Lorviqua (lorlatinib) vs Vegzelma (bevacizumab-adcd)

Lorviqua (lorlatinib) vs Vegzelma (bevacizumab-adcd)

Lorviqua (lorlatinib) is a targeted therapy specifically designed to treat ALK-positive non-small cell lung cancer (NSCLC) in patients who have specific genetic mutations and have progressed on other treatments. Vegzelma (bevacizumab-adcd) is a biosimilar to Avastin (bevacizumab) and is used to treat various forms of cancer, including colorectal, lung, glioblastoma, kidney, and cervical cancers, by inhibiting blood vessel growth that tumors need to grow and spread. When deciding between Lorviqua and Vegzelma, it is crucial to consider the type of cancer, the presence of specific genetic markers, previous treatments, and the overall treatment goals, as each medication has a distinct mechanism of action and is approved for different indications.

Difference between Lorviqua and Vegzelma

Metric Lorviqua (lorlatinib) Vegzelma (bevacizumab-adcd)
Generic name lorlatinib bevacizumab-adcd
Indications ALK-positive metastatic non-small cell lung cancer (NSCLC) Various types of cancer including colorectal, lung, glioblastoma, kidney, and cervical cancers
Mechanism of action ALK and ROS1 tyrosine kinase inhibitor Monoclonal antibody that inhibits angiogenesis by targeting VEGF-A
Brand names Lorviqua Vegzelma
Administrative route Oral Intravenous
Side effects Edema, peripheral neuropathy, cognitive effects, dyspnea, fatigue Hypertension, proteinuria, hemorrhage, arterial thromboembolism, gastrointestinal perforation
Contraindications Severe hypersensitivity to lorlatinib or any of its excipients Hypersensitivity to bevacizumab, its derivatives, or any component of the formulation
Drug class Tyrosine kinase inhibitor Monoclonal antibody
Manufacturer Pfizer Celltrion Healthcare

Efficacy

Lorviqua (lorlatinib) Efficacy in Lung Cancer

Lorviqua (lorlatinib) is a third-generation anaplastic lymphoma kinase (ALK) inhibitor specifically designed to inhibit the most common ALK mutations that drive resistance to earlier ALK inhibitors. It is used for the treatment of patients with ALK-positive metastatic non-small cell lung cancer (NSCLC) who have progressed on crizotinib and at least one other ALK inhibitor for metastatic disease, or whose disease has progressed on alectinib or ceritinib as the first ALK inhibitor therapy for metastatic disease. Clinical trials have demonstrated significant efficacy of lorlatinib in this patient population, with a high percentage of patients achieving partial or complete responses. The response rates and duration of response indicate that lorlatinib is a potent therapeutic option for patients with advanced ALK-positive NSCLC, especially those who have developed resistance to previous treatments.

Vegzelma (bevacizumab-adcd) Efficacy in Lung Cancer

Vegzelma (bevacizumab-adcd) is a biosimilar to the original bevacizumab product, which is a monoclonal antibody that inhibits vascular endothelial growth factor (VEGF). By blocking VEGF, Vegzelma helps prevent the growth of blood vessels that supply tumors with oxygen and nutrients, which is essential for their growth and survival. In the context of lung cancer, particularly non-squamous non-small cell lung cancer (NSCLC), Vegzelma has been shown to be effective when used in combination with chemotherapy. Clinical studies have indicated that adding Vegzelma to standard chemotherapy can extend the time before the cancer worsens (progression-free survival) and can also improve overall survival in some patients compared to chemotherapy alone.

Both Lorviqua and Vegzelma represent important components in the management of lung cancer. Their efficacy in improving outcomes for patients with specific types of lung cancer highlights the advances in targeted and biological therapies that are becoming increasingly important in the oncology field. As new data emerges, the role of these medications in the treatment landscape of lung cancer may continue to evolve, offering hope for improved survival and quality of life for patients affected by this challenging disease.

It is important to note that the efficacy of these medicines can vary based on individual patient factors, including the specific characteristics of the tumor, previous treatments, and overall health. Therefore, decisions regarding the use of Lorviqua or Vegzelma should be made by a healthcare professional, taking into account the unique circumstances of each patient. Ongoing research and clinical trials will further elucidate the efficacy and safety profiles of these drugs, potentially leading to expanded indications and improved patient outcomes in lung cancer treatment.

Regulatory Agency Approvals

Lorviqua
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
  • Therapeutic Goods Administration (TGA), Australia
Vegzelma
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA

Access Lorviqua or Vegzelma today

If Lorviqua or Vegzelma 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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