Keytruda (pembrolizumab) vs Xalkori (crizotinib)

Keytruda (pembrolizumab) vs Xalkori (crizotinib)

Keytruda (pembrolizumab) is an immune checkpoint inhibitor that works by blocking the PD-1 pathway, thereby enhancing the body's immune response against cancer cells, and is commonly used for a variety of cancers including melanoma, lung cancer, and head and neck cancers. Xalkori (crizotinib), on the other hand, is a targeted therapy that inhibits anaplastic lymphoma kinase (ALK) and ROS1 receptors, making it specifically effective for non-small cell lung cancer (NSCLC) patients who have these genetic mutations. When deciding between Keytruda and Xalkori, it is crucial to consider the specific type of cancer, its genetic makeup, and the patient's overall health, as Keytruda is more broadly applicable for different cancers, while Xalkori is tailored for cancers with specific mutations.

Difference between Keytruda and Xalkori

Metric Keytruda (pembrolizumab) Xalkori (crizotinib)
Generic name Pembrolizumab Crizotinib
Indications Various types of cancers including melanoma, lung cancer, head and neck cancer, Hodgkin lymphoma, and others Non-small cell lung cancer (NSCLC), ROS1-positive NSCLC, and ALK-positive metastatic NSCLC
Mechanism of action Programmed death receptor-1 (PD-1) blocking antibody Anaplastic lymphoma kinase (ALK) and ROS1 tyrosine kinase inhibitor
Brand names Keytruda Xalkori
Administrative route Intravenous infusion Oral
Side effects Fatigue, musculoskeletal pain, decreased appetite, pruritus, diarrhea, nausea, rash, fever, cough, dyspnea, constipation, pain in extremity, and headache Visual disorders, gastrointestinal effects, edema, elevated transaminases, fatigue, decreased appetite, upper respiratory infection, dizziness, and neuropathy
Contraindications None known beyond hypersensitivity to pembrolizumab or its excipients Hepatic impairment or severe renal impairment, concomitant use with strong CYP3A inhibitors or inducers
Drug class Anti-PD-1 monoclonal antibody Small molecule tyrosine kinase inhibitor
Manufacturer Merck & Co. Pfizer

Efficacy

Keytruda (Pembrolizumab) Efficacy in Lung Cancer

Keytruda, also known by its generic name pembrolizumab, is a highly effective treatment option for certain types of lung cancer. It is a type of immunotherapy that works by blocking the PD-1 pathway, which some cancer cells use to hide from the immune system. By inhibiting this pathway, Keytruda helps the immune system to detect and fight cancer cells. It has shown significant efficacy in treating non-small cell lung cancer (NSCLC), particularly in patients whose tumors express PD-L1 and who have not had prior chemotherapy, or have received previous treatments but have progressed.

In clinical trials, Keytruda has demonstrated an improvement in overall survival compared to chemotherapy alone. For instance, the KEYNOTE-024 study showed that pembrolizumab provided a median overall survival of 30 months compared to 14.2 months with chemotherapy in untreated metastatic NSCLC patients with high PD-L1 expression. In addition, Keytruda has been shown to have a durable response, meaning that the effects of the treatment last for a significant amount of time after the therapy has been administered.

Xalkori (Crizotinib) Efficacy in Lung Cancer

Xalkori, with the generic name crizotinib, is another targeted therapy that has shown efficacy in the treatment of lung cancer, specifically in patients with advanced NSCLC that is anaplastic lymphoma kinase (ALK) positive. Crizotinib targets and inhibits the activity of the ALK protein, which can drive the growth of cancer cells. By doing so, Xalkori can help to shrink or slow the growth of tumors.

Clinical trials have demonstrated that crizotinib is effective in improving progression-free survival in patients with ALK-positive NSCLC. The PROFILE 1014 study, for example, showed that crizotinib nearly doubled progression-free survival compared to standard chemotherapy (10.9 months vs. 7.0 months). Furthermore, the response rate to crizotinib was significantly higher than that seen with chemotherapy. Xalkori has become a standard of care for patients with ALK-positive NSCLC, offering a targeted approach that can lead to better outcomes for this specific genetic subset of lung cancer.

Regulatory Agency Approvals

Keytruda
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
  • 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 Keytruda or Xalkori today

If Keytruda 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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