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Registry Hub
mTOR Inhibitor Antineoplastic/Prescription

AFINITOR

AFINITOR

Clinical safety rating

caution

Comprehensive clinical and safety monograph for AFINITOR (AFINITOR).


What is AFINITOR?

Comprehensive clinical and safety monograph for AFINITOR (AFINITOR).

Indications & Uses

Advanced hormone receptor-positive, HER2-negative breast cancer in postmenopausal women in combination with exemestane after failure of letrozole or anastrozoleProgressive neuroendocrine tumors of pancreatic origin (PNET) in unresectable, locally advanced or metastatic diseaseAdvanced renal cell carcinoma (RCC) after failure of sunitinib or sorafenibSubependymal giant cell astrocytoma (SEGA) associated with tuberous sclerosis complex (TSC) in patients requiring therapeutic intervention but not amenable to curative resection

Side Effects

Weakness, Sinus inflammation, Infection, Fever, Cough, Fatigue, Stomatitis (Inflammation of the mouth), Otitis media (infection of ear), Diarrhea, Upper respiratory tract infection

Compare AFINITOR vs AFINITOR DISPERZ →View all mTOR Inhibitor Antineoplastic drugs →

Mechanism of Action

Inhibitor of mammalian target of rapamycin (mTOR), specifically the mTORC1 complex, by binding to the FKBP-12 protein, reducing cell proliferation, angiogenesis, and glucose uptake.

What the body does with it

MetabolismSubstrate of CYP3A4; metabolized primarily by CYP3A4; also a substrate of P-glycoprotein (P-gp).
ExcretionPrimarily fecal (80%) and renal (5%) as unchanged drug and metabolites. Biliary excretion is significant.
Half-lifeTerminal elimination half-life: 30 hours (range 15–40 hours) in healthy subjects; increases to 40–70 hours in moderate hepatic impairment.
Protein binding74% bound to plasma proteins (primarily albumin and α1-acid glycoprotein).
Volume of DistributionMean steady-state Vd: 342 L (approx. 4.9 L/kg in a 70 kg adult), indicating extensive tissue distribution.
BioavailabilityOral bioavailability: approximately 16% (low due to P-glycoprotein efflux and first-pass metabolism); food reduces variability but does not alter AUC significantly.
Onset of ActionOral: Peak concentration at 1–2 hours; clinical effect (e.g., mTOR inhibition) occurs within hours; tumor response may take weeks.
Duration of ActionTherapeutic effect persists throughout the dosing interval (once daily) due to sustained mTORC1 inhibition; pharmacodynamic effect lasts >24 hours.
Molecular Weight958.2 Da

Classification & Brands

Action ClassImmunosuppressant- mTOR inhibitors
Brand SubstitutesEvermil 5 Tablet, Everbliss 5mg Tablet, Rolimus 5 Tablet, Volantis 5mg Tablet, Evertor 5mg Tablet, Evermil 10 Tablet, Rolimus 10 Tablet, Everbliss 10mg Tablet, Volantis 10mg Tablet, Evertor 10mg Tablet

Dosing & administration

10 mg orally once daily for advanced breast cancer, neuroendocrine tumors, and renal cell carcinoma; 10 mg orally once daily for subependymal giant cell astrocytoma (SEGA) in adults; 5 mg/m^2 orally once daily for SEGA in pediatric patients (titrated to trough levels 5-15 ng/mL).

Dosage formTABLET
Renal impairmentNo dose adjustment for mild to moderate renal impairment (CrCl >=30 mL/min). For severe renal impairment (CrCl <30 mL/min): reduce dose to 5 mg once daily. End-stage renal disease (CrCl <15 mL/min): use with caution, no specific recommendation.
Liver impairmentChild-Pugh A: no adjustment; Child-Pugh B: reduce dose to 5 mg daily; Child-Pugh C: reduce dose to 2.5 mg daily, or consider alternate therapy.
Pediatric useFor SEGA: 5 mg/m^2 orally once daily, adjusted to achieve everolimus trough concentrations of 5-15 ng/mL. Dose adjustments per AUC or tolerability. Not approved for other indications in children.
Geriatric useNo specific dose adjustment; start at recommended adult dose. Monitor for increased risk of infections, stomatitis, and metabolic effects due to age-related decline in organ function.

