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TAZVERIK (tazemetostat) is an EZH2 methyltransferase inhibitor, primarily used to treat specific cancer types with EZH2 mutations, including epithelioid sarcoma and relapsed or refractory follicular lymphoma. It works by inhibiting the EZH2 enzyme, which regulates gene expression through histone methylation, a process that is often disrupted in certain cancers. This drug is FDA-approved under an accelerated approval pathway based on initial clinical data demonstrating a response to treatment. Its continued approval depends on the results of ongoing studies to confirm long-term clinical benefits.
TAZVERIK is administered orally, typically at a dose of 800 mg twice daily, and it is well-suited for patients who have already undergone prior treatments with limited options. However, patients must be monitored for potential adverse reactions, such as hematologic toxicity and lipid abnormalities, which could require dose adjustments.
Tazverik is indicated for the treatment of adults and pediatric patients aged 16 years and older with metastatic or locally advanced epithelioid sarcoma who are not eligible for complete surgical resection. It is also indicated for conditions where EZH2 mutations are observed, making the drug particularly relevant in certain sarcomas and tumors linked to histone modification disruptions.
The recommended dose of Tazverik is 800 mg (four 200 mg tablets) orally once daily.
