Xalkori (crizotinib) vs Zynlonta (loncastuximab tesirine-lpyl)

Xalkori (crizotinib) vs Zynlonta (loncastuximab tesirine-lpyl)

Xalkori (crizotinib) is an oral small molecule tyrosine kinase inhibitor primarily used to treat non-small cell lung cancer (NSCLC) with specific genetic alterations, such as ALK or ROS1 rearrangements. In contrast, Zynlonta (loncastuximab tesirine-lpyl) is an antibody-drug conjugate used intravenously for the treatment of relapsed or refractory diffuse large B-cell lymphoma (DLBCL) after two or more lines of systemic therapy. The choice between Xalkori and Zynlonta would depend on the type of cancer a patient has, the specific genetic markers of their cancer cells, and their previous treatments, as these medications are not interchangeable and target different diseases.

Difference between Xalkori and Zynlonta

Metric Xalkori (crizotinib) Zynlonta (loncastuximab tesirine-lpyl)
Generic name Crizotinib Loncastuximab tesirine-lpyl
Indications Non-small cell lung cancer (NSCLC), ALK or ROS1 positive Relapsed or refractory large B-cell lymphoma
Mechanism of action ALK and ROS1 tyrosine kinase inhibitor CD19-directed antibody and alkylating agent conjugate
Brand names Xalkori Zynlonta
Administrative route Oral Intravenous
Side effects Visual disorders, GI disturbances, edema, elevated liver enzymes, etc. Thrombocytopenia, neutropenia, anemia, fatigue, musculoskeletal pain, etc.
Contraindications Hepatic impairment, concurrent use of strong CYP3A inhibitors/inducers Hypersensitivity to loncastuximab tesirine-lpyl or its excipients
Drug class Tyrosine kinase inhibitor Antibody-drug conjugate
Manufacturer Pfizer ADC Therapeutics

Efficacy

Xalkori (Crizotinib) and Its Efficacy in Lymphoma

Xalkori, known by its generic name crizotinib, is primarily known for its efficacy in treating non-small cell lung cancer (NSCLC) that is ALK or ROS1-positive. However, its efficacy in lymphoma, particularly anaplastic large cell lymphoma (ALCL), which is ALK-positive, has been a subject of research. ALK-positive ALCL is a subtype of non-Hodgkin lymphoma, and crizotinib has shown promise in preclinical studies and some clinical cases in targeting ALK-positive cells. While the use of crizotinib in lymphoma is considered off-label, the results from these studies have indicated potential benefits, particularly for patients who may not have responded well to traditional chemotherapy regimens.

Zynlonta (Loncastuximab Tesirine-lpyl) and Its Efficacy in Lymphoma

Zynlonta, or loncastuximab tesirine-lpyl, is a CD19-directed antibody and alkylating agent conjugate that has been approved for the treatment of certain types of lymphoma. Specifically, it is indicated for adult patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL) after two or more lines of systemic therapy. The efficacy of Zynlonta was evaluated in a multicenter, open-label, single-arm trial where patients demonstrated a significant response rate, with a notable percentage achieving complete remission. This has marked Zynlonta as an important treatment option for patients with DLBCL who have limited therapeutic options after the failure of multiple lines of systemic therapy.

Comparative Efficacy in Lymphoma

When comparing the efficacy of Xalkori and Zynlonta in the context of lymphoma, it is important to note that they target different subtypes and mechanisms of the disease. Xalkori's efficacy in lymphoma is more exploratory, particularly in ALK-positive ALCL, and is not a standard treatment, whereas Zynlonta has been specifically approved for use in relapsed or refractory DLBCL. The efficacy of Zynlonta in its indicated population is supported by clinical trial data and its approval by regulatory agencies for this specific use.

Conclusion

In conclusion, while Xalkori shows potential off-label use in ALK-positive ALCL, Zynlonta is an approved and effective treatment for relapsed or refractory DLBCL. The use of these drugs must be carefully considered by healthcare professionals based on the specific type of lymphoma, the patient's previous treatment history, and the current evidence supporting their use. Ongoing research and clinical trials continue to inform the medical community about the efficacy and safety of these drugs in various forms of lymphoma.

Regulatory Agency Approvals

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

Access Xalkori or Zynlonta today

If Xalkori or Zynlonta 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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