Negative plasma Epstein-Barr virus DNA nasopharyngeal carcinoma in an endemic region and its influence on liquid biopsy screening programmes
-
Published:2019-09-17
Issue:8
Volume:121
Page:690-698
-
ISSN:0007-0920
-
Container-title:British Journal of Cancer
-
language:en
-
Short-container-title:Br J Cancer
Author:
Nicholls John Malcolm, Lee Victor Ho-FunORCID, Chan Sik-Kwan, Tsang Ka-Chun, Choi Cheuk-Wai, Kwong Dora Lai-Wan, Lam Ka-On, Chan Sum-Yin, Tong Chi-Chung, So Tsz-Him, Leung To-Wai, Luk Mai-Yee, Khong Pek-LanORCID, Lee Anne Wing-Mui
Abstract
Abstract
Background
Epstein-Barr virus (EBV)-associated nasopharyngeal carcinoma (NPC) in endemic regions may have undetectable plasma EBV DNA.
Methods
We 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.
Results
Seventy-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.
Conclusions
Patients 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 registration
Clinicaltrials.gov Identifier: NCT02476669.
Funder
Croucher Foundation
Publisher
Springer Science and Business Media LLC
Subject
Cancer Research,Oncology
Reference50 articles.
1. Lee, A. W., Ma, B. B., Ng, W. T. & Chan, A. T. Management of nasopharyngeal carcinoma: current practice and future perspective. J. Clin. Oncol. 33, 3356–3364 (2015). 2. Fung, S. Y., Lam, J. W. & Chan, K. C. Clinical utility of circulating Epstein-Barr virus DNA analysis for the management of nasopharyngeal carcinoma. Chin. Clin. Oncol. 5, 18 (2016). 3. Kim K. Y., Le Q. T., Yom S. S., Pinsky B. A., Bratman S. V., Ng R. H. et al. Current state of PCR-based Epstein-Barr virus DNA testing for nasopharyngeal cancer. J. Natl Cancer Inst. 109, djx007 (2017). 4. Le, Q. T., Zhang, Q., Cao, H., Cheng, A. J., Pinsky, B. A., Hong, R. L. et al. An international collaboration to harmonize the quantitative plasma Epstein-Barr virus DNA assay for future biomarker-guided trials in nasopharyngeal carcinoma. Clin. Cancer Res. 19, 2208–2215 (2013). 5. Zhang, W., Chen, Y., Chen, L., Guo, R., Zhou, G., Tang, L. et al. The clinical utility of plasma Epstein-Barr virus DNA assays in nasopharyngeal carcinoma: the dawn of a new era?: a systematic review and meta-analysis of 7836 cases. Med. (Baltim.) 94, e845 (2015).
Cited by
22 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
|
|