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Mainstreamed genetic testing of breast cancer patients in two hospitals in South Eastern Norway

Studies have shown that a significant number of eligible breast cancer patients are not offered genetic testing or referral to genetic counseling. To increase access to genetic testing in South Eastern Norway, testing has since 2014 been offered directly to breast cancer patients by surgeons and onc...

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Autores principales: Grindedal, Eli Marie, Jørgensen, Kjersti, Olsson, Pernilla, Gravdehaug, Berit, Lurås, Hilde, Schlichting, Ellen, Vamre, Tone, Wangensteen, Teresia, Heramb, Cecilie, Mæhle, Lovise
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7101297/
https://www.ncbi.nlm.nih.gov/pubmed/32002722
http://dx.doi.org/10.1007/s10689-020-00160-x
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author Grindedal, Eli Marie
Jørgensen, Kjersti
Olsson, Pernilla
Gravdehaug, Berit
Lurås, Hilde
Schlichting, Ellen
Vamre, Tone
Wangensteen, Teresia
Heramb, Cecilie
Mæhle, Lovise
author_facet Grindedal, Eli Marie
Jørgensen, Kjersti
Olsson, Pernilla
Gravdehaug, Berit
Lurås, Hilde
Schlichting, Ellen
Vamre, Tone
Wangensteen, Teresia
Heramb, Cecilie
Mæhle, Lovise
author_sort Grindedal, Eli Marie
collection PubMed
description Studies have shown that a significant number of eligible breast cancer patients are not offered genetic testing or referral to genetic counseling. To increase access to genetic testing in South Eastern Norway, testing has since 2014 been offered directly to breast cancer patients by surgeons and oncologists. This practice is termed “mainstreamed genetic testing”. The aim of this study was to investigate to what extent patients in South Eastern Norway are offered testing. Three hundred and sixty one patients diagnosed in 2016 and 2017 at one regional and one university hospital in South Eastern Norway were included. Data on whether the patients fulfilled the criteria, whether they had been offered testing and if they were tested were collected. In total, 26.6% (96/361) fulfilled the criteria for testing. Seventy five percent (69/92) of these were offered testing, and 71.7% (66/92) were tested. At the university hospital, 90.2% (37/41) of eligible patients were offered testing, and at the regional hospital 62.7% (32/51). Fifty two percent (12/23) of eligible patient not offered testing were younger than 50 years at time of diagnosis. As many as 95.4% (125/131) of all patients who were offered testing, wanted to be tested. The majority of patients who fulfilled the criteria were offered testing, supporting the practice of mainstreamed genetic testing. There were nevertheless differences in rates of testing between the hospitals that affected all groups of patients, indicating that genetic testing may not be equally accessible to all patients. We suggest that efforts should be made to increase awareness and improve routines for genetic testing of breast cancer patients in Norway.
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spelling pubmed-71012972020-03-30 Mainstreamed genetic testing of breast cancer patients in two hospitals in South Eastern Norway Grindedal, Eli Marie Jørgensen, Kjersti Olsson, Pernilla Gravdehaug, Berit Lurås, Hilde Schlichting, Ellen Vamre, Tone Wangensteen, Teresia Heramb, Cecilie Mæhle, Lovise Fam Cancer Original Article Studies have shown that a significant number of eligible breast cancer patients are not offered genetic testing or referral to genetic counseling. To increase access to genetic testing in South Eastern Norway, testing has since 2014 been offered directly to breast cancer patients by surgeons and oncologists. This practice is termed “mainstreamed genetic testing”. The aim of this study was to investigate to what extent patients in South Eastern Norway are offered testing. Three hundred and sixty one patients diagnosed in 2016 and 2017 at one regional and one university hospital in South Eastern Norway were included. Data on whether the patients fulfilled the criteria, whether they had been offered testing and if they were tested were collected. In total, 26.6% (96/361) fulfilled the criteria for testing. Seventy five percent (69/92) of these were offered testing, and 71.7% (66/92) were tested. At the university hospital, 90.2% (37/41) of eligible patients were offered testing, and at the regional hospital 62.7% (32/51). Fifty two percent (12/23) of eligible patient not offered testing were younger than 50 years at time of diagnosis. As many as 95.4% (125/131) of all patients who were offered testing, wanted to be tested. The majority of patients who fulfilled the criteria were offered testing, supporting the practice of mainstreamed genetic testing. There were nevertheless differences in rates of testing between the hospitals that affected all groups of patients, indicating that genetic testing may not be equally accessible to all patients. We suggest that efforts should be made to increase awareness and improve routines for genetic testing of breast cancer patients in Norway. Springer Netherlands 2020-01-30 2020 /pmc/articles/PMC7101297/ /pubmed/32002722 http://dx.doi.org/10.1007/s10689-020-00160-x Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Original Article
Grindedal, Eli Marie
Jørgensen, Kjersti
Olsson, Pernilla
Gravdehaug, Berit
Lurås, Hilde
Schlichting, Ellen
Vamre, Tone
Wangensteen, Teresia
Heramb, Cecilie
Mæhle, Lovise
Mainstreamed genetic testing of breast cancer patients in two hospitals in South Eastern Norway
title Mainstreamed genetic testing of breast cancer patients in two hospitals in South Eastern Norway
title_full Mainstreamed genetic testing of breast cancer patients in two hospitals in South Eastern Norway
title_fullStr Mainstreamed genetic testing of breast cancer patients in two hospitals in South Eastern Norway
title_full_unstemmed Mainstreamed genetic testing of breast cancer patients in two hospitals in South Eastern Norway
title_short Mainstreamed genetic testing of breast cancer patients in two hospitals in South Eastern Norway
title_sort mainstreamed genetic testing of breast cancer patients in two hospitals in south eastern norway
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7101297/
https://www.ncbi.nlm.nih.gov/pubmed/32002722
http://dx.doi.org/10.1007/s10689-020-00160-x
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