Bavencio (avelumab) vs Opdualag (nivolumab & relatlimab)

Bavencio (avelumab) vs Opdualag (nivolumab & relatlimab)

Bavencio (avelumab) is a PD-L1 inhibitor used primarily for the treatment of Merkel cell carcinoma, a rare type of skin cancer, and for urothelial carcinoma. Opdualag, on the other hand, is a combination of nivolumab, a PD-1 inhibitor, and relatlimab, a LAG-3 blocking antibody, recently approved for the treatment of melanoma. When deciding between these two treatments, a patient should consider the type of cancer they have, as each medication is targeted for different indications, and they should consult with their oncologist to discuss the specific benefits, side effects, and compatibility with their individual health profile.

Difference between Bavencio and Opdualag

Metric Bavencio (avelumab) Opdualag (nivolumab & relatlimab)
Generic name Avelumab Nivolumab & Relatlimab
Indications Merkel cell carcinoma, urothelial carcinoma, renal cell carcinoma Unresectable or metastatic melanoma
Mechanism of action PD-L1 blocking antibody Nivolumab: PD-1 blocking antibody; Relatlimab: LAG-3 blocking antibody
Brand names Bavencio Opdualag
Administrative route Intravenous Intravenous
Side effects Fatigue, musculoskeletal pain, diarrhea, nausea, infusion-related reactions, rash, decreased appetite Fatigue, rash, musculoskeletal pain, pruritus, diarrhea, nausea, arthralgia, pyrexia
Contraindications None known None known
Drug class Monoclonal antibody, Immune checkpoint inhibitor Combination of monoclonal antibodies, Immune checkpoint inhibitors
Manufacturer EMD Serono, Pfizer Bristol Myers Squibb

Efficacy

Bavencio (Avelumab) Efficacy in Skin Cancer Treatment

Bavencio (avelumab) is a programmed death ligand-1 (PD-L1) blocking antibody used in the treatment of Merkel cell carcinoma (MCC), a rare and aggressive form of skin cancer. It is the first FDA-approved treatment for metastatic MCC and is indicated for adult and pediatric patients 12 years and older. Clinical trials have demonstrated that avelumab can induce durable responses in a subset of patients with metastatic MCC. The efficacy of avelumab was shown in a pivotal phase II trial (JAVELIN Merkel 200), where the objective response rate (ORR) was reported to be around 33%, with 11.4% of patients achieving a complete response. The median duration of response had not been reached at the time of data cut-off, indicating potential long-term benefits.

Opdualag (Nivolumab & Relatlimab) Efficacy in Skin Cancer Treatment

Opdualag, a combination of nivolumab and relatlimab, targets two different immune checkpoints, PD-1 and LAG-3, respectively. This combination is designed to enhance the anti-tumor immune response more effectively than targeting PD-1 alone. In March 2022, the FDA approved Opdualag for the treatment of patients with unresectable or metastatic melanoma based on the results of the RELATIVITY-047 trial. This phase 2/3 trial demonstrated that the combination of nivolumab and relatlimab significantly improved progression-free survival (PFS) compared to nivolumab alone in patients with previously untreated metastatic or unresectable melanoma. The median PFS was 10.1 months for the combination therapy compared to 4.6 months for nivolumab alone, representing a significant improvement in delaying disease progression.

Furthermore, the overall response rate (ORR) was higher in the combination arm at 42.6% compared to 36.4% in the nivolumab monotherapy arm. These findings suggest that Opdualag may offer a more potent therapeutic option for patients with advanced melanoma, potentially leading to better clinical outcomes. It is important to note, however, that long-term data on overall survival and quality of life are still being collected to fully understand the benefits of Opdualag in this patient population.

In conclusion, both Bavencio and Opdualag have shown efficacy in the treatment of certain types of skin cancer, with Bavencio being particularly valuable for patients with metastatic MCC and Opdualag offering a new therapeutic approach for advanced melanoma. The use of these therapies represents a significant advancement in the management of skin cancers, providing hope for improved survival and quality of life for patients suffering from these challenging conditions. As with all therapies, the efficacy of these drugs should be evaluated on an individual basis, considering the specific characteristics of the patient's disease and their overall health status.

Regulatory Agency Approvals

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

Access Bavencio or Opdualag today

If Bavencio or Opdualag 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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