Tagrisso (osimertinib) vs Portrazza (necitumumab)

Tagrisso (osimertinib) vs Portrazza (necitumumab)

Tagrisso (osimertinib) is a third-generation, oral EGFR tyrosine kinase inhibitor specifically designed to target EGFR mutations in non-small cell lung cancer (NSCLC), and it is particularly effective against T790M mutation-positive cancers. Portrazza (necitumumab) is a monoclonal antibody given intravenously that targets the EGFR receptor, but it is used in combination with chemotherapy for the treatment of metastatic squamous NSCLC without EGFR mutations. The choice between Tagrisso and Portrazza would depend on the patient's specific type of NSCLC and the presence of EGFR mutations, as well as the overall health and treatment goals of the patient, which should be discussed with an oncologist.

Difference between Tagrisso and Portrazza

Metric Tagrisso (osimertinib) Portrazza (necitumumab)
Generic name Osimertinib Necitumumab
Indications Non-small cell lung cancer (NSCLC) with specific EGFR mutations Metastatic squamous non-small cell lung cancer in combination with chemotherapy
Mechanism of action EGFR tyrosine kinase inhibitor Epidermal growth factor receptor (EGFR) antagonist
Brand names Tagrisso Portrazza
Administrative route Oral Intravenous
Side effects Diarrhea, rash, dry skin, nail toxicity, stomatitis Electrolyte imbalances, rash, venous thromboembolism, dermatitis acneiform
Contraindications Patients with hypersensitivity to osimertinib or any excipients Patients with hypersensitivity to necitumumab or any excipients
Drug class Tyrosine kinase inhibitor Monoclonal antibody
Manufacturer AstraZeneca Eli Lilly and Company

Efficacy

Efficacy of Tagrisso (Osimertinib) in Lung Cancer

Tagrisso (osimertinib) is a third-generation, irreversible epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor specifically designed for the treatment of certain types of non-small cell lung cancer (NSCLC). It is particularly effective in patients whose tumors have specific mutations in the EGFR gene, known as T790M mutations, which are associated with resistance to earlier-generation EGFR inhibitors. Clinical trials have demonstrated that Tagrisso is effective in improving progression-free survival in patients with these mutations. Additionally, Tagrisso has shown efficacy in the first-line treatment of patients with metastatic NSCLC that have exon 19 deletions or exon 21 L858R mutations in the EGFR gene.

One of the pivotal phase III trials, the FLAURA study, compared osimertinib to standard EGFR tyrosine kinase inhibitors in the first-line treatment of patients with advanced NSCLC with EGFR mutations. The results showed a significant improvement in progression-free survival for patients treated with osimertinib. Moreover, Tagrisso has also been found to have central nervous system (CNS) activity, which is critical for treating patients with brain metastases, a common complication of advanced NSCLC.

Efficacy of Portrazza (Necitumumab) in Lung Cancer

Portrazza (necitumumab) is a recombinant human IgG1 monoclonal antibody that targets the epidermal growth factor receptor (EGFR). It is used in combination with gemcitabine and cisplatin for the first-line treatment of patients with metastatic squamous non-small cell lung cancer (NSCLC). The approval of necitumumab was based on a multicenter, randomized, open-label clinical trial, which demonstrated an improvement in overall survival when added to the standard chemotherapy regimen.

However, it is important to note that the efficacy of necitumumab is specific to squamous NSCLC and does not extend to non-squamous NSCLC. The SQUIRE trial, which led to the approval of necitumumab, showed a modest but statistically significant improvement in overall survival for patients with advanced squamous NSCLC when necitumumab was added to chemotherapy compared to chemotherapy alone. Despite this, the use of necitumumab is associated with certain adverse effects, and its use must be carefully considered against the potential benefits in the context of individual patient health profiles.

Regulatory Agency Approvals

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

Access Tagrisso or Portrazza today

If Tagrisso or Portrazza 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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