King Judy, Fakhouri Walid, Jarvis Rosalind, Badreldin Waleed, Harper Gavin, Palmieri Carlo, Nathan Mark
Royal Free London NHS Foundation Trust, London, UK.
Eli Lilly and Company, Indianapolis, USA.
BMC Cancer. 2025 Jul 19;25(1):1189. doi: 10.1186/s12885-025-14526-w.
Cyclin-dependent kinase 4/6 inhibitors combined with endocrine therapy are now standard of care in the first- or second-line settings for hormone receptor positive (HR+), human epidermal growth factor 2 negative (HER2-) patients with advanced / metastatic breast cancer (ABC/MBC). Abemaciclib was first authorised in the United Kingdom (UK) in 2018 via patient access schemes before approval for routine use. This study assessed the treatment patterns and outcomes of abemaciclib in combination with endocrine therapy in a real-world setting.
This was an observational, multi-centre retrospective chart review of women in the UK with HR+, HER2- ABC/MBC treated with abemaciclib plus endocrine therapy during 07/2021 to 05/2022 with [Formula: see text]3 months' follow-up data. Data were summarised using descriptive analyses. Kaplan-Meier methods estimated time to progression (TTP) with 95% confidence intervals (CIs).
One hundred seventy-four adult women from 9 institutions were included. Median patient age at abemaciclib initiation was 65.2 years. Best tumor response was recorded in 78.2% (n = 136) of patients; 0.7% had complete response, 27.9% had partial response, 59.6% had stable disease and 11.8% had disease progressed. Abemaciclib was associated with a 12-month TTP rate of 81.1% (first line), 68.2% (second line) and 58.2% (third line). The median TTP for patients who received abemaciclib in the first, second, and third line of treatment was: not reached, 27.7 months (95% CI: 11.7 months-not reached), and 19.3 months (95% CI: 7.7-21.9 months), respectively.
These findings support the benefit of abemaciclib in women with HR+, HER2- ABC/MBC in the real-world and complement data from MONARCH 2 and 3 clinical trials.
细胞周期蛋白依赖性激酶4/6抑制剂联合内分泌治疗现已成为激素受体阳性(HR+)、人表皮生长因子2阴性(HER2-)的晚期/转移性乳腺癌(ABC/MBC)患者一线或二线治疗的标准方案。阿贝西利于2018年在英国首次通过患者准入计划获得批准,之后才被批准常规使用。本研究评估了阿贝西利联合内分泌治疗在真实世界中的治疗模式和疗效。
这是一项观察性、多中心回顾性病历审查,研究对象为2021年7月至2022年5月期间在英国接受阿贝西利联合内分泌治疗的HR+、HER2- ABC/MBC女性患者,并收集了至少3个月的随访数据。数据采用描述性分析进行总结。采用Kaplan-Meier方法估计疾病进展时间(TTP)及95%置信区间(CI)。
纳入了来自9家机构的174名成年女性。开始使用阿贝西利时患者的中位年龄为65.2岁。78.2%(n = 136)的患者记录到最佳肿瘤反应;0.7%为完全缓解,27.9%为部分缓解,59.6%为疾病稳定,11.8%为疾病进展。阿贝西利治疗12个月时的TTP率在一线治疗中为81.1%,二线治疗中为68.2%,三线治疗中为58.2%。在一线、二线和三线治疗中接受阿贝西利治疗的患者的中位TTP分别为:未达到、27.7个月(95%CI:11.7个月 - 未达到)和19.3个月(95%CI:7.7 - 21.9个月)。
这些研究结果支持阿贝西利对HR+、HER2- ABC/MBC女性患者在真实世界中的益处,并补充了MONARCH 2和3临床试验的数据。