Abstract P1-19-12: Patterns of treatment with everolimus and exemestane in hormone receptor positive HER2 negative metastatic breast cancer in the era of targeted therapy

Mariya Rozenblit, L. Pusztai, K. Adelson, S. Mougalian
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Abstract

Background: In 2012 the FDA approved everolimus and exemestane (EE) as second line therapy for patients who have progressed on letrozole or anastrozole, based on the BOLERO-2 trial which showed improvement in PFS with EE compared to exemestane alone (6.9 vs 2.8 months). Currently, aromatase inhibitors (AI), or fulvestrant (F), alone or in combination with a CDK4/6 inhibitor (CDK4/6i) are the most commonly used first line endocrine therapies for hormone receptor (HR) positive HER2 negative metastatic breast cancer (mBC). There is currently no clinical trial data regarding the efficacy of EE in patients previously treated with CDK4/6i. The goal of this project was to explore the treatment patterns of EE in this contemporary patient population, with particular interest in those who had received prior CDK4/6i plus AI/F, as first, second, or third-line treatment. Methods: The Flatiron Health electronic health record-derived nationwide database selected de-identified patients with HR positive HER2 negative mBC and the first (1L), second (2L), and third line (3L) treatments they received. Duration of treatment (DOT) is defined as time from the date of initiation of a line of treatment to the day prior to initiation of subsequent line of treatment; prolonged DOT is defined as duration ≥ 6 months. Medical non-cancer co-morbidities listed as defined by the Charlson Comorbidity Index were included. Median DOT was compared using t-test, unadjusted for patient and disease characteristics. Statistical analysis was performed using Python v3.7. Results: A total of 8457 HR positive HER2 negative patients diagnosed with mBC between 1/2011 and 1/2019 were identified. Of these, 726 patients received EE in 1L (N=127), 2L (N=326), or 3L (N=273). In this cohort, 72.3% of patients were diagnosed between 2011-2014, and 27.7% were diagnosed after 1/2015, and most (94.6%) were treated in the community setting. The majority were female (98.4%), Caucasian (75.1%), and had no co-morbidities (79%); the mean age was 64. A quarter of patients (25%) had de novo mBC. The median DOT for 1L EE was 7.6 months (95% CI 5.6, 9.6); 56.7% received 1L EE for ≥6 months. The median DOT for 2L EE was 9.1 months (95% CI 7.6,10.6) following 1L AI/F and 10.7 months (95% CI 8.5,12.9) following 1L AI/F plus CDK4/6i (p Conclusion: In a cohort of patients with HR positive HER2 negative mBC who received EE in the 2L or 3L, a significant percentage of patients derived clinical benefit (DOT>6 months) from EE, even after CDK4/6i therapy. Patients who received CDK4/6i 1L had longer unadjusted DOT of 2L EE compared to those who received 1L AI/F alone. Citation Format: Mariya Rozenblit, Lajos Pusztai, Kerin Adelson, Sarah Mougalian. Patterns of treatment with everolimus and exemestane in hormone receptor positive HER2 negative metastatic breast cancer in the era of targeted therapy [abstract]. In: Proceedings of the 2019 San Antonio Breast Cancer Symposium; 2019 Dec 10-14; San Antonio, TX. Philadelphia (PA): AACR; Cancer Res 2020;80(4 Suppl):Abstract nr P1-19-12.
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摘要P1-19-12:靶向治疗时代依维莫司和依西美坦治疗激素受体阳性HER2阴性转移性乳腺癌的模式
背景:2012年,基于BOLERO-2试验,FDA批准依维莫司和依西美坦(EE)作为来曲唑或阿那曲唑进展患者的二线治疗,该试验显示,与单独依西美坦相比,EE可改善PFS(6.9个月vs 2.8个月)。目前,芳香化酶抑制剂(AI)或氟维strant (F)单独或联合CDK4/6抑制剂(CDK4/6i)是激素受体(HR)阳性HER2阴性转移性乳腺癌(mBC)最常用的一线内分泌治疗方法。目前还没有临床试验数据表明,EE对之前接受过CDK4/6i治疗的患者的疗效。该项目的目标是探索当代患者群体中EE的治疗模式,对那些先前接受过CDK4/6i + AI/F作为一线、二线或三线治疗的患者特别感兴趣。方法:从Flatiron Health电子健康记录衍生的全国数据库中选择未识别的HR阳性HER2阴性mBC患者,并对其进行一线(1L)、二线(2L)和三线(3L)治疗。治疗持续时间(DOT)定义为从开始治疗之日到开始后续治疗前一天的时间;延长DOT定义为持续时间≥6个月。根据Charlson合并症指数列出的医学非癌症合并症包括在内。中位DOT采用t检验进行比较,未对患者和疾病特征进行调整。使用Python v3.7进行统计分析。结果:2011年1月至2019年1月期间,共发现8457例HR阳性HER2阴性的mBC患者。其中,726例患者在1L (N=127)、2L (N=326)和3L (N=273)接受了EE治疗。在该队列中,72.3%的患者在2011-2014年期间被诊断,27.7%的患者在2015年1月之后被诊断,大多数(94.6%)在社区环境中接受治疗。多数为女性(98.4%),白种人(75.1%),无合并症(79%);平均年龄为64岁。四分之一的患者(25%)有新发mBC。1L EE的中位DOT为7.6个月(95% CI 5.6, 9.6);56.7%接受1L EE治疗≥6个月。在1L AI/F后,2L EE的中位DOT为9.1个月(95% CI 7.6,10.6),在1L AI/F + CDK4/6i后,2L EE的中位DOT为10.7个月(95% CI 8.5,12.9)。(p)结论:在2L或3L接受EE的HR阳性HER2阴性mBC患者队列中,即使在CDK4/6i治疗后,仍有显著比例的患者从EE中获得临床获益(DOT>6个月)。与单独接受1L AI/F的患者相比,接受CDK4/6i 1L的患者未调整DOT为2L EE的时间更长。引用格式:Mariya Rozenblit, Lajos Pusztai, Kerin Adelson, Sarah Mougalian。靶向治疗时代依维莫司和依西美坦治疗激素受体阳性HER2阴性转移性乳腺癌的模式[摘要]。摘自:2019年圣安东尼奥乳腺癌研讨会论文集;2019年12月10日至14日;费城(PA): AACR;中国癌症杂志,2020;31(增刊):1-19-12。
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