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新型靶向治疗时代下 HER2 阳性乳腺癌脑转移自然史的改变

Changing Natural History of HER2-Positive Breast Cancer Metastatic to the Brain in the Era of New Targeted Therapies.

机构信息

University of North Carolina School of Medicine, Chapel Hill, NC.

Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC.

出版信息

Clin Breast Cancer. 2018 Feb;18(1):29-37. doi: 10.1016/j.clbc.2017.07.017. Epub 2017 Aug 9.

Abstract

BACKGROUND

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 AND METHODS

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.

RESULTS

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).

CONCLUSION

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.

摘要

背景

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。

方法

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。

结果

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)。

结论

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。

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