Incidence and Survival by Human Epidermal Growth Factor Receptor 2 Status in Young Women With Stage I-III Breast Cancer: SEER, 2010-2016

被引:5
|
作者
Thomas, Alexandra [1 ]
Rhoads, Anthony [3 ]
Suhl, Jonathan [3 ]
Conway, Kristin M. [3 ]
Hundley, William G. [5 ]
McNally, Lacey R. [2 ]
Oleson, Jacob [4 ]
Melin, Susan A. [1 ]
Lynch, Charles F. [3 ]
Romitti, Paul A. [3 ,4 ]
机构
[1] Wake Forest Univ, Bowman Gray Sch Med, Dept Internal Med, Winston Salem, NC 27103 USA
[2] Wake Forest Univ, Bowman Gray Sch Med, Dept Canc Biol, Winston Salem, NC USA
[3] Univ Iowa, Dept Epidemiol, Iowa City, IA 52242 USA
[4] Univ Iowa, Dept Biostat, Iowa City, IA 52242 USA
[5] Virginia Commonwealth Univ, Dept Internal Med, Richmond, VA USA
关键词
Breast neoplasms; Incidence study; Neoplasm staging; Registries; Survival analysis; CLINICAL ONCOLOGY/COLLEGE; AMERICAN SOCIETY; PROGNOSIS; THERAPY; AGE; DIAGNOSIS; NONADHERENCE; GUIDELINES; PREGNANCY; PATTERNS;
D O I
10.1016/j.clbc.2020.01.014
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Contemporary data of breast cancer incidence and survival by human epidermal growth factor receptor 2 (HER2) status among premenopausal women are limited. In our analysis of 68,530 women in the Surveillance, Epidemiology, and End Results (SEER) database aged 20-49 years, HER2(+) cancer increased in incidence and was also associated with higher early survival within each hormone receptor status. Our findings provide insights to help inform preventive and therapeutic strategies for premenopausal women. Background: Young premenopausal women with breast cancer often experience more aggressive disease biology and poorer survival than older women. Diagnostic and therapeutic advances, including human epidermal growth factor receptor 2 (HER2)-directed therapy, may lessen treatment burden and improve survival for these young women, but contemporary incidence and survival data by HER2 status are limited. Patients and Methods: We identified women aged 20-49 years (n - 68,530) diagnosed with stage I-III breast cancer during 2010-2016 from the United States Surveillance, Epidemiology, and End Results 18 registries database. Age-adjusted average annual percent changes in incidence (diagnosis 2010-2016) and 5-year Kaplan-Meier survival curves (diagnosis 2010-2015) were estimated by HER2 and hormone receptor (HR) status and stratified independently by cancer stage and race/ethnicity. Results: With increasing age decade, proportions of HER2(-)/HR+ cancer increased, whereas proportions of HER2(+)/HR+, HER2(+)/HR-, and HER2(-)/HR- decreased. The greatest increases in incidence during 2010-2016 were observed for HER2(+) among women aged 20-49 years and HER2(-)/HR(- )among women aged 20-29 years. Incidence decreased for HER2(-)/HR- among women aged 40-49 years. Five-year survival was lowest for HER2(-)/HR- status compared to other receptor-based subtypes among women aged 20-49 years. HER2(+) status was more beneficial for 5-year survival than HR+ status among women aged 20-29 years, with the opposite observed among women aged 30-49 years, particularly those aged 40-49 years. Conclusion: HER2(+) breast cancer increased among premenopausal women and was also associated with higher early survival within each HR status. HER2(-)/HR- cancer also increased among women aged 20-29 years and was associated with lower early survival. Our contemporary data provide important insights to help inform preventive and therapeutic strategies for premenopausal women. (C) 2020 Elsevier Inc. All rights reserved.
引用
收藏
页码:E410 / E422
页数:13
相关论文
共 50 条
  • [1] Incidence and Survival Among Young Women With Stage I-III Breast Cancer: SEER 2000-2015
    Thomas, Alexandra
    Rhoads, Anthony
    Pinkerton, Elizabeth
    Schroeder, Mary C.
    Conway, Kristin M.
    Hundley, William G.
    McNally, Lacey R.
    Oleson, Jacob
    Lynch, Charles F.
    Romitti, Paul A.
    JNCI CANCER SPECTRUM, 2019, 3 (03)
  • [2] Incidence and survival among young women with stage I-III breast cancer
    Thomas, A.
    Rhoads, A.
    Pinkerton, E.
    Schroeder, M. C.
    Oelson, J. J.
    McNally, L. R.
    Hundley, W. G.
    Conway, K.
    Lynch, C. F.
    Romitti, P. A.
    ANNALS OF ONCOLOGY, 2018, 29
  • [3] Incidence of breast cancer among women in the United States, by human epidermal growth factor receptor-2 status: An analysis of National Registry data 2010
    Lang, Kathy
    Hao, Yanni
    Huang, Huan
    Federico, Victoria
    Menzin, Joseph
    JOURNAL OF CLINICAL ONCOLOGY, 2013, 31 (31)
  • [4] Survival by HER2 receptor status in stage IV breast cancer: SEER 2010-2012.
    Thomas, Alexandra
    Khan, Seema Ahsan
    Lynch, Charles
    Schroeder, Mary Chen
    JOURNAL OF CLINICAL ONCOLOGY, 2017, 35
  • [5] Racial disparities in women with triple-negative breast cancer: a 2010-2016 SEER-based survival analysis
    Makhani, Sarah
    Bouz, Antoun
    Zucker, Isaac
    Chung-Bridges, Katherine
    GYNECOLOGIC ONCOLOGY, 2021, 162 : S252 - S253
  • [6] Survival analysis based on human epidermal growth factor 2 status in stage II-III gastric cancer
    Cho, Jang Ho
    Lim, Jae Yun
    Cho, Jae Yong
    WORLD JOURNAL OF GASTROENTEROLOGY, 2017, 23 (41) : 7407 - 7414
  • [7] Outcomes of primary endocrine therapy in elderly women with stage I-III breast cancer: a SEER database analysis
    Yuan, Cai
    Xie, Zhigang
    Bian, Jiang
    Huo, Jinhai
    Daily, Karen
    BREAST CANCER RESEARCH AND TREATMENT, 2020, 180 (03) : 819 - 827
  • [8] Aspirin Exposure and Nodal Status at Diagnosis in Women with Stage I-III Breast Cancer.
    Barron, T. I.
    Sharp, L.
    Bennett, K.
    Visvanathan, K.
    CANCER RESEARCH, 2011, 71
  • [9] Survival analysis based on human epidermal growth factor 2 status in stage Ⅱ-Ⅲ gastric cancer
    Jang Ho Cho
    Jae Yun Lim
    Jae Yong Cho
    World Journal of Gastroenterology, 2017, (41) : 7407 - 7414
  • [10] Human epidermal growth factor receptor 2 status in breast cancer: A comparison between borderline positive human epidermal growth factor receptor 2 and strongly positive human epidermal growth factor receptor 2 tumors
    Huszno, Joanna
    Nowara, Elibieta
    CLINICAL CANCER INVESTIGATION JOURNAL, 2015, 4 (03): : 307 - 311