Abstract

PurposeTo investigate the long-term clinical outcome of nasopharyngeal carcinoma (NPC) patients with persistently detectable plasma EBV (pEBV) DNA after curative radiotherapy (RT).ResultsThe post-RT pEBV DNA levels were very lower copy number (median 21, interquartile range 8–206 copies/ml). After long-term follow-up, the relapse rate was 64.8%, the median time to progression 20 months, and 5-year overall survival (OS) 49.6%. Thirty-two of 39 (82.1%) patients with high viral load (≥ 100 copies/ml) developed tumor relapse, whereas 57.0% (49/86) patients with low viral load (< 100 copies/ml) had tumor relapse (P = 0.0065). The 5-year OS rates were 20.5% and 62.9% for patients with viral load ≥ and < 100 copies/ml (median survival, 20 vs. 100 months; P < 0.0001). Patients who received adjuvant chemotherapy (AdjCT) experienced significant reduction in distant failures (66.2% vs. 31.6%; P = 0.0001) but similar locoregional recurrences (P = 0.2337). The 5-year OS rates were 69.4% for patients who received AdjCT compared with 33.2% for those of without AdjCT (median survival, 111 vs. 32 months; P < 0.0001).MethodsWe screened 931 newly diagnosed NPC patients who finished curative RT and found 125 patients (13.4%) with detectable pEBV DNA one week after RT. The clinical characteristics, treatment modality, subsequent failure patterns and survivals were analyzed.ConclusionsNPC patients with persistently detectable pEBV DNA after curative RT have a higher rate of treatment failure and poor survivals. Levels of the post-RT pEBV DNA and administration of AdjCT affect the final outcome significantly.

Highlights

  • Nasopharyngeal carcinoma (NPC) has been demonstrated as a radio- and chemo-sensitive tumor

  • NPC patients with persistently detectable plasma EBV (pEBV) DNA after curative RT have a higher rate of treatment failure and poor survivals

  • Our previous studies found that the post-treatment plasma EBV DNA status dominated the effect of the pre-treatment viral load and had greater impact than the TNM staging [17,18,19]

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Summary

Introduction

Nasopharyngeal carcinoma (NPC) has been demonstrated as a radio- and chemo-sensitive tumor. Treatment failure in the past was due to a high rate of local recurrence and/ or distant metastasis. Advances in radiation oncology have improved the locoregional control, and treatment failure is due mainly to distant metastasis. The TNM staging (extent of local invasion, regional lymphatic spread, and distant metastasis) is the most important prognostic factors in NPC. Cell-free circulating EBV DNA can be detected in plasma and serum of NPC patients, and has been shown as a significant prognosticator at different time-points, including pre-treatment, post-treatment, and middle part of RT [12,13,14,15,16,17,18,19,20,21,22]. Other investigators confirmed our findings [20, 21]

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