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.
Kazuma FujitaDaiki TaguchiKoji FukudaTaichi YoshidaKazuhiro ShimazuHanae ShinozakiHiroyuki ShibataMasatomo MiuraPublished in: Investigational new drugs (2024)
The aim of the present study was to determine whether the trough plasma concentrations (C 0 ) 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 0 values of regorafenib and its major metabolites were measured by high-performance liquid chromatography on day 8 after treatment initiation. The C 0 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 0 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 0 of regorafenib is not maintained. Monitoring the C 0 of regorafenib regularly is necessary to guide dose adjustment.
Keyphrases
- end stage renal disease
- metastatic colorectal cancer
- ejection fraction
- low dose
- newly diagnosed
- chronic kidney disease
- ms ms
- peritoneal dialysis
- prognostic factors
- stem cells
- high performance liquid chromatography
- clinical trial
- mass spectrometry
- physical activity
- bone marrow
- patient reported
- solid phase extraction
- high intensity
- replacement therapy