Onureg (azacitidine) vs Asparlas (calaspargase pegol-mknl)

Onureg (azacitidine) vs Asparlas (calaspargase pegol-mknl)

Onureg (azacitidine) is an oral hypomethylating agent used to treat adults with acute myeloid leukemia (AML) who are in remission but still at high risk of relapse. Asparlas (calaspargase pegol-mknl) is a modified enzyme used as part of a multi-agent chemotherapeutic regimen for the treatment of acute lymphoblastic leukemia (ALL). When deciding between these medications, it is crucial to consider the specific type of leukemia being treated, as Onureg is indicated for AML, while Asparlas is used for ALL, and the choice of medication will depend on the patient's individual diagnosis and treatment plan as determined by their healthcare provider.

Difference between Onureg and Asparlas

Metric Onureg (azacitidine) Asparlas (calaspargase pegol-mknl)
Generic name Azacitidine Calaspargase pegol-mknl
Indications Continued treatment of acute myeloid leukemia (AML) in adult patients in first remission Used as a component of a multi-agent chemotherapeutic regimen for the treatment of acute lymphoblastic leukemia (ALL) in pediatric and young adult patients
Mechanism of action Cytidine nucleoside analog that inhibits DNA methylation leading to cell differentiation and apoptosis Modified enzyme that catalyzes the hydrolysis of asparagine to aspartic acid and ammonia, depriving leukemia cells of asparagine which is necessary for their growth
Brand names Onureg Asparlas
Administrative route Oral Intravenous
Side effects Nausea, vomiting, diarrhea, decreased appetite, constipation, fatigue, pneumonia, joint pain, dizziness, and decreased white blood cell count Allergic reactions, elevated liver enzymes, decreased blood pressure, hyperglycemia, pancreatitis, hemorrhage, thrombosis
Contraindications Advanced malignant hepatic tumors, hypersensitivity to azacitidine or mannitol Hypersensitivity to calaspargase pegol-mknl or pegaspargase, history of serious thrombosis with prior L-asparaginase therapy
Drug class Hypomethylating agent, antimetabolite Asparagine specific enzyme
Manufacturer Bristol Myers Squibb Servier Pharmaceuticals

Efficacy

Efficacy of Onureg (azacitidine) in Leukemia

Onureg (azacitidine) is a hypomethylating agent approved by the U.S. Food and Drug Administration (FDA) for the continued treatment of adult patients with acute myeloid leukemia (AML) who achieved first complete remission (CR) or complete remission with incomplete blood count recovery (CRi) following intensive induction chemotherapy and are not able to complete intensive curative therapy. Azacitidine has been shown to be effective in extending overall survival in this patient population. Clinical trials have demonstrated that patients receiving Onureg had a significant improvement in overall survival compared to those receiving a placebo. The efficacy of azacitidine is attributed to its ability to induce DNA hypomethylation, which can promote the reactivation of genes that are critical for the differentiation and proliferation of hematopoietic cells.

Efficacy of Asparlas (calaspargase pegol-mknl) in Leukemia

Asparlas (calaspargase pegol-mknl) is an asparagine-specific enzyme indicated as a component of a multi-agent chemotherapeutic regimen for the treatment of acute lymphoblastic leukemia (ALL) in pediatric and young adult patients. It is a novel formulation of L-asparaginase with a modified release profile, which allows for less frequent dosing compared to other forms of L-asparaginase. The efficacy of Asparlas is based on achieving a sustained asparagine depletion, which is essential for the treatment of ALL, as leukemic cells are unable to synthesize asparagine and rely on an external supply for survival. Clinical studies have shown that Asparlas is effective in maintaining therapeutic levels of asparagine depletion, which is associated with positive treatment outcomes in ALL.

Both Onureg and Asparlas have shown efficacy in the treatment of different types of leukemia, addressing specific needs within the leukemia patient population. Onureg serves as a maintenance therapy for AML patients in remission who are not candidates for intensive curative therapy, while Asparlas is part of the front-line treatment for pediatric and young adult patients with ALL. The use of these medications is a reflection of the ongoing advancement in targeted therapies for leukemia, aiming to improve patient outcomes and survival rates.

It is important for healthcare providers to consider the individual patient's type of leukemia, treatment history, and overall health when prescribing these medications. The efficacy of Onureg and Asparlas in the treatment of leukemia underscores the importance of personalized medicine in oncology, where treatments are increasingly tailored to the specific characteristics of the disease and the patient.

Regulatory Agency Approvals

Onureg
  • Food and Drug Administration (FDA), USA
Asparlas
  • Food and Drug Administration (FDA), USA

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