Skip to main content
Erschienen in: Breast Cancer Research and Treatment 1/2020

Open Access 16.08.2020 | Clinical Trial

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

verfasst von: C. Louwrens Braal, Koen G. A. M. Hussaarts, Lieke Seuren, Esther Oomen-de Hoop, Peter de Bruijn, Stefan A. J. Buck, Monique E. M. M. Bos, Martine F. Thijs-Visser, Hanneke J. M. Zuetenhorst, Daniëlle Mathijssen-van Stein, Mijntje B. Vastbinder, Roelof W. F. van Leeuwen, Teun van Gelder, Stijn L. W. Koolen, Agnes Jager, Ron H. J. Mathijssen

Erschienen in: Breast Cancer Research and Treatment | Ausgabe 1/2020

Einloggen, um Zugang zu erhalten

Abstract

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 (AUC0–24h), maximum concentration (Cmax) and minimum concentration (Ctrough) were obtained from individual plasma concentration–time curves.

Results

No difference was found in geometric mean endoxifen AUC0–24h in the period with green tea versus tamoxifen monotherapy (− 0.4%; 95% CI − 8.6 to 8.5%; p = 0.92). Furthermore, no differences in Cmax (− 2.8%; − 10.6 to 5.6%; p = 0.47) nor Ctrough (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.
Literatur
1.
Zurück zum Zitat Bray F et al (2018) (2018) Global Cancer Statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin 68(6):394–424CrossRef Bray F et al (2018) (2018) Global Cancer Statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin 68(6):394–424CrossRef
2.
Zurück zum Zitat Early Breast Cancer Trialists’ Collaborative Group (EBCTCG) (2005) Effects of chemotherapy and hormonal therapy for early breast cancer on recurrence and 15-year survival: an overview of the randomised trials. Lancet 365:1687–1717CrossRef Early Breast Cancer Trialists’ Collaborative Group (EBCTCG) (2005) Effects of chemotherapy and hormonal therapy for early breast cancer on recurrence and 15-year survival: an overview of the randomised trials. Lancet 365:1687–1717CrossRef
3.
Zurück zum Zitat Horneber M et al (2012) How many cancer patients use complementary and alternative medicine: a systematic review and metaanalysis. Integr Cancer Ther 11:187–203CrossRef Horneber M et al (2012) How many cancer patients use complementary and alternative medicine: a systematic review and metaanalysis. Integr Cancer Ther 11:187–203CrossRef
4.
Zurück zum Zitat Boon HS, Olatunde F, Zick SM (2007) Trends in complementary/alternative medicine use by breast cancer survivors: comparing survey data from 1998 and 2005. BMC Womens Health 7:4CrossRef Boon HS, Olatunde F, Zick SM (2007) Trends in complementary/alternative medicine use by breast cancer survivors: comparing survey data from 1998 and 2005. BMC Womens Health 7:4CrossRef
5.
Zurück zum Zitat Witt CM, Cardoso MJ (2016) Complementary and integrative medicine for breast cancer patients—evidence based practical recommendations. Breast 28:37–44CrossRef Witt CM, Cardoso MJ (2016) Complementary and integrative medicine for breast cancer patients—evidence based practical recommendations. Breast 28:37–44CrossRef
6.
Zurück zum Zitat Mathijssen RHJ, Sparreboom A, Verweij J (2014) Determining the optimal dose in the development of anticancer agents. Nat Rev Clin Oncol 11:272–281CrossRef Mathijssen RHJ, Sparreboom A, Verweij J (2014) Determining the optimal dose in the development of anticancer agents. Nat Rev Clin Oncol 11:272–281CrossRef
7.
Zurück zum Zitat Veerman GDM et al (2020) Clinical implications of food–drug interactions with small-molecule kinase inhibitors. Lancet Oncol 21:e265–e279CrossRef Veerman GDM et al (2020) Clinical implications of food–drug interactions with small-molecule kinase inhibitors. Lancet Oncol 21:e265–e279CrossRef
8.
Zurück zum Zitat Engdal S, Klepp O, Nilsen OG (2009) Identification and exploration of herb–drug combinations used by cancer patients. Integr Cancer Ther 8:29–36CrossRef Engdal S, Klepp O, Nilsen OG (2009) Identification and exploration of herb–drug combinations used by cancer patients. Integr Cancer Ther 8:29–36CrossRef
9.
Zurück zum Zitat Graham HN (1992) Green tea composition, consumption, and polyphenol chemistry. Prev Med 21:334–350CrossRef Graham HN (1992) Green tea composition, consumption, and polyphenol chemistry. Prev Med 21:334–350CrossRef
