Division of Hematology and Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA, 19104, USA.
Ontada, 6555 State Highway 161, Irving, TX, 75039, USA.
Target Oncol. 2023 Jul;18(4):543-558. doi: 10.1007/s11523-023-00979-1. Epub 2023 Jul 10.
Limited real-world data exist regarding the efficacy of palbociclib in combination with endocrine therapy in pre/perimenopausal women with metastatic breast cancer.
We aimed to compare real-world tumor responses among pre/perimenopausal women who initiated palbociclib plus an aromatase inhibitor (AI) or AI monotherapy as first-line treatment for hormone receptor-positive/human epidermal growth factor receptor 2-negative metastatic breast cancer.
This retrospective observational cohort study (NCT05012644) used electronic health record data from The US Oncology Network. Tumor responses were determined based on treating clinicians' assessments of radiologic evidence for changes in disease burden. Normalized inverse probability treatment weighting was used to balance baseline characteristics between treatment cohorts.
Of 196 pre/perimenopausal women, 116 and 80 were in the palbociclib plus AI cohort and AI cohort, respectively. Real-world response rates (complete or partial response) were 52.1% and 46.2%, respectively (odds ratio, 1.27 [95% confidence interval 0.72‒2.24]). Among patients with one or more tumor assessments on treatment, real-world response rates were 60.0% in the palbociclib plus AI cohort (n = 103) and 49.9% in the AI cohort (n = 71; odds ratio, 1.51 [95% confidence interval 0.82‒2.77]).
This real-world analysis suggests that pre/perimenopausal patients with hormone receptor-positive/human epidermal growth factor receptor 2-negative metastatic breast cancer appear more likely to respond to palbociclib plus AI versus AI alone as first-line therapy, which may support the combination as a standard-of-care treatment for this patient population.
关于转移性乳腺癌绝经前/围绝经期妇女中帕博西尼联合内分泌治疗的疗效,真实世界的数据有限。
我们旨在比较绝经前/围绝经期妇女中,作为激素受体阳性/人表皮生长因子受体 2 阴性转移性乳腺癌一线治疗,起始帕博西尼联合芳香化酶抑制剂(AI)或 AI 单药治疗的真实肿瘤应答情况。
这项回顾性观察性队列研究(NCT05012644)使用了美国肿瘤网络的电子健康记录数据。根据治疗临床医生评估疾病负担变化的放射学证据来确定肿瘤应答情况。使用标准化逆概率处理加权来平衡治疗队列之间的基线特征。
在 196 例绝经前/围绝经期妇女中,116 例和 80 例分别入组帕博西尼联合 AI 组和 AI 组。真实世界的反应率(完全或部分反应)分别为 52.1%和 46.2%(优势比,1.27[95%置信区间 0.72-2.24])。在接受治疗的患者中,有一个或多个肿瘤评估的患者中,帕博西尼联合 AI 组的真实世界反应率为 60.0%(n=103),AI 组为 49.9%(n=71;优势比,1.51[95%置信区间 0.82-2.77])。
这项真实世界分析表明,激素受体阳性/人表皮生长因子受体 2 阴性转移性乳腺癌绝经前/围绝经期妇女对帕博西尼联合 AI 治疗比 AI 单药治疗作为一线治疗更有可能产生应答,这可能支持该联合治疗作为该患者人群的标准治疗方案。