Alecensa (alectinib) vs Xalkori (crizotinib)

Alecensa (alectinib) vs Xalkori (crizotinib)

Alecensa (alectinib) and Xalkori (crizotinib) are both oral medications used to treat non-small cell lung cancer (NSCLC) with specific genetic mutations in the ALK gene. Alecensa is often preferred as a first-line treatment because it has shown higher efficacy and a lower risk of side effects, particularly in the central nervous system, compared to Xalkori. However, the choice between Alecensa and Xalkori should be made based on individual patient characteristics, potential drug interactions, specific ALK mutations, and the patient's overall health profile, with a healthcare provider's guidance.

Difference between Alecensa and Xalkori

Metric Alecensa (alectinib) Xalkori (crizotinib)
Generic name Alectinib Crizotinib
Indications ALK-positive non-small cell lung cancer (NSCLC) ALK or ROS1-positive NSCLC
Mechanism of action ALK inhibitor ALK and ROS1 inhibitor
Brand names Alecensa Xalkori
Administrative route Oral Oral
Side effects Constipation, fatigue, edema, myalgia, anemia Visual disorders, gastrointestinal effects, edema, elevated transaminases
Contraindications Hypersensitivity to alectinib or any component of the formulation Hypersensitivity to crizotinib or any component of the formulation
Drug class Tyrosine kinase inhibitor Tyrosine kinase inhibitor
Manufacturer Genentech (Roche) Pfizer

Efficacy

Alecensa (Alectinib) Efficacy in Lung Cancer

Alecensa (alectinib) is a targeted therapy approved for the treatment of ALK-positive non-small cell lung cancer (NSCLC). Its efficacy has been demonstrated in several clinical trials. Notably, the ALEX trial, which was a pivotal phase III study, showed that alectinib significantly improved progression-free survival (PFS) compared to crizotinib in the first-line treatment of ALK-positive NSCLC. Patients treated with alectinib had a median PFS of 34.8 months, compared to 10.9 months for those on crizotinib. Moreover, alectinib has shown high central nervous system (CNS) efficacy, reducing the risk of CNS progression or death by 84% compared to crizotinib.

Xalkori (Crizotinib) Efficacy in Lung Cancer

Xalkori (crizotinib) is another targeted therapy used in the treatment of ALK-positive NSCLC. It was the first ALK inhibitor approved for this indication. In clinical trials, crizotinib has demonstrated significant efficacy in shrinking tumors and prolonging PFS. The PROFILE 1014 study, which compared crizotinib with chemotherapy in previously untreated advanced ALK-positive NSCLC, showed a median PFS of 10.9 months for crizotinib versus 7 months for chemotherapy. However, crizotinib is associated with a higher rate of progression in the CNS, which is a common site of metastasis in ALK-positive NSCLC patients.

Comparison of Alecensa and Xalkori

When comparing Alecensa and Xalkori, the evidence suggests that Alecensa may offer superior efficacy, particularly in terms of PFS and CNS involvement. The ALEX trial directly compared alectinib to crizotinib and found that alectinib not only prolonged PFS but also had a more favorable safety profile and was less toxic than crizotinib. Additionally, alectinib's ability to better penetrate the CNS and prevent brain metastases is a significant advantage, as CNS metastases can significantly impact patient quality of life and prognosis.

Conclusion

Both Alecensa (alectinib) and Xalkori (crizotinib) have changed the treatment landscape for ALK-positive NSCLC, offering patients targeted options that can lead to better outcomes compared to traditional chemotherapy. While both drugs have shown efficacy in treating lung cancer, alectinib seems to have an edge over crizotinib, particularly in terms of progression-free survival and CNS efficacy. These findings underscore the importance of personalized medicine and the need for ongoing research to optimize treatment for lung cancer patients.

Regulatory Agency Approvals

Alecensa
  • 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
  • Medsafe (NZ)
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

Access Alecensa or Xalkori today

If Alecensa or Xalkori 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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