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Autoimmune diseases and hypersensitivities improve the prognosis in ER-negative breast cancer

INTRODUCTION: Breast cancer (BC) is one of the leading causes of death among women worldwide. Immunostimulatory treatment has increasingly been used as adjuvant therapy in the last few years, in patients with melanoma and other cancer forms, often with an induction of autoimmunity as a consequence o...

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Autores principales: Einefors, Rickard, Kogler, Ulrika, Ellberg, Carolina, Olsson, Håkan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3755812/
https://www.ncbi.nlm.nih.gov/pubmed/24010029
http://dx.doi.org/10.1186/2193-1801-2-357
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author Einefors, Rickard
Kogler, Ulrika
Ellberg, Carolina
Olsson, Håkan
author_facet Einefors, Rickard
Kogler, Ulrika
Ellberg, Carolina
Olsson, Håkan
author_sort Einefors, Rickard
collection PubMed
description INTRODUCTION: Breast cancer (BC) is one of the leading causes of death among women worldwide. Immunostimulatory treatment has increasingly been used as adjuvant therapy in the last few years, in patients with melanoma and other cancer forms, often with an induction of autoimmunity as a consequence of a successful treatment. We aimed at investigating if coexisting autoimmune diseases (AD) or hypersensitivities (HS) similarly to the side effects of immunostimulatory treatment resulted in a better overall survival, compared to patients without these disorders. MATERIAL AND METHODS: The patient material used was a consecutive clinical material consisting of 1705 patients diagnosed with BC between 1980 and 2010 in Sweden. The patients were stratified according to coexisting AD, HS or lack of both. Overall survival was calculated using Kaplan-Meier and the Cox proportional hazard model. RESULTS: Our main finding was that BC patients with estrogen receptor (ER) negative tumors together with preexisting AD or HS had a statistically significant better overall survival (HR=0.53; 95% CI= 0.30-0.96) compared to patients without. Premenopausal BC patients with a coexistence of AD or HS had a better overall survival, but this was not statistically significant. DISCUSSION: For patients with premenopausal or ER-negative BC, coexistence with AD or HS was associated with a better overall survival. Although these findings require validation, and the mechanisms responsible need to be found, they hint to possible new treatment strategies for BC, especially for those with ER-negative tumors and potentially for premenopausal patients. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/2193-1801-2-357) contains supplementary material, which is available to authorized users.
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spelling pubmed-37558122013-09-04 Autoimmune diseases and hypersensitivities improve the prognosis in ER-negative breast cancer Einefors, Rickard Kogler, Ulrika Ellberg, Carolina Olsson, Håkan Springerplus Research INTRODUCTION: Breast cancer (BC) is one of the leading causes of death among women worldwide. Immunostimulatory treatment has increasingly been used as adjuvant therapy in the last few years, in patients with melanoma and other cancer forms, often with an induction of autoimmunity as a consequence of a successful treatment. We aimed at investigating if coexisting autoimmune diseases (AD) or hypersensitivities (HS) similarly to the side effects of immunostimulatory treatment resulted in a better overall survival, compared to patients without these disorders. MATERIAL AND METHODS: The patient material used was a consecutive clinical material consisting of 1705 patients diagnosed with BC between 1980 and 2010 in Sweden. The patients were stratified according to coexisting AD, HS or lack of both. Overall survival was calculated using Kaplan-Meier and the Cox proportional hazard model. RESULTS: Our main finding was that BC patients with estrogen receptor (ER) negative tumors together with preexisting AD or HS had a statistically significant better overall survival (HR=0.53; 95% CI= 0.30-0.96) compared to patients without. Premenopausal BC patients with a coexistence of AD or HS had a better overall survival, but this was not statistically significant. DISCUSSION: For patients with premenopausal or ER-negative BC, coexistence with AD or HS was associated with a better overall survival. Although these findings require validation, and the mechanisms responsible need to be found, they hint to possible new treatment strategies for BC, especially for those with ER-negative tumors and potentially for premenopausal patients. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/2193-1801-2-357) contains supplementary material, which is available to authorized users. Springer International Publishing 2013-07-30 /pmc/articles/PMC3755812/ /pubmed/24010029 http://dx.doi.org/10.1186/2193-1801-2-357 Text en © Einefors et al.; licensee Springer. 2013 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Einefors, Rickard
Kogler, Ulrika
Ellberg, Carolina
Olsson, Håkan
Autoimmune diseases and hypersensitivities improve the prognosis in ER-negative breast cancer
title Autoimmune diseases and hypersensitivities improve the prognosis in ER-negative breast cancer
title_full Autoimmune diseases and hypersensitivities improve the prognosis in ER-negative breast cancer
title_fullStr Autoimmune diseases and hypersensitivities improve the prognosis in ER-negative breast cancer
title_full_unstemmed Autoimmune diseases and hypersensitivities improve the prognosis in ER-negative breast cancer
title_short Autoimmune diseases and hypersensitivities improve the prognosis in ER-negative breast cancer
title_sort autoimmune diseases and hypersensitivities improve the prognosis in er-negative breast cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3755812/
https://www.ncbi.nlm.nih.gov/pubmed/24010029
http://dx.doi.org/10.1186/2193-1801-2-357
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