File Download
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1038/s41416-019-0575-6
- Scopus: eid_2-s2.0-85073310068
- PMID: 31527689
- WOS: WOS:000490189300008
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: Negative plasma Epstein-Barr virus DNA nasopharyngeal carcinoma in an endemic region and its influence on liquid biopsy screening programmes
Title | Negative plasma Epstein-Barr virus DNA nasopharyngeal carcinoma in an endemic region and its influence on liquid biopsy screening programmes |
---|---|
Authors | |
Issue Date | 2019 |
Publisher | Springer Nature, published in association with Cancer Research UK. The Journal's web site is located at http://www.nature.com/bjc |
Citation | British Journal of Cancer, 2019, v. 121 n. 8, p. 690-698 How to Cite? |
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. |
Persistent Identifier | http://hdl.handle.net/10722/284045 |
ISSN | 2023 Impact Factor: 6.4 2023 SCImago Journal Rankings: 3.000 |
PubMed Central ID | |
ISI Accession Number ID |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Nicholls, JM | - |
dc.contributor.author | Lee, VHF | - |
dc.contributor.author | Chan, SK | - |
dc.contributor.author | Tsang, KC | - |
dc.contributor.author | Choi, CW | - |
dc.contributor.author | Kwong, DLW | - |
dc.contributor.author | Lam, KO | - |
dc.contributor.author | Chan, SY | - |
dc.contributor.author | Tong, CC | - |
dc.contributor.author | So, TH | - |
dc.contributor.author | Leung, TW | - |
dc.contributor.author | Luk, MY | - |
dc.contributor.author | Khong, PL | - |
dc.contributor.author | Lee, AWM | - |
dc.date.accessioned | 2020-07-20T05:55:39Z | - |
dc.date.available | 2020-07-20T05:55:39Z | - |
dc.date.issued | 2019 | - |
dc.identifier.citation | British Journal of Cancer, 2019, v. 121 n. 8, p. 690-698 | - |
dc.identifier.issn | 0007-0920 | - |
dc.identifier.uri | http://hdl.handle.net/10722/284045 | - |
dc.description.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. | - |
dc.language | eng | - |
dc.publisher | Springer Nature, published in association with Cancer Research UK. The Journal's web site is located at http://www.nature.com/bjc | - |
dc.relation.ispartof | British Journal of Cancer | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.title | Negative plasma Epstein-Barr virus DNA nasopharyngeal carcinoma in an endemic region and its influence on liquid biopsy screening programmes | - |
dc.type | Article | - |
dc.identifier.email | Nicholls, JM: jmnichol@hkucc.hku.hk | - |
dc.identifier.email | Lee, VHF: vhflee@hku.hk | - |
dc.identifier.email | Choi, CW: hcchoi@hku.hk | - |
dc.identifier.email | Kwong, DLW: dlwkwong@hku.hk | - |
dc.identifier.email | Lam, KO: lamkaon@hku.hk | - |
dc.identifier.email | Tong, CC: tccz01@hku.hk | - |
dc.identifier.email | So, TH: sth495@hku.hk | - |
dc.identifier.email | Leung, TW: ltw920@hkucc.hku.hk | - |
dc.identifier.email | Luk, MY: myluk@hkucc.hku.hk | - |
dc.identifier.email | Khong, PL: plkhong@hku.hk | - |
dc.identifier.email | Lee, AWM: awmlee@hkucc.hku.hk | - |
dc.identifier.authority | Nicholls, JM=rp00364 | - |
dc.identifier.authority | Lee, VHF=rp00264 | - |
dc.identifier.authority | Kwong, DLW=rp00414 | - |
dc.identifier.authority | Lam, KO=rp01501 | - |
dc.identifier.authority | So, TH=rp01981 | - |
dc.identifier.authority | Khong, PL=rp00467 | - |
dc.identifier.authority | Lee, AWM=rp02056 | - |
dc.description.nature | published_or_final_version | - |
dc.identifier.doi | 10.1038/s41416-019-0575-6 | - |
dc.identifier.pmid | 31527689 | - |
dc.identifier.pmcid | PMC6888810 | - |
dc.identifier.scopus | eid_2-s2.0-85073310068 | - |
dc.identifier.hkuros | 311326 | - |
dc.identifier.volume | 121 | - |
dc.identifier.issue | 8 | - |
dc.identifier.spage | 690 | - |
dc.identifier.epage | 698 | - |
dc.identifier.isi | WOS:000490189300008 | - |
dc.publisher.place | United Kingdom | - |
dc.identifier.issnl | 0007-0920 | - |