Truxima (rituximab) vs Elzonris (tagraxofusp-erzs)

Truxima (rituximab) vs Elzonris (tagraxofusp-erzs)

Truxima (rituximab) is a monoclonal antibody used to treat certain types of blood cancers, such as non-Hodgkin lymphoma and chronic lymphocytic leukemia, as well as autoimmune diseases like rheumatoid arthritis. Elzonris (tagraxofusp-erzs) is a targeted therapy known as a CD123-directed cytotoxin, specifically approved for the treatment of blastic plasmacytoid dendritic cell neoplasm (BPDCN), a rare and aggressive form of blood cancer. When deciding between these two medications, it is crucial to consider the specific type of cancer being treated, as Truxima is not indicated for BPDCN, while Elzonris is not a treatment option for the conditions that Truxima addresses.

Difference between Truxima and Elzonris

Metric Truxima (rituximab) Elzonris (tagraxofusp-erzs)
Generic name Rituximab Tagraxofusp-erzs
Indications Non-Hodgkin's lymphoma, chronic lymphocytic leukemia, rheumatoid arthritis, granulomatosis with polyangiitis, microscopic polyangiitis Blastic plasmacytoid dendritic cell neoplasm (BPDCN)
Mechanism of action CD20-directed cytolytic antibody CD123-directed cytotoxin
Brand names Truxima, Rituxan, MabThera Elzonris
Administrative route Intravenous infusion Intravenous infusion
Side effects Infusion reactions, infections, body aches, fatigue, skin rash Capillary leak syndrome, nausea, fatigue, swelling, pyrexia
Contraindications Severe infections, hepatitis B reactivation, severe cardiac disease Capillary leak syndrome, hypersensitivity to tagraxofusp-erzs or any component of the formulation
Drug class Monoclonal antibody CD123-targeted therapy
Manufacturer Celltrion, Genentech Stemline Therapeutics, Inc.

Efficacy

Truxima (Rituximab) Efficacy in Treating Leukemia

Truxima, a biosimilar to the original rituximab, is a monoclonal antibody that targets the CD20 antigen found on the surface of B-cells. It is not primarily approved for leukemia but has been used off-label in certain types of this disease, notably in chronic lymphocytic leukemia (CLL) and occasionally in acute lymphoblastic leukemia (ALL) as part of a combination therapy. In CLL, rituximab has been shown to improve overall survival and progression-free survival when used in combination with chemotherapy. The efficacy of Truxima in treating leukemia is considered comparable to that of the reference product, rituximab, based on totality of evidence from analytical, preclinical, and clinical studies.

In the case of ALL, rituximab is used off-label due to its ability to target B-cell precursors. Studies have indicated that when added to standard chemotherapy regimens, rituximab can improve outcomes for patients with CD20-positive ALL. However, it is important to note that the use of Truxima for leukemia is not universally standard and its efficacy can vary depending on the specific patient population, disease characteristics, and treatment regimen.

Elzonris (Tagraxofusp-erzs) Efficacy in Treating Leukemia

Elzonris (tagraxofusp-erzs) is a novel targeted therapy approved by the FDA for the treatment of blastic plasmacytoid dendritic cell neoplasm (BPDCN), a rare form of leukemia. It is a fusion protein composed of interleukin-3 (IL-3) linked to a truncated diphtheria toxin. This drug targets the IL-3 receptor, which is overexpressed on BPDCN cells, and delivers the toxin into the cells, leading to cell death. Clinical trials have demonstrated significant efficacy of Elzonris in BPDCN, with a sizable proportion of patients achieving complete remission or clinical benefit. This has been a particularly important advancement given the historically poor prognosis associated with BPDCN and the lack of other effective treatments.

While the primary indication for Elzonris is BPDCN, its efficacy in other forms of leukemia is an area of ongoing investigation. As of the current knowledge cutoff, Elzonris is not approved for other types of leukemia, but research into its potential application in diseases with similar pathophysiology or IL-3 receptor expression continues. The unique mechanism of action of Elzonris offers a promising therapeutic option for patients with BPDCN and potentially other leukemias in the future, subject to the results of further clinical trials and regulatory reviews.

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)
Elzonris
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA

Access Truxima or Elzonris today

If Truxima or Elzonris 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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