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Trends in incidence, mortality and survival of penile squamous cell carcinoma in Norway 1956–2015

We examine trends in incidence, mortality and survival of penile squamous cell carcinoma (SCC) in Norway over 60 years. Data on all cases of penile cancer diagnosed in Norway during 1956–2015 were obtained from the Cancer Registry of Norway. Trends in age‐standardized rates of penile SCC incidence,...

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Autores principales: Hansen, Bo T., Orumaa, Madleen, Lie, A. Kathrine, Brennhovd, Bjørn, Nygård, Mari
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5838782/
https://www.ncbi.nlm.nih.gov/pubmed/29205336
http://dx.doi.org/10.1002/ijc.31194
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author Hansen, Bo T.
Orumaa, Madleen
Lie, A. Kathrine
Brennhovd, Bjørn
Nygård, Mari
author_facet Hansen, Bo T.
Orumaa, Madleen
Lie, A. Kathrine
Brennhovd, Bjørn
Nygård, Mari
author_sort Hansen, Bo T.
collection PubMed
description We examine trends in incidence, mortality and survival of penile squamous cell carcinoma (SCC) in Norway over 60 years. Data on all cases of penile cancer diagnosed in Norway during 1956–2015 were obtained from the Cancer Registry of Norway. Trends in age‐standardized rates of penile SCC incidence, mortality and 5‐year relative survival were assessed by the annual percentage change statistic and joinpoint regression. A total of 1,596 penile cancer cases were diagnosed during 1956–2015, among which 1,474 (92.4%) were SCC. During 2011–2015, the age‐standardized incidence and mortality of penile SCC were 0.91 (95% confidence interval (CI): 0.78; 1.05) and 0.50 (0.42; 0.60) per 100,000, respectively, and the 5‐year relative survival was 61.6% (41.9; 76.4). The incidence of SCC increased during 1956–2015, with an average annual percentage change (AAPC) of 0.80% (0.46; 1.15). The increase was strongest among men diagnosed at a relatively early age (age<=64 years; AAPC: 1.47% (0.90; 2.05)). Mortality also increased over the study period (AAPC: 0.47% (0.10; 0.85)), whereas 5‐year relative survival did not change (AAPC: 0.08% (−0.19; 0.36)). We conclude that the incidence of penile SCC has increased at a moderate and constant rate during 1956–2015, and that the most consistent increase occurred among younger men. Mortality also increased during the study period. However, survival did not change, thus changes in diagnostics and treatment had little impact on survival from penile SCC. Since a substantial proportion of penile SCC is caused by human papillomavirus (HPV), the incidence increase may in part be attributed to increased exposure to HPV in the population.
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spelling pubmed-58387822018-03-12 Trends in incidence, mortality and survival of penile squamous cell carcinoma in Norway 1956–2015 Hansen, Bo T. Orumaa, Madleen Lie, A. Kathrine Brennhovd, Bjørn Nygård, Mari Int J Cancer Cancer Epidemiology We examine trends in incidence, mortality and survival of penile squamous cell carcinoma (SCC) in Norway over 60 years. Data on all cases of penile cancer diagnosed in Norway during 1956–2015 were obtained from the Cancer Registry of Norway. Trends in age‐standardized rates of penile SCC incidence, mortality and 5‐year relative survival were assessed by the annual percentage change statistic and joinpoint regression. A total of 1,596 penile cancer cases were diagnosed during 1956–2015, among which 1,474 (92.4%) were SCC. During 2011–2015, the age‐standardized incidence and mortality of penile SCC were 0.91 (95% confidence interval (CI): 0.78; 1.05) and 0.50 (0.42; 0.60) per 100,000, respectively, and the 5‐year relative survival was 61.6% (41.9; 76.4). The incidence of SCC increased during 1956–2015, with an average annual percentage change (AAPC) of 0.80% (0.46; 1.15). The increase was strongest among men diagnosed at a relatively early age (age<=64 years; AAPC: 1.47% (0.90; 2.05)). Mortality also increased over the study period (AAPC: 0.47% (0.10; 0.85)), whereas 5‐year relative survival did not change (AAPC: 0.08% (−0.19; 0.36)). We conclude that the incidence of penile SCC has increased at a moderate and constant rate during 1956–2015, and that the most consistent increase occurred among younger men. Mortality also increased during the study period. However, survival did not change, thus changes in diagnostics and treatment had little impact on survival from penile SCC. Since a substantial proportion of penile SCC is caused by human papillomavirus (HPV), the incidence increase may in part be attributed to increased exposure to HPV in the population. John Wiley and Sons Inc. 2017-12-15 2018-04-15 /pmc/articles/PMC5838782/ /pubmed/29205336 http://dx.doi.org/10.1002/ijc.31194 Text en © 2017 The Authors International Journal of Cancer published by John Wiley & Sons Ltd on behalf of UICC This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Cancer Epidemiology
Hansen, Bo T.
Orumaa, Madleen
Lie, A. Kathrine
Brennhovd, Bjørn
Nygård, Mari
Trends in incidence, mortality and survival of penile squamous cell carcinoma in Norway 1956–2015
title Trends in incidence, mortality and survival of penile squamous cell carcinoma in Norway 1956–2015
title_full Trends in incidence, mortality and survival of penile squamous cell carcinoma in Norway 1956–2015
title_fullStr Trends in incidence, mortality and survival of penile squamous cell carcinoma in Norway 1956–2015
title_full_unstemmed Trends in incidence, mortality and survival of penile squamous cell carcinoma in Norway 1956–2015
title_short Trends in incidence, mortality and survival of penile squamous cell carcinoma in Norway 1956–2015
title_sort trends in incidence, mortality and survival of penile squamous cell carcinoma in norway 1956–2015
topic Cancer Epidemiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5838782/
https://www.ncbi.nlm.nih.gov/pubmed/29205336
http://dx.doi.org/10.1002/ijc.31194
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