Lorviqua (lorlatinib) vs Enhertu (fam-trastuzumab deruxtecan-nxki)

Lorviqua (lorlatinib) vs Enhertu (fam-trastuzumab deruxtecan-nxki)

Lorviqua (lorlatinib) is a targeted therapy specifically designed for the treatment of patients with anaplastic lymphoma kinase (ALK)-positive non-small cell lung cancer (NSCLC), particularly for those who have developed resistance to other ALK inhibitors. Enhertu (fam-trastuzumab deruxtecan-nxki), on the other hand, is an antibody-drug conjugate used for the treatment of HER2-positive breast cancer and is not indicated for lung cancer. The choice between these two medications would be based on the specific type of cancer a patient has, as they target different molecular pathways and are not interchangeable; Lorviqua is for ALK-positive NSCLC, while Enhertu is for HER2-positive breast cancer.

Difference between Lorviqua and Enhertu

Metric Lorviqua (lorlatinib) Enhertu (fam-trastuzumab deruxtecan-nxki)
Generic name lorlatinib fam-trastuzumab deruxtecan-nxki
Indications ALK-positive metastatic non-small cell lung cancer (NSCLC) HER2-positive breast cancer, HER2-positive gastric or gastroesophageal junction adenocarcinoma
Mechanism of action ALK tyrosine kinase inhibitor HER2-directed antibody and topoisomerase inhibitor conjugate
Brand names Lorviqua Enhertu
Administrative route Oral Intravenous
Side effects Edema, neuropathy, cognitive effects, fatigue, weight gain Nausea, fatigue, vomiting, alopecia, constipation
Contraindications Hypersensitivity to lorlatinib Hypersensitivity to fam-trastuzumab deruxtecan-nxki or excipients
Drug class Tyrosine kinase inhibitor Antibody-drug conjugate
Manufacturer Pfizer Daiichi Sankyo and AstraZeneca

Efficacy

Lorviqua (lorlatinib) Efficacy in Lung Cancer

Lorviqua, also known by its generic name lorlatinib, is a medication specifically approved for the treatment of anaplastic lymphoma kinase (ALK)-positive metastatic non-small cell lung cancer (NSCLC) in patients who have progressed on prior ALK inhibitors. As a third-generation ALK inhibitor, lorlatinib has shown significant efficacy in overcoming resistance to first and second-generation ALK inhibitors. Clinical trials have demonstrated that lorlatinib is effective in patients with ALK-positive NSCLC, including those with central nervous system (CNS) metastases, which is a common complication in lung cancer and a significant challenge in treatment.

In clinical studies, lorlatinib has shown a high objective response rate (ORR) in patients with ALK-positive metastatic NSCLC, with responses observed in both systemic disease and CNS lesions. The duration of response and progression-free survival with lorlatinib have also been noteworthy, offering a valuable option for patients who have limited treatments available due to resistance or intolerance to earlier ALK inhibitors. The efficacy of lorlatinib highlights its role as a targeted therapy that can provide meaningful clinical benefits in a specific subset of lung cancer patients.

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

Enhertu, with the generic name fam-trastuzumab deruxtecan-nxki, is an antibody-drug conjugate that combines trastuzumab, a HER2-targeting antibody, with a cytotoxic topoisomerase inhibitor. Although initially developed and approved for HER2-positive breast cancer, Enhertu has also shown promising efficacy in HER2-mutant non-small cell lung cancer (NSCLC). This off-label use is based on the recognition that HER2 mutations are actionable targets in a subset of NSCLC patients.

In clinical trials, Enhertu has demonstrated significant antitumor activity in patients with HER2-mutant NSCLC. The ORR and disease control rate in these studies have been encouraging, suggesting that Enhertu can provide a new treatment avenue for patients with this specific molecular alteration in lung cancer. The duration of response and progression-free survival data further support the potential role of Enhertu as an effective treatment for patients with HER2-mutant NSCLC. As research continues, Enhertu may become an important addition to the targeted therapy options available for lung cancer patients with HER2 mutations.

Regulatory Agency Approvals

Lorviqua
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
  • Therapeutic Goods Administration (TGA), Australia
Enhertu
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Pharmaceuticals and Medical Devices Agency (PMDA), Japan

Access Lorviqua or Enhertu today

If Lorviqua or Enhertu 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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