Pharmacokinetic study of the oral fluorouracil antitumor agent S-1 in patients with impaired renal function.


Journal

Cancer science
ISSN: 1349-7006
Titre abrégé: Cancer Sci
Pays: England
ID NLM: 101168776

Informations de publication

Date de publication:
Jun 2019
Historique:
received: 02 07 2018
revised: 11 03 2019
accepted: 28 03 2019
pubmed: 17 4 2019
medline: 25 6 2019
entrez: 17 4 2019
Statut: ppublish

Résumé

Although dose reduction of S-1 is recommended for patients with impaired renal function, dose modification for such patients has not been prospectively evaluated. The aim of the present study was to investigate the pharmacokinetic parameters of 5-fluorouracil, 5-chloro-2,4 dihydroxypyridine and oteracil potassium, and to review the recommended dose modification of S-1 in patients with renal impairment. We classified patients receiving S-1 into 4 groups according to their renal function, as measured using the Japanese estimated glomerular filtration rate (eGFR) equation. The daily S-1 dose was adjusted based on the patient's eGFR and body surface area. Blood samples were collected for pharmacokinetic analysis. A total of 33 patients were enrolled and classified into 4 groups as follows: 10 patients in cohort 1 (eGFR ≥ 80 mL/min/1.73 m

Identifiants

pubmed: 30989775
doi: 10.1111/cas.14025
pmc: PMC6550132
doi:

Substances chimiques

Drug Combinations 0
S 1 (combination) 150863-82-4
Tegafur 1548R74NSZ
Oxonic Acid 5VT6420TIG
Fluorouracil U3P01618RT

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1987-1994

Subventions

Organisme : Ministry of Health, Labour and Welfare
ID : 23-A-16

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© 2019 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association.

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Auteurs

Keiko Goto (K)

Department of Thoracic Oncology, National Cancer Center Hospital, Tokyo, Japan.
Department of Medical Oncology and Hematology, Kobe University Graduate School of Medicine, Kobe, Japan.

Yutaka Fujiwara (Y)

Department of Thoracic Oncology, National Cancer Center Hospital, Tokyo, Japan.
Department of Experimental Therapeutics, National Cancer Center Hospital, Shimane, Tokyo.
Division of Respiratory Medicine, Mitsui Memorial Hospital, Tokyo, Japan.

Takeshi Isobe (T)

Division of Medical Oncology and Respiratory Medicine, Department of Internal Medicine, Faculty of Medicine, Shimane University, Shimane, Japan.

Naoko Chayahara (N)

Department of Medical Oncology and Hematology, Kobe University Graduate School of Medicine, Kobe, Japan.

Naomi Kiyota (N)

Department of Medical Oncology and Hematology, Kobe University Graduate School of Medicine, Kobe, Japan.

Toru Mukohara (T)

Department of Medical Oncology and Hematology, Kobe University Graduate School of Medicine, Kobe, Japan.
Department of Breast and Medical Oncology, National Cancer Center Hospital East, Kashiwa, Japan.

Yukari Tsubata (Y)

Division of Medical Oncology and Respiratory Medicine, Department of Internal Medicine, Faculty of Medicine, Shimane University, Shimane, Japan.

Takamasa Hotta (T)

Division of Medical Oncology and Respiratory Medicine, Department of Internal Medicine, Faculty of Medicine, Shimane University, Shimane, Japan.

Kenji Tamura (K)

Department of Breast and Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.

Noboru Yamamoto (N)

Department of Thoracic Oncology, National Cancer Center Hospital, Tokyo, Japan.
Department of Experimental Therapeutics, National Cancer Center Hospital, Shimane, Tokyo.

Hironobu Minami (H)

Department of Medical Oncology and Hematology, Kobe University Graduate School of Medicine, Kobe, Japan.

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Classifications MeSH