The Effect of Fucoidan on the Pharmacokinetics of Letrozole and Tamoxifen in Patients With Breast Cancer

Background: Although the use of complementary and alternative medicines is widespread in cancer patients, clinical evidence of their benefits is sparse. Furthermore, while they are often assumed to be safe with regard to concurrent use of anticancer therapies, few studies have been carried out to in...

Full description

Bibliographic Details
Main Authors: Shreya Tocaciu BDS, MBBS, Lesley J. Oliver BAppSc, Ray M. Lowenthal MD, FRACP, Gregory M. Peterson PhD, MBA, Rahul Patel PhD, Madhur Shastri PhD, Georgia McGuinness PhD, Inger Olesen MBBS, FRACP, J. Helen Fitton PhD
Format: Article
Language:English
Published: SAGE Publishing 2018-03-01
Series:Integrative Cancer Therapies
Online Access:https://doi.org/10.1177/1534735416684014
_version_ 1819292132962205696
author Shreya Tocaciu BDS, MBBS
Lesley J. Oliver BAppSc
Ray M. Lowenthal MD, FRACP
Gregory M. Peterson PhD, MBA
Rahul Patel PhD
Madhur Shastri PhD
Georgia McGuinness PhD
Inger Olesen MBBS, FRACP
J. Helen Fitton PhD
author_facet Shreya Tocaciu BDS, MBBS
Lesley J. Oliver BAppSc
Ray M. Lowenthal MD, FRACP
Gregory M. Peterson PhD, MBA
Rahul Patel PhD
Madhur Shastri PhD
Georgia McGuinness PhD
Inger Olesen MBBS, FRACP
J. Helen Fitton PhD
author_sort Shreya Tocaciu BDS, MBBS
collection DOAJ
description Background: Although the use of complementary and alternative medicines is widespread in cancer patients, clinical evidence of their benefits is sparse. Furthermore, while they are often assumed to be safe with regard to concurrent use of anticancer therapies, few studies have been carried out to investigate possible interactions. Fucoidans are a group of sulfated carbohydrates, derived from marine brown algae, which have long been used as dietary supplements due to their reported medicinal properties, including anticancer activity. The aim of this study was to investigate the effect of co-administration of fucoidan, derived from Undaria pinnatifida , on the pharmacokinetics of 2 commonly used hormonal therapies, letrozole and tamoxifen, in patients with breast cancer. Methods: This was an open label non-crossover study in patients with active malignancy taking letrozole or tamoxifen (n = 10 for each group). Patients took oral fucoidan, given in the form of Maritech extract, for a 3-week period (500 mg twice daily). Trough plasma concentrations of letrozole, tamoxifen, 4-hydroxytamoxifen, and endoxifen were measured using HPLC-CAD (high-performance liquid chromatography charged aerosol detector), at baseline and after concomitant administration with fucoidan. Results: No significant changes in steady-state plasma concentrations of letrozole, tamoxifen, or tamoxifen metabolites were detected after co-administration with fucoidan. In addition, no adverse effects of fucoidan were reported, and toxicity monitoring showed no significant differences in all parameters measured over the study period. Conclusions: Administration of Undaria pinnatifida fucoidan had no significant effect on the steady-state trough concentrations of letrozole or tamoxifen and was well tolerated. These results suggest that fucoidan in the studied form and dosage could be taken concomitantly with letrozole and tamoxifen without the risk of clinically significant interactions.
first_indexed 2024-12-24T03:49:41Z
format Article
id doaj.art-81e4a3a993354e9b86aef5f35d3c7bb4
institution Directory Open Access Journal
issn 1534-7354
1552-695X
language English
last_indexed 2024-12-24T03:49:41Z
publishDate 2018-03-01
publisher SAGE Publishing
record_format Article
series Integrative Cancer Therapies
spelling doaj.art-81e4a3a993354e9b86aef5f35d3c7bb42022-12-21T17:16:37ZengSAGE PublishingIntegrative Cancer Therapies1534-73541552-695X2018-03-011710.1177/1534735416684014The Effect of Fucoidan on the Pharmacokinetics of Letrozole and Tamoxifen in Patients With Breast CancerShreya Tocaciu BDS, MBBS0Lesley J. Oliver BAppSc1Ray M. Lowenthal MD, FRACP2Gregory M. Peterson PhD, MBA3Rahul Patel PhD4Madhur Shastri PhD5Georgia McGuinness PhD6Inger Olesen MBBS, FRACP7J. Helen Fitton PhD8Royal Hobart Hospital, Hobart, Tasmania, AustraliaRoyal Hobart Hospital, Hobart, Tasmania, AustraliaUniversity of Tasmania, Hobart, Tasmania, AustraliaUniversity of Tasmania, Hobart, Tasmania, AustraliaUniversity of Tasmania, Hobart, Tasmania, AustraliaUniversity of Tasmania, Hobart, Tasmania, AustraliaUniversity of Tasmania, Hobart, Tasmania, AustraliaAndrew Love Cancer Centre, Barwon Health, Geelong, Victoria, AustraliaMarinova Pty Ltd, Cambridge, Tasmania, AustraliaBackground: Although the use of complementary and alternative medicines is widespread in cancer patients, clinical evidence of their benefits is sparse. Furthermore, while they are often assumed to be safe with regard to concurrent use of anticancer