10.
Zurück zum Zitat Balentine DA, Wiseman SA, Bouwens LC (1997) The chemistry of tea flavonoids. Crit Rev Food Sci Nutr 37:693–704CrossRef Balentine DA, Wiseman SA, Bouwens LC (1997) The chemistry of tea flavonoids. Crit Rev Food Sci Nutr 37:693–704CrossRef
11.
Zurück zum Zitat Xu JZ, Yeung SYV, Chang Q, Huang Y, Chen Z-Y (2004) Comparison of antioxidant activity and bioavailability of tea epicatechins with their epimers. Br J Nutr 91(6):873–881CrossRef Xu JZ, Yeung SYV, Chang Q, Huang Y, Chen Z-Y (2004) Comparison of antioxidant activity and bioavailability of tea epicatechins with their epimers. Br J Nutr 91(6):873–881CrossRef
12.
Zurück zum Zitat Gormaz JG, Valls N, Sotomayor C, Turner T, Rodrigo R (2016) Potential role of polyphenols in the prevention of cardiovascular diseases: molecular bases. Curr Med Chem 23:115–128CrossRef Gormaz JG, Valls N, Sotomayor C, Turner T, Rodrigo R (2016) Potential role of polyphenols in the prevention of cardiovascular diseases: molecular bases. Curr Med Chem 23:115–128CrossRef
13.
Zurück zum Zitat Ju J, Lu G, Lambert JD, Yang CS (2007) Inhibition of carcinogenesis by tea constituents. Semin Cancer Biol 17:395–402CrossRef Ju J, Lu G, Lambert JD, Yang CS (2007) Inhibition of carcinogenesis by tea constituents. Semin Cancer Biol 17:395–402CrossRef
14.
Zurück zum Zitat Miyata Y, Shida Y, Hakariya T, Sakai H (2019) Anti-cancer effects of green tea polyphenols against prostate cancer. Molecules 24(1):193.CrossRef Miyata Y, Shida Y, Hakariya T, Sakai H (2019) Anti-cancer effects of green tea polyphenols against prostate cancer. Molecules 24(1):193.CrossRef
15.
Zurück zum Zitat Yang CS et al (2011) Cancer prevention by tea: evidence from laboratory studies. Pharmacol Res 64:113–122CrossRef Yang CS et al (2011) Cancer prevention by tea: evidence from laboratory studies. Pharmacol Res 64:113–122CrossRef
16.
Zurück zum Zitat Schröder L et al (2019) Effects of green tea, matcha tea and their components epigallocatechin gallate and quercetin on MCF-7 and MDA-MB-231 breast carcinoma cells. Oncol Rep 41(1):387–396PubMed Schröder L et al (2019) Effects of green tea, matcha tea and their components epigallocatechin gallate and quercetin on MCF-7 and MDA-MB-231 breast carcinoma cells. Oncol Rep 41(1):387–396PubMed
17.
Zurück zum Zitat Bigelow RLH, Cardelli JA (2006) The green tea catechins, (−)-Epigallocatechin-3-gallate (EGCG) and (−)-Epicatechin-3-gallate (ECG), inhibit HGF/Met signaling in immortalized and tumorigenic breast epithelial cells. Oncogene 25:1922–1930CrossRef Bigelow RLH, Cardelli JA (2006) The green tea catechins, (−)-Epigallocatechin-3-gallate (EGCG) and (−)-Epicatechin-3-gallate (ECG), inhibit HGF/Met signaling in immortalized and tumorigenic breast epithelial cells. Oncogene 25:1922–1930CrossRef
18.
Zurück zum Zitat Misaka S et al (2014) Green tea ingestion greatly reduces plasma concentrations of nadolol in healthy subjects. Clin Pharmacol Ther 95:432–438CrossRef Misaka S et al (2014) Green tea ingestion greatly reduces plasma concentrations of nadolol in healthy subjects. Clin Pharmacol Ther 95:432–438CrossRef
19.
Zurück zum Zitat Kim T-E et al (2018) Effect of green tea catechins on the pharmacokinetics of digoxin in humans. Drug Des Dev Ther 12:2139–2147CrossRef Kim T-E et al (2018) Effect of green tea catechins on the pharmacokinetics of digoxin in humans. Drug Des Dev Ther 12:2139–2147CrossRef
20.
Zurück zum Zitat Alemdaroglu NC, Dietz U, Wolffram S, Spahn-Langguth H, Langguth P (2008) Influence of green and black tea on folic acid pharmacokinetics in healthy volunteers: potential risk of diminished folic acid bioavailability. Biopharm Drug Dispos 29:335–348CrossRef Alemdaroglu NC, Dietz U, Wolffram S, Spahn-Langguth H, Langguth P (2008) Influence of green and black tea on folic acid pharmacokinetics in healthy volunteers: potential risk of diminished folic acid bioavailability. Biopharm Drug Dispos 29:335–348CrossRef
21.
