Adcetris (brentuximab vedotin) vs Xpovio (selinexor)

Adcetris (brentuximab vedotin) vs Xpovio (selinexor)

Adcetris (brentuximab vedotin) is an antibody-drug conjugate specifically targeting CD30-positive cells, commonly used in the treatment of Hodgkin lymphoma and systemic anaplastic large cell lymphoma. Xpovio (selinexor) is a selective inhibitor of nuclear export, used for multiple myeloma and diffuse large B-cell lymphoma, particularly in cases where other treatments have failed. When deciding between Adcetris and Xpovio, it is essential to consider the specific type of cancer, its progression, previous treatments, and the patient's overall health, as each medication has a distinct mechanism of action and side effect profile that may influence the choice of treatment.

Difference between Adcetris and Xpovio

Metric Adcetris (brentuximab vedotin) Xpovio (selinexor)
Generic name Brentuximab vedotin Selinexor
Indications Hodgkin lymphoma, systemic anaplastic large cell lymphoma, primary cutaneous anaplastic large cell lymphoma, and certain types of mycosis fungoides Multiple myeloma, diffuse large B-cell lymphoma
Mechanism of action Antibody-drug conjugate targeting CD30-expressing cells Selective inhibitor of nuclear export (SINE) compounds that inhibits exportin 1 (XPO1)
Brand names Adcetris Xpovio
Administrative route Intravenous injection Oral
Side effects Peripheral neuropathy, neutropenia, fatigue, nausea, fever, rash, thrombocytopenia Nausea, vomiting, fatigue, loss of appetite, weight loss, diarrhea, fever, anemia, thrombocytopenia
Contraindications Hypersensitivity to brentuximab vedotin or any of its excipients Hypersensitivity to selinexor or any of its excipients
Drug class Antineoplastic agent, monoclonal antibody Antineoplastic agent, exportin 1 inhibitor
Manufacturer Seattle Genetics Karyopharm Therapeutics

Efficacy

Efficacy of Adcetris (Brentuximab Vedotin) in Lymphoma

Adcetris (brentuximab vedotin) is a targeted therapy approved for the treatment of several types of lymphoma, including Hodgkin lymphoma and systemic anaplastic large cell lymphoma (ALCL). The efficacy of Adcetris in Hodgkin lymphoma was demonstrated in a pivotal phase 3 clinical trial which showed that the drug, when used as a consolidation therapy post-autologous stem cell transplant (ASCT), can significantly improve progression-free survival compared to placebo. This improvement in survival was seen without a corresponding increase in treatment-related mortality, indicating a favorable benefit-risk profile for patients with relapsed or refractory Hodgkin lymphoma.

For systemic anaplastic large cell lymphoma, Adcetris has shown efficacy as a monotherapy in patients who have relapsed after at least one prior multi-agent chemotherapy regimen. The objective response rate (ORR) in this patient population was high, with a significant proportion of patients achieving complete remission. The duration of response for those who achieved remission was also notable, suggesting that Adcetris can provide a meaningful clinical benefit in this setting.

Efficacy of Xpovio (Selinexor) in Lymphoma

Xpovio (selinexor) is a selective inhibitor of nuclear export (SINE) compound that has been studied for its efficacy in treating various types of lymphoma, including diffuse large B-cell lymphoma (DLBCL). In clinical trials, Xpovio, in combination with dexamethasone, was evaluated in patients with relapsed or refractory DLBCL who had received multiple prior lines of therapy. The results demonstrated a modest ORR, with a subset of patients achieving partial or complete responses. The median duration of response for these patients indicated that Xpovio could offer a therapeutic option for those with limited alternatives due to the refractory nature of their disease.

It is important to note that the efficacy of both Adcetris and Xpovio can vary based on the specific subtype of lymphoma, prior treatments, and individual patient factors. Clinical trials continue to explore the use of these drugs in various combinations and settings to optimize outcomes for patients with lymphoma. As with any medication, the decision to use Adcetris or Xpovio should be made in consultation with a healthcare provider, taking into account the potential benefits and risks for the individual patient.

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

Access Adcetris or Xpovio today

If Adcetris or Xpovio 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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