Enhertu (fam-trastuzumab deruxtecan-nxki) vs Exkivity (mobocertinib)

Enhertu (fam-trastuzumab deruxtecan-nxki) vs Exkivity (mobocertinib)

Enhertu (fam-trastuzumab deruxtecan-nxki) is a targeted therapy designed for the treatment of patients with HER2-positive breast cancer and has recently been approved for certain types of HER2-overexpressing or HER2-mutated non-small cell lung cancer. Exkivity (mobocertinib) is an oral medication specifically approved for the treatment of adult patients with non-small cell lung cancer (NSCLC) that has a specific mutation (EGFR Exon20 insertion) and has progressed on or after platinum-based chemotherapy. When deciding between Enhertu and Exkivity, it is crucial to consider the specific type and molecular profile of the cancer, as Enhertu is primarily used for HER2-positive cancers, while Exkivity is tailored for NSCLC with EGFR Exon20 insertion mutations.

Difference between Enhertu and Exkivity

Metric Enhertu (fam-trastuzumab deruxtecan-nxki) Exkivity (mobocertinib)
Generic name Fam-trastuzumab deruxtecan-nxki Mobocertinib
Indications HER2-positive breast cancer, HER2-positive gastric or gastroesophageal junction adenocarcinoma Non-small cell lung cancer (NSCLC) with EGFR exon 20 insertion mutations
Mechanism of action Antibody-drug conjugate targeting HER2 for cancer cell destruction Tyrosine kinase inhibitor targeting EGFR exon 20 insertion mutations
Brand names Enhertu Exkivity
Administrative route IV infusion Oral
Side effects Nausea, fatigue, vomiting, alopecia, constipation, decreased appetite, anemia, neutropenia, diarrhea, cough, etc. Diarrhea, rash, nausea, stomatitis, vomiting, decreased appetite, paronychia, fatigue, etc.
Contraindications Patients with a history of interstitial lung disease or pneumonitis, hypersensitivity to fam-trastuzumab deruxtecan-nxki Patients with a history of hypersensitivity to mobocertinib or excipients
Drug class Antibody-drug conjugate Tyrosine kinase inhibitor
Manufacturer Daiichi Sankyo and AstraZeneca Takeda Pharmaceutical Company

Efficacy

Enhertu (fam-trastuzumab deruxtecan-nxki) Efficacy in Lung Cancer

Enhertu (fam-trastuzumab deruxtecan-nxki) is a targeted therapy approved for the treatment of adults with unresectable or metastatic non-small cell lung cancer (NSCLC) that has a specific mutation known as HER2 (human epidermal growth factor receptor 2) overexpression. Clinical trials have shown that Enhertu can significantly improve the outcomes in patients with this type of lung cancer. In a pivotal phase 2 trial, patients treated with Enhertu demonstrated a notable response rate, indicating a reduction in tumor size. The duration of response and progression-free survival were also observed to be promising, providing a new avenue of hope for patients with HER2-mutant or HER2-overexpressing NSCLC.

It is important to note that Enhertu's efficacy is specifically linked to the presence of the HER2 mutation. As such, patients must undergo diagnostic testing to confirm HER2 overexpression or mutation before starting treatment with Enhertu. This personalized approach to cancer treatment ensures that the therapy is used in the population most likely to benefit from its mechanism of action, which combines antibody-drug conjugate technology with a potent cytotoxic agent.

Exkivity (mobocertinib) Efficacy in Lung Cancer

Exkivity (mobocertinib) is an oral medication approved for the treatment of adult patients with metastatic NSCLC harboring EGFR exon 20 insertion mutations, as detected by an FDA-approved test, who have received prior platinum-based chemotherapy. This kinase inhibitor has shown significant efficacy in shrinking tumors in patients with this specific genetic alteration. The approval of Exkivity was based on the results of a clinical trial that demonstrated a considerable response rate in patients with EGFR exon 20 insertion-positive NSCLC. The responses were durable, and the median progression-free survival indicated a meaningful clinical benefit for patients with this challenging-to-treat form of lung cancer.

Exkivity's approval underscores the importance of genetic testing in the management of NSCLC. The presence of EGFR exon 20 insertion mutations can be identified through molecular testing, which is critical for determining the appropriate treatment course. By targeting a specific mutation within the cancer cells, Exkivity offers a personalized treatment option that can lead to better outcomes for patients with this particular molecular profile of lung cancer.

Regulatory Agency Approvals

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

Access Enhertu or Exkivity today

If Enhertu 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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