File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1056/NEJMoa2301496
- Scopus: eid_2-s2.0-85168959839
- WOS: WOS:001086344300008
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: Anti–Epstein–Barr Virus BNLF2b for Mass Screening for Nasopharyngeal Cancer
Title | Anti–Epstein–Barr Virus BNLF2b for Mass Screening for Nasopharyngeal Cancer |
---|---|
Authors | |
Issue Date | 31-Aug-2023 |
Publisher | Massachusetts Medical Society |
Citation | New England Journal of Medicine, 2023, v. 389, n. 9, p. 808-819 How to Cite? |
Abstract | Background: Population screening of asymptomatic persons with Epstein-Barr virus (EBV) DNA or antibodies has improved the diagnosis of nasopharyngeal carcinoma and survival among affected persons. However, the positive predictive value of current screening strategies is unsatisfactory even in areas where nasopharyngeal carcinoma is endemic. Methods: We designed a peptide library representing highly ranked B-cell epitopes of EBV coding sequences to identify novel serologic biomarkers for nasopharyngeal carcinoma. After a retrospective case-control study, the performance of the novel biomarker anti-BNLF2b total antibody (P85-Ab) was validated through a large-scale prospective screening program and compared with that of the standard two-antibody-based screening method (EBV nuclear antigen 1 [EBNA1]-IgA and EBV-specific viral capsid antigen [VCA]-IgA). Results: P85-Ab was the most promising biomarker for nasopharyngeal carcinoma screening, with high sensitivity (94.4%; 95% confidence interval [CI], 86.4 to 97.8) and specificity (99.6%; 95% CI, 97.8 to 99.9) in the retrospective case-control study. Among the 24,852 eligible participants in the prospective cohort, 47 cases of nasopharyngeal carcinoma (38 at an early stage) were identified. P85-Ab showed higher sensitivity than the two-antibody method (97.9% vs. 72.3%; ratio, 1.4 [95% CI, 1.1 to 1.6]), higher specificity (98.3% vs. 97.0%; ratio, 1.01 [95% CI, 1.01 to 1.02]), and a higher positive predictive value (10.0% vs. 4.3%; ratio, 2.3 [95% CI, 1.8 to 2.8]). The combination of P85-Ab and the two-antibody method markedly increased the positive predictive value to 44.6% (95% CI, 33.8 to 55.9), with sensitivity of 70.2% (95% CI, 56.0 to 81.4). Conclusions: Our results suggest that P85-Ab is a promising novel biomarker for nasopharyngeal carcinoma screening, with higher sensitivity, specificity, and positive predictive value than the standard two-antibody method. (Funded by the National Key Research and Development Program of China and others; ClinicalTrials.gov number, NCT04085900.). |
Persistent Identifier | http://hdl.handle.net/10722/337748 |
ISSN | 2023 Impact Factor: 96.2 2023 SCImago Journal Rankings: 20.544 |
ISI Accession Number ID |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Li, Tingdong | - |
dc.contributor.author | Li, Fugui | - |
dc.contributor.author | Guo, Xiaoyi | - |
dc.contributor.author | Hong, Congming | - |
dc.contributor.author | Yu, Xia | - |
dc.contributor.author | Wu, Biaohua | - |
dc.contributor.author | Lian, Shifeng | - |
dc.contributor.author | Song, Liuwei | - |
dc.contributor.author | Tang, Jiabao | - |
dc.contributor.author | Wen, Shunhua | - |
dc.contributor.author | Gao, Kaimin | - |
dc.contributor.author | Hao, Mengling | - |
dc.contributor.author | Cheng, Weimin | - |
dc.contributor.author | Su, Yingying | - |
dc.contributor.author | Zhang, Shiyin | - |
dc.contributor.author | Huang, Shoujie | - |
dc.contributor.author | Fang, Mujin | - |
dc.contributor.author | Wang, Yingbin | - |
