Cargando…
Is There a Role for Post-Mastectomy Radiotherapy for T1-2N1 Breast Cancers With Node-Positive Pathology After Patients Become Node-Negative Pathology Following Neoadjuvant Chemotherapy?
Purpose: To assess the benefit of post-mastectomy radiotherapy (PMRT) in breast cancer (BC) patients with T1-2N1M0 who developed pathologically negative lymph nodes (ypN0) after undergoing neoadjuvant chemotherapy (NAC) and mastectomy. Patients and Materials: Patients with T1-2 tumors and positive l...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7338570/ https://www.ncbi.nlm.nih.gov/pubmed/32695661 http://dx.doi.org/10.3389/fonc.2020.00892 |
_version_ | 1783554708708786176 |
---|---|
author | Wang, Qian Zhao, Jingjing Han, Xiaowei Er, Puchun Meng, Xiangying Shi, Jinyan Sun, Huiru Zhu, Jingyang Zhu, Li Wu, Shikai Zhang, Wencheng Sun, Bing |
author_facet | Wang, Qian Zhao, Jingjing Han, Xiaowei Er, Puchun Meng, Xiangying Shi, Jinyan Sun, Huiru Zhu, Jingyang Zhu, Li Wu, Shikai Zhang, Wencheng Sun, Bing |
author_sort | Wang, Qian |
collection | PubMed |
description | Purpose: To assess the benefit of post-mastectomy radiotherapy (PMRT) in breast cancer (BC) patients with T1-2N1M0 who developed pathologically negative lymph nodes (ypN0) after undergoing neoadjuvant chemotherapy (NAC) and mastectomy. Patients and Materials: Patients with T1-2 tumors and positive lymph node(s) who became pN0 after NAC and mastectomy were screened from our prospectively maintained database. The primary endpoint was recurrence-free survival (RFS), and the secondary endpoints were local recurrence-free survival (LRFS) and overall survival (OS). Propensity-score matching (PSM) was conducted for the comparison between PMRT and non-PMRT groups. Results: Of the 142 eligible patients, 110 (77.5%) received PMRT, and 32 (22.5%) did not. The median follow-up time was 72 months. Univariate analyses showed that the 5-year RFS, LRFS, and OS rates were 88.7, 94.5, and 96.1, respectively, with PMRT and 72.4, 90.1, and 95.0% without PMRT (p = 0.028; p = 0.151; p = 0.971). Multivariate analyses established PMRT as a significant prognostic factor for RFS rate (HR, 0.411; 95% CI, 0.175–0.968; p = 0.042). After a PSM analysis (64 in the PMRT group vs. 32 in the non-PMRT group), PMRT remained significant, with improved RFS in univariate and multivariate analysis (with 5-year RFS rates of 90.1 vs. 72.4%, respectively, p = 0.016; HR, 0.323, 95%CI, 0.115–0.913, p = 0.033). In the subgroup of 48 (33.8%) patients with pathologic complete responses (pCR, ypT0, and ypN0) after NAC, PMRT did not affect RFS (HR, 0.226; 95% CI, 0.034–1.500; p = 0.123). Conclusions: PMRT might benefit pT1-2N1M0 patients with pN0 after NAC. Patients with pCR might consider omitting PMRT. Prospective studies are needed to assess the effect of PMRT on this specific patient population. |
format | Online Article Text |
id | pubmed-7338570 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73385702020-07-20 Is There a Role for Post-Mastectomy Radiotherapy for T1-2N1 Breast Cancers With Node-Positive Pathology After Patients Become Node-Negative Pathology Following Neoadjuvant Chemotherapy? Wang, Qian Zhao, Jingjing Han, Xiaowei Er, Puchun Meng, Xiangying Shi, Jinyan Sun, Huiru Zhu, Jingyang Zhu, Li Wu, Shikai Zhang, Wencheng Sun, Bing Front Oncol Oncology Purpose: To assess the benefit of post-mastectomy radiotherapy (PMRT) in breast cancer (BC) patients with T1-2N1M0 who developed pathologically negative lymph nodes (ypN0) after undergoing neoadjuvant chemotherapy (NAC) and mastectomy. Patients and Materials: Patients with T1-2 tumors and positive lymph node(s) who became pN0 after NAC and mastectomy were screened from our prospectively maintained database. The primary endpoint was recurrence-free survival (RFS), and the secondary endpoints were local recurrence-free survival (LRFS) and overall survival (OS). Propensity-score matching (PSM) was conducted for the comparison between PMRT and non-PMRT groups. Results: Of the 142 eligible patients, 110 (77.5%) received PMRT, and 32 (22.5%) did not. The median follow-up time was 72 months. Univariate analyses showed that the 5-year RFS, LRFS, and OS rates were 88.7, 94.5, and 96.1, respectively, with PMRT and 72.4, 90.1, and 95.0% without PMRT (p = 0.028; p = 0.151; p = 0.971). Multivariate analyses established PMRT as a significant prognostic factor for RFS rate (HR, 0.411; 95% CI, 0.175–0.968; p = 0.042). After a PSM analysis (64 in the PMRT group vs. 32 in the non-PMRT group), PMRT remained significant, with improved RFS in univariate