How long does it take Verzenio to work?
Verzenio (abemaciclib) is a targeted treatment that helps to reduce the growth and spread of cancer cells in the body. It may be used to treat adults with HR+ HER2-, node-positive, early breast cancer at high risk of recurrence in combination with endocrine treatment (tamoxifen or an aromatase inhibitor). It may also be used to treat advanced or metastatic HR+ HER2- breast cancer.
Verzenio belongs to the class of medicines known as CDK 4/6 inhibitors which help to reduce the growth and spread of cancer cells in the body.
Verzenio is usually taken twice daily. When taken regularly, consistent blood levels are achieved within five days.
Gastrointestinal side effects, such as diarrhea, typically occur in the first month of treatment and can affect up to 81% of patients. The average time to onset of diarrhea was 6 to 8 days. Diarrhea can be severe and requires monitoring and proper management.
Clinical trials have shown Verzenio improves invasive disease-free survival for men or women with early breast cancer and high-risk clinical and pathological factors:
For women taking Verzenio plus anastrozole or letrozole:
For women taking Verzenio in combination with fulvestrant:
For women taking Verzenio as monotherapy:
How does Verzenio work?
Verzenio belongs to the class of medicines known as CDK4/6 inhibitors. CDK4/6 inhibitors, such as Verzenio, target particular enzymes, called CDK4 and CDK6.
CDK stands for cyclin-dependent kinase, and it is an enzyme that is important for cell division. CDK4/6 inhibitors interrupt signals that stimulate the growth of cancerous cells. Certain cancers, for example, hormone-receptor-positive breast cancer, are more likely to have disturbances in CDK4/6, and CDK 4/6 inhibitors may form part of the treatment protocol.
Most often, CDK4/6 inhibitors are given at the same time as hormonal therapy (such as an aromatase inhibitor or fulvestrant), although Verzenio may be used alone to treat hormone receptor-positive, HER2-negative metastatic breast cancer in pre-treated patients.
Research suggests CDK4/6 inhibitors may increase the time people have before cancer spreads. More evidence is needed to determine their impact on overall survival.
Common side effects include fatigue and gastrointestinal disturbances, such as nausea, severe diarrhea, and vomiting. Bone marrow suppression resulting in neutropenia and leukopenia may also occur, although anemia and thrombocytopenia are less common. In general, the side effects associated with CDK4/6 inhibitor therapy are less severe than those experienced with chemotherapy.
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