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BSA and ABCB1 polymorphism affect the pharmacokinetics of sunitinib and its active metabolite in Asian mRCC patients receiving an attenuated sunitinib dosing regimen
Chungnam Natl Univ, Coll Pharm, Taejon 305764, South Korea.;Natl Univ Singapore, Dept Pharm, Fac Sci, 18 Sci Dr 4,Block S4A, Singapore 117543, Singapore..
Natl Univ Singapore, Dept Pharm, Fac Sci, 18 Sci Dr 4,Block S4A, Singapore 117543, Singapore..
Natl Univ Singapore, Dept Pharm, Fac Sci, 18 Sci Dr 4,Block S4A, Singapore 117543, Singapore..
Chungnam Natl Univ, Coll Pharm, Taejon 305764, South Korea..
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2016 (Engelska)Ingår i: Cancer Chemotherapy and Pharmacology, ISSN 0344-5704, E-ISSN 1432-0843, Vol. 78, nr 3, s. 623-632Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

An attenuated dosing (AD) sunitinib regimen of 37.5 mg daily has been suggested to reduce the toxicity reported with the standard dosing regimen to metastatic renal cell carcinoma (mRCC) patients. The aim of this study was to characterize the population pharmacokinetic (PK) properties of sunitinib and SU12662, the active metabolite, in patients receiving the AD regimen and to ascertain significant covariates influencing PK parameters. Thirty-one mRCC patients receiving AD sunitinib regimen were included. Plasma samples were collected on day 29 of each treatment cycle after the start of the therapy. Nonlinear mixed-effects modeling was applied to estimate the population PK properties of sunitinib and SU12662 as well as the effect of covariates on PK parameters. Monte Carlo simulation was also performed to predict the total trough level (TTL) of sunitinib and SU12662. Sunitinib population means for CL/F and V (d) /F (central) were 13.8 L/h and 1720 L, respectively. SU12662 population means for CL/F and V (d) /F were 42.1 L/h and 1410 L, respectively. Body surface area (BSA) and ABCB1 polymorphism significantly influenced the CL/F variability of sunitinib: CL/F (parent) = 13.8 x exp((BSA - 1.75) x 2.08 + (ABCB1 (genotype) - 0.67) x 0.61), ABCB1-0: wild genotype, 1: mutant genotype. The effect size of ABCB1 mutant genotype and BSA greater than 1.75 m(2) in relation to sunitinib clearance was 31.14 % (p = 0.006) and 22.11 % (p = 0.011), respectively, relative to the reference group. Adjusting doses of sunitinib according to BSA and ABCB1 polymorphism in Asian mRCC patients may be recommended for sufficient attainment of a target TTL of sunitinib and its metabolite.

Ort, förlag, år, upplaga, sidor
2016. Vol. 78, nr 3, s. 623-632
Nyckelord [en]
Sunitinib, SU12662, Population pharmacokinetics, Metastatic renal cell carcinoma, Attenuated sunitinib dosing regimen, Body surface area, ABCB1 polymorphism
Nationell ämneskategori
Cancer och onkologi Farmakologi och toxikologi
Identifikatorer
URN: urn:nbn:se:uu:diva-305488DOI: 10.1007/s00280-016-3104-9ISI: 000383083100020PubMedID: 27485537OAI: oai:DiVA.org:uu-305488DiVA, id: diva2:1038503
Tillgänglig från: 2016-10-18 Skapad: 2016-10-18 Senast uppdaterad: 2018-01-14Bibliografiskt granskad

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Karlsson, Mats O.
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Institutionen för farmaceutisk biovetenskap
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Cancer Chemotherapy and Pharmacology
Cancer och onkologiFarmakologi och toxikologi

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