Zurück zum Zitat Misaka S et al (2013) Green tea extract affects the cytochrome P450 3A activity and pharmacokinetics of simvastatin in rats. Drug Metab Pharmacokinet 28:514–518CrossRef Misaka S et al (2013) Green tea extract affects the cytochrome P450 3A activity and pharmacokinetics of simvastatin in rats. Drug Metab Pharmacokinet 28:514–518CrossRef
22.
Zurück zum Zitat Chung J-H, Choi D-H, Choi J-S (2009) Effects of oral epigallocatechin gallate on the oral pharmacokinetics of verapamil in rats. Biopharm Drug Dispos 30:90–93CrossRef Chung J-H, Choi D-H, Choi J-S (2009) Effects of oral epigallocatechin gallate on the oral pharmacokinetics of verapamil in rats. Biopharm Drug Dispos 30:90–93CrossRef
23.
Zurück zum Zitat Albassam AA, Markowitz JS (2017) An appraisal of drug–drug interactions with green tea (Camellia sinensis). Planta Med 83:496–508CrossRef Albassam AA, Markowitz JS (2017) An appraisal of drug–drug interactions with green tea (Camellia sinensis). Planta Med 83:496–508CrossRef
24.
Zurück zum Zitat Satoh T, Fujisawa H, Nakamura A, Takahashi N, Watanabe K (2016) Inhibitory effects of eight green tea catechins on cytochrome P450 1A2, 2C9, 2D6, and 3A4 activities. J Pharm 19:188–197 Satoh T, Fujisawa H, Nakamura A, Takahashi N, Watanabe K (2016) Inhibitory effects of eight green tea catechins on cytochrome P450 1A2, 2C9, 2D6, and 3A4 activities. J Pharm 19:188–197
25.
Zurück zum Zitat Nikaidou S et al (2005) Effect of components of green tea extracts, caffeine and catechins on hepatic drug metabolizing enzyme activities and mutagenic transformation of carcinogens. J Vet Res 52:185–192 Nikaidou S et al (2005) Effect of components of green tea extracts, caffeine and catechins on hepatic drug metabolizing enzyme activities and mutagenic transformation of carcinogens. J Vet Res 52:185–192
26.
Zurück zum Zitat Farabegoli F, Papi A, Bartolini G, Ostan R, Orlandi M (2010) (−)-Epigallocatechin-3-gallate downregulates Pg-P and BCRP in a tamoxifen resistant MCF-7 cell line. Phytomedicine 17(5):356–362CrossRef Farabegoli F, Papi A, Bartolini G, Ostan R, Orlandi M (2010) (−)-Epigallocatechin-3-gallate downregulates Pg-P and BCRP in a tamoxifen resistant MCF-7 cell line. Phytomedicine 17(5):356–362CrossRef
27.
Zurück zum Zitat Knop J et al (2015) Inhibitory effects of green tea and (−)-epigallocatechin gallate on transport by OATP1B1, OATP1B3, OCT1, OCT2, MATE1, MATE2-K and P-glycoprotein. PLoS ONE 10:e0139370CrossRef Knop J et al (2015) Inhibitory effects of green tea and (−)-epigallocatechin gallate on transport by OATP1B1, OATP1B3, OCT1, OCT2, MATE1, MATE2-K and P-glycoprotein. PLoS ONE 10:e0139370CrossRef
28.
Zurück zum Zitat Jordan VC (2007) New insights into the metabolism of tamoxifen and its role in the treatment and prevention of breast cancer. Steroids 72(13):829–842CrossRef Jordan VC (2007) New insights into the metabolism of tamoxifen and its role in the treatment and prevention of breast cancer. Steroids 72(13):829–842CrossRef
29.
Zurück zum Zitat Del Re M et al (2016) Pharmacogenetics of CYP2D6 and tamoxifen therapy: light at the end of the tunnel? Pharmacol Res 107:398–406CrossRef Del Re M et al (2016) Pharmacogenetics of CYP2D6 and tamoxifen therapy: light at the end of the tunnel? Pharmacol Res 107:398–406CrossRef
30.
Zurück zum Zitat Binkhorst L, Mathijssen RHJ, Jager A, van Gelder T (2015) Individualization of tamoxifen therapy: much more than just CYP2D6 genotyping. Cancer Treat Rev 41:289–299CrossRef Binkhorst L, Mathijssen RHJ, Jager A, van Gelder T (2015) Individualization of tamoxifen therapy: much more than just CYP2D6 genotyping. Cancer Treat Rev 41:289–299CrossRef
31.
Zurück zum Zitat Binkhorst L, van Gelder T, Mathijssen RH (2012) Individualization of tamoxifen treatment for breast carcinoma. Clin Pharmacol Ther 92(4):431–433CrossRef Binkhorst L, van Gelder T, Mathijssen RH (2012) Individualization of tamoxifen treatment for breast carcinoma. Clin Pharmacol Ther 92(4):431–433CrossRef
32.
Zurück zum Zitat Hussaarts KGAM et al (2019) Impact of curcumin (with or without piperine) on the pharmacokinetics of tamoxifen. Cancers (Basel) 11(3):403CrossRef Hussaarts KGAM et al (2019) Impact of curcumin (with or without piperine) on the pharmacokinetics of tamoxifen. Cancers (Basel) 11(3):403CrossRef
