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Osimertinib

TAGRISSO

Pronunciation: oe-sim-ER-ti-nib (ta-GRI-soe)

Osimertinib ballicule: receptor binding, kinetics and half-life diagram
Mechanism of action: Osimertinib ballicule

What it isThird-generation EGFR tyrosine kinase inhibitor; EGFR-mutant lung cancer.

Why this oneIt targets the T790M resistance mutation and penetrates the CNS, so it treats brain metastases.

What limits itQT prolongation and rare interstitial lung disease and cardiomyopathy. CYP3A4-dependent.

Osimertinib molecular structure (skeletal formula)
Molecular structure: Osimertinib

FDA-approved for

FDA label

FDA dosingPopulationStartTargetMax
Adjuvant early-stage NSCLC (EGFR ex19del/L858R)Adults80 mg QD80 mg QD80 mg QD
Stage III unresectable NSCLC after chemoradiation (EGFR ex19del/L858R)Adults80 mg QD80 mg QD80 mg QD
Metastatic NSCLC, incl. T790M+ (EGFR); monotherapy or + pemetrexed/platinumAdults80 mg QD80 mg QD80 mg QD

Renal No adjustment for CLcr 15-89 mL/min; no recommended dose for ESRD (CLcr <15)

Hepatic No adjustment for mild-moderate (Child-Pugh A/B); no recommended dose for severe

Instructions

Available strengths

Cautions

Adverse reactions

Pregnancy Can cause fetal harm; use effective contraception during and 6 wks (females)/4 mo (males) after last dose

Lactation Do not breastfeed during treatment and for 2 weeks after last dose

Cost

Osimertinib (TAGRISSO)
Strength#/mogeneric $/moCostPlus
40 mgtab30 qdnot offered
80 mgtab30 qdnot offered
NADAC is a voluntary CMS survey of what retail community pharmacies pay for the drugs they stock. Osimertinib is dispensed outside retail pharmacies, so it rarely appears on surveyed invoices.

Generic entry2035 est.

NO BOXED WARNINGS

Principal riskInterstitial lung disease; QT prolongation

Classes and tags

Clinical profile

Therapeutic safety burden3 / 4
Overdose danger2 / 4
Weight-gain liability0 / 4
Sedation liability0 / 4
QT / Torsades3 / 4
Direct muscarinic antagonism0 / 4
Embryofetal risk3 / 4

Legacy pregnancy categoryUnknown / historical label unavailable

Defining liabilityMyelosuppression and agent-specific hepatic, cardiac, pulmonary, neurologic or reproductive toxicity require oncology monitoring.

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