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在日本患者中,白蛋白-胆红素分级与regorafenib 及其代谢物 M-2 和 M-5 在稳态时的血浆谷浓度之间的关系。

Association between albumin-bilirubin grade and plasma trough concentrations of regorafenib and its metabolites M-2 and M-5 at steady-state in Japanese patients.

机构信息

Department of Pharmacy, Akita University Hospital, Akita, Japan.

Department of Clinical Oncology, Akita University, Akita, Japan.

出版信息

Invest New Drugs. 2024 Jun;42(3):252-260. doi: 10.1007/s10637-024-01429-z. Epub 2024 Mar 22.

Abstract

The aim of the present study was to determine whether the trough plasma concentrations (C) of regorafenib and its metabolites, the N-oxide metabolite (M-2) and the desmethyl N-oxide metabolite (M-5), in 21 patients receiving regorafenib therapy were affected by albumin-bilirubin (ALBI) grade. Regorafenib was administered at dosages ranging from 40 to 160 mg once daily on a 3-week-on, 1-week-off cycle. C values of regorafenib and its major metabolites were measured by high-performance liquid chromatography on day 8 after treatment initiation. The C values of regorafenib and metabolites M-2 and M-5 were significantly lower in patients with ALBI grade 2 as compared with grade 1 (P = 0.023, 0.003 and 0.017, respectively). The total C of regorafenib and its metabolites was significantly higher in ALBI grade 1 patients relative to grade 2 (3.489 μg/mL vs. 1.48 μg/mL; P = 0.009). The median relative dose intensity (RDI) of patients categorized as ALBI grade 2 was significantly lower than that of grade 1 patients (21.9% vs. 62.9%; P = 0.006). In 15 colorectal cancer patients among the total 21 patients, patients with ALBI grade 2 (n = 9) had a significantly shorter median overall survival time than patients with grade 1 (n = 6; P = 0.013). Administering a low dose of regorafenib to patients with ALBI grade 2 reduces the RDI of regorafenib and lowers treatment efficacy, as an appropriate C of regorafenib is not maintained. Monitoring the C of regorafenib regularly is necessary to guide dose adjustment.

摘要

本研究旨在确定接受regorafenib 治疗的 21 例患者的regorafenib 及其代谢物 N-氧化物代谢物(M-2)和去甲基 N-氧化物代谢物(M-5)的谷浓度(C)是否受白蛋白-胆红素(ALBI)分级的影响。regorafenib 剂量范围为 40-160mg,每日一次,每 3 周为一个周期,1 周停药。治疗开始后第 8 天,采用高效液相色谱法测定 regorafenib 及其主要代谢物的 C 值。与 ALBI 分级 1 相比,ALBI 分级 2 的患者 regorafenib 和代谢物 M-2 和 M-5 的 C 值显著降低(P=0.023、0.003 和 0.017)。ALBI 分级 1 患者的 regorafenib 和代谢物总 C 值明显高于 ALBI 分级 2 患者(3.489μg/ml 比 1.48μg/ml;P=0.009)。ALBI 分级 2 患者的中位相对剂量强度(RDI)明显低于 ALBI 分级 1 患者(21.9%比 62.9%;P=0.006)。在 21 例患者中,15 例为结直肠癌患者,其中 ALBI 分级 2 患者(n=9)的中位总生存期明显短于 ALBI 分级 1 患者(n=6;P=0.013)。对于 ALBI 分级 2 的患者,给予低剂量 regorafenib 可降低 regorafenib 的 RDI,并降低治疗效果,因为无法维持适当的 regorafenib C 值。需要定期监测 regorafenib 的 C 值,以指导剂量调整。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b205/11164767/311dd36d9dbe/10637_2024_1429_Fig1_HTML.jpg

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