and multivariate analysis (with 5-year RFS rates of 90.1 vs. 72.4%, respectively, p = 0.016; HR, 0.323, 95%CI, 0.115–0.913, p = 0.033). In the subgroup of 48 (33.8%) patients with pathologic complete responses (pCR, ypT0, and ypN0) after NAC, PMRT did not affect RFS (HR, 0.226; 95% CI, 0.034–1.500; p = 0.123). Conclusions: PMRT might benefit pT1-2N1M0 patients with pN0 after NAC. Patients with pCR might consider omitting PMRT. Prospective studies are needed to assess the effect of PMRT on this specific patient population. Frontiers Media S.A. 2020-06-30 /pmc/articles/PMC7338570/ /pubmed/32695661 http://dx.doi.org/10.3389/fonc.2020.00892 Text en Copyright © 2020 Wang, Zhao, Han, Er, Meng, Shi, Sun, Zhu, Zhu, Wu, Zhang and Sun. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Wang, Qian Zhao, Jingjing Han, Xiaowei Er, Puchun Meng, Xiangying Shi, Jinyan Sun, Huiru Zhu, Jingyang Zhu, Li Wu, Shikai Zhang, Wencheng Sun, Bing Is There a Role for Post-Mastectomy Radiotherapy for T1-2N1 Breast Cancers With Node-Positive Pathology After Patients Become Node-Negative Pathology Following Neoadjuvant Chemotherapy? |
title | Is There a Role for Post-Mastectomy Radiotherapy for T1-2N1 Breast Cancers With Node-Positive Pathology After Patients Become Node-Negative Pathology Following Neoadjuvant Chemotherapy? |
title_full | Is There a Role for Post-Mastectomy Radiotherapy for T1-2N1 Breast Cancers With Node-Positive Pathology After Patients Become Node-Negative Pathology Following Neoadjuvant Chemotherapy? |
title_fullStr | Is There a Role for Post-Mastectomy Radiotherapy for T1-2N1 Breast Cancers With Node-Positive Pathology After Patients Become Node-Negative Pathology Following Neoadjuvant Chemotherapy? |
title_full_unstemmed | Is There a Role for Post-Mastectomy Radiotherapy for T1-2N1 Breast Cancers With Node-Positive Pathology After Patients Become Node-Negative Pathology Following Neoadjuvant Chemotherapy? |
title_short | Is There a Role for Post-Mastectomy Radiotherapy for T1-2N1 Breast Cancers With Node-Positive Pathology After Patients Become Node-Negative Pathology Following Neoadjuvant Chemotherapy? |
title_sort | is there a role for post-mastectomy radiotherapy for t1-2n1 breast cancers with node-positive pathology after patients become node-negative pathology following neoadjuvant chemotherapy? |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7338570/ https://www.ncbi.nlm.nih.gov/pubmed/32695661 http://dx.doi.org/10.3389/fonc.2020.00892 |
work_keys_str_mv | AT wangqian istherearoleforpostmastectomyradiotherapyfort12n1breastcancerswithnodepositivepathologyafterpatientsbecomenodenegativepathologyfollowingneoadjuvantchemotherapy AT zhaojingjing istherearoleforpostmastectomyradiotherapyfort12n1breastcancerswithnodepositivepathologyafterpatientsbecomenodenegativepathologyfollowingneoadjuvantchemotherapy AT hanxiaowei istherearoleforpostmastectomyradiotherapyfort12n1breastcancerswithnodepositivepathologyafterpatientsbecomenodenegativepathologyfollowingneoadjuvantchemotherapy AT erpuchun istherearoleforpostmastectomyradiotherapyfort12n1breastcancerswithnodepositivepathologyafterpatientsbecomenodenegativepathologyfollowingneoadjuvantchemotherapy AT mengxiangying istherearoleforpostmastectomyradiotherapyfort12n1breastcancerswithnodepositivepathologyafterpatientsbecomenodenegativepathologyfollowingneoadjuvantchemotherapy AT shijinyan istherearoleforpostmastectomyradiotherapyfort12n1breastcancerswithnodepositivepathologyafterpatientsbecomenodenegativepathologyfollowingneoadjuvantchemotherapy AT sunhuiru istherearoleforpostmastectomyradiotherapyfort12n1breastcancerswithnodepositivepathologyafterpatientsbecomenodenegativepathologyfollowingneoadjuvantchemotherapy AT zhujingyang istherearoleforpostmastectomyradiotherapyfort12n1breastcancerswithnodepositivepathologyafterpatientsbecomenodenegativepathologyfollowingneoadjuvantchemotherapy AT zhuli istherearoleforpostmastectomyradiotherapyfort12n1breastcancerswithnodepositivepathologyafterpatientsbecomenodenegativepathologyfollowingneoadjuvantchemotherapy AT wushikai istherearoleforpostmastectomyradiotherapyfort12n1breastcancerswithnodepositivepathologyafterpatientsbecomenodenegativepathologyfollowingneoadjuvantchemotherapy AT zhangwencheng istherearoleforpostmastectomyradiotherapyfort12n1breastcancerswithnodepositivepathologyafterpatientsbecomenodenegativepathologyfollowingneoadjuvantchemotherapy AT sunbing istherearoleforpostmastectomyradiotherapyfort12n1breastcancerswithnodepositivepathologyafterpatientsbecomenodenegativepathologyfollowingneoadjuvantchemotherapy |