Second primary breast cancer after diagnosis of breast cancer among male patients: An examination of population characteristics and overall survival

被引:1
|
作者
Chowdhry, Amit K. [1 ]
Chowdhry, Divya N. [2 ]
Shayne, Michelle [3 ]
Milano, Michael T. [1 ]
机构
[1] Univ Rochester, Dept Radiat Oncol, Med Ctr, 601 Elmwood Ave,Box 647, Rochester, NY 14642 USA
[2] Univ Rochester, Med Ctr, Dept Imaging Sci, Rochester, NY 14642 USA
[3] Univ Rochester, Med Ctr, Dept Med Hematol Oncol, Rochester, NY 14642 USA
关键词
RADIOTHERAPY; RISK;
D O I
10.1016/j.eclinm.2020.100551
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Male patients with breast cancer (BrC) have increased risk of developing 2nd-primary BrC (2nd-BrC). Given the relative rarity of male BrC, population-based registries are needed to analyze overall survival (OS) outcomes for these patients. Methods: Using the Surveillance, Epidemiology and End Results registry of patients diagnosed from 1975 to 2016, a cohort study of men whose only malignancy was BrC (BrC-O; n = 6,475), and men who developed 2nd-BrC after initial BrC diagnosis (BrC-2; n = 85) was performed. The standardized incidence ratio (SIR) of 2nd-BrC, Kaplan-Meier OS and multivariable Cox regression modelling were performed. Findings: The SIR for 2nd-BrC was 32.95 (95%CI:[23.85-44.38],p < 0.05). The majority (88%) of 2nd-BrC for BrC-2 were contralateral from 1st-BrC; suggesting the unlikeliness of miscoding local recurrences as 2nd-BrC for most patients. There was no statistically significant difference between rates of hormone (reported in 44%) or HER-2 (reported in 33%) receptor status between BrC-O and BrC-2, albeit with limited data. The 2ndBrC for BrC-2 was significantly more likely to be localized or distant stage (rather than regional) than BrC-O. Median OS was 103 months (95% CI: [99, 108]) for BrC-O and 62 months (95% CI [49, 128] after 2nd-BrC. When sub-grouped by BrC stage, and when analyzed by Cox regression, there was no significant difference in OS between BrC-O and BrC-2. Interpretation: Patients with male BrC are at significantly increased risk of 2nd BrC, but they can expect similar post-BrC prognosis (versus those without 2nd-BrC), after adjusting for patient demographics and tumor characteristics known to affect OS. Funding: None. (C) 2020 The Author(s). Published by Elsevier Ltd.
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页数:9
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