34.
Zurück zum Zitat Qian F, Wei D, Zhang Q, Yang S (2005) Modulation of P-glycoprotein function and reversal of multidrug resistance by (−)-epigallocatechin gallate in human cancer cells. Biomed Pharmacother 59:64–69CrossRef Qian F, Wei D, Zhang Q, Yang S (2005) Modulation of P-glycoprotein function and reversal of multidrug resistance by (−)-epigallocatechin gallate in human cancer cells. Biomed Pharmacother 59:64–69CrossRef
35.
Zurück zum Zitat Shin S-C, Choi J-S (2009) Effects of epigallocatechin gallate on the oral bioavailability and pharmacokinetics of tamoxifen and its main metabolite, 4-hydroxytamoxifen, in rats. Anticancer Drugs 20:584–588CrossRef Shin S-C, Choi J-S (2009) Effects of epigallocatechin gallate on the oral bioavailability and pharmacokinetics of tamoxifen and its main metabolite, 4-hydroxytamoxifen, in rats. Anticancer Drugs 20:584–588CrossRef
36.
Zurück zum Zitat Hu J, Webster D, Cao J, Shao A (2018) The safety of green tea and green tea extract consumption in adults—results of a systematic review. Regul Toxicol Pharmacol 95:412–433CrossRef Hu J, Webster D, Cao J, Shao A (2018) The safety of green tea and green tea extract consumption in adults—results of a systematic review. Regul Toxicol Pharmacol 95:412–433CrossRef
37.
Zurück zum Zitat Crew KD et al (2012) Phase IB randomized, double-blinded, placebo-controlled, dose escalation study of polyphenon E in women with hormone receptor-negative breast cancer. Cancer Prev Res 5:1144–1154CrossRef Crew KD et al (2012) Phase IB randomized, double-blinded, placebo-controlled, dose escalation study of polyphenon E in women with hormone receptor-negative breast cancer. Cancer Prev Res 5:1144–1154CrossRef
39.
Zurück zum Zitat Stingl JC et al (2011) Protocol for minimizing the risk of metachronous adenomas of the colorectum with green tea extract (MIRACLE): a randomised controlled trial of green tea extract versus placebo for nutriprevention of metachronous colon adenomas in the elderly population. BMC Cancer 11:360CrossRef Stingl JC et al (2011) Protocol for minimizing the risk of metachronous adenomas of the colorectum with green tea extract (MIRACLE): a randomised controlled trial of green tea extract versus placebo for nutriprevention of metachronous colon adenomas in the elderly population. BMC Cancer 11:360CrossRef
40.
Zurück zum Zitat Bonkovsky HL (2006) Hepatotoxicity associated with supplements containing Chinese green tea (Camellia sinensis). Ann Intern Med 144:68–71CrossRef Bonkovsky HL (2006) Hepatotoxicity associated with supplements containing Chinese green tea (Camellia sinensis). Ann Intern Med 144:68–71CrossRef
41.
Zurück zum Zitat Scholl C et al (2018) Population nutrikinetics of green tea extract. PLoS ONE 13:e0193074CrossRef Scholl C et al (2018) Population nutrikinetics of green tea extract. PLoS ONE 13:e0193074CrossRef
42.
Zurück zum Zitat Lee M-J et al (2002) Pharmacokinetics of tea catechins after ingestion of green tea and (−)-epigallocatechin-3-gallate by humans: formation of different metabolites and individual variability. Cancer Epidemiol Biomark Prev 11:1025–1032 Lee M-J et al (2002) Pharmacokinetics of tea catechins after ingestion of green tea and (−)-epigallocatechin-3-gallate by humans: formation of different metabolites and individual variability. Cancer Epidemiol Biomark Prev 11:1025–1032
Metadaten
Titel
Influence of green tea consumption on endoxifen steady-state concentration in breast cancer patients treated with tamoxifen
verfasst von
C. Louwrens Braal
Koen G. A. M. Hussaarts
Lieke Seuren
Esther Oomen-de Hoop
Peter de Bruijn
Stefan A. J. Buck
Monique E. M. M. Bos
Martine F. Thijs-Visser
Hanneke J. M. Zuetenhorst
Daniëlle Mathijssen-van Stein
Mijntje B. Vastbinder
Roelof W. F. van Leeuwen
Teun van Gelder
Stijn L. W. Koolen
Agnes Jager
Ron H. J. Mathijssen
Publikationsdatum
16.08.2020
Verlag
Springer US
Erschienen in
Breast Cancer Research and Treatment / Ausgabe 1/2020
Print ISSN: 0167-6806
Elektronische ISSN: 1573-7217
DOI
https://doi.org/10.1007/s10549-020-05829-6

