Opdivo (Nivolumab) vs Adcetris (brentuximab vedotin)

Opdivo (Nivolumab) vs Adcetris (brentuximab vedotin)

Opdivo (nivolumab) is a PD-1 inhibitor used in immunotherapy to treat a variety of cancers, including melanoma, lung cancer, and kidney cancer, by helping the immune system recognize and attack cancer cells. Adcetris (brentuximab vedotin) is an antibody-drug conjugate specifically targeting CD30, a protein found on some cancer cells, and is primarily used to treat Hodgkin lymphoma and certain types of T-cell lymphomas. The choice between Opdivo and Adcetris would depend on the type of cancer a patient has, as they are designed to treat different conditions and work through distinct mechanisms within the body.

Difference between Opdivo and Adcetris

Metric Opdivo (Nivolumab) Adcetris (brentuximab vedotin)
Generic name Nivolumab Brentuximab vedotin
Indications Various types of cancers including melanoma, lung cancer, renal cell carcinoma, Hodgkin lymphoma, head and neck cancer, urothelial carcinoma, and more. Classical Hodgkin lymphoma, systemic anaplastic large cell lymphoma, and other CD30-expressing lymphomas.
Mechanism of action PD-1 immune checkpoint inhibitor that enables the immune system to attack cancer cells. Antibody-drug conjugate targeting CD30, which delivers a cytotoxic agent directly to CD30-expressing cells.
Brand names Opdivo Adcetris
Administrative route Intravenous infusion Intravenous infusion
Side effects Fatigue, rash, musculoskeletal pain, pruritus, diarrhea, nausea, decreased appetite, cough, dyspnea, constipation, vomiting, and others. Peripheral neuropathy, fatigue, nausea, fever, anemia, upper respiratory tract infection, diarrhea, rash, thrombocytopenia, cough, and others.
Contraindications Known hypersensitivity to nivolumab or any of its excipients. Known hypersensitivity to brentuximab vedotin, its excipients, or to bleomycin.
Drug class Monoclonal antibody, PD-1 inhibitor Antibody-drug conjugate, CD30-directed
Manufacturer Bristol-Myers Squibb Seagen Inc. (formerly Seattle Genetics) and Takeda Pharmaceutical Company

Efficacy

Efficacy of Opdivo (Nivolumab) in Lymphoma

Opdivo (Nivolumab) is an immune checkpoint inhibitor specifically targeting the PD-1 receptor on T cells. It is designed to overcome immune resistance by tumors, including lymphomas. The efficacy of Opdivo in lymphoma has been evaluated in several clinical trials. For instance, in patients with classical Hodgkin Lymphoma (cHL) that is relapsed or refractory, Opdivo has shown significant efficacy. The drug has been approved by the FDA for the treatment of cHL after failure of autologous stem cell transplant (ASCT) or after two or more lines of systemic therapy for those who are not ASCT candidates. Clinical studies have reported overall response rates ranging from 65% to 87% in this patient population, with a subset of patients achieving complete remission.

Efficacy of Opdivo in Other Lymphoma Subtypes

While the most compelling data for Nivolumab's efficacy in lymphoma is in cHL, studies are ongoing to determine its effectiveness in other lymphoma subtypes. For example, in non-Hodgkin lymphoma (NHL), including diffuse large B-cell lymphoma (DLBCL), follicular lymphoma, and other types, the response rates have been more variable and generally lower than in cHL. Opdivo continues to be investigated in various combinations and settings within the lymphoma category to better understand its full potential across different subtypes.

Efficacy of Adcetris (Brentuximab Vedotin) in Lymphoma

Adcetris (Brentuximab Vedotin) is an antibody-drug conjugate targeting CD30, a marker expressed on the surface of Hodgkin Lymphoma cells and some T-cell lymphomas. It has shown high efficacy in the treatment of relapsed or refractory Hodgkin Lymphoma, particularly after failure of ASCT or after two prior multi-agent chemotherapy regimens in patients who are not ASCT candidates. In pivotal clinical trials, Brentuximab Vedotin demonstrated an overall response rate of approximately 75% in patients with relapsed or refractory HL, with many patients achieving complete remission. The drug has also been approved for the treatment of systemic anaplastic large cell lymphoma (sALCL) based on the strength of its clinical trial results.

Adcetris in Other Lymphoma Settings

Adcetris has also been evaluated for its efficacy in frontline therapy when combined with chemotherapy. The ECHELON-1 study, for instance, demonstrated a significant improvement in modified progression-free survival when Adcetris was added to a chemotherapy regimen in patients with advanced Hodgkin Lymphoma. Additionally, Brentuximab Vedotin is being investigated for its potential in other CD30-expressing lymphomas, including certain subtypes of T-cell lymphoma. Its role in these settings is evolving as more data from clinical trials become available.

Regulatory Agency Approvals

Opdivo
  • 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
  • Medsafe (NZ)
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)

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If Opdivo or Adcetris 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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