Bavencio (avelumab) vs Padcev (enfortumab vedotin-ejfv)

Bavencio (avelumab) vs Padcev (enfortumab vedotin-ejfv)

Bavencio (avelumab) is a PD-L1 blocking antibody used primarily for the treatment of Merkel cell carcinoma, a rare type of skin cancer, and for urothelial carcinoma, which is a type of bladder cancer. Padcev (enfortumab vedotin-ejfv) is an antibody-drug conjugate specifically targeted against Nectin-4, a protein found on the surface of cells and is used to treat urothelial cancers, particularly when the disease has spread or cannot be removed by surgery. When deciding between the two, a patient should consider the specific type of cancer they have, the stage of the disease, previous treatments, and the side effect profile of each drug, in consultation with their healthcare provider to determine the most appropriate treatment option.

Difference between Bavencio and Padcev

Metric Bavencio (avelumab) Padcev (enfortumab vedotin-ejfv)
Generic name Avelumab Enfortumab vedotin-ejfv
Indications Merkel cell carcinoma, urothelial carcinoma, renal cell carcinoma Locally advanced or metastatic urothelial cancer
Mechanism of action PD-L1 blocking antibody Antibody-drug conjugate targeting Nectin-4
Brand names Bavencio Padcev
Administrative route Intravenous infusion Intravenous infusion
Side effects Fatigue, musculoskeletal pain, diarrhea, nausea, infusion-related reactions, rash, decreased appetite Peripheral neuropathy, fatigue, rash, decreased appetite, nausea, diarrhea, dry eye, pruritus, weight decreased
Contraindications None known specifically; use caution in patients with pre-existing autoimmune disease or those on immunosuppressive therapy None known specifically; contraindicated in patients with known severe hypersensitivity to enfortumab vedotin-ejfv
Drug class PD-L1 blocking antibody, Immuno-oncology agent Antibody-drug conjugate, Antineoplastic agent
Manufacturer Merck KGaA and Pfizer Astellas Pharma and Seagen Inc.

Efficacy

Bavencio (Avelumab) for Urothelial Carcinoma

Bavencio (avelumab) is a programmed death ligand-1 (PD-L1) blocking antibody used in the treatment of urothelial carcinoma, among other cancers. For urothelial carcinoma specifically, Bavencio has shown efficacy in patients with locally advanced or metastatic urothelial carcinoma who have disease progression during or following platinum-containing chemotherapy or within 12 months of neoadjuvant or adjuvant treatment with platinum-containing chemotherapy. In clinical trials, avelumab demonstrated a meaningful response rate in this patient population, with a portion of these responses being durable. The approval of Bavencio for this indication was based on the tumor response rate and duration of response; however, continued approval for this indication may be contingent upon verification and description of clinical benefit in confirmatory trials.

Padcev (Enfortumab Vedotin-ejfv) for Urothelial Carcinoma

Padcev (enfortumab vedotin-ejfv) is an antibody-drug conjugate directed against Nectin-4, a protein located on the surface of cells and highly expressed in urothelial carcinoma. Padcev has been approved for the treatment of adult patients with locally advanced or metastatic urothelial cancer who have previously received a PD-1 or PD-L1 inhibitor and a platinum-containing chemotherapy in the neoadjuvant/adjuvant, locally advanced or metastatic setting. Clinical trials have demonstrated that enfortumab vedotin-ejfv elicits significant antitumor activity in patients with advanced urothelial carcinoma, with a manageable safety profile. The objective response rate reported in these trials provides evidence of its efficacy for patients who have limited treatment options.

Comparative Efficacy in Urothelial Carcinoma

While direct comparative studies between Bavencio and Padcev for the treatment of urothelial carcinoma are limited, both agents represent important therapeutic options for patients with advanced disease. The selection of either Bavencio or Padcev as a treatment option depends on several factors, including prior treatments, PD-L1 status, and specific patient characteristics. Both treatments have been associated with improved outcomes in specific patient populations within the advanced urothelial carcinoma setting.

Conclusion

Both Bavencio and Padcev have added to the therapeutic landscape of urothelial carcinoma, offering hope to patients with advanced disease. Their efficacy has been demonstrated in clinical trials, leading to their respective approvals for use in patients with disease progression despite platinum-based chemotherapy and immunotherapy. As research continues, the role of these agents, either alone or in combination with other therapies, will be further defined, potentially improving outcomes for patients with urothelial carcinoma.

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
Padcev
  • Food and Drug Administration (FDA), USA

Access Bavencio or Padcev today

If Bavencio or Padcev 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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