therapies, few studies have been carried out to investigate possible interactions. Fucoidans are a group of sulfated carbohydrates, derived from marine brown algae, which have long been used as dietary supplements due to their reported medicinal properties, including anticancer activity. The aim of this study was to investigate the effect of co-administration of fucoidan, derived from Undaria pinnatifida , on the pharmacokinetics of 2 commonly used hormonal therapies, letrozole and tamoxifen, in patients with breast cancer. Methods: This was an open label non-crossover study in patients with active malignancy taking letrozole or tamoxifen (n = 10 for each group). Patients took oral fucoidan, given in the form of Maritech extract, for a 3-week period (500 mg twice daily). Trough plasma concentrations of letrozole, tamoxifen, 4-hydroxytamoxifen, and endoxifen were measured using HPLC-CAD (high-performance liquid chromatography charged aerosol detector), at baseline and after concomitant administration with fucoidan. Results: No significant changes in steady-state plasma concentrations of letrozole, tamoxifen, or tamoxifen metabolites were detected after co-administration with fucoidan. In addition, no adverse effects of fucoidan were reported, and toxicity monitoring showed no significant differences in all parameters measured over the study period. Conclusions: Administration of Undaria pinnatifida fucoidan had no significant effect on the steady-state trough concentrations of letrozole or tamoxifen and was well tolerated. These results suggest that fucoidan in the studied form and dosage could be taken concomitantly with letrozole and tamoxifen without the risk of clinically significant interactions.https://doi.org/10.1177/1534735416684014
spellingShingle Shreya Tocaciu BDS, MBBS
Lesley J. Oliver BAppSc
Ray M. Lowenthal MD, FRACP
Gregory M. Peterson PhD, MBA
Rahul Patel PhD
Madhur Shastri PhD
Georgia McGuinness PhD
Inger Olesen MBBS, FRACP
J. Helen Fitton PhD
The Effect of Fucoidan on the Pharmacokinetics of Letrozole and Tamoxifen in Patients With Breast Cancer
Integrative Cancer Therapies
title The Effect of Fucoidan on the Pharmacokinetics of Letrozole and Tamoxifen in Patients With Breast Cancer
title_full The Effect of Fucoidan on the Pharmacokinetics of Letrozole and Tamoxifen in Patients With Breast Cancer
title_fullStr The Effect of Fucoidan on the Pharmacokinetics of Letrozole and Tamoxifen in Patients With Breast Cancer
title_full_unstemmed The Effect of Fucoidan on the Pharmacokinetics of Letrozole and Tamoxifen in Patients With Breast Cancer
title_short The Effect of Fucoidan on the Pharmacokinetics of Letrozole and Tamoxifen in Patients With Breast Cancer
title_sort effect of fucoidan on the pharmacokinetics of letrozole and tamoxifen in patients with breast cancer
url https://doi.org/10.1177/1534735416684014
work_keys_str_mv AT shreyatocaciubdsmbbs theeffectoffucoidanonthepharmacokineticsofletrozoleandtamoxifeninpatientswithbreastcancer
AT lesleyjoliverbappsc theeffectoffucoidanonthepharmacokineticsofletrozoleandtamoxifeninpatientswithbreastcancer
AT raymlowenthalmdfracp theeffectoffucoidanonthepharmacokineticsofletrozoleandtamoxifeninpatientswithbreastcancer
AT gregorympetersonphdmba theeffectoffucoidanonthepharmacokineticsofletrozoleandtamoxifeninpatientswithbreastcancer
AT rahulpatelphd theeffectoffucoidanonthepharmacokineticsofletrozoleandtamoxifeninpatientswithbreastcancer
AT madhurshastriphd theeffectoffucoidanonthepharmacokineticsofletrozoleandtamoxifeninpatientswithbreastcancer
AT georgiamcguinnessphd theeffectoffucoidanonthepharmacokineticsofletrozoleandtamoxifeninpatientswithbreastcancer
AT ingerolesenmbbsfracp theeffectoffucoidanonthepharmacokineticsofletrozoleandtamoxifeninpatientswithbreastcancer
AT jhelenfittonphd theeffectoffucoidanonthepharmacokineticsofletrozoleandtamoxifeninpatientswithbreastcancer
AT shreyatocaciubdsmbbs effectoffucoidanonthepharmacokineticsofletrozoleandtamoxifeninpatientswithbreastcancer
AT lesleyjoliverbappsc effectoffucoidanonthepharmacokineticsofletrozoleandtamoxifeninpatientswithbreastcancer
AT raymlowenthalmdfracp effectoffucoidanonthepharmacokineticsofletrozoleandtamoxifeninpatientswithbreastcancer
AT gregorympetersonphdmba effectoffucoidanonthepharmacokineticsofletrozoleandtamoxifeninpatientswithbreastcancer
AT rahulpatelphd effectoffucoidanonthepharmacokineticsofletrozoleandtamoxifeninpatientswithbreastcancer
AT madhurshastriphd effectoffucoidanonthepharmacokineticsofletrozoleandtamoxifeninpatientswithbreastcancer
AT georgiamcguinnessphd effectoffucoidanonthepharmacokineticsofletrozoleandtamoxifeninpatientswithbreastcancer
AT ingerolesenmbbsfracp effectoffucoidanonthepharmacokineticsofletrozoleandtamoxifeninpatientswithbreastcancer
AT jhelenfittonphd effectoffucoidanonthepharmacokineticsofletrozoleandtamoxifeninpatientswithbreastcancer