12.0%) had 0 copy/ml. Only 23/78 (29.5%) plasma EBV DNA-negative patients with advanced NPC (stage III-IVA) had strong EBV encoded RNA (EBER) positivity (score 3) in their tumours compared to 342/440 (77.7%) EBV DNA-positive patients of the same stages (p < 0.001). Though EBV DNA-negative patients had more early-stage disease (p < 0.001) and smaller volumes of the primary tumour and the positive neck nodes (p < 0.001), they had similar 5-year overall survival and cancer-specific survival to those EBV DNA-positive counterparts by stage. Similar results were also seen when plasma EBV DNA cut-off was set at 0 copy/ml.ConclusionsPatients with low-volume NPC may not be identified by plasma/serum tumour markers and caution should be taken in its utility as a screening tool for NPC even in endemic regions.Clinical trial registrationClinicaltrials.gov Identifier: NCT02476669.

Highlights

  • Nasopharyngeal carcinoma (NPC) is endemic in southern China including Hong Kong.[1]

  • All patient blood samples contained in EDTA tubes were immediately stored in a 4 °C refrigerator after blood taking from patients and they were processed for subsequent Epstein-Barr virus (EBV) deoxyribonucleic acid (DNA) extraction within 4 h of blood taking in the single laboratory of our institution

  • Seventyeight (15.1%) patients were classified as pre-treatment plasma EBV DNA-negative (i.e. ≤20 copies/ml)

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Summary

Introduction

Nasopharyngeal carcinoma (NPC) is endemic in southern China including Hong Kong.[1] Over the past 20 years, plasma Epstein-Barr Virus (EBV) deoxyribonucleic acid (DNA) has been advocated for the diagnosis of NPC. The rationale for this methodology has been based on the concept that since EBV has been associated with. In. Epstein-Barr virus (EBV)-associated nasopharyngeal carcinoma (NPC) in endemic regions may have undetectable plasma EBV DNA. The stage distribution and prognosis between pre-treatment plasma EBV DNA-negative (0–20 copies/ml) and EBV DNA-positive (>20 copies/ml) patients following radical treatment were compared.

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