Opdivo (Nivolumab) vs Rybrevant (amivantamab-vmjw)

Opdivo (Nivolumab) vs Rybrevant (amivantamab-vmjw)

Opdivo (nivolumab) is an immune checkpoint inhibitor that targets the PD-1/PD-L1 pathway, enhancing the body's immune response against cancer cells, and is approved for various types of cancer, including melanoma, lung cancer, and kidney cancer. Rybrevant (amivantamab-vmjw) is a bispecific antibody that targets EGFR and MET receptors and is specifically approved for the treatment of non-small cell lung cancer (NSCLC) with EGFR exon 20 insertion mutations. The choice between Opdivo and Rybrevant would depend on the specific type and genetic profile of the cancer, as well as the patient's overall health, previous treatments, and potential side effects, and should be made in consultation with an oncologist.

Difference between Opdivo and Rybrevant

Metric Opdivo (Nivolumab) Rybrevant (amivantamab-vmjw)
Generic name Nivolumab Amivantamab-vmjw
Indications Various types of cancers including melanoma, lung cancer, kidney cancer, bladder cancer, head and neck cancer, and others. Non-small cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) exon 20 insertion mutations.
Mechanism of action Programmed death receptor-1 (PD-1) blocking antibody, enhancing the immune response against cancer cells. Bispecific antibody that targets EGFR and MET receptors, inhibiting tumor growth and cell proliferation.
Brand names Opdivo Rybrevant
Administrative route Intravenous infusion Intravenous infusion
Side effects Fatigue, rash, musculoskeletal pain, pruritus, diarrhea, nausea, and others. Infusion-related reactions, rash, paronychia, musculoskeletal pain, dyspnea, and others.
Contraindications Known hypersensitivity to nivolumab or any of its excipients. Known hypersensitivity to amivantamab-vmjw or any of its excipients.
Drug class Immune checkpoint inhibitor Bispecific antibody
Manufacturer Bristol Myers Squibb Janssen Biotech, Inc.

Efficacy

Overview of Opdivo (Nivolumab) in Lung Cancer Treatment

Opdivo (Nivolumab) is a medication that has shown efficacy in the treatment of lung cancer, specifically non-small cell lung cancer (NSCLC). It is a type of immunotherapy known as a checkpoint inhibitor, which works by blocking the PD-1 protein on the surface of immune cells, thereby enhancing the immune system's ability to detect and fight cancer cells. Clinical trials have demonstrated that Opdivo can lead to improved overall survival in patients with NSCLC compared to chemotherapy, particularly in those with high levels of PD-L1 expression. It has been approved for use in several scenarios, including as a first-line treatment in combination with other medications, and as a monotherapy for advanced or metastatic NSCLC after prior chemotherapy.

Efficacy of Opdivo in Advanced Lung Cancer

In advanced lung cancer, Opdivo has been shown to extend the lives of patients with previously treated metastatic squamous NSCLC. The CheckMate-017 and CheckMate-057 trials demonstrated a significant improvement in overall survival when compared to docetaxel, a standard chemotherapy drug. These trials have cemented Opdivo's role as a standard treatment option in the second-line setting for advanced NSCLC. Furthermore, the CheckMate-227 and CheckMate-9LA studies have provided evidence supporting the use of Opdivo in combination with other agents as a first-line treatment, offering new hope for patients with advanced lung cancer.

Rybrevant (amivantamab-vmjw) and Its Role in Lung Cancer

Rybrevant (amivantamab-vmjw) is a newer therapeutic agent approved for the treatment of adult patients with NSCLC characterized by epidermal growth factor receptor (EGFR) exon 20 insertion mutations, whose disease has progressed on or after platinum-based chemotherapy. This bispecific antibody targets both EGFR and MET pathways, which are often implicated in the growth and spread of cancer cells. In the pivotal CHRYSALIS trial, Rybrevant demonstrated a significant clinical benefit, with a notable percentage of patients achieving partial responses and a median duration of response that supports its use in this specific patient population.

Comparative Efficacy and Considerations

While both Opdivo and Rybrevant offer significant advancements in the treatment of different subsets of NSCLC, their efficacy cannot be directly compared due to their use in different patient populations and lines of therapy. Opdivo has a broader indication for NSCLC patients, whereas Rybrevant is specifically for those with EGFR exon 20 insertion mutations. Physicians must consider the molecular profile of the tumor, prior treatments, and overall patient health when deciding between these therapies. Both drugs represent important components of the evolving landscape of lung cancer treatment, offering targeted approaches that can lead to better patient outcomes.

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

Access Opdivo or Rybrevant today

If Opdivo or Rybrevant 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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