Cargando…

Incidence of Second Malignancies for Prostate Cancer

INTRODUCTION: There is a need to assess risk of second primary cancers in prostate cancer (PCa) patients, especially since PCa treatment may be associated with increased risk of second primary tumours. METHODS: We calculated standardized incidence ratios (SIRs) for second primary tumours comparing m...

Descripción completa

Detalles Bibliográficos
Autores principales: Van Hemelrijck, Mieke, Feller, Anita, Garmo, Hans, Valeri, Fabio, Korol, Dimitri, Dehler, Silvia, Rohrmann, Sabine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4105414/
https://www.ncbi.nlm.nih.gov/pubmed/25047238
http://dx.doi.org/10.1371/journal.pone.0102596
_version_ 1782327361566408704
author Van Hemelrijck, Mieke
Feller, Anita
Garmo, Hans
Valeri, Fabio
Korol, Dimitri
Dehler, Silvia
Rohrmann, Sabine
author_facet Van Hemelrijck, Mieke
Feller, Anita
Garmo, Hans
Valeri, Fabio
Korol, Dimitri
Dehler, Silvia
Rohrmann, Sabine
author_sort Van Hemelrijck, Mieke
collection PubMed
description INTRODUCTION: There is a need to assess risk of second primary cancers in prostate cancer (PCa) patients, especially since PCa treatment may be associated with increased risk of second primary tumours. METHODS: We calculated standardized incidence ratios (SIRs) for second primary tumours comparing men diagnosed with PCa between 1980 and 2010 in the Canton of Zurich, Switzerland (n = 20,559), and the general male population in the Canton. RESULTS: A total of 1,718 men developed a second primary tumour after PCa diagnosis, with lung and colon cancer being the most common (15 and 13% respectively). The SIR for overall second primary cancer was 1.11 (95%CI: 1.06–1.17). Site-specific SIRs varied from 1.19 (1.05–1.34) to 2.89 (2.62–4.77) for lung and thyroid cancer, respectively. When stratified by treatment, the highest SIR was observed for thyroid cancer (3.57 (1.30–7.76)) when undergoing surgery, whereas liver cancer was common when treated with radiotherapy (3.21 (1.54–5.90)) and kidney bladder was most prevalent for those on hormonal treatment (3.15 (1.93–4.87)). Stratification by time since PCa diagnosis showed a lower risk of cancer for men with PCa compared to the general population for the first four years, but then a steep increase in risk was observed. CONCLUSION: In the Canton of Zurich, there was an increased risk of second primary cancers among men with PCa compared to the general population. Increased diagnostic activity after PCa diagnosis may partly explain increased risks within the first years of diagnosis, but time-stratified analyses indicated that increased risks remained and even increased over time.
format Online
Article
Text
id pubmed-4105414
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-41054142014-07-23 Incidence of Second Malignancies for Prostate Cancer Van Hemelrijck, Mieke Feller, Anita Garmo, Hans Valeri, Fabio Korol, Dimitri Dehler, Silvia Rohrmann, Sabine PLoS One Research Article INTRODUCTION: There is a need to assess risk of second primary cancers in prostate cancer (PCa) patients, especially since PCa treatment may be associated with increased risk of second primary tumours. METHODS: We calculated standardized incidence ratios (SIRs) for second primary tumours comparing men diagnosed with PCa between 1980 and 2010 in the Canton of Zurich, Switzerland (n = 20,559), and the general male population in the Canton. RESULTS: A total of 1,718 men developed a second primary tumour after PCa diagnosis, with lung and colon cancer being the most common (15 and 13% respectively). The SIR for overall second primary cancer was 1.11 (95%CI: 1.06–1.17). Site-specific SIRs varied from 1.19 (1.05–1.34) to 2.89 (2.62–4.77) for lung and thyroid cancer, respectively. When stratified by treatment, the highest SIR was observed for thyroid cancer (3.57 (1.30–7.76)) when undergoing surgery, whereas liver cancer was common when treated with radiotherapy (3.21 (1.54–5.90)) and kidney bladder was most prevalent for those on hormonal treatment (3.15 (1.93–4.87)). Stratification by time since PCa diagnosis showed a lower risk of cancer for men with PCa compared to the general population for the first four years, but then a steep increase in risk was observed. CONCLUSION: In the Canton of Zurich, there was an increased risk of second primary cancers among men with PCa compared to the general population. Increased diagnostic activity after PCa diagnosis may partly explain increased risks within the first years of diagnosis, but time-stratified analyses indicated that increased risks remained and even increased over time. Public Library of Science 2014-07-21 /pmc/articles/PMC4105414/ /pubmed/25047238 http://dx.doi.org/10.1371/journal.pone.0102596 Text en © 2014 Van Hemelrijck et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Van Hemelrijck, Mieke
Feller, Anita
Garmo, Hans
Valeri, Fabio
Korol, Dimitri
Dehler, Silvia
Rohrmann, Sabine
Incidence of Second Malignancies for Prostate Cancer
title Incidence of Second Malignancies for Prostate Cancer
title_full Incidence of Second Malignancies for Prostate Cancer
title_fullStr Incidence of Second Malignancies for Prostate Cancer
title_full_unstemmed Incidence of Second Malignancies for Prostate Cancer
title_short Incidence of Second Malignancies for Prostate Cancer
title_sort incidence of second malignancies for prostate cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4105414/
https://www.ncbi.nlm.nih.gov/pubmed/25047238
http://dx.doi.org/10.1371/journal.pone.0102596
work_keys_str_mv AT vanhemelrijckmieke incidenceofsecondmalignanciesforprostatecancer
AT felleranita incidenceofsecondmalignanciesforprostatecancer
AT garmohans incidenceofsecondmalignanciesforprostatecancer
AT valerifabio incidenceofsecondmalignanciesforprostatecancer
AT koroldimitri incidenceofsecondmalignanciesforprostatecancer
AT dehlersilvia incidenceofsecondmalignanciesforprostatecancer
AT rohrmannsabine incidenceofsecondmalignanciesforprostatecancer