Division of Pharmaceutical Care Sciences, Center for Social Pharmacy and Pharmaceutical Care Sciences, Keio University Faculty of Pharmacy, Tokyo, Japan.
Department of Industrial Engineering and Economics, Tokyo Institute of Technology, Tokyo, Japan.
Oncologist. 2024 Jun 3;29(6):e741-e749. doi: 10.1093/oncolo/oyae015.
Proton pump inhibitors (PPIs) reduce the bioavailability of several anticancer drugs. The impact of PPIs co-administered with cyclin-dependent kinase 4 and 6 inhibitors is controversial. We aimed to clarify whether the concomitant use of PPIs impacts palbociclib and abemaciclib effectiveness in breast cancer treatment.
This multicenter, retrospective, observational study, conducted across 4 medical institutions in Japan, consecutively included patients with endocrine-resistant metastatic breast cancer, receiving palbociclib or abemaciclib between December 2017 and August 2022. Propensity score-matched analyses were performed. Treatment efficacy and safety with and without PPIs were compared. Progression-free survival and overall survival were estimated using the Kaplan-Meier method and compared using a log-rank test. A Cox proportional hazards model was used to estimate the hazard ratio.
The study included 240 patients. After 1:1 matching, 112 patients were treated with and without PPIs. The median progression-free survival period was 1.2 years in the PPI group and 1.3 years in the non-PPI group (hazard ratio, 1.19; 95% CI, 0.70-2.02). The median overall survival period was 3.6 years in the PPI group, whereas it was not reached in the non-PPI group (hazard ratio, 1.23; 95% CI, 0.61-2.47). Consistent results were obtained for subgroups receiving palbociclib (n = 177) and abemaciclib (n = 63) without propensity score matching. Adverse event incidence and severity were similar in both groups.
The effectiveness of cyclin-dependent kinase 4/6 inhibitors is unlikely to be affected by concomitant PPI use. Future prospective pharmacokinetic studies are warranted.
质子泵抑制剂(PPIs)会降低几种抗癌药物的生物利用度。与细胞周期蛋白依赖性激酶 4 和 6 抑制剂联合使用的影响存在争议。我们旨在阐明 PPI 的联合使用是否会影响 CDK4/6 抑制剂在乳腺癌治疗中的疗效。
这是一项在日本 4 家医疗机构进行的多中心、回顾性、观察性研究,连续纳入了 2017 年 12 月至 2022 年 8 月期间接受帕博西尼或阿贝西利治疗的内分泌耐药转移性乳腺癌患者。进行了倾向评分匹配分析。比较了有无 PPI 时的治疗效果和安全性。采用 Kaplan-Meier 法估计无进展生存期和总生存期,并采用对数秩检验进行比较。采用 Cox 比例风险模型估计风险比。
该研究纳入了 240 例患者。经过 1:1 匹配后,有 112 例患者接受了 PPI 治疗和无 PPI 治疗。PPI 组的中位无进展生存期为 1.2 年,无 PPI 组为 1.3 年(风险比,1.19;95%CI,0.70-2.02)。PPI 组的中位总生存期为 3.6 年,而无 PPI 组尚未达到(风险比,1.23;95%CI,0.61-2.47)。在未进行倾向评分匹配的情况下,接受帕博西尼(n=177)和阿贝西利(n=63)治疗的亚组也得到了一致的结果。两组的不良事件发生率和严重程度相似。
细胞周期蛋白依赖性激酶 4/6 抑制剂的疗效不太可能受到同时使用 PPI 的影响。需要进一步开展前瞻性药代动力学研究。