Opdivo (Nivolumab) vs Padcev (enfortumab vedotin-ejfv)

Opdivo (Nivolumab) vs Padcev (enfortumab vedotin-ejfv)

Opdivo (Nivolumab) is an immune checkpoint inhibitor that works by enhancing the body's immune response against cancer cells, and it is commonly used for various types of cancer, including melanoma, lung cancer, and kidney cancer. Padcev (enfortumab vedotin-ejfv) is an antibody-drug conjugate specifically designed to target and kill cancer cells in patients with locally advanced or metastatic urothelial cancer, and it is often used when other treatments have failed. The choice between Opdivo and Padcev would largely depend on the type of cancer being treated, the patient's overall health, prior treatments, and the specific recommendations of the oncologist.

Difference between Opdivo and Padcev

Metric Opdivo (Nivolumab) Padcev (enfortumab vedotin-ejfv)
Generic name Nivolumab Enfortumab vedotin-ejfv
Indications Used for various types of cancers, including melanoma, lung cancer, kidney cancer, bladder cancer, head and neck cancer, and others. Used for the treatment of urothelial cancer.
Mechanism of action PD-1 inhibitor that enhances the immune response against cancer cells. Antibody-drug conjugate that targets Nectin-4, a protein on the surface of cancer cells, and delivers a cytotoxic agent.
Brand names Opdivo Padcev
Administrative route Intravenous infusion Intravenous infusion
Side effects Includes fatigue, skin rash, musculoskeletal pain, itching, diarrhea, nausea, and potential immune-related adverse reactions. Includes fatigue, peripheral neuropathy, decreased appetite, rash, alopecia, nausea, diarrhea, dry eye, pruritus, and others.
Contraindications Should not be used in patients with a history of severe hypersensitivity to nivolumab or any of its excipients. Should not be used in patients with a history of severe hypersensitivity to enfortumab vedotin-ejfv or any of its excipients.
Drug class Immune checkpoint inhibitor Antibody-drug conjugate
Manufacturer Bristol Myers Squibb Astellas Pharma US, Inc., and Seagen Inc.

Efficacy

Opdivo (Nivolumab) in the Treatment of Urothelial Carcinoma

Opdivo (Nivolumab) is an immune checkpoint inhibitor that has been shown to be effective in the treatment of urothelial carcinoma, which is a type of bladder cancer. It is a programmed death-1 (PD-1) inhibitor that works by enhancing the body's immune response against cancer cells. The efficacy of Opdivo in urothelial carcinoma was demonstrated in a phase II study (CheckMate 275) where it was used in patients with metastatic or surgically unresectable urothelial carcinoma who had progressed on or after platinum-based chemotherapy. The study showed a meaningful objective response rate, indicating that the drug can shrink tumors or slow their growth in a significant number of patients.

Further, the phase III study (CheckMate 032) evaluated nivolumab in combination with another immunotherapy agent, ipilimumab, showing promising response rates and a manageable safety profile. This combination is particularly considered for patients with a poor prognosis or those who have a lower likelihood of responding to single-agent immunotherapy. The results from these studies have supported the use of Opdivo as a second-line treatment for advanced urothelial carcinoma.

Padcev (Enfortumab Vedotin-ejfv) in the Management of Urothelial Carcinoma

Padcev (Enfortumab Vedotin-ejfv) is an antibody-drug conjugate specifically approved for the treatment of advanced urothelial carcinoma. It targets Nectin-4, a protein that is highly expressed in urothelial carcinoma cells, and delivers a cytotoxic agent directly to the cancer cells. The efficacy of Padcev was evaluated in a pivotal phase II clinical trial (EV-201) involving patients with locally advanced or metastatic urothelial carcinoma who had previously received a PD-1 or PD-L1 inhibitor and a platinum-containing chemotherapy. The trial demonstrated a significant objective response rate, with a portion of these responses being complete responses, indicating a complete disappearance of the tumor in those patients.

Moreover, the EV-301 phase III trial compared Padcev to chemotherapy in patients with previously treated advanced urothelial carcinoma. The results showed a significant improvement in overall survival for patients treated with Padcev compared to chemotherapy. These findings have established Padcev as a valuable treatment option for patients with advanced urothelial carcinoma who have limited treatment options due to prior therapies. Both Opdivo and Padcev represent important advancements in the management of urothelial carcinoma, offering hope for improved outcomes in this challenging disease.

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)
Padcev
  • Food and Drug Administration (FDA), USA

Access Opdivo or Padcev today

If Opdivo 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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