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- Scopus: eid_2-s2.0-0034671947
- PMID: 11156384
- WOS: WOS:000166201500023
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Article: Molecular prognostication of nasopharyngeal carcinoma by quantitative analysis of circulating epstein-barr virus DNA
Title | Molecular prognostication of nasopharyngeal carcinoma by quantitative analysis of circulating epstein-barr virus DNA |
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Authors | |
Issue Date | 2000 |
Publisher | American Association for Cancer Research. The Journal's web site is located at http://cancerres.aacrjournals.org/ |
Citation | Cancer Research, 2000, v. 60 n. 24, p. 6878-6881 How to Cite? |
Abstract | We investigated the prognostic implication of pretreatment plasma/ serum EBV DNA concentration, as measured by real-time quantitative PCR, in nasopharyngeal carcinoma (NPC). In 91 prospectively recruited NPC patients, those with recurrence or metastasis within the first year after treatment had a higher median plasma EBV DNA concentration than those without events (41,756 copies/ml versus 5,807 copies/ml; P < 0.001, Mann-Whitney rank-sum test). In multivariate logistic regression analysis, plasma EBV DNA was an independent prognostic indicator for early clinical events [relative risk = 3.8 (95% confidence interval, 1.6-9.2 for each 10-fold increase in plasma EBV DNA concentration; P = 0.003)]. In a second cohort of 139 NPC patients followed-up for a median period of 2,027 days (interquartile range, 597-2,335 days), serum EBV DNA was found to be a significant variable associated with NPC-related death in multivariate Cox's regression analysis [relative risk = 1.6 (95% confidence interval, 1.1-2.1 for each 10-fold increase in serum EBV DNA concentration; P = 0.007)]. The quantitation of circulating EBV DNA may thus allow improved prognostication of NPC. |
Persistent Identifier | http://hdl.handle.net/10722/148216 |
ISSN | 2023 Impact Factor: 12.5 2023 SCImago Journal Rankings: 3.468 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Lo, YMD | en_US |
dc.contributor.author | Chan, ATC | en_US |
dc.contributor.author | Chan, LYS | en_US |
dc.contributor.author | Leung, SF | en_US |
dc.contributor.author | Lam, CW | en_US |
dc.contributor.author | Huang, DP | en_US |
dc.contributor.author | Johnson, PJ | en_US |
dc.date.accessioned | 2012-05-29T06:11:33Z | - |
dc.date.available | 2012-05-29T06:11:33Z | - |
dc.date.issued | 2000 | en_US |
dc.identifier.citation | Cancer Research, 2000, v. 60 n. 24, p. 6878-6881 | en_US |
dc.identifier.issn | 0008-5472 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/148216 | - |
dc.description.abstract | We investigated the prognostic implication of pretreatment plasma/ serum EBV DNA concentration, as measured by real-time quantitative PCR, in nasopharyngeal carcinoma (NPC). In 91 prospectively recruited NPC patients, those with recurrence or metastasis within the first year after treatment had a higher median plasma EBV DNA concentration than those without events (41,756 copies/ml versus 5,807 copies/ml; P < 0.001, Mann-Whitney rank-sum test). In multivariate logistic regression analysis, plasma EBV DNA was an independent prognostic indicator for early clinical events [relative risk = 3.8 (95% confidence interval, 1.6-9.2 for each 10-fold increase in plasma EBV DNA concentration; P = 0.003)]. In a second cohort of 139 NPC patients followed-up for a median period of 2,027 days (interquartile range, 597-2,335 days), serum EBV DNA was found to be a significant variable associated with NPC-related death in multivariate Cox's regression analysis [relative risk = 1.6 (95% confidence interval, 1.1-2.1 for each 10-fold increase in serum EBV DNA concentration; P = 0.007)]. The quantitation of circulating EBV DNA may thus allow improved prognostication of NPC. | en_US |
dc.language | eng | en_US |
dc.publisher | American Association for Cancer Research. The Journal's web site is located at http://cancerres.aacrjournals.org/ | en_US |
dc.relation.ispartof | Cancer Research | en_US |
dc.subject.mesh | Adult | en_US |
dc.subject.mesh | Carcinoma - Blood - Diagnosis - Genetics - Mortality | en_US |
dc.subject.mesh | Dna - Analysis | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Herpesvirus 4, Human - Genetics - Metabolism | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Logistic Models | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Middle Aged | en_US |
dc.subject.mesh | Multivariate Analysis | en_US |
dc.subject.mesh | Nasopharyngeal Neoplasms - Blood - Diagnosis - Genetics - Mortality | en_US |
dc.subject.mesh | Polymerase Chain Reaction | en_US |
dc.subject.mesh | Prognosis | en_US |
dc.subject.mesh | Time Factors | en_US |
dc.title | Molecular prognostication of nasopharyngeal carcinoma by quantitative analysis of circulating epstein-barr virus DNA | en_US |
dc.type | Article | en_US |
dc.identifier.email | Lam, CW:ching-wanlam@pathology.hku.hk | en_US |
dc.identifier.authority | Lam, CW=rp00260 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.pmid | 11156384 | - |
dc.identifier.scopus | eid_2-s2.0-0034671947 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-0034671947&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 60 | en_US |
dc.identifier.issue | 24 | en_US |
dc.identifier.spage | 6878 | en_US |
dc.identifier.epage | 6881 | en_US |
dc.identifier.isi | WOS:000166201500023 | - |
dc.publisher.place | United States | en_US |
dc.identifier.issnl | 0008-5472 | - |