Efficacy and Safety of Peginterferon in ET and PV.

Launched by ZHENYA HONG · Dec 11, 2024

Keywords

ClinConnect Summary

This clinical trial is studying a medication called Peginterferon α-2b to see how effective and safe it is for patients with Essential Thrombocythemia (ET) and Polycythemia Vera (PV), which are conditions that affect blood cell production. The trial plans to enroll 40 participants who meet specific health criteria, such as having high platelet counts for ET or specific blood measurements for PV. Eligible participants will receive a weekly injection of the medication and will have regular follow-ups to monitor their health.

To join the trial, participants need to be between the ages of 65 and 74 and must meet certain medical guidelines that confirm they have ET or PV. Those who have previously received Peginterferon treatment or have certain health issues, like severe heart disease or liver problems, will not be eligible. Participants can expect to receive careful monitoring throughout the study to assess how well the treatment works and whether it is safe for them. If you're considering participating, it's important to discuss any questions or concerns with your healthcare provider.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • 1. Meet the 2016 WHO diagnostic criteria for ET (Essential Thrombocythemia) and PV (Polycythemia Vera)
• * ET (Essential Thrombocythemia) major criteria:
• • 1. Platelet count \> 450 \* 10\^9/L; (2) Bone marrow biopsy shows marked megakaryocytic proliferation with increased mature megakaryocyte volume and increased nuclear lobulation. There is no significant granulocytic proliferation, left shift, or erythroid proliferation, with grade 1 fibrosis observed in a few cases; (3) Does not meet the WHO diagnostic criteria for BCR-ABL1+ CML, PV, PMF, MDS, or other myeloproliferative neoplasms; (4) JAK2, CALR, or MPL mutation positive.
• • Secondary criteria: (1) Presence of a clonal marker or absence of evidence for reactive thrombocytosis.
• • The diagnosis of ET requires the fulfillment of all four main criteria, or the first three main criteria plus one secondary criterion.
• • PV (Polycythemia Vera) main criteria: (1) Hemoglobin \> 16.5 g/dL in males, \> 16 g/dL in females, or Hematocrit \> 49% in males, \> 48% in females, or an increase in red cell volume of 25% or more above the normal value; (2) Bone marrow biopsy shows increased cellularity inappropriate for age, with marked erythroid, granulocytic, and megakaryocytic proliferation, and the presence of mature megakaryocytes of varying sizes and morphologies; (3) JAK2 V617F mutation positive or JAK2 exon 12 mutation positive.
• • Secondary criteria: Serum Epo (Erythropoietin) level below the lower limit of the normal range.
• • The diagnosis of PV requires the fulfillment of three major criteria, or the first two main criteria plus one secondary criterion.
• 2. For ET patients, the criteria for cytoreductive therapy must be met, as follows:
• • (1) For patients without a history of thrombosis: Age ≥ 60 years, regardless of the presence of cardiovascular risk (CVR) or JAK2V617 mutation; Any age with a platelet count \> 1500 × 109/L. (2) For patients with a history of arterial thrombosis: Any age, regardless of the presence of CVR and JAK2V617 mutation; (3) For patients with a history of venous thrombosis: Any age, regardless of the presence of CVR and JAK2V617 mutation; 3.ECOG score ≤ 2. 4.Cardiac ejection fraction (EF) ≥ 60%. 5.The participant voluntarily signs the informed consent form.
• Exclusion Criteria:
• • Previous treatment with Peginterferon α-2b.
• • ET patients who do not meet the criteria for cytoreductive therapy as per the 2016 Chinese Expert Consensus on Primary Thrombocythemia.
• • Allergy to the active ingredient, α-interferon, or any excipients of this product.
• • History of psychiatric illness, or allergy to interferon.
• • Plasma total bilirubin greater than twice the normal value.
• • Severe cardiac disease, liver insufficiency, chronic kidney disease, and neurological disorders (such as depression or mania).
• • History of other malignant tumors within the past three years.
• • Autoimmune chronic hepatitis.
• • Any condition deemed unsuitable for inclusion by the investigator.