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Drug Interactions between dehydroepiandrosterone and tamoxifen

This report displays the potential drug interactions for the following 2 drugs:

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Interactions between your drugs

Major

tamoxifen dehydroepiandrosterone (prasterone)

Applies to: tamoxifen and dehydroepiandrosterone

GENERALLY AVOID: Theoretically, high levels of dehydroepiandrosterone (also known as prasterone or DHEA) may negate the pharmacologic effects of selective estrogen receptor modulators (SERMs) like tamoxifen and estrogen receptor antagonists like fulvestrant when they are used to treat estrogen receptor positive cancer. In vitro studies have demonstrated that the sulfate conjugate of DHEA (DHEA-S) is estrogenic in a low-estrogen environment, allowing it to compete with SERMs and estrogen receptor antagonists to bind to the estrogen receptor and promote cell growth in estrogen receptor positive breast cancer cells. The in vitro study that analyzed this potential interaction with tamoxifen found that tamoxifen's ability to inhibit cell growth could be circumvented by DHEA-S at concentrations >= 90 mcg/dL; while the study analyzing DHEA-S with fulvestrant used a concentration of 900 mcg/dL.

MANAGEMENT: The use of dehydroepiandrosterone (also known as prasterone or DHEA) should be generally avoided in patients using SERMs like tamoxifen or estrogen receptor antagonists like fulvestrant. Some authorities consider the use of DHEA to be contraindicated in patients with a known or suspected estrogen dependent tumor as well as in patients with a known or suspected history of breast cancer. Consultation with an oncologist as well as a gynecologist should be considered prior to starting this combination.

References

  1. (2023) "Product Information. Intrarosa (prasterone)." Theramex Australia Pty Ltd, 1
  2. (2022) "Product Information. Intrarosa (prasterone)." Theramex HQ UK Ltd
  3. (2021) "Product Information. Intrarosa (dehydroepiandrosterone (prasterone))." Endoceutics, Inc.
  4. (2020) "Product Information. Intrarosa (dehydroepiandrosterone (prasterone))." Millicent Pharma
  5. Calhoun KE, pommier rf, Muller P, et al. (2023) Dehydroepiandrosterone sulfate causes proliferation of estrogen receptor-positive breast cancer cells despite treatment with fulvestrant https://jamanetwork.com/journals/jamasurgery/fullarticle/395314
  6. Calhoun K, pommier r, Cheek J, Fletcher W, Toth-Fejel S (2023) The effect of high dehydroepiandrosterone sulfate levels on tamoxifen blockade and breast cancer progression. https://pubmed.ncbi.nlm.nih.gov/12727558/
View all 6 references

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Drug and food interactions

Moderate

tamoxifen food

Applies to: tamoxifen

GENERALLY AVOID: Due to their estrogenic effect, isoflavones present in soy such as genistein and daidzein may stimulate breast tumor growth and antagonize the antiproliferative action of tamoxifen. Supportive data are derived primarily from in vitro and animal studies. In vitro, low concentrations of these phytoestrogens have been found to promote DNA synthesis and reverse the inhibitory effect of tamoxifen on estrogen-dependent breast cancer cell proliferation. In contrast, high concentrations of genistein greater than 10 microM/L have been found to enhance tamoxifen effects by inhibiting breast cancer cell growth. It is not known if these high concentrations are normally achieved in humans. Plasma concentrations below 4 microM/L have been observed in healthy volunteers given a soy diet for one month or large single doses of genistein. These concentrations are comparable to the low plasma concentrations associated with tumor stimulation reported in animals. In a study of 155 female breast cancer survivors with substantially bothersome hot flashes, a product containing 50 mg of soy isoflavones (40% to 45% genistein; 40% to 45% daidzein; 10% to 20% glycitein) taken three times a day was found to be no more effective than placebo in reducing hot flashes. No toxicity or recurrence of breast cancer was reported during the 9-week study period.

Green tea does not appear to have significant effects on the pharmacokinetics of tamoxifen or its primary active metabolite, endoxifen. In a study consisting of 14 patients who have been receiving tamoxifen treatment at a stable dose of 20 mg (n=13) or 40 mg (n=1) once daily for at least 3 months, coadministration with green tea supplements twice daily for 14 days resulted in no significant differences in the pharmacokinetics of either tamoxifen or endoxifen with respect to peak plasma concentration (Cmax), systemic exposure (AUC), and trough plasma concentration (Cmin) compared to administration of tamoxifen alone. The combination was well tolerated, with all reported adverse events categorized as mild (grade 1) and none categorized as serious or severe (grade 3 or higher) during the entire study. Although some adverse events such as headache, polyuria, gastrointestinal side effects (e.g., constipation, dyspepsia), and minor liver biochemical disturbances were reported more often during concomitant treatment with green tea, most can be attributed to the high dose of green tea used or to the caffeine in green tea. The green tea supplements used were 1000 mg in strength and contained 150 mg of epigallocatechin-3-gallate (EGCG), the most abundant and biologically active catechin in green tea. According to the investigators, the total daily dose of EGCG taken by study participants is equivalent to the amount contained in approximately 5 to 6 cups of regular green tea. However, it is not known to what extent the data from this study may be applicable to other preparations of green tea such as infusions, since the bioavailability of EGCG and other catechins may vary between preparations.

MANAGEMENT: Until more information is available, patients treated with tamoxifen may consider avoiding or limiting the consumption of soy-containing products. Consumption of green tea and green tea extracts during tamoxifen therapy appears to be safe.

References

  1. Therapeutic Research Faculty (2008) Natural Medicines Comprehensive Database. http://www.naturaldatabase.com
  2. Braal CL, Hussaarts KGAM, Seuren L, et al. (2020) "Influence of green tea consumption on endoxifen steady-state concentration in breast cancer patients treated with tamoxifen." Breast Cancer Res Treat, 184, p. 107-13

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Therapeutic duplication warnings

No warnings were found for your selected drugs.

Therapeutic duplication warnings are only returned when drugs within the same group exceed the recommended therapeutic duplication maximum.


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Drug Interaction Classification

These classifications are only a guideline. The relevance of a particular drug interaction to a specific individual is difficult to determine. Always consult your healthcare provider before starting or stopping any medication.
Major Highly clinically significant. Avoid combinations; the risk of the interaction outweighs the benefit.
Moderate Moderately clinically significant. Usually avoid combinations; use it only under special circumstances.
Minor Minimally clinically significant. Minimize risk; assess risk and consider an alternative drug, take steps to circumvent the interaction risk and/or institute a monitoring plan.
Unknown No interaction information available.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.