Abstract P6-18-19: Real-world survival of heavily pretreated patients with refractory HR+, HER2- metastatic breast cancer receiving single-agent chemotherapy - A comparison with MONARCH 1

H. Rugo, V. Diéras, J. Cortes, D. Patt, H. Wildiers, J. O’Shaughnessy, E. Zamora, D. Yardley, G. Carter, K. Sheffield, Liming Li, V. André, Re Derbyshire, Xi Li, Martin Frenzel, Y. Huang, M. Dickler, S. Tolaney
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Abstract

Background In MONARCH 1 (NCT02102490), abemaciclib demonstrated promising single-agent activity and tolerability in a population of heavily pretreated women with refractory HR+, HER2- metastatic breast cancer (MBC). 1 Confirmed objective response rate (ORR) was 19.7% (95% CI: 13.3, 27.5) and at 18 months minimum follow-up median overall survival (OS) was 22.3 months. Due to the single-arm trial design of MONARCH 1, there is a need to view these results in clinical context relative to available treatment options. This study compared the OS results of abemaciclib in MONARCH 1 vs that in a real-world single-agent chemotherapy cohort with similar patient and disease characteristics. Methods MONARCH 1 study design and key eligibility criteria were previously described. 1 The real-world cohort was based on Flatiron Health electronic health records-derived, nationally representative (USA-based) database comprising patient-level structured and unstructured data, curated via technology-enabled abstraction, for patients with MBC between January 1, 2011 through February 28, 2018. A real-world single-agent chemotherapy cohort was created based on the key eligibility criteria of MONARCH 1 and included patients diagnosed with HR+, HER2- MBC who received single-agent chemotherapy (eribulin, capecitabine, gemcitabine, or vinorelbine) following 1-2 prior chemotherapy regimens in the metastatic setting, had an ECOG PS of 0-1, and no prior CDK4 & 6 therapy. The index date was the start of the eligible single-agent chemotherapy, and patients were followed from the index date until date of death, loss to follow-up, or end of the database, whichever occurred earlier. OS results were adjusted using 2 methods (Mahalanobis distance matching and entropy balancing with bootstrapping) to account for baseline demographic and clinical differences between the real-world and trial cohorts. Results A real-world cohort (n=281) with eligibility criteria similar to the MONARCH 1 population (n=132) was identified. A subsequent matching based on Mahalanobis distance was performed to match MONARCH 1 population (n=108) with the real-world cohort (n=108). The matched cohorts demonstrated similar patient and disease characteristics. Median OS was 22.3 months in the abemaciclib arm vs 13.6 months in the matched cohort with an estimated hazard ratio (HR) of 0.54 (95% CI: 0.37, 0.77). Results of a sensitivity analysis performed using entropy balancing were consistent with an adjusted median OS of 12.7 months in the real-world cohort (n=281)with HR of 0.57 (95% CI from bootstrapping: 0.44, 0.78). Conclusion Methodological advances to adjust for potential biases, and improvements in data quality, have evolved enabling the ability to leverage a real-world cohort as an external comparator arm. This study demonstrates the ability to create a real-world chemotherapy cohort suitable to serve as a comparator for MONARCH 1. These exploratory results suggest a survival advantage and adequately place the clinical benefit of abemaciclib monotherapy in clinical context. References Dickler et al, CCR 2017 Citation Format: Rugo H, Dieras V, Cortes J, Patt D, Wildiers H, O9Shaughnessy J, Zamora E, Yardley DY, Carter GC, Sheffield KM, Li L, Andre VA, Derbyshire RE, Li XI, Frenzel M, Huang Y-J, Dickler MN, Tolaney SM. Real-world survival of heavily pretreated patients with refractory HR+, HER2- metastatic breast cancer receiving single-agent chemotherapy - A comparison with MONARCH 1 [abstract]. In: Proceedings of the 2018 San Antonio Breast Cancer Symposium; 2018 Dec 4-8; San Antonio, TX. Philadelphia (PA): AACR; Cancer Res 2019;79(4 Suppl):Abstract nr P6-18-19.
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P6-18-19:重度预处理的难治性HR+, HER2-转移性乳腺癌患者接受单药化疗的真实生存-与MONARCH 1的比较
在MONARCH 1 (NCT02102490)中,abemaciclib在重度预处理的难治性HR+、HER2-转移性乳腺癌(MBC)患者中显示出了良好的单药活性和耐受性。1 .确认的客观缓解率(ORR)为19.7% (95% CI: 13.3, 27.5),最低随访18个月时中位总生存期(OS)为22.3个月。由于MONARCH 1的单臂试验设计,有必要将这些结果与可用的治疗方案在临床背景下进行比较。本研究比较了abemaciclib在MONARCH 1中的OS结果与在具有相似患者和疾病特征的现实世界单药化疗队列中的OS结果。方法先前描述了MONARCH 1研究的设计和主要入选标准。1真实世界队列基于Flatiron Health电子健康记录衍生的全国代表性(美国)数据库,该数据库包括患者级别的结构化和非结构化数据,通过技术支持的抽象管理,用于2011年1月1日至2018年2月28日期间的MBC患者。基于MONARCH 1的关键资格标准,建立了一个真实世界的单药化疗队列,包括在1-2次转移性化疗方案后接受单药化疗(艾瑞布林、卡培他滨、吉西他滨或维诺瑞滨)的HR+、HER2- MBC患者,ECOG PS为0-1,既往未接受CDK4和cdk6治疗。索引日期为符合条件的单药化疗的开始,从索引日期开始对患者进行随访,直至患者死亡、失去随访或数据库结束(以较早者为准)。使用两种方法(马氏距离匹配和熵平衡与自引导)调整OS结果,以解释现实世界和试验队列之间的基线人口统计学和临床差异。结果确定了一个真实世界的队列(n=281),其资格标准与MONARCH 1人群(n=132)相似。随后根据马氏距离进行匹配,将MONARCH 1种群(n=108)与现实世界队列(n=108)进行匹配。匹配的队列显示出相似的患者和疾病特征。abemaciclib组的中位生存期为22.3个月,而匹配队列的中位生存期为13.6个月,估计风险比(HR)为0.54 (95% CI: 0.37, 0.77)。使用熵平衡进行的敏感性分析结果与现实世界队列(n=281)的调整中位OS 12.7个月一致,HR为0.57 (bootstrapping的95% CI: 0.44, 0.78)。方法上的进步调整了潜在的偏差,数据质量也得到了改善,这使得我们能够利用现实世界的队列作为外部比较指标。这项研究证明了创建一个适合作为君主1比较物的真实化疗队列的能力。这些探索性结果表明,在临床背景下,abemaciclib单药治疗具有生存优势和充分的临床益处。重度预处理的难治性HR+, HER2-转移性乳腺癌患者接受单药化疗的真实生存-与MONARCH 1的比较[摘要]。2018年圣安东尼奥乳腺癌研讨会论文集;2018年12月4-8日;费城(PA): AACR;癌症杂志,2019;79(4增刊):P6-18-19。
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