Truxima (rituximab) vs Tazverik (tazemetostat)

Truxima (rituximab) vs Tazverik (tazemetostat)

Truxima (rituximab) is a monoclonal antibody that targets the CD20 protein found on the surface of B cells and is commonly used in the treatment of certain types of non-Hodgkin lymphoma, chronic lymphocytic leukemia, and rheumatoid arthritis. Tazverik (tazemetostat) is a small molecule inhibitor that targets the EZH2 enzyme, used for the treatment of epithelioid sarcoma and certain types of non-Hodgkin lymphoma with an EZH2 gene mutation. When deciding between Truxima and Tazverik, it is important to consider the specific type and genetic characteristics of the cancer, as well as the patient's overall health and treatment history, since each medication has a different mechanism of action and is approved for different indications.

Difference between Truxima and Tazverik

Metric Truxima (rituximab) Tazverik (tazemetostat)
Generic name Rituximab Tazemetostat
Indications Non-Hodgkin's lymphoma, chronic lymphocytic leukemia, rheumatoid arthritis, granulomatosis with polyangiitis, microscopic polyangiitis Epithelioid sarcoma, follicular lymphoma
Mechanism of action CD20-directed cytolytic antibody EZH2 inhibitor
Brand names Truxima, Rituxan, MabThera Tazverik
Administrative route Intravenous infusion Oral
Side effects Infusion reactions, infections, body aches, fatigue, skin rash Nausea, vomiting, constipation, pain, fatigue, anemia, decreased appetite
Contraindications Severe infections, hepatitis B reactivation, severe cardiac disease None known that are specific to tazemetostat
Drug class Monoclonal antibody Small molecule inhibitor
Manufacturer Celltrion Healthcare, Genentech Epizyme, Inc.

Efficacy

Truxima (Rituximab) for Lymphoma

Truxima, a biosimilar to the original rituximab product, is a monoclonal antibody that targets the CD20 antigen on the surface of pre-B and mature B lymphocytes. It is approved for the treatment of non-Hodgkin lymphoma (NHL), including follicular lymphoma and diffuse large B-cell lymphoma, as well as chronic lymphocytic leukemia. Studies have demonstrated that Truxima is effective in reducing tumor burden and improving survival rates in patients with these types of lymphoma. When used in combination with chemotherapy, Truxima has been shown to improve overall response rates and prolong progression-free survival compared to chemotherapy alone.

Tazverik (Tazemetostat) for Lymphoma

Tazverik (tazemetostat) is a selective inhibitor of the EZH2 enzyme, which is often mutated or overexpressed in various types of cancer, including some forms of lymphoma. It has been approved for the treatment of adults with relapsed or refractory follicular lymphoma whose tumors are positive for an EZH2 mutation and for those with no satisfactory alternative treatment options. Tazverik has shown efficacy in shrinking tumors and achieving partial or complete responses in a subset of these patients. The drug's effectiveness in treating follicular lymphoma was evaluated in a clinical trial where it demonstrated a meaningful proportion of patients achieving objective response rates, with a small number also reaching complete remission.

Comparison of Efficacy in Lymphoma Treatment

When comparing the efficacy of Truxima and Tazverik, it is important to consider the specific type of lymphoma and the patient's individual characteristics. Truxima has a broad indication for various types of B-cell non-Hodgkin lymphoma and is often used as a first-line treatment in combination with chemotherapy. Tazverik, on the other hand, is used for a more specific patient population with relapsed or refractory follicular lymphoma, particularly those with an EZH2 mutation. The choice between these medications would depend on the lymphoma subtype, previous treatments, and the presence of specific genetic markers.

Conclusion

Both Truxima and Tazverik play significant roles in the management of lymphoma. Truxima has a well-established efficacy profile in treating various B-cell lymphomas, especially when combined with chemotherapy. Tazverik offers a targeted approach for patients with EZH2-mutated follicular lymphoma who have limited treatment options. Ongoing research and clinical trials continue to refine the understanding of how best to use these drugs in the treatment of lymphoma, aiming to improve patient outcomes and quality of life.

Regulatory Agency Approvals

Truxima
  • 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

Access Truxima or Tazverik today

If Truxima 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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