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Published in: Cancer Chemotherapy and Pharmacology 2/2021

Open Access 01-08-2021 | Solid Tumor | Original Article

Pharmacokinetics and safety of rucaparib in patients with advanced solid tumors and hepatic impairment

Authors: Nikolay Grechko, Viera Skarbova, Monika Tomaszewska-Kiecana, Rodryg Ramlau, Piotr Centkowski, Yvette Drew, Rafal Dziadziuszko, Milada Zemanova, Jeri Beltman, Eileen Nash, Jenn Habeck, Mingxiang Liao, Jim Xiao

Published in: Cancer Chemotherapy and Pharmacology | Issue 2/2021

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Abstract

Purpose

The poly(ADP-ribose) polymerase inhibitor rucaparib is approved for the treatment of patients with recurrent ovarian and metastatic castration-resistant prostate cancer; however, limited data are available on its use in patients with hepatic dysfunction. This study investigated whether hepatic impairment affects the pharmacokinetics, safety, and tolerability of rucaparib in patients with advanced solid tumors.

Methods

Patients with normal hepatic function or moderate hepatic impairment according to the National Cancer Institute Organ Dysfunction Working Group (NCI-ODWG) criteria were enrolled and received a single oral dose of rucaparib 600 mg. Concentrations of rucaparib and its metabolite M324 in plasma and urine were measured. Pharmacokinetic parameters were compared between hepatic function groups, and safety and tolerability were assessed.

Results

Sixteen patients were enrolled (n = 8 per group). Rucaparib maximum concentration (Cmax) was similar, while the area under the concentration–time curve from time 0 to infinity (AUC0–inf) was mildly higher in the moderate hepatic impairment group than in the normal control group (geometric mean ratio, 1.446 [90% CI 0.668–3.131]); similar trends were observed for M324. Eight (50%) patients experienced ≥ 1 treatment-emergent adverse event (TEAE); 2 had normal hepatic function and 6 had moderate hepatic impairment.

Conclusion

Patients with moderate hepatic impairment showed mildly increased AUC0–inf for rucaparib compared to patients with normal hepatic function. Although more patients with moderate hepatic impairment experienced TEAEs, only 2 TEAEs were considered treatment related. These results suggest no starting dose adjustment is necessary for patients with moderate hepatic impairment; however, close safety monitoring is warranted.
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Literature
8.
go back to reference Xiao JJ, Green M, Ma SC, Goble S, Giordano H, Maloney L, Harding TC (2017) Population pharmacokinetics (PK) of rucaparib (CO-338) in patients with advanced ovarian cancer (AOC) or other solid tumors. Presented at: American Society for Clinical Pharmacology and Therapeutics (ASCPT) 2017 Annual Meeting; March 15–18, 2017; Washington, DC Xiao JJ, Green M, Ma SC, Goble S, Giordano H, Maloney L, Harding TC (2017) Population pharmacokinetics (PK) of rucaparib (CO-338) in patients with advanced ovarian cancer (AOC) or other solid tumors. Presented at: American Society for Clinical Pharmacology and Therapeutics (ASCPT) 2017 Annual Meeting; March 15–18, 2017; Washington, DC
Metadata
Title
Pharmacokinetics and safety of rucaparib in patients with advanced solid tumors and hepatic impairment
Authors
Nikolay Grechko
Viera Skarbova
Monika Tomaszewska-Kiecana
Rodryg Ramlau
Piotr Centkowski
Yvette Drew
Rafal Dziadziuszko
Milada Zemanova
Jeri Beltman
Eileen Nash
Jenn Habeck
Mingxiang Liao
Jim Xiao
Publication date
01-08-2021
Publisher
Springer Berlin Heidelberg
Published in
Cancer Chemotherapy and Pharmacology / Issue 2/2021
Print ISSN: 0344-5704
Electronic ISSN: 1432-0843
DOI
https://doi.org/10.1007/s00280-021-04278-2

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