Çağlayan Dilek, Koçak Mehmet Zahid, Geredeli Çağlayan, Tatlı Ali Murat, Göksu Sema Sezgin, Eryılmaz Melek Karakurt, Araz Murat, Artaç Mehmet
Department of Medical Oncology, Meram Faculty of Medicine, Necmettin Erbakan University, Konya, Turkey.
Department of Medical Oncology, Okmeydani Training and Research Hospital, Istanbul, Turkey.
Eur J Clin Pharmacol. 2023 Feb;79(2):243-248. doi: 10.1007/s00228-022-03435-7. Epub 2022 Dec 15.
To evaluate the difference of progression free survival between the patients using concomitant proton pump inhibitors and non-users in the patients using CDK 4/6 inhibitors with HR + and HER2 negative mBC.
We included 86 patients with HR + and HER 2 negative mBC treated with CDK 4/6 inhibitors in this study. Patients were divided into two categories according to their status of PPI use. The primary end points was progression free survival (PFS). We compared PPI users and non-users.
Forty-five (52.3%) patients used a PPI concomitantly with a CDK 4/6 inhibitor, and 41 (47.7%) did not. The median duration of follow-up was 10.68 (1.94-27.56) months. Of the patients, 50 (58.1%) palbociclib and 36 (41.9%) received ribociclib. The median progression free survival (mPFS) was 10.9 months (95% CI: 7.5-14.27) in the group with concomitant PPI use with a CDK 4/6 inhibitor, whereas the median progression free survival could not be reached in the group without concomitant PPI use (p = 0.04). In addition, concomitant PPI use with palbociclib was associated with a shorter PFS; there was no significant difference between the concomitant PPI users and non-users in terms of PFS in the patients using ribociclib.
Palbociclib and ribociclib are weak base drugs so their bioavailability is pH-dependent. PPIs can affect their solubility and their concentration in the plasma. Therefore, we must avoid concomitant use of PPIs and CDK 4/6 inhibitors. If we need to use concomitant PPI and CDK 4/6 inhibitors, we should prefer ribociclib than palbociclib.
评估在使用细胞周期蛋白依赖性激酶4/6(CDK 4/6)抑制剂的激素受体阳性(HR +)、人表皮生长因子受体2阴性(HER2阴性)转移性乳腺癌(mBC)患者中,同时使用质子泵抑制剂(PPI)的患者与未使用PPI的患者之间无进展生存期的差异。
本研究纳入了86例接受CDK 4/6抑制剂治疗的HR +、HER2阴性mBC患者。根据患者使用PPI的情况将其分为两类。主要终点是无进展生存期(PFS)。我们比较了使用PPI的患者和未使用PPI的患者。
45例(52.3%)患者在使用CDK 4/6抑制剂的同时使用了PPI,41例(47.7%)未使用。中位随访时间为10.68(1.94 - 27.56)个月。在这些患者中,50例(58.1%)使用了哌柏西利,36例(41.9%)使用了瑞博西尼。在同时使用PPI和CDK 4/6抑制剂的组中,中位无进展生存期(mPFS)为10.9个月(95%置信区间:7.5 - 14.27),而在未同时使用PPI的组中,中位无进展生存期未达到(p = 0.04)。此外,同时使用PPI和哌柏西利与较短的PFS相关;在使用瑞博西尼的患者中,同时使用PPI的患者和未使用PPI的患者在PFS方面无显著差异。
哌柏西利和瑞博西尼是弱碱性药物,因此它们的生物利用度依赖于pH值。PPI会影响它们的溶解度及其在血浆中的浓度。因此,我们必须避免同时使用PPI和CDK 4/6抑制剂。如果需要同时使用PPI和CDK 4/6抑制剂,与哌柏西利相比,我们应优先选择瑞博西尼。