University of California San Francisco Helen Diller Family Comprehensive Cancer Center, San Francisco, CA, USA.
Pfizer Inc, New York, NY, USA.
Breast. 2023 Jun;69:375-381. doi: 10.1016/j.breast.2023.03.015. Epub 2023 Mar 27.
Palbociclib, the first available cyclin-dependent kinase 4/6 inhibitor, plus endocrine therapy is approved for hormone receptor-positive/human epidermal growth factor receptor 2-negative (HR+/HER2-) metastatic breast cancer (MBC). This study compared real-world effectiveness of palbociclib plus letrozole versus letrozole in older patients with MBC in US clinical practice.
This retrospective analysis included patients from the Flatiron Health longitudinal database. Overall, 796 women with HR+/HER2- MBC aged ≥65 years starting palbociclib plus letrozole or letrozole as first-line therapy between February 2015 and September 2018 were included. Patients were evaluated from treatment start until December 2018, death, or last visit, whichever came first. Real-world progression-free survival (rwPFS), overall survival (OS), and real-world best tumor responses (rwBTR) were endpoints. Stabilized inverse probability treatment weighting (sIPTW) balanced patient characteristics.
After sIPTW, 450 patients treated with palbociclib plus letrozole and 335 treated with letrozole were included; median age was 74.0 years. Median rwPFS was 22.2 (95% CI, 20.0-30.4) months for palbociclib plus letrozole versus 15.8 (12.9-18.9) months for letrozole (hazard ratio, 0.59 [0.47-0.74]; P<0.001). Median OS was not reached for palbociclib plus letrozole versus 43.4 months (30.0-not estimable) with letrozole (hazard ratio, 0.55 [0.42-0.72]; P<0.001). No interactions between age groups (65-74 and ≥75 years) and treatment groups were observed for rwPFS or OS. Rate of rwBTR was significantly higher for palbociclib plus letrozole (52.4%) versus letrozole (22.1%; odds ratio, 2.0 [1.4-2.7]; P<0.001).
This analysis demonstrates the effectiveness of palbociclib combination therapy as standard-of-care for older patients with HR+/HER2- MBC in the first-line setting.
帕博西尼是首个被批准用于治疗激素受体阳性/人表皮生长因子受体 2 阴性(HR+/HER2-)转移性乳腺癌(MBC)的细胞周期蛋白依赖性激酶 4/6 抑制剂,联合内分泌治疗。本研究比较了帕博西尼联合来曲唑与来曲唑在真实世界中治疗美国临床实践中老年 HR+/HER2-MBC 患者的疗效。
本回顾性分析纳入了来自 Flatiron Health 纵向数据库的患者。共纳入 796 例年龄≥65 岁、接受帕博西尼联合来曲唑或来曲唑作为一线治疗的 HR+/HER2-MBC 患者。从治疗开始到 2018 年 12 月死亡或最后一次就诊,以先发生者为准,对患者进行评估。真实世界无进展生存期(rwPFS)、总生存期(OS)和真实世界最佳肿瘤缓解率(rwBTR)是主要终点。稳定的逆概率治疗加权(sIPTW)平衡了患者特征。
经过 sIPTW,纳入 450 例接受帕博西尼联合来曲唑治疗和 335 例接受来曲唑治疗的患者;中位年龄为 74.0 岁。帕博西尼联合来曲唑组 rwPFS 中位数为 22.2(95%CI,20.0-30.4)个月,来曲唑组为 15.8(12.9-18.9)个月(风险比,0.59[0.47-0.74];P<0.001)。帕博西尼联合来曲唑组中位 OS 未达到,来曲唑组为 43.4 个月(30.0-无法评估)(风险比,0.55[0.42-0.72];P<0.001)。rwPFS 和 OS 均未观察到年龄组(65-74 岁和≥75 岁)与治疗组之间的交互作用。帕博西尼联合来曲唑组 rwBTR 率显著高于来曲唑组(52.4% vs 22.1%;比值比,2.0[1.4-2.7];P<0.001)。
本分析表明,在一线治疗中,帕博西尼联合治疗是 HR+/HER2-MBC 老年患者的标准治疗选择。