TUKYSA 150MG /200MG /250MG TAB (TUCATINIB)
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Tukysa
- Generic Name: tucatinib tablets
- Brand Name: Tukysa
- Drug Class: Antineoplastic Tyrosine Kinase Inhibitors
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Tukysa (tucatinib) is a kinase inhibitor used in combination with trastuzumab and capecitabine to treat adult patients with advanced unresectable or metastatic HER2-positive breast cancer, including patients with brain metastases, who have received one or more prior anti-HER2-based regimens in the metastatic setting.
Generic Name: Tucatinib
Brand Name: Tukysa
Manufacturer: Seagen Inc. & licensed by Pfizer
Drug Class: HER2-selective tyrosine kinase inhibitor
Indications:
HER2‑positive metastatic breast cancer — in combination with trastuzumab and capecitabine, including those with brain metastases, after prior anti-HER2 therapy .
RAS wild-type, HER2-positive metastatic colorectal cancer — combined with trastuzumab after progression on fluoropyrimidine, oxaliplatin, and irinotecan .
Standard adult dose: 300 mg orally twice daily, ~12 hours apart, with or without food .
With capecitabine/trastuzumab (breast cancer): Capecitabine is dosed at 1,000 mg/m² twice daily with meals .
Dose adjustments:
1st reduction: 250 mg twice daily
2nd: 200 mg twice daily
3rd: 150 mg twice daily; discontinue if still not tolerated .
Very Common:
Diarrhea (up to 81%; ~12% grade 3–4)
Nausea, vomiting
Palmar‑plantar erythrodysesthesia (hand‑foot rash)
Rash
Stomatitis (mouth sores)
Fatigue
Elevated liver enzymes (AST/ALT)
Anemia, decreased appetite
Other Possible Effects:
Fever, infusion reactions (colorectal cancer regimen)
Diarrhea: Severe diarrhea may cause dehydration, hypotension, kidney injury, or death. Monitor closely and manage promptly with anti-diarrheals. Interrupt or reduce dose if grade ≥3.
Hepatotoxicity: Monitor liver enzymes before treatment and every 3 weeks; dose reductions or discontinuation may be needed
Fertility: May impair fertility—both males and females should use contraception during treatment and for 1 week afterward
Contraindications/cautions:
Severe hepatic impairment: dose adjustment recommended.
Severe renal impairment in capecitabine regimen not recommended .
Breastfeeding: avoid during and 1 week after last dose .
Tukysa is a potent, targeted oral therapy for advanced HER2-positive cancers, either breast or colorectal, offering benefits even in patients with brain metastases. However, vigilant monitoring for severe diarrhea and liver toxicity, as well as dose adjustments, are essential. Discuss potential benefits and risks with your oncologist to ensure safe and optimal use.
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