Beleodaq (belinostat) vs Xalkori (crizotinib)

Beleodaq (belinostat) vs Xalkori (crizotinib)

Beleodaq (belinostat) is a histone deacetylase inhibitor used for the treatment of patients with relapsed or refractory peripheral T-cell lymphoma, a type of non-Hodgkin lymphoma. Xalkori (crizotinib), on the other hand, is an ALK and ROS1 inhibitor indicated for the treatment of certain types of non-small cell lung cancer (NSCLC) that are ALK or ROS1-positive as detected by an FDA-approved test. The choice between Beleodaq and Xalkori would be based on the specific type of cancer a patient has and the presence of certain genetic markers, as these medications are not interchangeable and target different pathways involved in cancer cell growth.

Difference between Beleodaq and Xalkori

Metric Beleodaq (belinostat) Xalkori (crizotinib)
Generic name Belinostat Crizotinib
Indications Peripheral T-cell lymphoma (PTCL) Non-small cell lung cancer (NSCLC), ROS1-positive and ALK-positive metastatic NSCLC
Mechanism of action HDAC inhibitor ALK and ROS1 tyrosine kinase inhibitor
Brand names Beleodaq Xalkori
Administrative route Intravenous Oral
Side effects Nausea, vomiting, fatigue, fever, anemia Visual disorders, nausea, diarrhea, vomiting, edema, constipation, elevated transaminases
Contraindications Known hypersensitivity to belinostat or any component of the formulation Hepatic impairment, concurrent use with strong CYP3A inhibitors or inducers
Drug class Antineoplastic agent, histone deacetylase inhibitor Antineoplastic agent, tyrosine kinase inhibitor
Manufacturer Spectrum Pharmaceuticals Pfizer

Efficacy

Beleodaq (Belinostat) for the Treatment of Lymphoma

Beleodaq, also known by its generic name belinostat, is a histone deacetylase inhibitor approved by the U.S. Food and Drug Administration (FDA) for the treatment of relapsed or refractory peripheral T-cell lymphoma (PTCL). This is a rare and aggressive form of non-Hodgkin lymphoma that affects the T-cells of the immune system. The efficacy of Beleodaq was evaluated in a multicenter, single-arm clinical trial where patients received the drug intravenously over a period of five days in a 21-day cycle. The overall response rate, which includes complete and partial responses, was observed to be approximately 25-30% in patients who had previously received treatment for PTCL.

The duration of response for those who benefited from Beleodaq treatment varied, with some patients experiencing prolonged responses. However, it is important to note that while Beleodaq can induce responses in a subset of patients with PTCL, it is not considered a cure and the long-term survival benefit of the drug is still under investigation. Physicians may consider Beleodaq as a second-line therapy or beyond for patients with PTCL who have not responded to other treatments.

Xalkori (Crizotinib) and Its Efficacy in Lymphoma

Xalkori, with the generic name crizotinib, is primarily known as a targeted therapy for the treatment of non-small cell lung cancer (NSCLC) that harbors specific genetic alterations. However, its efficacy in lymphoma, particularly in anaplastic large cell lymphoma (ALCL) that carries the anaplastic lymphoma kinase (ALK) gene rearrangement, has been a subject of clinical interest. ALCL is a subtype of non-Hodgkin lymphoma, and the presence of ALK rearrangement in lymphoma cells is a potential target for crizotinib.

While crizotinib is not FDA-approved for the treatment of lymphoma, early-phase clinical trials and case reports have suggested that crizotinib may have activity in ALK-positive lymphomas. The results from these studies indicate that some patients with ALK-positive ALCL may respond to crizotinib treatment, with a subset achieving complete remission. Nevertheless, these findings are preliminary, and more extensive clinical trials are necessary to fully establish the efficacy and safety profile of crizotinib for the treatment of ALK-positive lymphomas.

Regulatory Agency Approvals

Beleodaq
  • Food and Drug Administration (FDA), USA
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 Beleodaq or Xalkori today

If Beleodaq 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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