Opdivo (Nivolumab) vs Polivy (polatuzumab vedotin-piiq)

Opdivo (Nivolumab) vs Polivy (polatuzumab vedotin-piiq)

Opdivo (Nivolumab) is an immune checkpoint inhibitor that works by blocking the PD-1 protein on T cells, thereby enhancing the immune system's ability to attack cancer cells, and is commonly used in the treatment of various cancers including melanoma, lung cancer, and kidney cancer. Polivy (polatuzumab vedotin-piiq), on the other hand, is an antibody-drug conjugate that targets CD79b, a protein expressed on the surface of B cells, and is used specifically for the treatment of diffuse large B-cell lymphoma (DLBCL), often in combination with other chemotherapy drugs. The choice between Opdivo and Polivy would largely depend on the type of cancer being treated, as their mechanisms of action and approved indications differ significantly; therefore, a healthcare provider would recommend the most appropriate medication based on the patient's specific cancer diagnosis and overall health condition.

Difference between Opdivo and Polivy

Metric Opdivo (Nivolumab) Polivy (polatuzumab vedotin-piiq)
Generic name Nivolumab Polatuzumab vedotin-piiq
Indications Various types of cancer, including melanoma, lung cancer, and renal cell carcinoma Treatment of diffuse large B-cell lymphoma
Mechanism of action PD-1 inhibitor that enhances the immune response against cancer cells Antibody-drug conjugate targeting CD79b, delivering a cytotoxic agent to B-cells
Brand names Opdivo Polivy
Administrative route Intravenous infusion Intravenous infusion
Side effects Fatigue, rash, musculoskeletal pain, nausea, and pruritus Neutropenia, thrombocytopenia, anemia, peripheral neuropathy, and diarrhea
Contraindications Known hypersensitivity to nivolumab or any of its excipients Known hypersensitivity to polatuzumab vedotin-piiq, or any of its excipients
Drug class Immune checkpoint inhibitor Antibody-drug conjugate
Manufacturer Bristol-Myers Squibb Genentech, Inc.

Efficacy

Efficacy of Opdivo (Nivolumab) in Lymphoma

Opdivo (Nivolumab) is a PD-1 (Programmed Death-1) immune checkpoint inhibitor that has shown efficacy in the treatment of certain types of lymphoma. Specifically, it has been approved by the FDA for the treatment of classical Hodgkin lymphoma (cHL) after failure of autologous hematopoietic stem cell transplantation (HSCT) or after two or more lines of systemic therapy for those who are not HSCT candidates. Clinical trials have demonstrated that nivolumab can induce a durable response in relapsed or refractory cHL, with a significant proportion of patients achieving partial or complete remission. The efficacy of Opdivo in other lymphoma subtypes continues to be investigated in clinical trials.

Efficacy of Polivy (Polatuzumab Vedotin-piiq) in Lymphoma

Polivy (Polatuzumab Vedotin-piiq) is an antibody-drug conjugate targeting CD79b, a protein expressed on the surface of B cells, and is used in the treatment of certain types of non-Hodgkin lymphoma (NHL). It has been granted accelerated approval by the FDA for use in combination with bendamustine and a rituximab product (BR) for the treatment of adult patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL), not otherwise specified, after at least two prior therapies. Clinical studies have shown that the addition of Polivy to BR significantly improves overall response rates and can lead to complete remissions in a subset of patients with this aggressive form of lymphoma.

Comparative Efficacy in Lymphoma Treatment

While both Opdivo and Polivy have demonstrated efficacy in the treatment of different types of lymphoma, their mechanisms of action and indications differ. Opdivo works by blocking the PD-1 pathway, enhancing the immune system's ability to fight cancer cells, and is used in cHL. On the other hand, Polivy delivers a cytotoxic agent directly to B cells in NHL, particularly DLBCL. Both drugs represent important advancements in the management of these hematologic malignancies and offer hope for patients who have limited treatment options due to disease relapse or refractoriness to previous therapies.

Considerations and Ongoing Research

It is important to note that while these medications have shown promise, their efficacy can vary among individuals, and they are not without potential side effects. Ongoing research continues to evaluate the long-term efficacy and safety of Opdivo and Polivy, as well as their potential use in other lymphoma subtypes or in combination with other therapies. Clinical trials are essential for understanding the full potential and optimal use of these drugs in the diverse landscape of lymphoma treatment.

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

Access Opdivo or Polivy today

If Opdivo 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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