Truxima (rituximab) vs Xospata (gilteritinib)

Truxima (rituximab) vs Xospata (gilteritinib)

Truxima (rituximab) is a monoclonal antibody used primarily to treat certain types of blood cancers, such as non-Hodgkin's lymphoma and chronic lymphocytic leukemia, as well as autoimmune diseases like rheumatoid arthritis. Xospata (gilteritinib) is a tyrosine kinase inhibitor specifically indicated for the treatment of adult patients who have relapsed or refractory acute myeloid leukemia (AML) with a FLT3 mutation. The choice between Truxima and Xospata would depend on the specific type and characteristics of the cancer a patient has, as they target different diseases and work through distinct mechanisms of action.

Difference between Truxima and Xospata

Metric Truxima (rituximab) Xospata (gilteritinib)
Generic name Rituximab Gilteritinib
Indications Non-Hodgkin's lymphoma, chronic lymphocytic leukemia, rheumatoid arthritis, granulomatosis with polyangiitis, and microscopic polyangiitis Acute myeloid leukemia (AML) with a FLT3 mutation
Mechanism of action Monoclonal antibody that targets CD20 antigen on B cells Tyrosine kinase inhibitor that targets FLT3/AXL
Brand names Truxima, Rituxan, MabThera Xospata
Administrative route Intravenous infusion Oral
Side effects Infusion reactions, infections, cytopenias, cardiac arrhythmias, renal toxicity Fatigue, increased transaminase levels, diarrhea, dyspnea, edema, rash, differentiation syndrome
Contraindications Known hypersensitivity to rituximab or any of its components Known hypersensitivity to gilteritinib or any of its components
Drug class Monoclonal antibody, CD20-directed cytolytic antibody Tyrosine kinase inhibitor
Manufacturer Celltrion Healthcare, Teva Pharmaceuticals, Genentech (Roche) Astellas Pharma

Efficacy

Truxima (rituximab) Efficacy in Leukemia

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. In the context of leukemia, rituximab has been studied for its efficacy primarily in chronic lymphocytic leukemia (CLL) and, to a lesser extent, in acute lymphoblastic leukemia (ALL). In CLL, rituximab is often used in combination with chemotherapy and has been shown to improve overall survival and progression-free survival compared to chemotherapy alone. The addition of rituximab to standard chemotherapy regimens has become a standard of care in the treatment of CLL.

For ALL, the use of rituximab is more selective and is typically reserved for patients with CD20-positive B-cell precursor ALL. In this subset of patients, rituximab has demonstrated an improvement in event-free survival when added to chemotherapy. However, the use of rituximab in ALL is considered off-label, and the efficacy can vary based on the specific patient population and the chemotherapy regimen used.

Xospata (gilteritinib) Efficacy in Leukemia

Xospata (gilteritinib) is a targeted therapy approved for the treatment of adult patients who have relapsed or refractory acute myeloid leukemia (AML) with a FLT3 mutation as detected by an FDA-approved test. In clinical trials, gilteritinib has shown efficacy in inducing remissions in a proportion of patients with this specific genetic mutation. The response rates for patients treated with gilteritinib have been encouraging, with a significant number of patients achieving complete remission with full or partial hematologic recovery.

The efficacy of gilteritinib is particularly notable given that FLT3 mutations are associated with a poor prognosis in AML, and patients with relapsed or refractory AML have limited treatment options. Gilteritinib's role in improving outcomes for this challenging subset of AML patients represents a significant advancement in the treatment landscape. However, the long-term efficacy and survival benefits of gilteritinib are still under investigation, and ongoing clinical trials continue to evaluate its role in combination with other therapies and in different settings of AML treatment.

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)
Xospata
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
  • Therapeutic Goods Administration (TGA), Australia

Access Truxima or Xospata today

If Truxima or Xospata 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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