Xospata (gilteritinib) vs Scemblix (asciminib)

Xospata (gilteritinib) vs Scemblix (asciminib)

Xospata (gilteritinib) is a targeted therapy known as a FLT3 inhibitor, used specifically for the treatment of adult patients with relapsed or refractory acute myeloid leukemia (AML) with a FLT3 mutation. Scemblix (asciminib), on the other hand, is a kinase inhibitor indicated for the treatment of adult patients with Philadelphia chromosome-positive chronic myeloid leukemia (CML) in chronic phase who have received two or more prior lines of therapy, or those with the T315I mutation. When deciding between these two medications, it's crucial to consider the specific type of leukemia and its genetic mutations, as Xospata is tailored for FLT3-mutated AML, while Scemblix is for specific cases of CML, highlighting the importance of genetic testing and a healthcare provider's guidance in the decision-making process.

Difference between Xospata and Scemblix

Metric Xospata (gilteritinib) Scemblix (asciminib)
Generic name Gilteritinib Asciminib
Indications Acute myeloid leukemia (AML) with a FLT3 mutation Chronic myeloid leukemia (CML)
Mechanism of action FLT3/AXL tyrosine kinase inhibitor STAMP (Specifically Targeting the ABL Myristoyl Pocket) inhibitor
Brand names Xospata Scemblix
Administrative route Oral Oral
Side effects Fatigue, elevated liver enzymes, musculoskeletal pain, fever, rash, etc. Thrombocytopenia, neutropenia, anemia, musculoskeletal pain, fatigue, etc.
Contraindications Hypersensitivity to gilteritinib or any component of the formulation Hypersensitivity to asciminib or any component of the formulation
Drug class Tyrosine kinase inhibitor Tyrosine kinase inhibitor
Manufacturer Astellas Pharma Novartis

Efficacy

Xospata (Gilteritinib) Efficacy in Treating Leukemia

Xospata, known by its generic name gilteritinib, is a medication specifically approved for the treatment of adult patients who have relapsed or refractory acute myeloid leukemia (AML) with a FLT3 mutation as detected by an FDA-approved test. The efficacy of Xospata for this indication was studied in a clinical trial that involved patients with relapsed or refractory AML with a FLT3 mutation. The trial demonstrated that treatment with Xospata led to a significant improvement in the rate of complete remission with full or partial hematologic recovery. Additionally, there was an extension in the overall survival of patients compared to those who received alternative chemotherapy regimens.

The FLT3 mutation is known to be associated with a poor prognosis in AML, which makes the efficacy of Xospata particularly noteworthy. The drug works by inhibiting the activity of the FLT3 gene mutation, thereby reducing the proliferation of abnormal cells that contribute to the progression of AML. Gilteritinib has been shown to induce responses even in patients who have failed prior therapies, including those with resistance to other FLT3 inhibitors, which underscores its value in the management of this challenging form of leukemia.

Scemblix (Asciminib) Efficacy in Treating Leukemia

Scemblix, with the generic name asciminib, is another newer medication that has shown efficacy in the treatment of chronic myeloid leukemia (CML). It is specifically indicated for the treatment of adult patients with Philadelphia chromosome-positive CML in the chronic phase who have received two or more prior lines of tyrosine kinase inhibitor (TKI) therapy, or those with the T315I mutation, which is resistant to most other TKIs. In clinical trials, asciminib has demonstrated the ability to achieve hematologic and cytogenetic remissions in a significant proportion of patients, including those with the T315I mutation.

Asciminib represents a novel class of TKIs that binds to a different site on the BCR-ABL protein than previous drugs, which may account for its activity in patients who have developed resistance to other TKIs. The drug has been associated with deep and durable responses in patients with CML, offering a new line of treatment for those who have exhausted other options. The approval of Scemblix for the treatment of CML is based on its efficacy in achieving and maintaining remission, which is critical for the long-term management of this chronic form of leukemia.

Regulatory Agency Approvals

Xospata
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
  • Therapeutic Goods Administration (TGA), Australia
Scemblix
  • Food and Drug Administration (FDA), USA

Access Xospata or Scemblix today

If Xospata or Scemblix 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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