Adcetris (brentuximab vedotin) vs Columvi (glofitamab-gxbm)

Adcetris (brentuximab vedotin) vs Columvi (glofitamab-gxbm)

Adcetris (brentuximab vedotin) is an antibody-drug conjugate specifically targeting CD30, a marker on lymphoma cells, and is approved for several types of lymphomas, including Hodgkin lymphoma and systemic anaplastic large cell lymphoma. On the other hand, Glofitamab (Columvi) is a bispecific monoclonal antibody that redirects T cells to target and eliminate CD20-expressing B cells, and it's being investigated for the treatment of B-cell malignancies. When deciding between these two medications, it is crucial to consider the specific type of lymphoma being treated, as well as the individual patient's medical history, as each drug targets different antigens and may have different indications, side effect profiles, and administration schedules.

Difference between Adcetris and Columvi

Metric Adcetris (brentuximab vedotin) Columvi (glofitamab-gxbm)
Generic name Brentuximab vedotin Glofitamab-gxbm
Indications Hodgkin lymphoma, systemic anaplastic large cell lymphoma, primary cutaneous anaplastic large cell lymphoma, and certain types of mycosis fungoides Currently being investigated for the treatment of B-cell non-Hodgkin lymphoma
Mechanism of action Antibody-drug conjugate targeting CD30 on lymphoma cells Bispecific antibody targeting CD20 on B-cells and CD3 on T-cells
Brand names Adcetris Columvi
Administrative route Intravenous infusion Intravenous infusion
Side effects Peripheral neuropathy, neutropenia, fatigue, nausea, fever, rash, thrombocytopenia Not fully characterized; clinical trials are ongoing
Contraindications Concomitant use of bleomycin due to pulmonary toxicity Not fully established; clinical trials are ongoing
Drug class Antineoplastic agent, monoclonal antibody, antibody-drug conjugate Monoclonal antibody, bispecific antibody
Manufacturer Seagen Inc. (formerly Seattle Genetics) and Takeda Pharmaceutical Company Roche

Efficacy

Efficacy of Adcetris (Brentuximab Vedotin) in Lymphoma Treatment

Adcetris (brentuximab vedotin) is an antibody-drug conjugate specifically designed to target CD30, a protein expressed on the surface of some lymphoma cells. In the treatment of lymphoma, particularly Hodgkin lymphoma (HL) and systemic anaplastic large cell lymphoma (sALCL), Adcetris has shown significant efficacy. Clinical trials have demonstrated that Adcetris, when used as a single agent, can induce complete remission in a substantial proportion of patients with relapsed or refractory HL and sALCL. Additionally, when combined with chemotherapy, Adcetris has improved the outcomes for patients with previously untreated advanced HL, leading to its approval for frontline therapy in this setting.

The pivotal phase III trial known as the ECHELON-1 study further solidified the role of Adcetris in treating Hodgkin lymphoma. In this study, a combination of Adcetris and chemotherapy demonstrated a statistically significant improvement in the modified progression-free survival compared to the standard chemotherapy regimen alone. This supported the use of Adcetris as a part of the first-line treatment regimen for advanced Hodgkin lymphoma, offering a new hope for patients with this type of lymphoma.

Efficacy of Columvi (Glofitamab-gxbm) in Lymphoma Treatment

Columvi (glofitamab-gxbm) is a novel bispecific monoclonal antibody that targets both CD20, a protein commonly found on B-cells, and CD3, a protein found on T-cells. This dual targeting mechanism facilitates the destruction of B-cell lymphomas by bringing cytotoxic T-cells into close proximity with the malignant B-cells. Although Columvi is a relatively new therapeutic agent, early clinical trials have shown promising results in the treatment of various types of non-Hodgkin lymphoma (NHL), including diffuse large B-cell lymphoma (DLBCL) and follicular lymphoma.

In these early phase clinical studies, Columvi has been evaluated as a monotherapy and in combination with other treatments. The data have indicated that Columvi can induce rapid and durable responses in patients with relapsed or refractory B-cell lymphomas. The efficacy of Columvi is particularly noteworthy in the context of heavily pre-treated patients, where traditional treatment options may be limited. As research continues, Columvi may become an important addition to the therapeutic arsenal against lymphoma, offering a new mechanism of action that could potentially overcome resistance to existing therapies.

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

Access Adcetris or Columvi today

If Adcetris or Columvi 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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