Drug Interactions between abiraterone and eplerenone
This report displays the potential drug interactions for the following 2 drugs:
- abiraterone
- eplerenone
Interactions between your drugs
eplerenone abiraterone
Applies to: eplerenone and abiraterone
MONITOR: Concomitant use of abiraterone and eplerenone may increase prostate specific antigen (PSA) levels and shorten progression free survival time in patients undergoing treatment for prostate cancer. The exact mechanism is unknown. Approximately 15% to 45% of patients undergoing therapy for castration-resistant prostate cancer have point mutations in their androgen receptors, which may increase the receptor's ability to bind different substances. The non-steroidal mineralocorticoid antagonist eplerenone has not demonstrated an ability to bind to the wild-type androgen receptor, but in vitro studies have shown that it is able to bind to at least one type of mutated androgen receptor (T877A). One retrospective study of men undergoing treatment for metastatic castration refractory prostate cancer with prednisone (10 mg daily) and abiraterone (n=66) or eplerenone (50 mg daily) and abiraterone (n=40) found that both options were well tolerated and there was no difference in the progression free survival time. Unfortunately, this trial was not powered to compare the survival outcomes between the two cohorts. Additionally, the progression free survival intervals were notably shorter in both treatment groups when compared to those observed in phase III trials with abiraterone and prednisone.
MANAGEMENT: If abiraterone and eplerenone are used together, monitoring for worsening clinical symptoms and increased levels of biochemical markers for prostate cancer such as PSA and alkaline phosphatase levels should be considered. Some authorities suggest using a combination of amiloride with hydrochlorothiazide if medications that do not activate androgen receptors, but can potentially treat symptoms of increased mineralocorticoid levels (e.g., hypertension, hypokalemia, fluid retention) are needed.
References (12)
- (2023) "Product Information. Akeega (abiraterone-niraparib)." Janssen Biotech, Inc.
- (2021) "Product Information. Zytiga (abiraterone)." Janssen Biotech, Inc.
- (2022) "Product Information. Yonsa (abiraterone)." Sun Pharmaceutical Industries
- (2023) "Product Information. Apo-Abiraterone (abiraterone)." Apotex Inc
- (2021) "Product Information. Zytiga (abiraterone)." Janssen-Cilag Pty Ltd
- (2023) "Product Information. Abiraterone (abiraterone)." Wockhardt UK Ltd
- (2023) "Product Information. Yonsa Mpred (abiraterone-methylprednisolone)." Sun Pharma ANZ Pty Ltd
- Vicente-Valor J, Escudero-Vilaplana V, Collado-Borrell R, et al. (2022) "Potential negative pharmacodynamic interaction of spironolactone and abiraterone in two prostate cancer patients." J Oncol Pharm Pract, 28, p. 1259-63
- Dhondt B, Buelens S, Van Besien J, et al. (2023) Abiraterone and spironolactone in prostate cancer: a combination to avoid. https://www.tandfonline.com/doi/abs/10.1080/17843286.2018.1543827
- Richards J, lim ac, Hay CW, et al. (2012) "Interactions of abiraterone, eplerenone and prednisolone with wild-type and mutant androgen receptor: a rationale for increasing abiraterone exposure or combining with MDV3100." Cancer Res, 72, p. 2176-82
- gill d, Gaston D, bailey e, et al. (2017) "Efficacy of eplerenone in the management of mineralocorticoid excess in men with metastatic castration resistant prostate cancer treated with abiraterone without prednisone." Clin Genitourin Cancer, 15, e599-2
- Decamps S, Lis R, Ekanayake P (2023) "Abirateron-induced endocrinopathies." JCEM Case Reports, 1, p. 1-4
Drug and food interactions
eplerenone food
Applies to: eplerenone
GENERALLY AVOID: Coadministration with grapefruit juice may increase the plasma concentrations of eplerenone. The primary mechanism is inhibition of CYP450 3A4-mediated first-pass metabolism in the gut wall by certain compounds present in grapefruits. Inhibition of hepatic CYP450 3A4 may also contribute. In drug interaction studies, administration of a single 100 mg dose of eplerenone in combination with grapefruit juice resulted in a 25% increase in eplerenone systemic exposure (AUC). High blood levels of eplerenone can increase the risk of side effects including hyperkalemia. In general, the effect of grapefruit juice is concentration-, dose- and preparation-dependent, and can vary widely among brands. Certain preparations of grapefruit juice (e.g., high dose, double strength) have sometimes demonstrated potent inhibition of CYP450 3A4, while other preparations (e.g., low dose, single strength) have typically demonstrated moderate inhibition.
MANAGEMENT: It may be advisable for patients to avoid the consumption of grapefruit, grapefruit juice, or supplements that contain grapefruit during treatment with eplerenone.
References (3)
- (2002) "Product Information. Inspra (eplerenone)." Searle
- (2021) "Product Information. Eplerenone (eplerenone)." MSN Laboratories Europe Ltd
- (2023) "Product Information. Eplerenone (Apotex) (eplerenone)." Apotex Pty Ltd
abiraterone food
Applies to: abiraterone
ADJUST DOSING INTERVAL: Food may significantly increase the oral bioavailability of some formulations of abiraterone acetate. Compared to administration in the fasted state, abiraterone peak plasma concentration (Cmax) and systemic exposure (AUC) were approximately 7- and 5-fold higher, respectively, when a single dose of abiraterone acetate was administered with a low-fat meal (7% fat; 300 calories) and approximately 17- and 10-fold higher, respectively, when it was administered with a high-fat meal (57% fat; 825 calories). Given the normal variation in the content and composition of meals, taking abiraterone acetate with meals has the potential to result in increased and highly variable exposures. The safety of these increased exposures during multiple dosing has not been assessed. However, the abiraterone acetate 125 mg tablet, commonly marketed as Yonsa, was found to have an approximately 6.5-fold higher Cmax and 4.4-fold higher AUC when a single dose of 500 mg (4 tablets) was administered with a high-fat meal (56% - 60% fat, 900 - 1000 calories) compared to overnight fasting in healthy volunteers. These differences were not considered clinically significant for this formulation.
MANAGEMENT: Some formulations of abiraterone acetate must be taken on an empty stomach. No food should be consumed for at least two hours before and one hour after the abiraterone acetate dose. However, the abiraterone acetate 125 mg tablet, commonly marketed as Yonsa, can be taken with or without food. The manufacturer's product labeling should be consulted for specific guidance.
References (9)
- (2011) "Product Information. Zytiga (abiraterone)." Centocor Inc
- (2023) "Product Information. Akeega (abiraterone-niraparib)." Janssen Biotech, Inc.
- (2023) "Product Information. Akeega (abiraterone-niraparib)." Janssen Inc
- (2021) "Product Information. Zytiga (abiraterone)." Janssen Biotech, Inc.
- (2022) "Product Information. Yonsa (abiraterone)." Sun Pharmaceutical Industries
- (2023) "Product Information. Apo-Abiraterone (abiraterone)." Apotex Inc
- (2021) "Product Information. Zytiga (abiraterone)." Janssen-Cilag Pty Ltd
- (2023) "Product Information. Abiraterone (abiraterone)." Wockhardt UK Ltd
- (2023) "Product Information. Yonsa Mpred (abiraterone-methylprednisolone)." Sun Pharma ANZ Pty Ltd
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.
See also
Drug Interaction Classification
Highly clinically significant. Avoid combinations; the risk of the interaction outweighs the benefit. | |
Moderately clinically significant. Usually avoid combinations; use it only under special circumstances. | |
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. | |
No interaction information available. |
Further information
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