Weitere Artikel der Ausgabe 1/2020

Breast Cancer Research and Treatment 1/2020 Zur Ausgabe

Erhebliches Risiko für Kehlkopfkrebs bei mäßiger Dysplasie

29.05.2024 Larynxkarzinom Nachrichten

Fast ein Viertel der Personen mit mäßig dysplastischen Stimmlippenläsionen entwickelt einen Kehlkopftumor. Solche Personen benötigen daher eine besonders enge ärztliche Überwachung.

15% bedauern gewählte Blasenkrebs-Therapie

29.05.2024 Urothelkarzinom Nachrichten

Ob Patienten und Patientinnen mit neu diagnostiziertem Blasenkrebs ein Jahr später Bedauern über die Therapieentscheidung empfinden, wird einer Studie aus England zufolge von der Radikalität und dem Erfolg des Eingriffs beeinflusst.

Erhöhtes Risiko fürs Herz unter Checkpointhemmer-Therapie

28.05.2024 Nebenwirkungen der Krebstherapie Nachrichten

Kardiotoxische Nebenwirkungen einer Therapie mit Immuncheckpointhemmern mögen selten sein – wenn sie aber auftreten, wird es für Patienten oft lebensgefährlich. Voruntersuchung und Monitoring sind daher obligat.

Costims – das nächste heiße Ding in der Krebstherapie?

28.05.2024 Onkologische Immuntherapie Nachrichten

„Kalte“ Tumoren werden heiß – CD28-kostimulatorische Antikörper sollen dies ermöglichen. Am besten könnten diese in Kombination mit BiTEs und Checkpointhemmern wirken. Erste klinische Studien laufen bereits.

Update Onkologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.