Gabos Zsolt, Sinha Richie, Hanson John, Chauhan Nitin, Hugh Judith, Mackey John R, Abdulkarim Bassam
Department of Oncology, Cross Cancer Institute and University of Alberta, Edmonton, Alberta, Canada.
J Clin Oncol. 2006 Dec 20;24(36):5658-63. doi: 10.1200/JCO.2006.07.0250. Epub 2006 Nov 13.
As survival in breast cancer patients is improving, brain metastases are becoming increasingly prevalent. The risk of brain metastases in newly diagnosed human epidermal growth factor receptor 2 (HER-2) -overexpressing breast cancer patients is not yet fully defined. We aimed to analyze the risk of brain metastasis in newly diagnosed HER-2-positive breast cancer patients in comparison with HER-2-negative patients.
To determine the incidence of brain metastases in HER-2-overexpressing patients, we analyzed a cohort of newly diagnosed 301 HER-2-positive and 363 HER-2-negative patients identified between January 1998 and December 2003. The association between histologic features and the occurrence of brain metastases was evaluated with univariate and multivariate Cox regression analysis.
Median follow-up was 3.9 years. Brain metastases were identified in 9% (27 patients) with HER-2-overexpressing breast cancer compared with only 1.9% (7 patients) in the HER-2 negative patients (hazard ratio 4.23 [1.84-9.74], P = .0007). HER-2 overexpression, tumor size larger than 2 cm, at least one positive node, and grade 2/3 disease were predictors of brain metastases in univariate analysis. In multivariate analysis, HER-2 overexpression, tumor size larger than 2 cm, and hormone-receptor negativity were independent prognostic factors for the development of brain metastases, whereas hormone-receptor expression was protective.
Our study shows that newly diagnosed HER-2-overexpressing breast cancer patients are at increased risk for brain metastases. Because most brain metastases occur after the development of systemic disease, these findings prompt consideration of brain prophylaxis strategies with HER-2-inhibiting small molecules able to cross the blood-brain barrier and/or radiologic screening to detect asymptomatic brain metastases.
随着乳腺癌患者生存率的提高,脑转移变得越来越普遍。新诊断的人表皮生长因子受体2(HER-2)过表达乳腺癌患者发生脑转移的风险尚未完全明确。我们旨在分析新诊断的HER-2阳性乳腺癌患者与HER-2阴性患者相比发生脑转移的风险。
为确定HER-2过表达患者脑转移的发生率,我们分析了1998年1月至2003年12月期间新诊断的301例HER-2阳性和363例HER-2阴性患者组成的队列。采用单因素和多因素Cox回归分析评估组织学特征与脑转移发生之间的关联。
中位随访时间为3.9年。HER-2过表达乳腺癌患者中有9%(27例)发生脑转移,而HER-2阴性患者中仅有1.9%(7例)发生脑转移(风险比4.23[1.84 - 9.74],P = 0.0007)。在单因素分析中,HER-2过表达、肿瘤大小大于2 cm、至少一个阳性淋巴结以及2/3级疾病是脑转移的预测因素。在多因素分析中,HER-2过表达、肿瘤大小大于2 cm以及激素受体阴性是脑转移发生的独立预后因素,而激素受体表达具有保护作用。
我们的研究表明,新诊断的HER-2过表达乳腺癌患者发生脑转移的风险增加。由于大多数脑转移发生在全身疾病发展之后,这些发现促使人们考虑采用能够穿过血脑屏障的HER-2抑制小分子进行脑预防策略和/或进行影像学筛查以检测无症状脑转移。