Letrozole (letrozole)

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Last reviewed · Source: First Databank (FDB) drug data

Overview

Letrozole, an aromatase inhibitor, is an antineoplastic agent.

Letrozole, a benzyltriazole derivative, is a selective, nonsteroidal aromatase inhibitor. Letrozole differs structurally from aminoglutethimide but shares the pharmacologic activity of competitive aromatase inhibition; although both drugs are selective nonsteroidal inhibitors, letrozole is more potent and selective on a molar basis. Competitive aromatase inhibitors also have been referred to as type II inhibitors of the enzyme.

Like anastrozole, letrozole is a triazole derivative. The N-4 nitrogen of the triazole ring, which coordinates with the heme iron atom of the aromatase enzyme complex, is thought to be responsible for the high affinity of the drug for the estrogen synthetase enzyme.

The growth of some breast cancers is stimulated or maintained by estrogens; in these cancers, decreasing estrogen levels or inhibiting estrogen effects can lead to decreased tumor mass or delayed cancer progression. In postmenopausal women, estrogens are primarily produced through the action of aromatase enzymes, which convert adrenal androgens (e.g., androstenedione, testosterone) to estrone and estradiol. Letrozole selectively inhibits synthesis of estrogens via inhibition of the aromatase enzyme; it does not affect synthesis of adrenal corticosteroid, aldosterone, or thyroid hormone.

Suppression of plasma concentrations of estradiol, estrone, and estrone sulfate by 75-95% from baseline, with maximal suppression achieved within 2-3 days, has been observed in postmenopausal women with advanced breast cancer receiving daily letrozole doses of 0.1-5 mg. Suppression was dose-related, and letrozole doses equal to or exceeding 0.5 mg resulted in suppression to estrone and estrone sulfate concentrations below the lower limit of detection in many cases. Suppression of serum estrogen concentrations was maintained throughout treatment in all patients receiving daily letrozole doses equal to or exceeding 0.5 mg.

Letrozole is rapidly and completely absorbed from the GI tract following oral administration. Steady-state plasma concentrations of the drug are reached in 2-6 weeks in patients receiving letrozole 2.5 mg daily. Letrozole exhibits slightly nonlinear pharmacokinetics with repeated administration of 2.5 mg daily, with steady-state plasma concentrations 1.5-2 times higher than predicted based on plasma concentrations measured after a single dose.

However, continuous accumulation of letrozole does not occur, and steady-state concentrations are maintained over extended periods of daily drug administration. Food does not affect the oral absorption of the drug.

Letrozole is weakly bound to plasma proteins. It has a terminal elimination half-life of about 2 days. The primary elimination pathway of letrozole consists of slow metabolism in the liver to a pharmacologically inactive carbinol metabolite (4,4'-methanol-bisbenzonitrile) followed by renal excretion of the glucuronide conjugate of this metabolite.

Formation of the carbinol metabolite is mediated by cytochrome P-450 (CYP) isoenzymes 3A4 and 2A6, and formation of the ketone analog of the carbinol metabolite is mediated by isoenzyme 2A6.

Following oral administration of radiolabeled letrozole, 90% of the administered dose was excreted in the urine. Of the radiolabeled drug recovered in urine, at least 75% was the glucuronide of the carbinol metabolite, about 9% consisted of 2 unidentified metabolites, and 6% was unchanged drug.

Age-related differences in pharmacokinetics over the range of 35 years of age to greater than 80 years of age have not been observed in patients receiving letrozole in clinical trials. Age-related differences between adults and children or race-related differences in the pharmacokinetics of letrozole have not been evaluated.

USES: This medication is used to treat certain types of breast cancer (such as hormone-receptor-positive breast cancer) in women after menopause. Letrozole is also used to help prevent the cancer from returning. Some breast cancers are made to grow faster by a natural hormone called estrogen.

Letrozole decreases the amount of estrogen the body makes and helps to slow or reverse the growth of these breast cancers.

Generic name: letrozole
Pronunciation: (LET-tro-zole)

Reference product & biosimilars

No reference, biosimilar or interchangeable associated with this drug.

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Indications

The following indications are listed for Letrozole:

  • Early Breast Cancer Hormone Receptor Positive And Postmenopausal
  • Hormone Receptor Positive Postmenopausal Advanced Breast Cancer
  • Hormone Receptor Positive Postmenopausal Early Breast Cancer After Adjuvant Tamoxifen

Dosing

No dosing information is available for this tab.

Drug interactions

Letrozole is a substrate of cytochrome P-450 (CYP) 3A4 and CYP2A6. Letrozole has been shown to inhibit CYP2A6 and CYP2C19 in human liver microsomes, but the clinical significance of this is not known.

Contraindications

*Pregnancy.

*Known hypersensitivity to letrozole or any ingredient in the formulation.

Adverse reactions

The most common adverse effects (occurring in greater than 20% of patients) are hot flashes, arthralgia, flushing, asthenia, edema, headache, dizziness, hypercholesterolemia, increased sweating, bone pain, and musculoskeletal effects.

Precautions

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ICD codes

No ICD codes are available for this drug.

Formulary status

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Last reviewed · Source: First Databank (FDB) drug data