Elzonris (tagraxofusp-erzs) vs Brukinsa (zanubrutinib)

Elzonris (tagraxofusp-erzs) vs Brukinsa (zanubrutinib)

Elzonris (tagraxofusp-erzs) is a targeted therapy known as a CD123-directed cytotoxin, approved for the treatment of blastic plasmacytoid dendritic cell neoplasm (BPDCN), a rare and aggressive form of blood cancer. Brukinsa (zanubrutinib) is a Bruton's tyrosine kinase (BTK) inhibitor used for the treatment of mantle cell lymphoma (MCL) and other B-cell malignancies, which works by blocking BTK and inhibiting cancer cell growth and survival. When deciding between Elzonris and Brukinsa, it is crucial to consider the specific type of blood cancer being treated, as each medication is targeted for different conditions and their use would be determined by a healthcare professional based on the patient's diagnosis and overall health profile.

Difference between Elzonris and Brukinsa

Metric Elzonris (tagraxofusp-erzs) Brukinsa (zanubrutinib)
Generic name tagraxofusp-erzs zanubrutinib
Indications Blastic plasmacytoid dendritic cell neoplasm (BPDCN) Mantle cell lymphoma (MCL), Waldenström's macroglobulinemia, Marginal zone lymphoma (MZL)
Mechanism of action CD123-directed cytotoxin Bruton's tyrosine kinase (BTK) inhibitor
Brand names Elzonris Brukinsa
Administrative route Intravenous Oral
Side effects Capillary leak syndrome, nausea, fatigue, edema, pyrexia Neutropenia, thrombocytopenia, anemia, diarrhea, bruising
Contraindications Hypersensitivity to tagraxofusp-erzs or any of its components Hypersensitivity to zanubrutinib or any of its components, severe bleeding, infection
Drug class Cytotoxin BTK inhibitor
Manufacturer Stemline Therapeutics, Inc. BeiGene, Ltd.

Efficacy

Elzonris (Tagraxofusp-erzs) Efficacy in Treating Leukemia

Elzonris (tagraxofusp-erzs) is a targeted therapy approved by the U.S. Food and Drug Administration (FDA) specifically for the treatment of blastic plasmacytoid dendritic cell neoplasm (BPDCN), a rare form of leukemia. The efficacy of Elzonris for treating BPDCN was demonstrated in clinical trials that led to its approval. In a pivotal trial, Elzonris showed a clinically meaningful response rate in patients with BPDCN. The majority of patients treated with Elzonris achieved a complete response or clinical complete response, indicating a significant reduction or disappearance of signs of the cancer.

While Elzonris is not approved for other types of leukemia, its mechanism of action, which involves targeting and delivering a cytotoxic agent to CD123-expressing cells, suggests potential utility in other CD123-positive hematologic malignancies. However, the efficacy of Elzonris in other forms of leukemia beyond BPDCN has not been established in large-scale, definitive clinical trials, and its use would be considered off-label in these contexts.

Brukinsa (Zanubrutinib) Efficacy in Treating Leukemia

Brukinsa (zanubrutinib) is a Bruton's tyrosine kinase (BTK) inhibitor that is FDA-approved for the treatment of mantle cell lymphoma (MCL). Although MCL is a type of non-Hodgkin lymphoma, there is interest in the potential efficacy of BTK inhibitors like zanubrutinib in chronic lymphocytic leukemia (CLL) and small lymphocytic lymphoma (SLL), which are both considered types of leukemia. Clinical trials have shown that Brukinsa is effective in achieving a high rate of response in patients with CLL and SLL, with a favorable safety profile compared to other BTK inhibitors.

It is important to note that while Brukinsa has shown promise in early clinical trials for CLL and SLL, its use in these indications would currently be off-label. Further large-scale clinical trials are necessary to fully establish the efficacy and safety of Brukinsa in the treatment of these and potentially other types of leukemia. As with any off-label use of medication, it is essential to weigh the potential benefits against the risks and to consider the evidence from clinical research and expert opinion.

Regulatory Agency Approvals

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

Access Elzonris or Brukinsa today

If Elzonris or Brukinsa 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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