Keytruda (pembrolizumab) vs Vizimpro (dacomitinib)

Keytruda (pembrolizumab) vs Vizimpro (dacomitinib)

Keytruda (pembrolizumab) is an immune checkpoint inhibitor that works by blocking the PD-1 pathway, which helps the immune system to detect and fight cancer cells, and is commonly used in various types of cancers, including melanoma, lung cancer, and head and neck cancer. Vizimpro (dacomitinib) is a tyrosine kinase inhibitor that targets the epidermal growth factor receptor (EGFR), and is specifically approved 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. The choice between Keytruda and Vizimpro would depend on the specific type and genetic characteristics of the cancer, as well as the patient's overall health, potential side effects, and the treatment goals discussed with their healthcare provider.

Difference between Keytruda and Vizimpro

Metric Keytruda (pembrolizumab) Vizimpro (dacomitinib)
Generic name Pembrolizumab Dacomitinib
Indications Various types of cancer including melanoma, lung cancer, head and neck cancer, Hodgkin lymphoma, and others First-line treatment of patients with metastatic non-small cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) exon 19 deletion or exon 21 L858R mutations
Mechanism of action Programmed death receptor-1 (PD-1) blocking antibody Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor
Brand names Keytruda Vizimpro
Administrative route Intravenous infusion Oral
Side effects Fatigue, musculoskeletal pain, decreased appetite, pruritus, diarrhea, nausea, rash, pyrexia, cough, dyspnea, constipation, pain in extremity, and headache Diarrhea, rash, paronychia, stomatitis, decreased appetite, dry skin, decreased weight, alopecia, cough, and pruritus
Contraindications Individuals with hypersensitivity to pembrolizumab or any of its excipients Individuals with hypersensitivity to dacomitinib or any of its excipients
Drug class Anti-PD-1 monoclonal antibody EGFR tyrosine kinase inhibitor
Manufacturer Merck & Co. Pfizer Inc.

Efficacy

Keytruda (pembrolizumab) Efficacy in Lung Cancer

Keytruda, known generically as pembrolizumab, is a highly effective immunotherapy drug used in the treatment of certain types of lung cancer. Specifically, it has shown efficacy in treating non-small cell lung cancer (NSCLC), which is the most common form of lung cancer. Pembrolizumab works by targeting the PD-1/PD-L1 pathway, a mechanism that tumors use to evade the immune system. By blocking this pathway, Keytruda enables the immune system to better recognize and destroy cancer cells.

Clinical trials have demonstrated that Keytruda can significantly improve survival rates in patients with metastatic NSCLC whose tumors express PD-L1 with a proportion score of 1% or more. When used as a first-line treatment, pembrolizumab has been shown to extend overall survival and progression-free survival compared to traditional chemotherapy regimens. Moreover, the benefits of Keytruda have been observed across various subgroups of lung cancer patients, including those with different histological subtypes and varying levels of PD-L1 expression.

Vizimpro (dacomitinib) Efficacy in Lung Cancer

Vizimpro, or dacomitinib, is a targeted therapy approved for the first-line treatment of patients with metastatic NSCLC with epidermal growth factor receptor (EGFR) exon 19 deletion or exon 21 L858R substitution mutations as detected by an FDA-approved test. Vizimpro is a tyrosine kinase inhibitor that works by blocking the activity of the EGFR, which is often overactive in NSCLC cells with these mutations and promotes their growth and survival.

In clinical studies, Vizimpro has shown a significant improvement in progression-free survival when compared to another EGFR-targeting medication, gefitinib, in patients with previously untreated, EGFR-mutated NSCLC. The efficacy of Vizimpro in terms of overall survival, however, has been more variable, with some studies showing a benefit and others not reaching statistical significance. It is important to note that the effectiveness of Vizimpro is largely limited to patients whose tumors have specific EGFR mutations, and it is not effective in NSCLC without these mutations.

Regulatory Agency Approvals

Keytruda
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
  • Therapeutic Goods Administration (TGA), Australia
  • Medsafe (NZ)
Vizimpro
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA

Access Keytruda or Vizimpro today

If Keytruda or Vizimpro 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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