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Strengthening health data on a rare and heterogeneous disease: sarcoma incidence and histological subtypes in Germany
BACKGROUND: The population-based incidence of sarcoma and its histological subtypes in Germany is unknown. Up-to-date information on a disease with an incidence comparable to other cancer entities is of high public health relevance. The aim of this study was to determine this incidence and to detect...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5809940/ https://www.ncbi.nlm.nih.gov/pubmed/29433465 http://dx.doi.org/10.1186/s12889-018-5131-4 |
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author | Ressing, Meike Wardelmann, Eva Hohenberger, Peter Jakob, Jens Kasper, Bernd Emrich, Katharina Eberle, Andrea Blettner, Maria Zeissig, Sylke Ruth |
author_facet | Ressing, Meike Wardelmann, Eva Hohenberger, Peter Jakob, Jens Kasper, Bernd Emrich, Katharina Eberle, Andrea Blettner, Maria Zeissig, Sylke Ruth |
author_sort | Ressing, Meike |
collection | PubMed |
description | BACKGROUND: The population-based incidence of sarcoma and its histological subtypes in Germany is unknown. Up-to-date information on a disease with an incidence comparable to other cancer entities is of high public health relevance. The aim of this study was to determine this incidence and to detect significant changes in incidence trends using data from German epidemiological cancer registries. METHODS: Pooled data from the German Centre for Cancer Registry Data with a primary diagnosis occurring in 2013 were used. To date, this is the latest data on cancer incidence available for Germany. All German cancer registries with sufficient completeness were included (10 out of 11), covering a population of 70.0 million people, representing 87% of the German population. All malignant sarcomas according to the RARECARE Project and the WHO classification 2002 were considered for analysis and, above all, gastrointestinal stromal tumours (GIST) of uncertain behaviour. Sensitivity analysis was performed excluding certain histologies. RESULTS: The analysis included 3404 cases in men and 3442 cases in women diagnosed in 2013. The age adjusted sarcoma incidence (European standard) was 7.4 (men) and 6.6 (women) per 100,000 inhabitants. About 70% of sarcomas were soft tissue sarcomas, about 22% GIST, and about 9% bone sarcomas. The most common histological subtypes besides GIST were fibrosarcomas (14%) and liposarcomas (12%) in men and complex mixed and stromal neoplasms (22%), non-uterine leiomysarcomas (10%) and fibrosarcomas (9%) in women. Considering the trend for the years of diagnosis 2004 to 2013, there was a significant increase in incidence for GIST while the incidence of soft tissue sarcomas (only men) as well as of bone sarcoma stayed constant over time. As to soft tissue sarcoma in women, the incidence stayed constant up to the year 2009 and significantly decreased afterwards. CONCLUSION: This study is the first detailed analysis of a German-wide population-based sarcoma incidence showing results comparable to the incidence detected in the RARECARE Project. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12889-018-5131-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5809940 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-58099402018-02-16 Strengthening health data on a rare and heterogeneous disease: sarcoma incidence and histological subtypes in Germany Ressing, Meike Wardelmann, Eva Hohenberger, Peter Jakob, Jens Kasper, Bernd Emrich, Katharina Eberle, Andrea Blettner, Maria Zeissig, Sylke Ruth BMC Public Health Research Article BACKGROUND: The population-based incidence of sarcoma and its histological subtypes in Germany is unknown. Up-to-date information on a disease with an incidence comparable to other cancer entities is of high public health relevance. The aim of this study was to determine this incidence and to detect significant changes in incidence trends using data from German epidemiological cancer registries. METHODS: Pooled data from the German Centre for Cancer Registry Data with a primary diagnosis occurring in 2013 were used. To date, this is the latest data on cancer incidence available for Germany. All German cancer registries with sufficient completeness were included (10 out of 11), covering a population of 70.0 million people, representing 87% of the German population. All malignant sarcomas according to the RARECARE Project and the WHO classification 2002 were considered for analysis and, above all, gastrointestinal stromal tumours (GIST) of uncertain behaviour. Sensitivity analysis was performed excluding certain histologies. RESULTS: The analysis included 3404 cases in men and 3442 cases in women diagnosed in 2013. The age adjusted sarcoma incidence (European standard) was 7.4 (men) and 6.6 (women) per 100,000 inhabitants. About 70% of sarcomas were soft tissue sarcomas, about 22% GIST, and about 9% bone sarcomas. The most common histological subtypes besides GIST were fibrosarcomas (14%) and liposarcomas (12%) in men and complex mixed and stromal neoplasms (22%), non-uterine leiomysarcomas (10%) and fibrosarcomas (9%) in women. Considering the trend for the years of diagnosis 2004 to 2013, there was a significant increase in incidence for GIST while the incidence of soft tissue sarcomas (only men) as well as of bone sarcoma stayed constant over time. As to soft tissue sarcoma in women, the incidence stayed constant up to the year 2009 and significantly decreased afterwards. CONCLUSION: This study is the first detailed analysis of a German-wide population-based sarcoma incidence showing results comparable to the incidence detected in the RARECARE Project. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12889-018-5131-4) contains supplementary material, which is available to authorized users. BioMed Central 2018-02-12 /pmc/articles/PMC5809940/ /pubmed/29433465 http://dx.doi.org/10.1186/s12889-018-5131-4 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Ressing, Meike Wardelmann, Eva Hohenberger, Peter Jakob, Jens Kasper, Bernd Emrich, Katharina Eberle, Andrea Blettner, Maria Zeissig, Sylke Ruth Strengthening health data on a rare and heterogeneous disease: sarcoma incidence and histological subtypes in Germany |
title | Strengthening health data on a rare and heterogeneous disease: sarcoma incidence and histological subtypes in Germany |
title_full | Strengthening health data on a rare and heterogeneous disease: sarcoma incidence and histological subtypes in Germany |
title_fullStr | Strengthening health data on a rare and heterogeneous disease: sarcoma incidence and histological subtypes in Germany |
title_full_unstemmed | Strengthening health data on a rare and heterogeneous disease: sarcoma incidence and histological subtypes in Germany |
title_short | Strengthening health data on a rare and heterogeneous disease: sarcoma incidence and histological subtypes in Germany |
title_sort | strengthening health data on a rare and heterogeneous disease: sarcoma incidence and histological subtypes in germany |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5809940/ https://www.ncbi.nlm.nih.gov/pubmed/29433465 http://dx.doi.org/10.1186/s12889-018-5131-4 |
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