Warner Erica T, Tamimi Rulla M, Hughes Melissa E, Ottesen Rebecca A, Wong Yu-Ning, Edge Stephen B, Theriault Richard L, Blayney Douglas W, Niland Joyce C, Winer Eric P, Weeks Jane C, Partridge Ann H
Erica T. Warner and Rulla M. Tamimi, Harvard School of Public Health; Erica T. Warner, Rulla M. Tamimi, Melissa E. Hughes, Eric P. Winer, Jane C. Weeks, and Ann H. Partridge, Brigham and Women's Hospital; Melissa E. Hughes, Eric P. Winer, Jane C. Weeks, and Ann H. Partridge, Dana-Farber Cancer Institute, Boston, MA; Rebecca A. Ottesen and Joyce C. Niland, City of Hope Comprehensive Cancer Center, Duarte; Douglas W. Blayney, Stanford University Cancer Center, Palo Alto, CA; Yu-Ning Wong, Fox Chase Cancer Center, Philadelphia, PA; Stephen B. Edge, Baptist Cancer Center, Memphis, TN; and Richard L. Theriault, University of Texas MD Anderson Cancer Center, Houston, TX.
J Clin Oncol. 2015 Jul 10;33(20):2254-61. doi: 10.1200/JCO.2014.57.1349. Epub 2015 May 11.
To evaluate the relationship between race/ethnicity and breast cancer-specific survival according to subtype and explore mediating factors.
Participants were women presenting with stage I to III breast cancer between January 2000 and December 2007 at National Comprehensive Cancer Network centers with survival follow-up through December 2009. Cox proportional hazards regression was used to compare breast cancer-specific survival among Asians (n = 533), Hispanics (n = 1,122), and blacks (n = 1,345) with that among whites (n = 14,268), overall and stratified by subtype (luminal A like, luminal B like, human epidermal growth factor receptor 2 type, and triple negative). Model estimates were used to derive mediation proportion and 95% CI for selected risk factors.
In multivariable adjusted models, overall, blacks had 21% higher risk of breast cancer-specific death (hazard ratio [HR], 1.21; 95% CI, 1.00 to 1.45). For estrogen receptor-positive tumors, black and white survival differences were greatest within 2 years of diagnosis (years 0 to 2: HR, 2.65; 95% CI, 1.34 to 5.24; year 2 to end of follow-up: HR, 1.50; 95% CI, 1.12 to 2.00). Blacks were 76% and 56% more likely to die as a result of luminal A-like and luminal B-like tumors, respectively. No disparities were observed for triple-negative or human epidermal growth factor receptor 2-type tumors. Asians and Hispanics were less likely to die as a result of breast cancer compared with whites (Asians: HR, 0.56; 95% CI, 0.37 to 0.85; Hispanics: HR, 0.74; 95% CI, 0.58 to 0.95). For blacks, tumor characteristics and stage at diagnosis were significant disparity mediators. Body mass index was an important mediator for blacks and Asians.
Racial disparities in breast cancer survival vary by tumor subtype. Interventions are needed to reduce disparities, particularly in the first 2 years after diagnosis among black women with estrogen receptor-positive tumors.
根据乳腺癌亚型评估种族/民族与乳腺癌特异性生存之间的关系,并探索中介因素。
研究对象为2000年1月至2007年12月期间在国家综合癌症网络中心就诊的I至III期乳腺癌女性患者,随访至2009年12月。采用Cox比例风险回归比较亚洲人(n = 533)、西班牙裔(n = 1122)和黑人(n = 1345)与白人(n = 14268)的乳腺癌特异性生存情况,总体及按亚型(luminal A样、luminal B样、人表皮生长因子受体2型和三阴性)分层比较。模型估计用于得出选定危险因素的中介比例和95%置信区间。
在多变量调整模型中,总体而言,黑人乳腺癌特异性死亡风险高21%(风险比[HR],1.21;95%置信区间,1.00至1.45)。对于雌激素受体阳性肿瘤,黑人和白人的生存差异在诊断后2年内最大(0至2年:HR,2.65;95%置信区间,1.34至5.24;2年至随访结束:HR,1.50;95%置信区间,1.12至2.00)。黑人因luminal A样和luminal B样肿瘤死亡的可能性分别高76%和56%。三阴性或人表皮生长因子受体2型肿瘤未观察到差异。与白人相比,亚洲人和西班牙裔因乳腺癌死亡的可能性较小(亚洲人:HR,0.56;95%置信区间,0.37至0.85;西班牙裔:HR,0.74;95%置信区间,0.58至0.95)。对于黑人,肿瘤特征和诊断时的分期是显著的差异中介因素。体重指数是黑人和亚洲人的重要中介因素。
乳腺癌生存的种族差异因肿瘤亚型而异。需要采取干预措施以减少差异,特别是在诊断后前2年中雌激素受体阳性肿瘤的黑人女性中。