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High risk of in-breast tumor recurrence after BRCA1/2-associated breast cancer

The purpose of the study was to compare breast-conserving therapy (BCT) and mastectomy (M) in BRCA1/2 mutation carriers. Women with invasive breast cancer and a pathogenic mutation in BRCA1 or BRCA2 were included in the study (n = 162). Patients treated with BCT (n = 45) were compared with patients...

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Autores principales: Nilsson, Martin P., Hartman, Linda, Kristoffersson, Ulf, Johannsson, Oskar T., Borg, Åke, Henriksson, Karin, Lanke, Elsa, Olsson, Håkan, Loman, Niklas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4174291/
https://www.ncbi.nlm.nih.gov/pubmed/25187270
http://dx.doi.org/10.1007/s10549-014-3115-3
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author Nilsson, Martin P.
Hartman, Linda
Kristoffersson, Ulf
Johannsson, Oskar T.
Borg, Åke
Henriksson, Karin
Lanke, Elsa
Olsson, Håkan
Loman, Niklas
author_facet Nilsson, Martin P.
Hartman, Linda
Kristoffersson, Ulf
Johannsson, Oskar T.
Borg, Åke
Henriksson, Karin
Lanke, Elsa
Olsson, Håkan
Loman, Niklas
author_sort Nilsson, Martin P.
collection PubMed
description The purpose of the study was to compare breast-conserving therapy (BCT) and mastectomy (M) in BRCA1/2 mutation carriers. Women with invasive breast cancer and a pathogenic mutation in BRCA1 or BRCA2 were included in the study (n = 162). Patients treated with BCT (n = 45) were compared with patients treated with M (n = 118). Endpoints were local recurrence as first recurrence (LR), overall survival (OS), breast cancer death, and distant recurrence. Cumulative incidence was calculated in the presence of competing risks. For calculation of hazard ratios and for multivariable analysis, cause-specific Cox proportional hazards regression was used. Compared to M, BCT was associated with an increased risk of LR in univariable analysis (HR 4.0; 95 % CI 1.6–9.8) and in multivariable analysis adjusting for tumor stage, age, and use of adjuvant chemotherapy (HR 2.9; CI 1.1–7.8). Following M, all local recurrences were seen in the first 5 years after breast cancer diagnosis. Following BCT, the rate of LR continued to be high also after the first 5 years. The cumulative incidence of LR in the BCT group was 15, 25, and 32 % after 5, 10, and 15 years, respectively. There were no significant differences between BCT and M for OS, breast cancer death, or distant recurrence. BRCA1/2 mutation carriers treated with BCT have a high risk of LR, many of which are new primary breast cancers. This must be thoroughly discussed with the patient and is an example of how rapid treatment-focused genetic testing could influence choice of treatment.
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spelling pubmed-41742912014-09-25 High risk of in-breast tumor recurrence after BRCA1/2-associated breast cancer Nilsson, Martin P. Hartman, Linda Kristoffersson, Ulf Johannsson, Oskar T. Borg, Åke Henriksson, Karin Lanke, Elsa Olsson, Håkan Loman, Niklas Breast Cancer Res Treat Clinical Trial The purpose of the study was to compare breast-conserving therapy (BCT) and mastectomy (M) in BRCA1/2 mutation carriers. Women with invasive breast cancer and a pathogenic mutation in BRCA1 or BRCA2 were included in the study (n = 162). Patients treated with BCT (n = 45) were compared with patients treated with M (n = 118). Endpoints were local recurrence as first recurrence (LR), overall survival (OS), breast cancer death, and distant recurrence. Cumulative incidence was calculated in the presence of competing risks. For calculation of hazard ratios and for multivariable analysis, cause-specific Cox proportional hazards regression was used. Compared to M, BCT was associated with an increased risk of LR in univariable analysis (HR 4.0; 95 % CI 1.6–9.8) and in multivariable analysis adjusting for tumor stage, age, and use of adjuvant chemotherapy (HR 2.9; CI 1.1–7.8). Following M, all local recurrences were seen in the first 5 years after breast cancer diagnosis. Following BCT, the rate of LR continued to be high also after the first 5 years. The cumulative incidence of LR in the BCT group was 15, 25, and 32 % after 5, 10, and 15 years, respectively. There were no significant differences between BCT and M for OS, breast cancer death, or distant recurrence. BRCA1/2 mutation carriers treated with BCT have a high risk of LR, many of which are new primary breast cancers. This must be thoroughly discussed with the patient and is an example of how rapid treatment-focused genetic testing could influence choice of treatment. Springer US 2014-09-04 2014 /pmc/articles/PMC4174291/ /pubmed/25187270 http://dx.doi.org/10.1007/s10549-014-3115-3 Text en © The Author(s) 2014 https://creativecommons.org/licenses/by-nc/4.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Clinical Trial
Nilsson, Martin P.
Hartman, Linda
Kristoffersson, Ulf
Johannsson, Oskar T.
Borg, Åke
Henriksson, Karin
Lanke, Elsa
Olsson, Håkan
Loman, Niklas
High risk of in-breast tumor recurrence after BRCA1/2-associated breast cancer
title High risk of in-breast tumor recurrence after BRCA1/2-associated breast cancer
title_full High risk of in-breast tumor recurrence after BRCA1/2-associated breast cancer
title_fullStr High risk of in-breast tumor recurrence after BRCA1/2-associated breast cancer
title_full_unstemmed High risk of in-breast tumor recurrence after BRCA1/2-associated breast cancer
title_short High risk of in-breast tumor recurrence after BRCA1/2-associated breast cancer
title_sort high risk of in-breast tumor recurrence after brca1/2-associated breast cancer
topic Clinical Trial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4174291/
https://www.ncbi.nlm.nih.gov/pubmed/25187270
http://dx.doi.org/10.1007/s10549-014-3115-3
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