Real-world treatment patterns and outcomes of abemaciclib for the treatment of HR+, HER2− metastatic breast cancer

医学 富维斯特朗 内科学 四分位间距 转移性乳腺癌 真实世界数据 芳香化酶抑制剂 危险系数 肿瘤科 乳腺癌 置信区间 癌症 阿那曲唑 三苯氧胺 计算机科学 数据科学
作者
Gebra Cuyún Carter,Kristin M. Sheffield,Anala Gossai,Yu‐Jing Huang,Yajun Emily Zhu,Lee Bowman,Emily Nash Smyth,Raina Mathur,Aaron B. Cohen,Erik Rasmussen,Shreya Balakrishna,Claudia Morato Guimaraes,Sarah Rybowski,Andrew D. Seidman
出处
期刊:Current Medical Research and Opinion [Taylor & Francis]
卷期号:37 (7): 1179-1187 被引量:18
标识
DOI:10.1080/03007995.2021.1923468
摘要

This retrospective observational study described baseline characteristics, real-world treatment patterns, and outcomes among patients with metastatic breast cancer treated with abemaciclib in the United States.De-identified electronic health record-derived data were used to describe patients who began abemaciclib treatment on or after 30 June 2016 and ≥4 months before data cutoff (31 December 2018). Real-world response (rwR) and real-world progression assessments were abstracted from clinical documentation. Descriptive statistics were used to calculate the real-world best response. The Kaplan-Meier method estimated real-world time to first response (rwTTFR) and real-world progression-free survival (rwPFS).The median age of 118 female patients at abemaciclib initiation was 66.5 years (interquartile range, 57.0, 73.0). The breakdown of patients who received abemaciclib in first, second, third, or later lines was 28.8%, 21.2%, 20.3%, and 29.7%, respectively. Patients received abemaciclib as monotherapy (12.7%) or in combination with endocrine therapy: fulvestrant (59.3%); aromatase inhibitor (22.9%); aromatase inhibitor and fulvestrant (5.1%). There were 68 patients (57.6%) with ≥1 rwR assessment: 41.2% with a real-world complete response or real-world partial response. Median rwTTFR was 3.6 months (95% confidence interval, 3.5, 5.2). Twelve-month rwPFS probability was 61.7%.This study represents utilization and outcomes associated with abemaciclib approximately 1 year following FDA approval. Treatment patterns demonstrated heterogeneity and, as in clinical trials, patients appeared to benefit from abemaciclib treatment in the real world. More research investigating outcomes associated with abemaciclib treatment is needed, with larger samples and longer follow-up to enable closer evaluation by subgroup, regimen, and line of therapy.

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