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Clinicopathologic analysis of 722 breast cancer patients who met the inclusion criteria of the TAILORx trial

BACKGROUND: The results of the Trial Assigning IndividuaLized Options for Treatment (TAILORx) suggested that approximately 70% of T1-2N0M0, hormone receptor-positive, human epidermal growth factor receptor 2 (HER2)-negative breast cancer patients can avoid chemotherapy and receive only adjuvant endo...

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Autores principales: Xiang, Hong-Yu, Liu, Yin-Hua, Zhang, Hong, Zhang, Shuang, Xin, Ling, Xu, Ling, Ye, Jing-Ming, Li, Ting, Duan, Xue-Ning, Liu, Qian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6964955/
https://www.ncbi.nlm.nih.gov/pubmed/31809316
http://dx.doi.org/10.1097/CM9.0000000000000548
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author Xiang, Hong-Yu
Liu, Yin-Hua
Zhang, Hong
Zhang, Shuang
Xin, Ling
Xu, Ling
Ye, Jing-Ming
Li, Ting
Duan, Xue-Ning
Liu, Qian
author_facet Xiang, Hong-Yu
Liu, Yin-Hua
Zhang, Hong
Zhang, Shuang
Xin, Ling
Xu, Ling
Ye, Jing-Ming
Li, Ting
Duan, Xue-Ning
Liu, Qian
author_sort Xiang, Hong-Yu
collection PubMed
description BACKGROUND: The results of the Trial Assigning IndividuaLized Options for Treatment (TAILORx) suggested that approximately 70% of T1-2N0M0, hormone receptor-positive, human epidermal growth factor receptor 2 (HER2)-negative breast cancer patients can avoid chemotherapy and receive only adjuvant endocrine therapy. We conducted a retrospective analysis of the clinicopathologic features and prognostic factors of patients with breast cancer who met the inclusion criteria of the TAILORx trial. METHODS: According to the enrollment criteria of the TAILORx trial, a retrospective analysis was performed on patients with breast cancer who were treated from January 2008 to December 2015 at Peking University First Hospital. The clinicopathologic characteristics of all patients were analyzed, and prognoses were calculated using the Kaplan-Meier method and a Cox proportionate hazards model. RESULTS: A total of 2430 patients with early stage breast cancer who were admitted at our hospital had complete clinicopathologic data and follow-up information. Of these patients, 722 met the inclusion criteria and were enrolled in the present study, accounting for 29.7% of all patients. Among them, 417 (57.8%) patients received only adjuvant endocrine therapy (the non-chemo group), and 305 (42.2%) patients received adjuvant chemotherapy followed by adjuvant endocrine therapy (the chemo group). No statistically significant difference was observed in overall survival (OS) between the two groups (non-chemo vs. chemo: 5-year OS: 97.9% vs. 97.9%, χ(2) = 1.00, P = 0.995; hazard ratio [HR] = 1.00, 95% confidence interval [CI]: 0.46–2.21). A significant difference was observed in disease-free survival (DFS) between the two groups (non-chemo vs. chemo: 5-year DFS: 97.9% vs. 94.7%, χ(2) = 8.65, P = 0.003; HR = 3.05, 95% CI: 1.40–6.67). The choice of adjuvant therapy was associated with clinicopathologic factors, such as the age at diagnosis, T stage, histologic grade, the Ki67 index, the presence of intravascular tumor thrombus (P < 0.001), pathologic type, and menstrual status (P = 0.014). CONCLUSIONS: In the absence of internationally recognized multigene testing methods, for patients with early hormone receptor-positive, HER2-negative breast cancer, clinicians can develop a treatment plan based on clinicopathologic features only, which can effectively screen some patients who do not need adjuvant chemotherapy. However, nearly half of patients still receive adjuvant chemotherapy, and whether these patients can be exempted from chemotherapy warrants further exploration.
