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Treatment and survival outcomes of lobular carcinoma in situ of the breast: a SEER population based study
Lobular carcinoma in situ (LCIS) represents 5.3% of in situ specimens, and is thought to carry a low risk for developing to the invasive lobular breast cancer (ILC). There is still no standard care approach for patients with LCIS. We aimed to define the impacts of surgical and radiation intervention...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5732709/ https://www.ncbi.nlm.nih.gov/pubmed/29262543 http://dx.doi.org/10.18632/oncotarget.21461 |
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author | Cheng, Pu Huang, Qi Shou, Jiafeng Hu, Guoming Han, Mengjiao Huang, Jian |
author_facet | Cheng, Pu Huang, Qi Shou, Jiafeng Hu, Guoming Han, Mengjiao Huang, Jian |
author_sort | Cheng, Pu |
collection | PubMed |
description | Lobular carcinoma in situ (LCIS) represents 5.3% of in situ specimens, and is thought to carry a low risk for developing to the invasive lobular breast cancer (ILC). There is still no standard care approach for patients with LCIS. We aimed to define the impacts of surgical and radiation intervention on survival outcomes of LCIS. LCIS cases from 2004 to 2013 of the recent Surveillance, Epidemiology, and End Results (SEER) database were analyzed. Clinicopathologic features were analyzed in 16002 patients between 2004 and 2013. Treatment modalities included no surgery (NS), lumpectomy alone (LA), lumpectomy with radiation treatment (LRT), mastectomy alone (MA) and mastectomy with radiation treatment (MRT). The overall survival (OS) was calculated by the Kaplan-Meier method. Univariate and multivariate analyses were performed using the variables of treatment, race, hormone receptor status, grade and age. Among 16002 patients, median follow-up was 54 months. Patients treated with LA had superior OS for NS (P = 0.001), MA (P < 0.001) and MRT P = 0.018). LRT only had superior OS for MRT (P = 0.009). There was no statistically significance between LA and LRT (P = 0.317). Improved OS was also correlated with younger age (P < 0.001), progesterone receptor positive (P = 0.001). Black patients had the worst OS (P < 0.001). There was no obvious survival difference among grade groups (P = 0.536). The LCIS patients treated with LA or LRT had better survival comparing with other groups. Considering the medical expense and the risk of radiotherapy, LA may be the most appropriate therapy for patients with LCIS. |
format | Online Article Text |
id | pubmed-5732709 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-57327092017-12-19 Treatment and survival outcomes of lobular carcinoma in situ of the breast: a SEER population based study Cheng, Pu Huang, Qi Shou, Jiafeng Hu, Guoming Han, Mengjiao Huang, Jian Oncotarget Research Paper Lobular carcinoma in situ (LCIS) represents 5.3% of in situ specimens, and is thought to carry a low risk for developing to the invasive lobular breast cancer (ILC). There is still no standard care approach for patients with LCIS. We aimed to define the impacts of surgical and radiation intervention on survival outcomes of LCIS. LCIS cases from 2004 to 2013 of the recent Surveillance, Epidemiology, and End Results (SEER) database were analyzed. Clinicopathologic features were analyzed in 16002 patients between 2004 and 2013. Treatment modalities included no surgery (NS), lumpectomy alone (LA), lumpectomy with radiation treatment (LRT), mastectomy alone (MA) and mastectomy with radiation treatment (MRT). The overall survival (OS) was calculated by the Kaplan-Meier method. Univariate and multivariate analyses were performed using the variables of treatment, race, hormone receptor status, grade and age. Among 16002 patients, median follow-up was 54 months. Patients treated with LA had superior OS for NS (P = 0.001), MA (P < 0.001) and MRT P = 0.018). LRT only had superior OS for MRT (P = 0.009). There was no statistically significance between LA and LRT (P = 0.317). Improved OS was also correlated with younger age (P < 0.001), progesterone receptor positive (P = 0.001). Black patients had the worst OS (P < 0.001). There was no obvious survival difference among grade groups (P = 0.536). The LCIS patients treated with LA or LRT had better survival comparing with other groups. Considering the medical expense and the risk of radiotherapy, LA may be the most appropriate therapy for patients with LCIS. Impact Journals LLC 2017-10-03 /pmc/articles/PMC5732709/ /pubmed/29262543 http://dx.doi.org/10.18632/oncotarget.21461 Text en Copyright: © 2017 Cheng et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Cheng, Pu Huang, Qi Shou, Jiafeng Hu, Guoming Han, Mengjiao Huang, Jian Treatment and survival outcomes of lobular carcinoma in situ of the breast: a SEER population based study |
title | Treatment and survival outcomes of lobular carcinoma in situ of the breast: a SEER population based study |
title_full | Treatment and survival outcomes of lobular carcinoma in situ of the breast: a SEER population based study |
title_fullStr | Treatment and survival outcomes of lobular carcinoma in situ of the breast: a SEER population based study |
title_full_unstemmed | Treatment and survival outcomes of lobular carcinoma in situ of the breast: a SEER population based study |
title_short | Treatment and survival outcomes of lobular carcinoma in situ of the breast: a SEER population based study |
title_sort | treatment and survival outcomes of lobular carcinoma in situ of the breast: a seer population based study |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5732709/ https://www.ncbi.nlm.nih.gov/pubmed/29262543 http://dx.doi.org/10.18632/oncotarget.21461 |
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