Tagrisso (osimertinib) vs Tabrecta (capmatinib)

Tagrisso (osimertinib) vs Tabrecta (capmatinib)

Tagrisso (osimertinib) is a third-generation, irreversible EGFR tyrosine kinase inhibitor specifically designed to treat non-small cell lung cancer (NSCLC) with certain EGFR mutations, and it is effective in both first-line treatment and in patients who have developed resistance to earlier EGFR inhibitors. Tabrecta (capmatinib), on the other hand, is a selective MET inhibitor indicated for adult patients with metastatic NSCLC harboring MET exon 14 skipping mutations. The choice between Tagrisso and Tabrecta would depend on the specific genetic alterations present in the tumor, with Tagrisso being appropriate for EGFR mutations and Tabrecta for MET exon 14 alterations, necessitating molecular testing to guide the decision.

Difference between Tagrisso and Tabrecta

Metric Tagrisso (osimertinib) Tabrecta (capmatinib)
Generic name Osimertinib Capmatinib
Indications Non-small cell lung cancer (NSCLC) with specific EGFR mutations Metastatic non-small cell lung cancer (NSCLC) with MET exon 14 skipping mutations
Mechanism of action EGFR tyrosine kinase inhibitor MET kinase inhibitor
Brand names Tagrisso Tabrecta
Administrative route Oral Oral
Side effects Diarrhea, rash, dry skin, nail toxicity, stomatitis, fatigue Nausea, vomiting, fatigue, edema, decreased appetite
Contraindications Hypersensitivity to osimertinib or any excipients in the formulation Hypersensitivity to capmatinib or any excipients in the formulation
Drug class Antineoplastic agent, tyrosine kinase inhibitor Antineoplastic agent, kinase inhibitor
Manufacturer AstraZeneca Novartis

Efficacy

Tagrisso (Osimertinib) Efficacy in Lung Cancer

Tagrisso (osimertinib) is a third-generation, irreversible epidermal growth factor receptor tyrosine kinase inhibitor (EGFR TKI) that has shown significant efficacy in the treatment of non-small cell lung cancer (NSCLC) with specific EGFR mutations. Clinical trials have demonstrated that osimertinib is effective in patients with NSCLC harboring exon 19 deletions or exon 21 L858R mutations, which are common EGFR mutations in this cancer type. In the FLAURA trial, osimertinib significantly improved progression-free survival (PFS) compared to standard EGFR TKIs (gefitinib or erlotinib) in the first-line treatment setting for patients with these mutations.

Moreover, osimertinib has shown efficacy in patients with central nervous system (CNS) metastases, a common and challenging complication of NSCLC. Osimertinib's ability to penetrate the blood-brain barrier allows for effective targeting of CNS lesions, which was demonstrated in the AURA3 trial where it improved PFS compared to platinum-based therapy in patients with T790M-positive NSCLC and brain metastases who had progressed after initial EGFR TKI therapy.

Tabrecta (Capmatinib) Efficacy in Lung Cancer

Tabrecta (capmatinib) is a selective inhibitor of the MET proto-oncogene, which has been identified as a driver in certain types of non-small cell lung cancer (NSCLC), particularly those with MET exon 14 skipping mutations. The GEOMETRY mono-1 trial evaluated the efficacy of capmatinib in patients with MET exon 14-altered advanced NSCLC. The results showed a notable objective response rate (ORR) in both treatment-naive patients and those who had received prior treatment, indicating capmatinib's potential as an effective targeted therapy for this patient population.

Capmatinib's approval was based on the efficacy outcomes from this trial, which highlighted its role in addressing a previously unmet need for patients with MET exon 14 skipping mutation-positive NSCLC. The treatment has been associated with rapid and durable responses, offering a new therapeutic option for a subset of NSCLC patients with limited targeted treatment alternatives. As research continues, the efficacy of capmatinib in broader NSCLC populations and in combination with other therapies is being explored to further understand its potential benefits in lung cancer management.

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)
Tabrecta
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Pharmaceuticals and Medical Devices Agency (PMDA), Japan

Access Tagrisso or Tabrecta today

If Tagrisso or Tabrecta 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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