Tagrisso (osimertinib) vs Exkivity (mobocertinib)

Tagrisso (osimertinib) vs Exkivity (mobocertinib)

Tagrisso (osimertinib) is an EGFR inhibitor specifically designed for the treatment of non-small cell lung cancer (NSCLC) with certain mutations in the EGFR gene, and it is often used as a first-line treatment due to its effectiveness and safety profile. Exkivity (mobocertinib), on the other hand, is also an EGFR inhibitor but is specifically indicated for NSCLC with EGFR Exon 20 insertion mutations, which are less common and often resistant to other EGFR-targeted therapies. When deciding between Tagrisso and Exkivity, it is crucial to have a molecular diagnosis of the tumor to determine which specific EGFR mutation is present, as this will guide the choice of therapy for optimal effectiveness.

Difference between Tagrisso and Exkivity

Metric Tagrisso (osimertinib) Exkivity (mobocertinib)
Generic name Osimertinib Mobocertinib
Indications Non-small cell lung cancer (NSCLC) with specific EGFR mutations Non-small cell lung cancer (NSCLC) with specific EGFR exon 20 insertion mutations
Mechanism of action EGFR tyrosine kinase inhibitor EGFR tyrosine kinase inhibitor
Brand names Tagrisso Exkivity
Administrative route Oral Oral
Side effects Diarrhea, rash, dry skin, nail toxicity, stomatitis, etc. Diarrhea, rash, nausea, vomiting, decreased appetite, etc.
Contraindications Patients with hypersensitivity to osimertinib or any excipient Patients with hypersensitivity to mobocertinib or any excipient
Drug class Antineoplastic agent Antineoplastic agent
Manufacturer AstraZeneca Takeda Oncology

Efficacy

Overview of Tagrisso (Osimertinib) in Treating Lung Cancer

Tagrisso (osimertinib) is a third-generation, irreversible epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor designed to treat non-small cell lung cancer (NSCLC) with specific EGFR mutations. Clinical trials have demonstrated its efficacy in patients with metastatic EGFR T790M mutation-positive NSCLC, particularly after the failure of first-line EGFR-TKI therapy. Tagrisso has shown a significant improvement in progression-free survival (PFS) compared to standard chemotherapy in this patient population. Furthermore, it has been approved as a first-line treatment for NSCLC with EGFR exon 19 deletions or exon 21 L858R mutations due to its superior PFS and overall survival (OS) compared to earlier-generation EGFR-TKIs.

Efficacy of Tagrisso in Advanced Stages of Lung Cancer

In advanced stages of NSCLC, Tagrisso has been pivotal in providing a new treatment avenue for patients with central nervous system (CNS) metastases, a common complication of lung cancer. The drug's ability to cross the blood-brain barrier allows it to be effective in treating CNS lesions, which is a significant advantage over some other targeted therapies. Studies have shown a notable CNS objective response rate, indicating its potential in controlling disease progression within the brain.

Introduction to Exkivity (Mobocertinib) for Lung Cancer

Exkivity (mobocertinib) is an oral tyrosine kinase inhibitor targeting EGFR exon 20 insertion mutations in metastatic NSCLC. This mutation accounts for a small subset of EGFR mutations but is associated with poor prognosis and limited treatment options. Exkivity has been granted approval based on the results of a phase 1/2 clinical trial, which demonstrated promising efficacy in patients with EGFR exon 20 insertion-positive NSCLC who had previously been treated with platinum-based chemotherapy. The trial reported a meaningful objective response rate and disease control rate, indicating its potential as a targeted therapy for this challenging mutation.

Effectiveness of Exkivity in a Challenging Patient Population

The efficacy of Exkivity in the treatment of NSCLC with EGFR exon 20 insertion mutations is particularly noteworthy given the limited options available for this patient population. The clinical trial results showed not only an objective response rate but also a duration of response that underscores the potential benefit of this therapy. While the treatment landscape for NSCLC continues to evolve, Exkivity offers a new hope for patients with specific genetic alterations that are not amenable to other EGFR-targeted treatments.

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)
Exkivity
  • Food and Drug Administration (FDA), USA

Access Tagrisso or Exkivity today

If Tagrisso or Exkivity 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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