dc.contributor.author | Ng, Mun-Hon | - |
dc.contributor.author | Chen, Honglin | - |
dc.contributor.author | Luo, Wenxin | - |
dc.contributor.author | Ge, Shengxiang | - |
dc.contributor.author | Zhang, Jun | - |
dc.contributor.author | Xia, Ningshao | - |
dc.contributor.author | Ji, Mingfang | - |
dc.date.accessioned | 2024-03-11T10:23:35Z | - |
dc.date.available | 2024-03-11T10:23:35Z | - |
dc.date.issued | 2023-08-31 | - |
dc.identifier.citation | New England Journal of Medicine, 2023, v. 389, n. 9, p. 808-819 | - |
dc.identifier.issn | 0028-4793 | - |
dc.identifier.uri | http://hdl.handle.net/10722/337748 | - |
dc.description.abstract | <p><strong>Background: </strong>Population screening of asymptomatic persons with Epstein-Barr virus (EBV) DNA or antibodies has improved the diagnosis of nasopharyngeal carcinoma and survival among affected persons. However, the positive predictive value of current screening strategies is unsatisfactory even in areas where nasopharyngeal carcinoma is endemic.</p><p><strong>Methods: </strong>We designed a peptide library representing highly ranked B-cell epitopes of EBV coding sequences to identify novel serologic biomarkers for nasopharyngeal carcinoma. After a retrospective case-control study, the performance of the novel biomarker anti-BNLF2b total antibody (P85-Ab) was validated through a large-scale prospective screening program and compared with that of the standard two-antibody-based screening method (EBV nuclear antigen 1 [EBNA1]-IgA and EBV-specific viral capsid antigen [VCA]-IgA).</p><p><strong>Results: </strong>P85-Ab was the most promising biomarker for nasopharyngeal carcinoma screening, with high sensitivity (94.4%; 95% confidence interval [CI], 86.4 to 97.8) and specificity (99.6%; 95% CI, 97.8 to 99.9) in the retrospective case-control study. Among the 24,852 eligible participants in the prospective cohort, 47 cases of nasopharyngeal carcinoma (38 at an early stage) were identified. P85-Ab showed higher sensitivity than the two-antibody method (97.9% vs. 72.3%; ratio, 1.4 [95% CI, 1.1 to 1.6]), higher specificity (98.3% vs. 97.0%; ratio, 1.01 [95% CI, 1.01 to 1.02]), and a higher positive predictive value (10.0% vs. 4.3%; ratio, 2.3 [95% CI, 1.8 to 2.8]). The combination of P85-Ab and the two-antibody method markedly increased the positive predictive value to 44.6% (95% CI, 33.8 to 55.9), with sensitivity of 70.2% (95% CI, 56.0 to 81.4).</p><p><strong>Conclusions: </strong>Our results suggest that P85-Ab is a promising novel biomarker for nasopharyngeal carcinoma screening, with higher sensitivity, specificity, and positive predictive value than the standard two-antibody method. (Funded by the National Key Research and Development Program of China and others; ClinicalTrials.gov number, <a href="http://clinicaltrials.gov/show/NCT04085900" title="See in ClinicalTrials.gov">NCT04085900</a>.).</p> | - |
dc.language | eng | - |
dc.publisher | Massachusetts Medical Society | - |
dc.relation.ispartof | New England Journal of Medicine | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.title | Anti–Epstein–Barr Virus BNLF2b for Mass Screening for Nasopharyngeal Cancer | - |
dc.type | Article | - |
dc.identifier.doi | 10.1056/NEJMoa2301496 | - |
dc.identifier.scopus | eid_2-s2.0-85168959839 | - |
dc.identifier.volume | 389 | - |
dc.identifier.issue | 9 | - |
dc.identifier.spage | 808 | - |
dc.identifier.epage | 819 | - |
dc.identifier.eissn | 1533-4406 | - |
dc.identifier.isi | WOS:001086344300008 | - |
dc.identifier.issnl | 0028-4793 | - |