Rydapt (midostaurin) vs Bosulif (bosutinib)

Rydapt (midostaurin) vs Bosulif (bosutinib)

Rydapt (midostaurin) is a multi-targeted kinase inhibitor approved for the treatment of adult patients with newly diagnosed acute myeloid leukemia (AML) that is FLT3 mutation-positive, as detected by an FDA-approved test, used in combination with standard chemotherapy. It is also indicated for adults with certain types of mastocytosis. In contrast, Bosulif (bosutinib) is a tyrosine kinase inhibitor specifically indicated for the treatment of adult patients with chronic, accelerated, or blast phase Philadelphia chromosome-positive chronic myelogenous leukemia (CML) who are resistant to or intolerant to prior therapy. The choice between Rydapt and Bosulif would depend on the specific type of leukemia a patient has and the presence of certain genetic mutations, as well as their previous treatments and overall health condition.

Difference between Rydapt and Bosulif

Metric Rydapt (midostaurin) Bosulif (bosutinib)
Generic name Midostaurin Bosutinib
Indications Acute Myeloid Leukemia (AML), Mastocytosis Chronic Myelogenous Leukemia (CML)
Mechanism of action Protein kinase inhibitor Tyrosine kinase inhibitor
Brand names Rydapt Bosulif
Administrative route Oral Oral
Side effects Febrile neutropenia, nausea, mucositis, vomiting, headache Diarrhea, nausea, thrombocytopenia, rash, increased liver enzymes
Contraindications Hypersensitivity to midostaurin or any component of the formulation Hypersensitivity to bosutinib or any component of the formulation
Drug class Protein kinase inhibitor Tyrosine kinase inhibitor
Manufacturer Novartis Pharmaceuticals Corporation Pfizer Inc.

Efficacy

Efficacy of Rydapt (Midostaurin) in Treating Leukemia

Rydapt, known generically as midostaurin, is a medication that has been approved for the treatment of acute myeloid leukemia (AML) in adult patients with a specific genetic mutation known as FLT3. This mutation is present in approximately one-third of AML cases and is associated with a poor prognosis. Clinical trials have demonstrated that when Rydapt is combined with standard chemotherapy, it can significantly improve overall survival rates compared to chemotherapy alone. The efficacy of Rydapt in AML was established in a large, randomized, placebo-controlled trial, which showed a substantial improvement in survival outcomes for patients who received Rydapt in addition to standard chemotherapy.

Furthermore, Rydapt is also indicated for the treatment of adults with newly diagnosed systemic mastocytosis, which includes aggressive systemic mastocytosis (ASM), systemic mastocytosis with associated hematological neoplasm (SM-AHN), and mast cell leukemia (MCL). However, its use in MCL is based on the number of patients who achieved a complete or partial response, and not on improvement in disease-related symptoms or increased survival.

Efficacy of Bosulif (Bosutinib) in Treating Leukemia

Bosulif, with the active ingredient bosutinib, is a tyrosine kinase inhibitor that is used to treat chronic myelogenous leukemia (CML). It is specifically indicated for adult patients with newly diagnosed chronic phase Philadelphia chromosome-positive CML, as well as for those who are resistant or intolerant to prior therapy. Clinical trials have shown that Bosulif is effective in achieving major cytogenetic response (MCyR) and complete cytogenetic response (CCyR) in a significant number of patients who were previously treated with other tyrosine kinase inhibitors. The efficacy of Bosulif in newly diagnosed chronic phase CML patients was demonstrated in a randomized trial comparing it to imatinib, where Bosulif showed superior rates of CCyR and major molecular response (MMR) at 12 months.

For patients with CML who are resistant or intolerant to prior therapy, Bosulif has been shown to induce MCyR and CCyR in a substantial proportion of patients, with some achieving a durable response. The drug's efficacy in this context was established through a single-arm trial that evaluated the long-term outcomes for patients treated with Bosulif after resistance or intolerance to previous treatments. It is important to note that while Bosulif is effective in treating CML, it may not be suitable for all patients, and its use should be based on an individual's specific condition and medical history.

Regulatory Agency Approvals

Rydapt
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
  • Therapeutic Goods Administration (TGA), Australia
  • Medsafe (NZ)
Bosulif
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA

Access Rydapt or Bosulif today

If Rydapt or Bosulif 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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