Vizimpro (dacomitinib) vs Rybrevant (amivantamab-vmjw)

Vizimpro (dacomitinib) vs Rybrevant (amivantamab-vmjw)

Vizimpro (dacomitinib) is an oral, once-daily, irreversible pan-human epidermal growth factor receptor (HER) tyrosine kinase inhibitor (TKI) used for the first-line treatment of patients with metastatic non-small cell lung cancer (NSCLC) with EGFR exon 19 deletion or exon 21 L858R substitution mutations. Rybrevant (amivantamab-vmjw), on the other hand, is a bispecific antibody administered through intravenous infusion, targeting both EGFR and MET receptors, and is approved for adult patients with NSCLC with EGFR exon 20 insertion mutations whose disease has progressed on or after platinum-based chemotherapy. The choice between Vizimpro and Rybrevant would depend on the patient's specific EGFR mutation, previous treatments, and the mode of administration preference, as well as the patient's overall health and treatment goals discussed with their healthcare provider.

Difference between Vizimpro and Rybrevant

Metric Vizimpro (dacomitinib) Rybrevant (amivantamab-vmjw)
Generic name Dacomitinib Amivantamab-vmjw
Indications First-line treatment for patients with metastatic non-small cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) exon 19 deletion or exon 21 L858R substitution mutations Treatment for adult patients with locally advanced or metastatic NSCLC with EGFR exon 20 insertion mutations, whose disease has progressed on or after platinum-based chemotherapy
Mechanism of action Irreversible inhibitor of the kinase activity of EGFR (ErbB1), HER2 (ErbB2), and HER4 (ErbB4) with activity against EGFR mutations Bispecific antibody that targets both EGFR and MET receptor tyrosine kinases
Brand names Vizimpro Rybrevant
Administrative route Oral Intravenous infusion
Side effects Diarrhea, rash, paronychia, stomatitis, decreased appetite, dry skin, decreased weight, alopecia, cough, pruritus Infusion-related reactions, skin rash, paronychia, musculoskeletal pain, dyspnea, nausea, edema, stomatitis, vomiting, decreased appetite
Contraindications None known None known
Drug class Tyrosine kinase inhibitor Bispecific antibody
Manufacturer Pfizer Janssen Biotech, Inc.

Efficacy

Vizimpro (dacomitinib) Efficacy in Lung Cancer

Vizimpro (dacomitinib) is a kinase inhibitor specifically designed to target the epidermal growth factor receptor (EGFR) which is a common mutation found in non-small cell lung cancer (NSCLC). The efficacy of Vizimpro for the first-line treatment of patients with NSCLC was established in a multicenter, international, open-label, randomized, controlled trial known as ARCHER 1050. In this study, Vizimpro demonstrated a significant improvement in progression-free survival (PFS) compared to gefitinib, another EGFR inhibitor. Patients treated with Vizimpro had a median PFS of 14.7 months compared to 9.2 months for those on gefitinib. This marked a substantial advancement in the treatment of EGFR-mutated NSCLC.

Rybrevant (amivantamab-vmjw) Efficacy in Lung Cancer

Rybrevant (amivantamab-vmjw) is a bispecific antibody that targets both EGFR and MET receptors and is used for the treatment of NSCLC. It is specifically indicated for adult patients with NSCLC with EGFR exon 20 insertion mutations, as detected by an FDA-approved test, whose disease has progressed on or after platinum-based chemotherapy. The efficacy of Rybrevant was evaluated in a multicohort, multicenter, open-label, non-randomized clinical trial. Results showed that the overall response rate (ORR) was 40%, with a median duration of response (DoR) of 11.1 months. These results indicate that Rybrevant provides a new treatment option for patients with this specific and difficult-to-treat form of lung cancer.

Comparative Efficacy in Lung Cancer Treatment

When comparing the efficacy of Vizimpro and Rybrevant, it is important to note that they are used to treat different mutations within NSCLC. Vizimpro is used primarily for the first-line treatment of patients with NSCLC harboring EGFR exon 19 deletions or exon 21 L858R mutations, while Rybrevant is for patients with EGFR exon 20 insertion mutations. Both medications have shown significant efficacy in their respective indications, improving outcomes for patients with these specific genetic alterations in NSCLC.

Conclusion

In conclusion, both Vizimpro and Rybrevant have demonstrated efficacy in the treatment of non-small cell lung cancer with specific genetic mutations. Vizimpro's role in improving progression-free survival in patients with EGFR exon 19 deletions or exon 21 L858R mutations and Rybrevant's ability to elicit responses in patients with EGFR exon 20 insertion mutations represent significant advancements in personalized cancer therapy. As treatment paradigms in lung cancer continue to evolve, the continued evaluation and understanding of these targeted therapies will be crucial in optimizing patient outcomes.

Regulatory Agency Approvals

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

Access Vizimpro or Rybrevant today

If Vizimpro 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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