Use during pregnancy

1st trimesterAvoid. Teratogenic effects observed in animal studies; risk of fetal harm.
2nd trimesterAvoid. Inhibits mTOR pathway critical for fetal development; oligohydramnios reported.
3rd trimesterAvoid. Risk of fetal and neonatal toxicities, including myelosuppression and infections.

Clinical note

Comprehensive clinical and safety monograph for AFINITOR (AFINITOR).

Placental transferYes. Crosses placenta in animals; human data show transfer based on molecular size and lipophilicity.
BreastfeedingContraindicated. Excreted in animal milk; potential for serious adverse reactions in nursing infants.
Lactation RatingL5
Teratogenic RiskPregnancy Category D. Positive evidence of human fetal risk. Based on its mechanism of action (mTOR inhibitor) and animal studies, AFINITOR (everolimus) is embryotoxic and fetotoxic. First trimester exposure carries risk of structural anomalies; second and third trimester exposure may cause fetal growth restriction, oligohydramnios, and renal impairment. Use only if benefit outweighs risk.
Fetal MonitoringMonitor maternal blood pressure, renal function, blood glucose, and lipid profile. Monitor fetal growth by ultrasound every 4 weeks after viability. Assess amniotic fluid volume. Monitor for signs of mTOR inhibitor toxicity in the mother (e.g., pneumonitis, infections, stomatitis).
Fertility EffectsMay impair fertility in females and males based on animal studies. In females, everolimus may cause menstrual irregularities, anovulation, and ovarian failure. In males, may cause azoospermia or oligospermia. Reversibility uncertain.

Warnings & precautions

■ FDA Black Box Warning

No black box warnings.

Side Effect Profile

Serious Effects

Absolute Contraindications

Hypersensitivity to everolimus or sirolimus derivativesSevere hepatic impairment (Child-Pugh class C)

Clinical Precautions

PrecautionsNon-infectious pneumonitis, Infections (including opportunistic infections), Hypersensitivity reactions including anaphylaxis, Angioedema, Renal failure, Impaired wound healing, Metabolic effects (hyperglycemia, dyslipidemia), Myelosuppression, Immunosuppression leading to increased risk of infections, Cases of fatal hemorrhage in patients with history of bleeding, Radiation sensitization and recall reactions, especially in patients with previous radiation therapy, Increased risk of pneumocystis jirovecii pneumonia (PJP) and other opportunistic infections; consider prophylaxis, Avoid live vaccines
Food/DietaryAvoid grapefruit, grapefruit juice, and Seville oranges (including marmalade) due to CYP3A4 inhibition increasing everolimus levels. Take consistently with or without food, but high-fat meals reduce absorption. Avoid St. John's wort.

Clinical Tips & Counseling

Clinical PearlsMonitor renal function and blood glucose regularly; Afinitor (everolimus) can cause non-infectious pneumonitis, so obtain baseline chest imaging and assess for new or worsening respiratory symptoms. Adjust dose for moderate hepatic impairment (Child-Pugh B). Avoid live vaccines during treatment.
Patient AdviceTake Afinitor at the same time each day, consistently either with or without food. · Avoid grapefruit, grapefruit juice, and Seville oranges during treatment. · Report any new or worsening cough, chest pain, or difficulty breathing immediately. · Monitor for signs of infection such as fever, chills, or sore throat; avoid large crowds and sick individuals. · Use effective contraception during treatment and for 8 weeks after stopping. · Do not crush or chew tablets; swallow whole with a glass of water.

AFINITOR Interactions

Loading safety data…

This overview is compiled from peer-reviewed clinical sources and FDA labeling. It's here to support — not replace — clinical judgment. Always verify dosing against your institution's current protocols before prescribing.

On this page

Mechanism of ActionDosing & administrationUse during pregnancyWarnings & precautionsDrug interactions

Compare with

AFINITOR DISPERZ

External sources

DailyMed (NIH) PubMed OpenFDA