Verzenio/Verzenios (abemaciclib) vs Tukysa (tucatinib)

Verzenio/Verzenios (abemaciclib) vs Tukysa (tucatinib)

Verzenio (abemaciclib) and Tukysa (tucatinib) are both targeted therapies used in the treatment of certain types of cancer, but they are used for different indications and work through different mechanisms. Verzenio is primarily used in the treatment of HR-positive, HER2-negative advanced or metastatic breast cancer and functions as a CDK4/6 inhibitor, which helps to slow down the growth of cancer cells. On the other hand, Tukysa is used to treat HER2-positive breast cancer, particularly in patients with advanced unresectable or metastatic disease, and works by specifically inhibiting the HER2 protein, which can promote the growth of cancer cells. For a patient deciding on which medicine is right for them, it is essential to consider the specific subtype of breast cancer they have, as well as the medicine's mechanism of action, potential side effects, and any other individual health considerations that may influence treatment efficacy and safety. Consulting with a healthcare professional who can evaluate the patient's unique medical history and cancer characteristics is crucial in making an informed decision.

Difference between Verzenio/Verzenios and Tukysa

Metric Verzenio/Verzenios (abemaciclib) Tukysa (tucatinib)
Generic name Abemaciclib Tucatinib
Indications HR-positive, HER2-negative advanced or metastatic breast cancer HER2-positive breast cancer
Mechanism of action CDK4 & CDK6 inhibitor Tyrosine kinase inhibitor
Brand names Verzenio, Verzenios Tukysa
Administrative route Oral Oral
Side effects Diarrhea, neutropenia, nausea, abdominal pain, infections Diarrhea, palmar-plantar erythrodysesthesia, nausea, fatigue, hepatotoxicity
Contraindications None known specific to abemaciclib None known specific to tucatinib
Drug class Antineoplastic agent Antineoplastic agent
Manufacturer Eli Lilly and Company Seagen Inc.

Efficacy

Verzenio (Abemaciclib) Efficacy in Breast Cancer

Verzenio, also known by its generic name abemaciclib, is a targeted therapy medication used in the treatment of certain types of breast cancer. Specifically, it is indicated for hormone receptor-positive (HR+), human epidermal growth factor receptor 2-negative (HER2-) advanced or metastatic breast cancer. Verzenio works as a CDK4/6 inhibitor, disrupting the cell cycle and thereby inhibiting the proliferation of cancer cells. Clinical trials have demonstrated that Verzenio, particularly when used in combination with an aromatase inhibitor or fulvestrant, improves progression-free survival in patients with HR+, HER2- advanced or metastatic breast cancer. These improvements in survival rates represent a significant advancement in the management of this breast cancer subtype.

Moreover, the MONARCH 2 and MONARCH 3 clinical trials have shown that Verzenio, in combination with standard endocrine therapy, leads to a delay in disease progression and an increase in overall survival rates. Patients receiving Verzenio have experienced a median progression-free survival that was notably longer than those receiving placebo plus endocrine therapy. This efficacy underlines the importance of Verzenio as a part of the treatment regimen for postmenopausal women with advanced HR+, HER2- breast cancer.

Tukysa (Tucatinib) Efficacy in Breast Cancer

Tukysa, with the generic name tucatinib, is another novel medication used in the treatment of breast cancer. Tukysa is a tyrosine kinase inhibitor that specifically targets HER2-positive breast cancer, a subtype characterized by the overexpression of the HER2 protein. The drug is used in combination with trastuzumab and capecitabine for the treatment of adults with advanced unresectable or metastatic HER2-positive breast cancer, including those with brain metastases, who have received one or more prior anti-HER2-based regimens in the metastatic setting.

The efficacy of Tukysa was evaluated in the HER2CLIMB trial, which showcased a significant improvement in progression-free and overall survival in patients with HER2-positive metastatic breast cancer, including those with brain metastases. The addition of Tukysa to trastuzumab and capecitabine was shown to reduce the risk of disease progression or death by 46% compared to the placebo group. Furthermore, patients treated with Tukysa experienced a 34% reduction in the risk of death. These results highlight Tukysa's role as an effective treatment option for patients with this aggressive form of breast cancer, offering hope for improved outcomes.

Regulatory Agency Approvals

Verzenio/Verzenios
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
  • Therapeutic Goods Administration (TGA), Australia
Tukysa
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
  • Therapeutic Goods Administration (TGA), Australia
  • Swissmedic (CH)

Access Verzenio/Verzenios or Tukysa today

If Verzenio/Verzenios or Tukysa are not approved or available in your country (e.g. due to supply issues), you can access them via Everyone.org.

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