Effect of pathologic stages on postmastectomy radiation therapy in breast cancer receiving neoadjuvant chemotherapy and total mastectomy: A Cancer Database Analysis

被引:24
|
作者
Zhang, Jiaqiang [1 ]
Lu, Chang-Yun [2 ]
Chen, Chien-Hsin [3 ]
Chen, Ho-Min [4 ]
Wu, Szu-Yuan [4 ,5 ,6 ,7 ,8 ]
机构
[1] Zhengzhou Univ, Dept Anesthesiol & Perioperat Med, Henan Prov Peoples Hosp, Peoples Hosp, Zhengzhou, Henan, Peoples R China
[2] Lotung Poh Ai Hosp, Lo Hsu Med Fdn, Dept Gen Surg, Yilan, Taiwan
[3] Taipei Med Univ, Wan Fang Hosp, Dept Colorectal Surg, Taipei, Taiwan
[4] Lotung Poh Ai Hosp, Lo Hsu Med Fdn, Big Data Ctr, Yilan, Taiwan
[5] Asia Univ, Dept Food Nutr & Hlth Biotechnol, Coll Med & Hlth Sci, Taichung, Taiwan
[6] Lotung Poh Ai Hosp, Lo Hsu Med Fdn, Div Radiat Oncol, Yilan, Taiwan
[7] Asia Univ, Dept Healthcare Adm, Coll Med & Hlth Sci, Taichung, Taiwan
[8] Taipei Med Univ, Coll Oral Med, Sch Dent, Taipei, Taiwan
来源
BREAST | 2020年 / 54卷
关键词
Breast cancer; Postmastectomy radiation therapy; Survival; Pathologic response; Neoadjuvant chemotherapy; LOCAL-REGIONAL CONTROL; LOCOREGIONAL RECURRENCE; SYSTEMIC THERAPY; RADIOTHERAPY; PREDICTORS; SURGERY; IMPACT; METAANALYSIS; COMORBIDITY; MORTALITY;
D O I
10.1016/j.breast.2020.08.017
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To use pathologic indicators to determine which patients benefit from postmastectomy radiation therapy (PMRT) for breast cancer after neoadjuvant chemotherapy (NACT) and total mastectomy (TM). Patients and methods: We enrolled 4236 patients with breast invasive ductal carcinoma who received NACT followed by TM. Cox regression analysis was used to calculate hazard ratios (HRs) and confidence intervals; independent predictors were controlled for or stratified in the analysis. Results: After multivariate Cox regression analyses, the adjusted HRs derived for PMRT for all-cause mortality were 0.65 (0.52-0.81, P < 0.0001) and 0.58 (0.47-0.71, P < 0.0001) in postchemotherapy pathologic tumor stages T2-4 (ypT3-4) and postchemotherapy pathologic nodal stages N2-3 (ypN2-3), respectively. Moreover, adjusted HRs derived for PMRT with all-cause mortality were 0.51 (0.38-0.69, P < 0.0001), 0.60 (0.40-0.88, P = 0.0096), and 0.64 (0.48-0.86, P = 0.0024) in pathological stages IIIA, IIIB, and IIIC, respectively. Additionally, the PMRT group showed significant locoregional control irrespective of the pathologic response, even ypT0, ypN0, or pathological complete response (pCR), compared with the No-PMRT group. The multivariate analysis showed no statistical differences between the PMRT and No-PMRT groups for distant metastasis-free survival in any pathologic response of ypT0-4, ypN0-3, and pathologic American Joint Committee on Cancer stages pCR to IIIC. Conclusion: For patients with breast cancer ypT3-4, ypN2-3, or pathologic stages IIIAeIIIC receiving NACT and TM, benefit from PMRT if it is associated with OS benefits, regardless of the clinical stage of the disease. Compared with No-PMRT, PMRT improved locoregional recurrence-free survival, even pCR, in patients with breast cancer receiving NACT and TM. (C) 2020 The Author(s). Published by Elsevier Ltd.
引用
收藏
页码:70 / 78
页数:9
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