Influence of green tea consumption on endoxifen steady-state concentration in breast cancer patients treated with tamoxifen

被引:16
作者
Braal, C. Louwrens [1 ]
Hussaarts, Koen G. A. M. [1 ]
Seuren, Lieke [1 ]
Oomen-de Hoop, Esther [1 ]
de Bruijn, Peter [1 ]
Buck, Stefan A. J. [1 ]
Bos, Monique E. M. M. [1 ]
Thijs-Visser, Martine F. [2 ]
Zuetenhorst, Hanneke J. M. [3 ]
Mathijssen-van Stein, Danielle [3 ]
Vastbinder, Mijntje B. [4 ]
van Leeuwen, Roelof W. F. [1 ,5 ]
van Gelder, Teun [6 ]
Koolen, Stijn L. W. [1 ,5 ]
Jager, Agnes [1 ]
Mathijssen, Ron H. J. [1 ]
机构
[1] Erasmus MC Canc Inst, Dept Med Oncol, Dr Molewaterpl 40,CN,POB 2040, NL-3015 CN Rotterdam, Netherlands
[2] Ikazia Hosp, Dept Med Oncol, Rotterdam, Netherlands
[3] Franciscus Gasthuis & Vlietland, Dept Internal Med, Schiedam, Netherlands
[4] IJsselland Hosp, Dept Internal Med, Capelle Aan Den Ijssel, Netherlands
[5] Erasmus MC, Dept Hosp Pharm, Rotterdam, Netherlands
[6] Leiden Univ, Med Ctr, Dept Clin Pharm & Toxicol, Leiden, Netherlands
关键词
Tamoxifen; Green tea extract; Epigallocatechin-3-gallate (EGCG); Herb-drug interaction; Pharmacokinetics; Toxicities; Breast cancer; EPIGALLOCATECHIN GALLATE; DRUG INTERACTIONS; PHARMACOKINETICS; CATECHINS; (-)-EPIGALLOCATECHIN-3-GALLATE; INDIVIDUALIZATION; BIOAVAILABILITY; COMPLEMENTARY; PREVENTION; INGESTION;
D O I
10.1007/s10549-020-05829-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Many cancer patients use additional herbs or supplements in combination with their anti-cancer therapy. Green tea-active ingredient epigallocatechin-3-gallate (EGCG)-is one of the most commonly used dietary supplements among breast cancer patients. EGCG may alter the metabolism of tamoxifen. Therefore, the aim of this study was to investigate the influence of green tea supplements on the pharmacokinetics of endoxifen; the most relevant active metabolite of tamoxifen. Methods In this single-center, randomized cross-over trial, effects of green tea capsules on endoxifen levels were evaluated. Patients treated with tamoxifen for at least 3 months were eligible for this study. After inclusion, patients were consecutively treated with tamoxifen monotherapy for 28 days and in combination with green tea supplements (1 g twice daily; containing 300 mg EGCG) for 14 days (or vice versa). Blood samples were collected on the last day of monotherapy or combination therapy. Area under the curve (AUC(0-24h)), maximum concentration (C-max) and minimum concentration (C-trough) were obtained from individual plasma concentration-time curves. Results No difference was found in geometric mean endoxifen AUC(0-24h)in the period with green tea versus tamoxifen monotherapy (- 0.4%; 95% CI - 8.6 to 8.5%;p = 0.92). Furthermore, no differences inC(max)(- 2.8%; - 10.6 to 5.6%;p = 0.47) norC(trough)(1.2%; - 7.3 to 10.5%;p = 0.77) were found. Moreover, no severe toxicity was reported during the whole study period. Conclusions This study demonstrated the absence of a pharmacokinetic interaction between green tea supplements and tamoxifen. Therefore, the use of green tea by patients with tamoxifen does not have to be discouraged.
引用
收藏
页码:107 / 113
页数:7
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