Adcetris (brentuximab vedotin) vs Polivy (polatuzumab vedotin-piiq)

Adcetris (brentuximab vedotin) vs Polivy (polatuzumab vedotin-piiq)

Adcetris (brentuximab vedotin) and Polivy (polatuzumab vedotin-piiq) are both antibody-drug conjugates used in the treatment of certain types of lymphoma, but they target different antigens on the cancer cells. Adcetris targets CD30, a marker found on the surface of Hodgkin lymphoma cells and some T-cell non-Hodgkin lymphomas, and is approved for several indications including after failure of other treatments or as a first-line therapy in combination with chemotherapy. Polivy targets CD79b, which is present on B-cells, and is used in combination with other drugs for the treatment of relapsed or refractory diffuse large B-cell lymphoma (DLBCL) after at least two prior therapies. The choice between these medications would depend on the specific type of lymphoma, its expression of CD30 or CD79b, and the patient's previous treatments and overall health condition.

Difference between Adcetris and Polivy

Metric Adcetris (brentuximab vedotin) Polivy (polatuzumab vedotin-piiq)
Generic name Brentuximab vedotin Polatuzumab vedotin-piiq
Indications Hodgkin lymphoma, systemic anaplastic large cell lymphoma, primary cutaneous anaplastic large cell lymphoma, and certain types of mycosis fungoides Relapsed or refractory diffuse large B-cell lymphoma, in combination with bendamustine and a rituximab product
Mechanism of action CD30-directed antibody-drug conjugate CD79b-directed antibody-drug conjugate
Brand names Adcetris Polivy
Administrative route Intravenous infusion Intravenous infusion
Side effects Peripheral neuropathy, neutropenia, fatigue, nausea, anemia, upper respiratory tract infection, diarrhea, fever, rash, thrombocytopenia, cough, and vomiting Neutropenia, thrombocytopenia, anemia, peripheral neuropathy, fatigue, diarrhea, fever, decreased appetite, pneumonia, and cough
Contraindications Hypersensitivity to brentuximab vedotin or any of its excipients Hypersensitivity to polatuzumab vedotin-piiq or any of its excipients
Drug class Antineoplastic agent, monoclonal antibody Antineoplastic agent, monoclonal antibody
Manufacturer Seattle Genetics Genentech, Inc.

Efficacy

Efficacy of Adcetris (brentuximab vedotin) in Lymphoma

Adcetris (brentuximab vedotin) is an antibody-drug conjugate specifically indicated for the treatment of certain 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). The pivotal phase II study demonstrated an overall response rate (ORR) of 75% in this patient population, with a complete remission (CR) rate of 34%. For patients with sALCL, Adcetris achieved an ORR of 86% and a CR rate of 57% in a phase II clinical trial. These results have established Adcetris as an effective treatment option for patients with relapsed or refractory HL and sALCL.

Efficacy of Adcetris in Combination Therapies for Lymphoma

Adcetris has also been evaluated in combination with other chemotherapeutic agents. A phase III trial assessing the efficacy of Adcetris in combination with chemotherapy for frontline treatment of advanced classical HL showed a significant improvement in modified progression-free survival compared to the standard chemotherapy regimen alone. The combination therapy led to a two-year modified progression-free survival rate of 82.1% compared to 77.2% with standard therapy, highlighting the potential of Adcetris in improving treatment outcomes when used as part of a combination regimen in newly diagnosed HL.

Efficacy of Polivy (polatuzumab vedotin-piiq) in Lymphoma

Polivy (polatuzumab vedotin-piiq) is another antibody-drug conjugate approved for the treatment of diffuse large B-cell lymphoma (DLBCL), the most common type of non-Hodgkin lymphoma. It is indicated for use in combination with bendamustine and a rituximab product in patients who have relapsed or refractory DLBCL after at least two prior therapies. In a pivotal phase Ib/II clinical trial, the combination including Polivy showed an ORR of 40% with a CR rate of 24% in patients with relapsed or refractory DLBCL. These outcomes are particularly noteworthy considering the poor prognosis associated with this patient population and the limited treatment options available.

Conclusion

Both Adcetris and Polivy have demonstrated efficacy in the treatment of different types of lymphoma, with Adcetris being particularly effective in HL and sALCL, and Polivy showing promise in DLBCL. Their roles as part of combination therapies have also been established, leading to improved outcomes in patients with these challenging conditions. Continued research and clinical trials are expected to further define the utility of these antibody-drug conjugates in the management of lymphoma and potentially expand their indications.

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)
Polivy
  • Food and Drug Administration (FDA), USA
  • Pharmaceuticals and Medical Devices Agency (PMDA), Japan
  • Therapeutic Goods Administration (TGA), Australia

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If Adcetris or Polivy 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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