Elzonris (tagraxofusp-erzs) vs Lumoxiti (moxetumomab pasudotox)

Elzonris (tagraxofusp-erzs) vs Lumoxiti (moxetumomab pasudotox)

Elzonris (tagraxofusp-erzs) is a targeted therapy approved for the treatment of blastic plasmacytoid dendritic cell neoplasm (BPDCN), a rare and aggressive form of blood cancer, and works by targeting and attaching to a protein called CD123 on the surface of cancer cells, delivering a toxin that kills these cells. Lumoxiti (moxetumomab pasudotox) is also a targeted therapy, but it is used for the treatment of hairy cell leukemia, another rare type of blood cancer, and it targets a different protein called CD22, also delivering a toxin to kill cancer cells. The choice between Elzonris and Lumoxiti would depend on the specific type of blood cancer a patient has, as they are each designed to target different diseases and are not interchangeable.

Difference between Elzonris and Lumoxiti

Metric Elzonris (tagraxofusp-erzs) Lumoxiti (moxetumomab pasudotox)
Generic name Tagraxofusp-erzs Moxetumomab pasudotox-tdfk
Indications Blastic plasmacytoid dendritic cell neoplasm (BPDCN) Hairy cell leukemia (HCL)
Mechanism of action CD123-directed cytotoxin CD22-directed cytotoxin
Brand names Elzonris Lumoxiti
Administrative route Intravenous infusion Intravenous infusion
Side effects Capillary leak syndrome, nausea, fatigue, edema, pyrexia Nausea, fatigue, headache, pyrexia, peripheral edema
Contraindications Hypersensitivity to tagraxofusp-erzs or any of its components Hypersensitivity to moxetumomab pasudotox or any of its components
Drug class Fusion protein toxin Recombinant immunotoxin
Manufacturer Stemline Therapeutics, Inc. AstraZeneca Pharmaceuticals LP

Efficacy

Efficacy of Elzonris (tagraxofusp-erzs) in Treating Leukemia

Elzonris (tagraxofusp-erzs) is a targeted therapy approved by the U.S. Food and Drug Administration (FDA) for the treatment of blastic plasmacytoid dendritic cell neoplasm (BPDCN), a rare form of leukemia. The efficacy of Elzonris for the treatment of BPDCN was demonstrated in clinical trials, where it showed significant therapeutic effects. Patients treated with Elzonris experienced a clinically meaningful response rate, with some achieving complete remission. The treatment has been particularly beneficial for newly diagnosed patients, offering a novel therapeutic option for a disease that previously had no standardized treatment approach.

While Elzonris is specifically indicated for BPDCN, its efficacy for other types of leukemia is not well established. As an off-label use, it may be considered in certain cases, but healthcare professionals typically rely on clinical trial data and published case reports to guide these decisions. The use of Elzonris for conditions other than BPDCN would require careful consideration of the potential benefits and risks, and it is not currently a standard treatment for other forms of leukemia.

Efficacy of Lumoxiti (moxetumomab pasudotox) in Treating Leukemia

Lumoxiti (moxetumomab pasudotox) is an FDA-approved medication for the treatment of hairy cell leukemia (HCL), a rare type of leukemia. Lumoxiti has shown significant efficacy in patients with HCL, particularly in those who have relapsed or are refractory to other treatments. In clinical trials, Lumoxiti demonstrated a high rate of durable complete remission, which is a key goal in the treatment of HCL. The drug's mechanism of action, which involves targeting and killing cancer cells, has proven to be effective in reducing the disease burden in affected patients.

While Lumoxiti's approval and demonstrated efficacy are specific to hairy cell leukemia, its use in other types of leukemia has not been established. The drug's unique mechanism of action suggests potential for broader applications, but further research would be required to evaluate its effectiveness in other leukemic conditions. As with any medication, the off-label use of Lumoxiti would need to be supported by clinical evidence and considered on a case-by-case basis, weighing the potential benefits against the risks.

Regulatory Agency Approvals

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

Access Elzonris or Lumoxiti today

If Elzonris or Lumoxiti 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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