The prognostic contribution of clinical breast cancer subtype, age, and race among patients with breast cancer brain metastases.
The prognostic contribution of clinical breast cancer subtype, age, and race among patients with breast cancer brain metastases.
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DOI:
10.1002/cncr.25746
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发表时间:
2011-04-15
期刊:
影响因子:
6.2
通讯作者:
Carey, Lisa A.
中科院分区:
文献类型:
--
作者:
Anders, Carey K.;Deal, Allison M.;Miller, C. Ryan;Khorram, Carmen;Meng, Hong;Burrows, Emily;Livasy, Chad;Fritchie, Karen;Ewend, Matthew G.;Perou, Charles M.;Carey, Lisa A.
Brain metastases (BM) arising from Triple-negative breast cancer (TNBC) portend poor prognosis. TNBC is more common in premenopausal and African-American (AA) patients; both also confer poor prognosis. In a single institution cohort study, we sought to determine if inferior outcome of TN BCBM is more reflective of a higher-risk population or subtype itself. The UNC Breast Cancer Database identified pts with BCBM diagnosed 1988 – 2008. BC subtype was assigned by IHC: HR+ (hormone receptor, ER+ and/or PR+)/HER2−, HR+/HER2+, HR−/HER2+ and TN (ER−/PR−/HER2−). Survival and recurrence patterns were evaluated by subtype, age (< vs ≥ 40 years) and race (AA vs non-AA) using the Kaplan-Meier method and Cox regression. Among 119 patients with BCBM, 33% were AA and 31% aged < 40 yrs. BC subtype was confirmed in 98 patients: 30% HR+/HER2−, 21% HR+/HER2+, 18% HR−/HER2+, 31% TN. Survival after BM was impacted by subtype (p=0.002), shortest for TNBC (0.24 yrs, CI 0.17 – 0.48). There were no age- (p=0.84) or race-specific (p=0.09) differences in survival after BM; stratification of subtypes by age and race revealed no difference (all, p > 0.1). Receipt of systemic therapy after BCBM was an important predictor of survival following BCBM (HR = 0.29, p=0.002) when adjusted for race, age, number of CNS lesions and BC subtype. TNBC confers a high risk of death following BM regardless of race and age supporting the need for novel agents capable of controlling both intra- and extracranial TNBC across all races and ages.
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影响因子:
11.2
作者:
Smid, Marcel;Wang, Yixin;Martens, John W. M.
通讯作者:
Martens, John W. M.
DOI:
10.1073/pnas.0932692100
发表时间:
2003-07-08
影响因子:
11.1
作者:
Sorlie, T;Tibshirani, R;Botstein, D
通讯作者:
Botstein, D
DOI:
10.1016/s0360-3016(02)04476-0
发表时间:
2003-04-01
影响因子:
7
作者:
Engel, J;Eckel, R;Hölzel, D
通讯作者:
Hölzel, D
影响因子:
45.3
作者:
Harvey, JM;Clark, GM;Allred, DC
通讯作者:
Allred, DC
影响因子:
--
作者:
Li, CI;Malone, KE;Daling, JR
通讯作者:
Daling, JR