Keytruda (pembrolizumab) vs Tazverik (tazemetostat)

Keytruda (pembrolizumab) vs Tazverik (tazemetostat)

Keytruda (pembrolizumab) is an immune checkpoint inhibitor that works by blocking the PD-1 protein on the surface of immune cells, thereby enhancing the immune system's ability to detect and fight cancer cells. It is widely used for various types of cancer, including melanoma, lung cancer, head and neck cancer, and others. In contrast, Tazverik (tazemetostat) is a selective inhibitor of the EZH2 enzyme, used primarily for the treatment of epithelioid sarcoma and certain types of non-Hodgkin lymphoma, and it works by modifying gene expression to inhibit cancer cell proliferation. For someone deciding which medicine is right for them, it is crucial to consult with a healthcare professional to determine the specific type of cancer they have, its genetic makeup, and the overall treatment goals, as these factors are essential in choosing between medications like Keytruda and Tazverik.

Difference between Keytruda and Tazverik

Metric Keytruda (pembrolizumab) Tazverik (tazemetostat)
Generic name Pembrolizumab Tazemetostat
Indications Various types of cancer including melanoma, lung cancer, head and neck cancer, Hodgkin lymphoma, and others Epithelioid sarcoma, follicular lymphoma
Mechanism of action Programmed death receptor-1 (PD-1) blocking antibody EZH2 inhibitor
Brand names Keytruda Tazverik
Administrative route Injection (IV) Oral
Side effects Fatigue, musculoskeletal pain, decreased appetite, itching, diarrhea, nausea, rash, fever, cough, difficulty breathing, constipation, pain, and abdominal pain Fatigue, pain, nausea, anemia, vomiting, constipation, and decreased appetite
Contraindications Individuals with hypersensitivity to pembrolizumab or its excipients Individuals with hypersensitivity to tazemetostat or its excipients
Drug class Immune checkpoint inhibitor Epigenetic therapy
Manufacturer Merck & Co. Epizyme, Inc.

Efficacy

Efficacy of Keytruda (Pembrolizumab) in Lymphoma

Keytruda, also known by its generic name pembrolizumab, is a type of immunotherapy that has shown efficacy in treating certain types of lymphoma. Specifically, it has been approved by the FDA for the treatment of adult and pediatric patients with refractory classical Hodgkin lymphoma (cHL), or those who have relapsed after three or more prior lines of therapy. Pembrolizumab is a programmed death receptor-1 (PD-1) blocking antibody, which helps the immune system to detect and fight cancer cells. Clinical trials have demonstrated that pembrolizumab can induce a significant response in a subset of patients with cHL, leading to partial or complete remission of the disease. However, the response rates and duration of response can vary widely among patients.

Efficacy of Tazverik (Tazemetostat) in Lymphoma

Tazverik, with the generic name tazemetostat, is an orally administered small molecule inhibitor of the EZH2 enzyme, which is often mutated or overexpressed in certain types of cancer, including lymphoma. The FDA has granted accelerated approval to tazemetostat for the treatment of adults and pediatric patients aged 16 years and older with relapsed or refractory follicular lymphoma (FL), whose tumors are positive for an EZH2 mutation as detected by an FDA-approved test and who have received at least two prior systemic therapies. It is also approved for FL patients who have no satisfactory alternative treatment options. Tazemetostat has shown a clinically meaningful and durable response in these patients, with a manageable safety profile.

Comparative Efficacy in Lymphoma

When comparing the efficacy of Keytruda and Tazverik, it is important to note that they are approved for different types of lymphoma and their mechanisms of action are distinct. Keytruda targets the PD-1 pathway to enhance the body's immune response against cancer cells, while Tazverik inhibits the activity of the EZH2 enzyme, which is implicated in the oncogenic process of certain lymphomas. Therefore, their efficacy is not directly comparable, and the choice of treatment would depend on the specific type of lymphoma, the presence of certain genetic mutations, the patient's prior treatment history, and overall health status.

Considerations for Treatment Selection

When considering treatment with either Keytruda or Tazverik for lymphoma, healthcare providers evaluate several factors, including the specific subtype of lymphoma, the presence of biomarkers such as PD-1 or EZH2 mutations, previous treatments, and the patient's performance status. Both drugs are generally used in cases where the disease has not responded to standard treatments, indicating a more aggressive or refractory disease course. As with all cancer therapies, the efficacy of these drugs must be balanced with their side effect profiles, and treatment decisions should be made in the context of a multidisciplinary team approach, taking into account the most current clinical guidelines and evidence.

Regulatory Agency Approvals

Keytruda
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
  • Therapeutic Goods Administration (TGA), Australia
  • Medsafe (NZ)
Tazverik
  • Food and Drug Administration (FDA), USA
  • Pharmaceuticals and Medical Devices Agency (PMDA), Japan

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If Keytruda or Tazverik 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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