Xpovio (selinexor) vs Lunsumio (mosunetuzumab-axgb)

Xpovio (selinexor) vs Lunsumio (mosunetuzumab-axgb)

Xpovio (selinexor) is an oral selective inhibitor of nuclear export, approved for the treatment of multiple myeloma and certain types of diffuse large B-cell lymphoma, working by blocking the export of tumor suppressor proteins. Lunsumio (mosunetuzumab-axgb), on the other hand, is a bispecific T-cell engager antibody approved for the treatment of follicular lymphoma, designed to redirect T-cells to engage and eliminate B-cells. When deciding between these medications, it is important to consider the specific type and stage of lymphoma, previous treatments, potential side effects, and the mode of administration, as Xpovio is taken orally while Lunsumio is given intravenously.

Difference between Xpovio and Lunsumio

Metric Xpovio (selinexor) Lunsumio (mosunetuzumab-axgb)
Generic name Selinexor Mosunetuzumab-axgb
Indications Multiple myeloma, diffuse large B-cell lymphoma Follicular lymphoma
Mechanism of action Selective inhibitor of nuclear export Bispecific T-cell engager antibody
Brand names Xpovio Lunsumio
Administrative route Oral Intravenous
Side effects Nausea, vomiting, fatigue, anorexia, weight loss Cytokine release syndrome, infections, fatigue, diarrhea
Contraindications Thrombocytopenia, neutropenia, pregnancy None known
Drug class Antineoplastic agent Monoclonal antibody
Manufacturer Karyopharm Therapeutics Genentech

Efficacy

Xpovio (Selinexor) Efficacy in Treating Lymphoma

Xpovio (selinexor) is a prescription medication that functions as a selective inhibitor of nuclear export, specifically targeting the exportin 1 (XPO1) protein. It has been approved by the U.S. Food and Drug Administration (FDA) for use in combination with dexamethasone for the treatment of adult patients with relapsed or refractory multiple myeloma and, as of 2020, for certain types of relapsed or refractory diffuse large B-cell lymphoma (DLBCL). In clinical trials, selinexor has shown efficacy in patients with DLBCL, particularly in those who have received at least two prior therapies and have not responded or have relapsed. The efficacy of selinexor in this setting is measured by the overall response rate (ORR) and duration of response (DOR), with studies showing a meaningful proportion of patients achieving partial or complete responses to the treatment.

Lunsumio (Mosunetuzumab-axgb) Efficacy in Treating Lymphoma

Lunsumio (mosunetuzumab-axgb) is a bispecific antibody that targets CD20 on B-cells and CD3 on T-cells, thereby redirecting T-cells to engage and eliminate B-cell lymphomas. As of the knowledge cutoff date, mosunetuzumab-axgb has been investigated in clinical trials for the treatment of various types of non-Hodgkin lymphoma, including follicular lymphoma and DLBCL. The efficacy of mosunetuzumab-axgb has been demonstrated in terms of ORR, complete response rates, and DOR. In a pivotal phase I/II study, mosunetuzumab-axgb showed promising results in heavily pretreated patients with relapsed or refractory follicular lymphoma, achieving high complete response rates and durable responses.

Both Xpovio and Lunsumio represent advances in the treatment of lymphoma, offering new options for patients who have limited responses to conventional therapies. While Xpovio targets nuclear export to induce apoptosis in cancer cells, Lunsumio engages the patient's own immune system to target and destroy lymphoma cells. The efficacy of these drugs in clinical trials underscores the potential of targeted therapies and immunotherapies in improving outcomes for patients with lymphoma.

It is important to note that the efficacy of these medications can vary based on individual patient characteristics and disease subtypes. Therefore, healthcare providers consider a range of factors, including previous treatments and specific lymphoma characteristics, when determining the appropriateness of Xpovio or Lunsumio for their patients. Ongoing research and clinical trials continue to refine the understanding of how best to use these medications in the treatment of lymphoma.

Regulatory Agency Approvals

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

Access Xpovio or Lunsumio today

If Xpovio or Lunsumio 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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