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Article: Multiple oral cancer development—Clinico‐pathological features in the Hong Kong population

TitleMultiple oral cancer development—Clinico‐pathological features in the Hong Kong population
Authors
KeywordsHong Kong population study
multiple tumours
oral cancer
Issue Date2020
PublisherWiley-Blackwell Publishing Ltd. The Journal's web site is located at http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1600-0714
Citation
Journal of Oral Pathology & Medicine, 2020, v. 49 n. 2, p. 145-149 How to Cite?
AbstractBackground: Multiple squamous cell carcinoma (SCC) development within the oral cavity is an important consequence of mucosal field cancerization. We have previously profiled contemporaneous demographics and confirmed a rising incidence of oral cancer within the Hong Kong population. In this further study, we sought to characterize the presenting clinico‐pathological features and clinical outcome consequent upon multiple primary tumour (PT) development. Methods: Having accessed the Hong Kong Hospital Authority (HA) database to identify new cases of oral SCC diagnosed during an 18‐year period (November 1999 to October 2018), specific clinico‐pathological data were retrieved for patients who developed multiple oral SCCs during the study period. Results: Out of 6706 identified SCC cases, 769 patients (11.5%) developed multiple PTs, most commonly 2 (663) but 3 (91), 4 (12), 5 (2) and 6 (1) were also observed. The male to female ratio was 2.25 to 1 (P = .004), with female patients significantly older at first tumour presentation (P = .002), demonstrating longer periods before second PT development (P = .001) and better long‐term survival than males (P = .001). Buccal mucosa (143), oropharynx (134) and tongue (112) were the sites most frequently affected by second tumours. Whilst buccal SCC showed a propensity for subsequent buccal tumour development (60), oropharynx primaries developed second PTs most frequently on the tonsil (28) and tongue (27). Tongue primaries were associated with second PTs on the floor of mouth (61) and oropharynx (57). Conclusion: Development of multiple oral cancers is a significant risk in Hong Kong, particularly for male patients. Following initial tumour management, regular and careful patient follow‐up is important for early recognition of multiple SCC development.
Persistent Identifierhttp://hdl.handle.net/10722/280261
ISSN
2023 Impact Factor: 2.7
2023 SCImago Journal Rankings: 0.716
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorChoi, S-W-
dc.contributor.authorThomson, P-
dc.date.accessioned2020-01-21T11:50:54Z-
dc.date.available2020-01-21T11:50:54Z-
dc.date.issued2020-
dc.identifier.citationJournal of Oral Pathology & Medicine, 2020, v. 49 n. 2, p. 145-149-
dc.identifier.issn0904-2512-
dc.identifier.urihttp://hdl.handle.net/10722/280261-
dc.description.abstractBackground: Multiple squamous cell carcinoma (SCC) development within the oral cavity is an important consequence of mucosal field cancerization. We have previously profiled contemporaneous demographics and confirmed a rising incidence of oral cancer within the Hong Kong population. In this further study, we sought to characterize the presenting clinico‐pathological features and clinical outcome consequent upon multiple primary tumour (PT) development. Methods: Having accessed the Hong Kong Hospital Authority (HA) database to identify new cases of oral SCC diagnosed during an 18‐year period (November 1999 to October 2018), specific clinico‐pathological data were retrieved for patients who developed multiple oral SCCs during the study period. Results: Out of 6706 identified SCC cases, 769 patients (11.5%) developed multiple PTs, most commonly 2 (663) but 3 (91), 4 (12), 5 (2) and 6 (1) were also observed. The male to female ratio was 2.25 to 1 (P = .004), with female patients significantly older at first tumour presentation (P = .002), demonstrating longer periods before second PT development (P = .001) and better long‐term survival than males (P = .001). Buccal mucosa (143), oropharynx (134) and tongue (112) were the sites most frequently affected by second tumours. Whilst buccal SCC showed a propensity for subsequent buccal tumour development (60), oropharynx primaries developed second PTs most frequently on the tonsil (28) and tongue (27). Tongue primaries were associated with second PTs on the floor of mouth (61) and oropharynx (57). Conclusion: Development of multiple oral cancers is a significant risk in Hong Kong, particularly for male patients. Following initial tumour management, regular and careful patient follow‐up is important for early recognition of multiple SCC development.-
dc.languageeng-
dc.publisherWiley-Blackwell Publishing Ltd. The Journal's web site is located at http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1600-0714-
dc.relation.ispartofJournal of Oral Pathology & Medicine-
dc.rightsPreprint This is the pre-peer reviewed version of the following article: [FULL CITE], which has been published in final form at [Link to final article using the DOI]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. Postprint This is the peer reviewed version of the following article: [FULL CITE], which has been published in final form at [Link to final article using the DOI]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.-
dc.subjectHong Kong population study-
dc.subjectmultiple tumours-
dc.subjectoral cancer-
dc.titleMultiple oral cancer development—Clinico‐pathological features in the Hong Kong population-
dc.typeArticle-
dc.identifier.emailChoi, S-W: htswchoi@hku.hk-
dc.identifier.emailThomson, P: thomsonp@hku.hk-
dc.identifier.authorityChoi, S-W=rp02552-
dc.identifier.authorityThomson, P=rp02327-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1111/jop.12962-
dc.identifier.pmid31544259-
dc.identifier.scopuseid_2-s2.0-85073962209-
dc.identifier.hkuros308924-
dc.identifier.volume49-
dc.identifier.issue2-
dc.identifier.spage145-
dc.identifier.epage149-
dc.identifier.isiWOS:000513487700007-
dc.publisher.placeDenmark-
dc.identifier.issnl0904-2512-

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