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Survival following radiotherapy in young women with localized early‐stage breast cancer according to molecular subtypes

BACKGROUND: To evaluate the significance and benefit of radiotherapy (RT) in young early‐stage breast cancer patients according to different molecular subtypes. METHODS: We conducted a retrospective cohort study utilizing the Surveillance, Epidemiology, and End Results database with known hormone re...

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Autores principales: Liu, Qi‐Qi, Sun, He‐Fen, Yang, Xue‐Li, Chen, Meng‐Ting, Liu, Yang, Zhao, Yang, Zhao, Yuan‐Yuan, Jin, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6558475/
https://www.ncbi.nlm.nih.gov/pubmed/31016890
http://dx.doi.org/10.1002/cam4.2186
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author Liu, Qi‐Qi
Sun, He‐Fen
Yang, Xue‐Li
Chen, Meng‐Ting
Liu, Yang
Zhao, Yang
Zhao, Yuan‐Yuan
Jin, Wei
author_facet Liu, Qi‐Qi
Sun, He‐Fen
Yang, Xue‐Li
Chen, Meng‐Ting
Liu, Yang
Zhao, Yang
Zhao, Yuan‐Yuan
Jin, Wei
author_sort Liu, Qi‐Qi
collection PubMed
description BACKGROUND: To evaluate the significance and benefit of radiotherapy (RT) in young early‐stage breast cancer patients according to different molecular subtypes. METHODS: We conducted a retrospective cohort study utilizing the Surveillance, Epidemiology, and End Results database with known hormone receptor (HoR) and human epidermal growth factor receptor 2 (HER2) status. Female patients aged 18‐45, received RT treatment, and diagnosed with stage T1‐3, N0‐3, M0 primary breast cancer between 2010 and 2013 were identified. RESULTS: Of all the 23 148 included patients, 14 708 (63.54%), 3385 (14.62%), 1225 (5.29%), and 3830 (16.55%) were diagnosed with luminal‐A (HoR + HER2‐), luminal‐B (HoR + HER2+), HER2‐enriched (HoR‐HER2+), and triple‐negative (HoR‐HER2‐) breast cancer, respectively. RT was significantly correlated with improved overall survival (OS, HR: 0.295; 95% CI:0.138‐0.63, P = 0.002) and breast cancer‐specific survival (BCSS, HR: 0.328; 95% CI: 0.153‐0.702, P = 0.004) in HER2‐enriched patients. In addition, a significantly prolonged OS was also observed when RT was given to luminal‐A (HR: 0.696; 95% CI: 0.538‐0.902, P = 0.006) and luminal‐B (HR: 0.385; 95% CI:0.199‐0.744, P = 0.005) breast cancer patients compared to those without RT. Multivariable‐adjusted analyses showed that HER2 was a significant favorable factor for RT benefit in breast cancer patients. CONCLUSIONS: RT could offer significant survival benefit in luminal‐A, luminal‐B, and especially HER2‐enriched young early‐stage breast cancer female patients. The results enabled clinicians to predict the benefits of RT and improve evidence‐based treatment for breast cancer patients.
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spelling pubmed-65584752019-06-13 Survival following radiotherapy in young women with localized early‐stage breast cancer according to molecular subtypes Liu, Qi‐Qi Sun, He‐Fen Yang, Xue‐Li Chen, Meng‐Ting Liu, Yang Zhao, Yang Zhao, Yuan‐Yuan Jin, Wei Cancer Med Clinical Cancer Research BACKGROUND: To evaluate the significance and benefit of radiotherapy (RT) in young early‐stage breast cancer patients according to different molecular subtypes. METHODS: We conducted a retrospective cohort study utilizing the Surveillance, Epidemiology, and End Results database with known hormone receptor (HoR) and human epidermal growth factor receptor 2 (HER2) status. Female patients aged 18‐45, received RT treatment, and diagnosed with stage T1‐3, N0‐3, M0 primary breast cancer between 2010 and 2013 were identified. RESULTS: Of all the 23 148 included patients, 14 708 (63.54%), 3385 (14.62%), 1225 (5.29%), and 3830 (16.55%) were diagnosed with luminal‐A (HoR + HER2‐), luminal‐B (HoR + HER2+), HER2‐enriched (HoR‐HER2+), and triple‐negative (HoR‐HER2‐) breast cancer, respectively. RT was significantly correlated with improved overall survival (OS, HR: 0.295; 95% CI:0.138‐0.63, P = 0.002) and breast cancer‐specific survival (BCSS, HR: 0.328; 95% CI: 0.153‐0.702, P = 0.004) in HER2‐enriched patients. In addition, a significantly prolonged OS was also observed when RT was given to luminal‐A (HR: 0.696; 95% CI: 0.538‐0.902, P = 0.006) and luminal‐B (HR: 0.385; 95% CI:0.199‐0.744, P = 0.005) breast cancer patients compared to those without RT. Multivariable‐adjusted analyses showed that HER2 was a significant favorable factor for RT benefit in breast cancer patients. CONCLUSIONS: RT could offer significant survival benefit in luminal‐A, luminal‐B, and especially HER2‐enriched young early‐stage breast cancer female patients. The results enabled clinicians to predict the benefits of RT and improve evidence‐based treatment for breast cancer patients. John Wiley and Sons Inc. 2019-04-23 /pmc/articles/PMC6558475/ /pubmed/31016890 http://dx.doi.org/10.1002/cam4.2186 Text en © 2019 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Cancer Research
Liu, Qi‐Qi
Sun, He‐Fen
Yang, Xue‐Li
Chen, Meng‐Ting
Liu, Yang
Zhao, Yang
Zhao, Yuan‐Yuan
Jin, Wei
Survival following radiotherapy in young women with localized early‐stage breast cancer according to molecular subtypes
title Survival following radiotherapy in young women with localized early‐stage breast cancer according to molecular subtypes
title_full Survival following radiotherapy in young women with localized early‐stage breast cancer according to molecular subtypes
title_fullStr Survival following radiotherapy in young women with localized early‐stage breast cancer according to molecular subtypes
title_full_unstemmed Survival following radiotherapy in young women with localized early‐stage breast cancer according to molecular subtypes
title_short Survival following radiotherapy in young women with localized early‐stage breast cancer according to molecular subtypes
title_sort survival following radiotherapy in young women with localized early‐stage breast cancer according to molecular subtypes
topic Clinical Cancer Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6558475/
https://www.ncbi.nlm.nih.gov/pubmed/31016890
http://dx.doi.org/10.1002/cam4.2186
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