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

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.
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| FDA dosing | Population | Start | Target | Max |
|---|---|---|---|---|
| HER2+ metastatic breast cancer (with trastuzumab + capecitabine) | Adults | 300 mg BID | 300 mg BID | 300 mg BID |
| RAS wild-type, HER2+ unresectable/metastatic colorectal cancer (with trastuzumab) | Adults | 300 mg BID | 300 mg BID | 300 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
Available strengths
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
| Strength | #/mo | generic $/mo | CostPlus | |
|---|---|---|---|---|
| 50 mg | tab | 60 BID | not offered | |
| 150 mg | tab | 60 BID | not offered |
Generic entry2038 est.
NO BOXED WARNINGS
Principal riskDiarrhea and hepatotoxicity
Legacy pregnancy categoryNot assigned — PLLR-era drug
Defining liabilityMyelosuppression and agent-specific hepatic, cardiac, pulmonary, neurologic or reproductive toxicity require oncology monitoring.