Drug Interactions between Cerianna and elacestrant
This report displays the potential drug interactions for the following 2 drugs:
- Cerianna (fluoroestradiol F 18)
- elacestrant
Interactions between your drugs
fluoroestradiol F 18 elacestrant
Applies to: Cerianna (fluoroestradiol F 18) and elacestrant
GENERALLY AVOID: Coadministration of the radioactive diagnostic agent fluoroestradiol F 18 with drugs that block the estrogen receptor (ER), such as tamoxifen and fulvestrant, may reduce the uptake of fluoroestradiol F 18 into ER-positive tumors. This may therefore reduce its potential to detect ER-positive non-primary breast cancer lesions. Fluoroestradiol F 18 binds to the ER and its uptake in human tumors is dependent on ER density and function in tumors and physiologic issue, including in the liver, ovaries, and uterus. The effect of selective ER modulators such as tamoxifen and ER down-regulators such as fulvestrant may persist for up to 8 and 28 weeks, respectively. In clinical studies, treatment with ER modulators or fulvestrant was discontinued 60 days prior to the administration of fluoroestradiol F 18. However, concurrent use of aromatase inhibitors was permitted in these clinical studies.
MANAGEMENT: Concomitant use of fluoroestradiol F 18 with systemic endocrine therapy that targets estrogen receptors, including estrogen receptor modulators such as tamoxifen and estrogen receptor down-regulators such as fulvestrant is not recommended. Administration of fluoroestradiol F 18 is recommended prior to starting treatment with these drugs. However, the manufacturer advises that treatment with estrogen receptor modulators or down-regulators should not be delayed in order to administer fluoroestradiol F 18.
References (1)
- (2022) "Product Information. Cerianna (fluoroestradiol F 18)." GE Healthcare
Drug and food interactions
elacestrant food
Applies to: elacestrant
GENERALLY AVOID: Grapefruit juice may increase the plasma concentrations of elacestrant, which is primarily metabolized by CYP450 3A4. The proposed mechanism is inhibition of CYP450 3A4-mediated first-pass metabolism in the gut wall by certain compounds present in grapefruit. Inhibition of hepatic CYP450 3A4 may also contribute. The interaction has not been studied with grapefruit juice but has been reported for other CYP450 3A4 inhibitors. When elacestrant (172 mg once daily) was administered with itraconazole, a potent CYP450 3A4 inhibitor, elacestrant peak plasma concentration (Cmax) and systemic exposure (AUC) increased by 4.4-fold and 5.3-fold, respectively. Concomitant use of fluconazole, a moderate CYP450 3A4 inhibitor, is predicted to increase elacestrant (345 mg single dose) Cmax and AUC by 1.6-fold and 2.3-fold, respectively. 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. Increased exposure to elacestrant may increase the risk of adverse reactions such as musculoskeletal pain, nausea, dyslipidemia, increased liver enzymes, fatigue, decreased hemoglobin, and vomiting.
Administration of elacestrant (345 mg) with a high-fat meal (800 to 1000 calories, 50% fat) increased elacestrant Cmax and AUC by 42% and 22%, respectively, compared to fasted conditions.
MANAGEMENT: It may be advisable for patients to avoid consumption of grapefruit, grapefruit juice, or supplements that contain grapefruit during treatment with elacestrant. Elacestrant should be taken with food at approximately the same time each day.
References (1)
- (2023) "Product Information. Orserdu (elacestrant)." Stemline Therapeutics
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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