University of North Carolina School of Medicine, Chapel Hill, NC.
Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC.
Clin Breast Cancer. 2018 Feb;18(1):29-37. doi: 10.1016/j.clbc.2017.07.017. Epub 2017 Aug 9.
Given the wide adoption of human epidermal growth factor receptor 2 (HER2)-targeted therapies for advanced HER2-positive breast cancer, we studied the natural history of patients with HER2-positive breast cancer brain metastases (BCBM) over time.
Patients with HER2-positive BCBM identified from a prospectively maintained database at the University of North Carolina were divided into 3 cohorts by year of BCBM diagnosis. Cohorts were selected by year of HER2-targeted therapy US Food and Drug Administration approval. Overall survival (OS), time to first metastasis, time to BCBM, and BCBM survival were estimated by the Kaplan-Meier method. Associations between OS after BCBM and clinical variables were assessed by Cox proportional hazards regression models.
One hundred twenty-three patients were identified. Median age was 51 years, and 58% were white and 31% African American. OS from initial breast cancer diagnosis improved over time: 3.6 years (95% confidence interval [CI], 2.8-6.1) in the 1998-2007 cohort, 6.6 years (95% CI, 4.5-8.6) in the 2008-2012 cohort, and 7.6 years (95% CI, 4.4-9.6) in the 2013-2015 cohort (P = .05). While time from initial diagnosis to first metastasis did not differ (P = .12), time to BCBM increased over time (2.6 years [95% CI, 1.3-3.5] for 1998-2007; 2.6 years [95% CI, 2.1-4.3] for 2008-2012, and 3.3 years [95% CI, 2.2-6] for 2013-2015; P = .05). Although OS from BCBM did not significantly differ by cohort, patients who received HER2-targeted therapy after BCBM had a prolonged OS (2.1 years [95% CI, 1.6-2.6] vs. 0.65 years [95% CI, 0.4-1.3]; P = .001).
OS from initial breast cancer diagnosis significantly improved over time for patients with HER2-positive breast cancer who develop BCBM, now exceeding 7 years; survival from BCBM diagnosis may now exceed 2 years.
鉴于人表皮生长因子受体 2(HER2)靶向治疗在晚期 HER2 阳性乳腺癌中的广泛应用,我们研究了 HER2 阳性乳腺癌脑转移(BCBM)患者随时间推移的自然病史。
从北卡罗来纳大学前瞻性维护的数据库中确定了 HER2 阳性 BCBM 患者,然后根据 BCBM 诊断年份将患者分为 3 个队列。队列根据 HER2 靶向治疗美国食品和药物管理局批准年份选择。通过 Kaplan-Meier 方法估计总生存期(OS)、首次转移时间、BCBM 时间和 BCBM 生存时间。通过 Cox 比例风险回归模型评估 BCBM 后 OS 与临床变量之间的关系。
共确定了 123 名患者。中位年龄为 51 岁,58%为白人,31%为非裔美国人。从初始乳腺癌诊断到 OS 的时间随着时间的推移而改善:1998-2007 队列为 3.6 年(95%置信区间[CI],2.8-6.1),2008-2012 队列为 6.6 年(95%CI,4.5-8.6),2013-2015 队列为 7.6 年(95%CI,4.4-9.6)(P=0.05)。虽然从初始诊断到首次转移的时间没有差异(P=0.12),但 BCBM 发生的时间随着时间的推移而增加(1998-2007 年为 2.6 年[95%CI,1.3-3.5];2008-2012 年为 2.6 年[95%CI,2.1-4.3];2013-2015 年为 3.3 年[95%CI,2.2-6];P=0.05)。尽管各个队列之间的 OS 没有显著差异,但在 BCBM 后接受 HER2 靶向治疗的患者 OS 延长(2.1 年[95%CI,1.6-2.6] vs. 0.65 年[95%CI,0.4-1.3];P=0.001)。
对于发生 HER2 阳性乳腺癌脑转移的患者,从初始乳腺癌诊断到 OS 的时间随着时间的推移显著改善,现在超过 7 年;BCBM 诊断后的生存时间可能超过 2 年。