Bosulif (bosutinib) vs Vanflyta (quizartinib)

Bosulif (bosutinib) vs Vanflyta (quizartinib)

Bosulif (bosutinib) and Vanflyta (quizartinib) are both oral medications used to treat different types of leukemia, but they target different genetic mutations and are used in different patient populations. Bosulif is a tyrosine kinase inhibitor specifically indicated for the treatment of chronic myelogenous leukemia (CML) with resistance or intolerance to prior therapy, and it targets the BCR-ABL kinase. In contrast, Vanflyta is designed for the treatment of adults with relapsed or refractory acute myeloid leukemia (AML) with FLT3-ITD mutations, targeting the FLT3 kinase. Patients should consult with their healthcare provider to determine which medication is appropriate based on their specific type of leukemia, genetic mutation profile, and overall health condition.

Difference between Bosulif and Vanflyta

Metric Bosulif (bosutinib) Vanflyta (quizartinib)
Generic name bosutinib quizartinib
Indications Chronic myelogenous leukemia (CML) Acute myeloid leukemia (AML)
Mechanism of action Tyrosine kinase inhibitor Tyrosine kinase inhibitor
Brand names Bosulif Vanflyta
Administrative route Oral Oral
Side effects Diarrhea, nausea, thrombocytopenia, rash, increased liver enzymes QT prolongation, myelosuppression, nausea, vomiting, fatigue
Contraindications Hypersensitivity to bosutinib or any component of the formulation Hypersensitivity to quizartinib or any component of the formulation
Drug class Tyrosine kinase inhibitor Tyrosine kinase inhibitor
Manufacturer Pfizer Daiichi Sankyo

Efficacy

Bosulif (bosutinib) Efficacy in Leukemia

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 or intolerant to prior therapy. Clinical trials have demonstrated the efficacy of bosutinib in achieving hematologic and cytogenetic responses in this patient population. In a pivotal phase 3 study, bosutinib was shown to be effective in inducing major cytogenetic response in patients with chronic phase CML who had not responded to or could not tolerate previous treatments, including imatinib. Additionally, bosutinib has shown efficacy in patients with advanced phases of the disease, although the response rates tend to be lower compared to those in the chronic phase.

The efficacy of Bosulif in treating CML is measured by its ability to achieve and maintain complete hematologic remission, as well as cytogenetic and molecular responses. The drug works by inhibiting the Bcr-Abl kinase that promotes the growth of abnormal cells in CML patients. Clinical outcomes have shown that bosutinib can lead to long-term disease control and has become an important treatment option for patients with CML, particularly for those who have not benefited from other therapies.

Vanflyta (quizartinib) Efficacy in Leukemia

Vanflyta (quizartinib) is an oral selective FLT3 inhibitor used in the treatment of acute myeloid leukemia (AML) with a specific focus on patients with FLT3-ITD, a common and often aggressive subtype of AML. The efficacy of quizartinib has been evaluated in clinical trials involving patients with relapsed or refractory AML. In these studies, quizartinib demonstrated a significant improvement in overall survival compared to chemotherapy in patients with FLT3-ITD AML. The drug's ability to target the FLT3 mutation, which is present in approximately 25-30% of AML cases, allows for a more personalized approach to treatment.

Quizartinib's effectiveness in AML is assessed through its impact on survival rates, the duration of remissions, and the rate of response to treatment. The clinical data suggest that quizartinib can induce complete remissions in a subset of patients with this challenging form of leukemia. It is particularly noteworthy for offering a treatment option for patients who have limited therapies available due to the aggressive nature of FLT3-ITD AML. While quizartinib provides a targeted approach for patients with this mutation, its use is generally associated with a specific patient population and is not considered a universal treatment for all AML patients.

Regulatory Agency Approvals

Bosulif
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
Vanflyta
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA

Access Bosulif or Vanflyta today

If Bosulif or Vanflyta 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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