Adcetris (brentuximab vedotin) vs Ukoniq (umbralisib)

Adcetris (brentuximab vedotin) vs Ukoniq (umbralisib)

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. Ukoniq (umbralisib) is a PI3K inhibitor and dual inhibitor of CK1ε, designed for the treatment of marginal zone lymphoma and follicular lymphoma after at least one prior anti-cancer therapy. When choosing between these medications, it is crucial to consider the specific type of lymphoma being treated, as well as the individual patient's previous treatments and overall health profile, since each drug is tailored for different indications and has its own side effect profile.

Difference between Adcetris and Ukoniq

Metric Adcetris (brentuximab vedotin) Ukoniq (umbralisib)
Generic name Brentuximab vedotin Umbralisib
Indications Hodgkin lymphoma, systemic anaplastic large cell lymphoma, primary cutaneous anaplastic large cell lymphoma, and certain types of mycosis fungoides Marginal zone lymphoma, follicular lymphoma
Mechanism of action Antibody-drug conjugate targeting CD30 on lymphoma cells PI3K delta and CK1 epsilon inhibitor
Brand names Adcetris Ukoniq
Administrative route Intravenous infusion Oral
Side effects Peripheral neuropathy, neutropenia, fatigue, nausea, fever, rash, thrombocytopenia Nausea, diarrhea, fatigue, increased liver enzymes, musculoskeletal pain
Contraindications Hypersensitivity to brentuximab vedotin or any excipients Hypersensitivity to umbralisib or any excipients
Drug class Antineoplastic agent, monoclonal antibody Antineoplastic agent, PI3K inhibitor
Manufacturer Seagen Inc. TG Therapeutics, Inc.

Efficacy

Efficacy of Adcetris (Brentuximab Vedotin) in Lymphoma

Adcetris (brentuximab vedotin) is an antibody-drug conjugate specifically indicated for the treatment of several types of lymphoma, including Hodgkin lymphoma (HL) and systemic anaplastic large cell lymphoma (sALCL). In clinical trials, Adcetris has shown significant efficacy in patients with relapsed or refractory HL after autologous hematopoietic stem cell transplantation (HSCT). In a pivotal phase 2 clinical trial, the overall response rate (ORR) was approximately 75% with a complete remission (CR) rate of 34% in this patient population. For sALCL, the ORR was around 86% with a CR rate of 57%, demonstrating Adcetris's potent activity against these lymphoma subtypes.

Adcetris's mechanism of action involves targeting CD30, a cell surface antigen expressed on lymphoma cells. Upon binding to CD30-positive cells, the agent is internalized and releases monomethyl auristatin E, a cytotoxic agent that disrupts the microtubule network, leading to cell cycle arrest and apoptosis. This targeted approach allows for direct delivery of the chemotherapeutic agent to the cancer cells, potentially reducing systemic exposure and toxicity.

Efficacy of Ukoniq (Umbralisib) in Lymphoma

Ukoniq (umbralisib) is a novel medication that has been approved for the treatment of marginal zone lymphoma (MZL) and follicular lymphoma (FL) after at least one prior anti-CD20-based therapy. Umbralisib is a dual inhibitor of PI3K-delta and CK1-epsilon, which are enzymes involved in the proliferation and survival of malignant B-cells. In clinical trials for MZL, umbralisib achieved an ORR of 49% with a CR rate of 16%. For patients with FL, the ORR was reported to be 43% with a CR rate of 3%. These results indicate that umbralisib can induce meaningful tumor shrinkage in a significant proportion of patients with relapsed or refractory MZL and FL.

Umbralisib's dual inhibitory action not only impedes the signaling pathways essential for the growth and survival of lymphoma cells but also affects the tumor microenvironment, which may contribute to its therapeutic effects. The clinical outcomes with umbralisib have been particularly encouraging in the relapsed or refractory setting, where treatment options are limited. The efficacy data from the trials underline the potential of umbralisib as a valuable treatment option for patients with these challenging forms 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)
Ukoniq
  • Food and Drug Administration (FDA), USA

Access Adcetris or Ukoniq today

If Adcetris or Ukoniq 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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