TY - JOUR
T1 - Relationships between sunitinib plasma concentration and clinical outcomes in Japanese patients with metastatic renal cell carcinoma
AU - Takasaki, Shinya
AU - Kawasaki, Yoshihide
AU - Kikuchi, Masafumi
AU - Tanaka, Masaki
AU - Suzuka, Masato
AU - Noda, Aoi
AU - Sato, Yuji
AU - Yamashita, Shinichi
AU - Mitsuzuka, Koji
AU - Saito, Hideo
AU - Ito, Akihiro
AU - Yamaguchi, Hiroaki
AU - Arai, Yoichi
AU - Mano, Nariyasu
N1 - Publisher Copyright:
© 2018, Japan Society of Clinical Oncology.
PY - 2018/10/1
Y1 - 2018/10/1
N2 - Background: The aim was to investigate the relationships between total sunitinib plasma concentrations (sunitinib plus its active metabolite; N-desethyl sunitinib) and clinical outcomes in Japanese patients with metastatic renal cell carcinoma (mRCC). Methods: Twenty patients with mRCC were enrolled following treatment with sunitinib. To assess safety, the total sunitinib concentration range up to discontinuation of treatment and dosage reduction associated with adverse events within 6 weeks from initiating administration were analyzed. The longest administered sunitinib dosage was defined as the maintenance dose, and the relationship between total sunitinib concentration at the maintenance dosage and sunitinib efficacy was investigated. Results: Total sunitinib concentration was significantly higher in patients who discontinued treatment or had dosage reduction due to adverse events within 6 weeks after initiation of sunitinib than in patients who continued treatment with the initial dosage. The time to treatment failure, progression-free survival, and overall survival were better in patients with total sunitinib concentrations < 50 ng/mL than in those with concentrations ≥ 50 ng/mL. Conclusions: The present study demonstrated that the effective range of total sunitinib concentration in Japanese patients with mRCC was lower than 50–100 ng/mL which was previously reported. These results indicate that therapeutic drug monitoring could maintain the therapeutic effect of sunitinib while minimizing adverse events by personalizing sunitinib dosages for Japanese patients with mRCC.
AB - Background: The aim was to investigate the relationships between total sunitinib plasma concentrations (sunitinib plus its active metabolite; N-desethyl sunitinib) and clinical outcomes in Japanese patients with metastatic renal cell carcinoma (mRCC). Methods: Twenty patients with mRCC were enrolled following treatment with sunitinib. To assess safety, the total sunitinib concentration range up to discontinuation of treatment and dosage reduction associated with adverse events within 6 weeks from initiating administration were analyzed. The longest administered sunitinib dosage was defined as the maintenance dose, and the relationship between total sunitinib concentration at the maintenance dosage and sunitinib efficacy was investigated. Results: Total sunitinib concentration was significantly higher in patients who discontinued treatment or had dosage reduction due to adverse events within 6 weeks after initiation of sunitinib than in patients who continued treatment with the initial dosage. The time to treatment failure, progression-free survival, and overall survival were better in patients with total sunitinib concentrations < 50 ng/mL than in those with concentrations ≥ 50 ng/mL. Conclusions: The present study demonstrated that the effective range of total sunitinib concentration in Japanese patients with mRCC was lower than 50–100 ng/mL which was previously reported. These results indicate that therapeutic drug monitoring could maintain the therapeutic effect of sunitinib while minimizing adverse events by personalizing sunitinib dosages for Japanese patients with mRCC.
KW - Pharmacokinetics
KW - Renal cell carcinoma
KW - Sunitinib
KW - Therapeutic drug monitoring
KW - Tyrosine kinase inhibitor
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U2 - 10.1007/s10147-018-1302-7
DO - 10.1007/s10147-018-1302-7
M3 - Article
C2 - 29860539
AN - SCOPUS:85047933564
SN - 1341-9625
VL - 23
SP - 936
EP - 943
JO - International Journal of Clinical Oncology
JF - International Journal of Clinical Oncology
IS - 5
ER -