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Tucatinib

TUKYSA

Pronunciation: too-KA-ti-nib (too-KYE-sa)

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

What it isHER2-selective tyrosine-kinase inhibitor; HER2-positive metastatic breast cancer, including brain metastases.

Why this oneHER2 selectivity spares EGFR, reducing the rash and diarrhea of less selective agents while preserving CNS activity.

What limits itDiarrhea and hepatotoxicity require monitoring. Strong CYP2C8 inhibitors raise exposure, and tucatinib strongly inhibits CYP3A4.

Tucatinib molecular structure (skeletal formula)
Molecular structure: Tucatinib

FDA-approved for

FDA label

FDA dosingPopulationStartTargetMax
HER2+ metastatic breast cancer (with trastuzumab + capecitabine)Adults300 mg BID300 mg BID300 mg BID
RAS wild-type, HER2+ unresectable/metastatic colorectal cancer (with trastuzumab)Adults300 mg BID300 mg BID300 mg BID

Renal No adjustment for mild–moderate (CLcr 30–89). With capecitabine: not recommended in severe (CLcr <30), as capecitabine is contraindicated

Hepatic Severe (Child-Pugh C): reduce to 200 mg BID. Mild–moderate: no adjustment

Instructions

Available strengths

Cautions

Adverse reactions

Pregnancy Can cause fetal harm (animal embryo-fetal mortality, reduced weight, malformations); advise contraception

Lactation Do not breastfeed during treatment and for 1 week after last dose

Cost

Tucatinib (TUKYSA)
Strength#/mogeneric $/moCostPlus
50 mgtab60 BIDnot offered
150 mgtab60 BIDnot offered
NADAC is a voluntary CMS survey of what retail community pharmacies pay for the drugs they stock. Tucatinib is dispensed outside retail pharmacies, so it rarely appears on surveyed invoices.

Generic entry2038 est.

NO BOXED WARNINGS

Principal riskDiarrhea and hepatotoxicity

Classes and tags

Clinical profile

Therapeutic safety burden3 / 4
Overdose danger2 / 4
Weight-gain liability0 / 4
Sedation liability0 / 4
QT / Torsades0 / 4
Direct muscarinic antagonism0 / 4
Embryofetal risk3 / 4

Legacy pregnancy categoryNot assigned — PLLR-era drug

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

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