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spelling pubmed-69649552020-02-10 Clinicopathologic analysis of 722 breast cancer patients who met the inclusion criteria of the TAILORx trial Xiang, Hong-Yu Liu, Yin-Hua Zhang, Hong Zhang, Shuang Xin, Ling Xu, Ling Ye, Jing-Ming Li, Ting Duan, Xue-Ning Liu, Qian Chin Med J (Engl) Original Articles BACKGROUND: The results of the Trial Assigning IndividuaLized Options for Treatment (TAILORx) suggested that approximately 70% of T1-2N0M0, hormone receptor-positive, human epidermal growth factor receptor 2 (HER2)-negative breast cancer patients can avoid chemotherapy and receive only adjuvant endocrine therapy. We conducted a retrospective analysis of the clinicopathologic features and prognostic factors of patients with breast cancer who met the inclusion criteria of the TAILORx trial. METHODS: According to the enrollment criteria of the TAILORx trial, a retrospective analysis was performed on patients with breast cancer who were treated from January 2008 to December 2015 at Peking University First Hospital. The clinicopathologic characteristics of all patients were analyzed, and prognoses were calculated using the Kaplan-Meier method and a Cox proportionate hazards model. RESULTS: A total of 2430 patients with early stage breast cancer who were admitted at our hospital had complete clinicopathologic data and follow-up information. Of these patients, 722 met the inclusion criteria and were enrolled in the present study, accounting for 29.7% of all patients. Among them, 417 (57.8%) patients received only adjuvant endocrine therapy (the non-chemo group), and 305 (42.2%) patients received adjuvant chemotherapy followed by adjuvant endocrine therapy (the chemo group). No statistically significant difference was observed in overall survival (OS) between the two groups (non-chemo vs. chemo: 5-year OS: 97.9% vs. 97.9%, χ(2) = 1.00, P = 0.995; hazard ratio [HR] = 1.00, 95% confidence interval [CI]: 0.46–2.21). A significant difference was observed in disease-free survival (DFS) between the two groups (non-chemo vs. chemo: 5-year DFS: 97.9% vs. 94.7%, χ(2) = 8.65, P = 0.003; HR = 3.05, 95% CI: 1.40–6.67). The choice of adjuvant therapy was associated with clinicopathologic factors, such as the age at diagnosis, T stage, histologic grade, the Ki67 index, the presence of intravascular tumor thrombus (P < 0.001), pathologic type, and menstrual status (P = 0.014). CONCLUSIONS: In the absence of internationally recognized multigene testing methods, for patients with early hormone receptor-positive, HER2-negative breast cancer, clinicians can develop a treatment plan based on clinicopathologic features only, which can effectively screen some patients who do not need adjuvant chemotherapy. However, nearly half of patients still receive adjuvant chemotherapy, and whether these patients can be exempted from chemotherapy warrants further exploration. Wolters Kluwer Health 2019-12-20 2019-12-20 /pmc/articles/PMC6964955/ /pubmed/31809316 http://dx.doi.org/10.1097/CM9.0000000000000548 Text en Copyright © 2019 The Chinese Medical Association, produced by Wolters Kluwer, Inc. under the CC-BY-NC-ND license. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle Original Articles
Xiang, Hong-Yu
Liu, Yin-Hua
Zhang, Hong
Zhang, Shuang
Xin, Ling
Xu, Ling
Ye, Jing-Ming
Li, Ting
Duan, Xue-Ning
Liu, Qian
Clinicopathologic analysis of 722 breast cancer patients who met the inclusion criteria of the TAILORx trial
title Clinicopathologic analysis of 722 breast cancer patients who met the inclusion criteria of the TAILORx trial
title_full Clinicopathologic analysis of 722 breast cancer patients who met the inclusion criteria of the TAILORx trial
title_fullStr Clinicopathologic analysis of 722 breast cancer patients who met the inclusion criteria of the TAILORx trial
title_full_unstemmed Clinicopathologic analysis of 722 breast cancer patients who met the inclusion criteria of the TAILORx trial
title_short Clinicopathologic analysis of 722 breast cancer patients who met the inclusion criteria of the TAILORx trial
title_sort clinicopathologic analysis of 722 breast cancer patients who met the inclusion criteria of the tailorx trial
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6964955/
https://www.ncbi.nlm.nih.gov/pubmed/31809316
http://dx.doi.org/10.1097/CM9.0000000000000548
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