Adcetris (brentuximab vedotin) vs Rylaze (asparaginase erwinia chrysanthemi (recombinant)-rywn)

Adcetris (brentuximab vedotin) vs Rylaze (asparaginase erwinia chrysanthemi (recombinant)-rywn)

Adcetris (brentuximab vedotin) is an antibody-drug conjugate specifically designed to treat certain types of lymphomas, including Hodgkin lymphoma and systemic anaplastic large cell lymphoma, by targeting the CD30 antigen on cancer cells. Rylaze (asparaginase erwinia chrysanthemi (recombinant)-rywn), on the other hand, is an asparagine-specific enzyme used to treat acute lymphoblastic leukemia (ALL) by depleting the amino acid asparagine, which is essential for the growth of leukemia cells. The choice between Adcetris and Rylaze would depend on the specific type and characteristics of the patient's hematologic cancer, as they are used to treat different diseases and work through distinct mechanisms.

Difference between Adcetris and Rylaze

Metric Adcetris (brentuximab vedotin) Rylaze (asparaginase erwinia chrysanthemi (recombinant)-rywn)
Generic name Brentuximab vedotin Asparaginase erwinia chrysanthemi (recombinant)-rywn
Indications Hodgkin lymphoma, systemic anaplastic large cell lymphoma, primary cutaneous anaplastic large cell lymphoma, and certain types of mycosis fungoides Acute lymphoblastic leukemia (ALL) as a component of a multi-agent chemotherapeutic regimen
Mechanism of action CD30-directed antibody-drug conjugate Enzyme that catalyzes the conversion of L-asparagine to aspartic acid and ammonia, depriving leukemia cells of an essential amino acid for protein synthesis
Brand names Adcetris Rylaze
Administrative route Intravenous infusion Intramuscular injection
Side effects Peripheral neuropathy, neutropenia, fatigue, nausea, fever, rash, thrombocytopenia Hypersensitivity reactions, pancreatitis, thrombosis, hemorrhage, hepatotoxicity, hyperglycemia
Contraindications Hypersensitivity to brentuximab vedotin or any excipient in the formulation Hypersensitivity to asparaginase erwinia chrysanthemi or any component of the formulation
Drug class Antineoplastic agent, monoclonal antibody, antibody-drug conjugate Antineoplastic agent, enzyme
Manufacturer Seattle Genetics Jazz Pharmaceuticals

Efficacy

Efficacy of Adcetris (Brentuximab Vedotin) in Lymphoma Treatment

Adcetris (brentuximab vedotin) is an antibody-drug conjugate specifically indicated for the treatment of several types of lymphoma, including Hodgkin lymphoma and systemic anaplastic large cell lymphoma (ALCL). Its efficacy in Hodgkin lymphoma has been demonstrated in clinical trials where it was used in patients with relapsed or refractory disease. The drug has shown a significant impact on overall response rates and progression-free survival, particularly when used in combination with other chemotherapy agents. In the pivotal trial, which led to its approval, a considerable percentage of patients achieved complete remission, indicating the potent activity of brentuximab vedotin against this type of lymphoma.

For systemic anaplastic large cell lymphoma, Adcetris has been shown to be effective as a monotherapy in patients who have relapsed or are refractory to other treatments. The response rates in clinical trials have been encouraging, with many patients experiencing tumor reduction and extended periods without disease progression. The targeted nature of brentuximab vedotin, which combines an anti-CD30 antibody with a cytotoxic agent, allows for direct delivery of the drug to the malignant cells, thereby enhancing its efficacy while minimizing systemic exposure.

Efficacy of Rylaze (Asparaginase Erwinia Chrysanthemi (Recombinant)-rywn) in Lymphoma

Rylaze, also known as asparaginase Erwinia chrysanthemi (recombinant)-rywn, is not directly indicated for the treatment of lymphoma. Instead, Rylaze is approved for use as a component of a multi-agent chemotherapeutic regimen for acute lymphoblastic leukemia (ALL). Its efficacy in lymphoma has not been established as it is not typically used for this type of cancer. Asparaginase enzymes are primarily utilized in the treatment of ALL due to their ability to deplete asparagine, an amino acid that is essential for the survival of leukemia cells. The role of asparaginase in lymphoma treatment is not well-defined, and therefore, Rylaze is not commonly part of lymphoma treatment protocols.

In summary, while Adcetris has proven efficacy in the treatment of certain types of lymphoma, Rylaze does not have an established role in the management of lymphoma. It is important for healthcare providers to use these medications within their approved indications and to consider the evidence base supporting their use in specific diseases. Patients should discuss with their oncologists the most appropriate treatment options for their specific type of lymphoma.

Regulatory Agency Approvals

Adcetris
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
  • Pharmaceuticals and Medical Devices Agency (PMDA), Japan
  • Therapeutic Goods Administration (TGA), Australia
  • NMPA (China)
Rylaze
  • Food and Drug Administration (FDA), USA

Access Adcetris or Rylaze today

If Adcetris or Rylaze 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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