AROMASIN
Pronunciation: ex-e-MES-tayn (a-ROEM-a-sin)

What it isSteroidal, irreversible aromatase inhibitor; hormone-receptor-positive breast cancer after menopause.
Why this oneUnlike anastrozole and letrozole, it permanently inactivates aromatase and can be used after a nonsteroidal inhibitor.
What limits itAccelerated bone loss and arthralgia limit treatment. It is ineffective before menopause unless ovarian function is suppressed.
Read the full label on DailyMed ↗
| FDA dosing | Population | Start | Target | Max |
|---|---|---|---|---|
| Adjuvant early breast cancer (ER+, after 2–3 yr tamoxifen) | Postmenopausal women | 25 mg QD after a meal | 25 mg QD after a meal | 25 mg QD |
| Advanced breast cancer (progressed after tamoxifen) | Postmenopausal women | 25 mg QD after a meal | 25 mg QD after a meal | 25 mg QD |
Renal No adjustment needed
Hepatic No adjustment needed
Available strengths
Pregnancy Can cause fetal harm (abortions, embryo-fetal toxicity in animals); advise risk to fetus
Lactation Advise not to breastfeed during treatment and for 1 month after final dose
| Strength | #/mo | generic $/mo | CostPlus | |
|---|---|---|---|---|
| 25 mg | tab | 30 qd | $22.43 | offered |
Generic entry2011
NO BOXED WARNINGS
Principal riskAccelerated bone loss and arthralgia
Legacy pregnancy categoryMultiple / indication-, trimester- or formulation-dependent
Defining liabilityThrombotic, metabolic, hepatic, skeletal or reproductive toxicity varies by hormonal target.