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Ropeginterferon Alfa 2b for Early MyelofibrosisDIPSS Low/Intermediate-1 Risk Myelofibrosis

Ropeginterferon Alfa 2b for Early MyelofibrosisDIPSS Low/Intermediate-1 Risk Myelofibrosis

Recruiting
20 years and older
All
Phase 2

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Overview

This is a multi-centre phase 2 open-label prospective study designed to assess the efficacy and safety of ropeg patients with pre-fibrotic primary myelofibrosis or DIPSS low/intermediate-1 risk myelofibrosis after 24 months of treatment.

Description

This is a multi-centre phase 2 open-label prospective study designed to assess the efficacy and safety of ropeg patients with pre-fibrotic primary myelofibrosis or DIPSS low/intermediate-1 risk myelofibrosis after 24 months of treatment. . In patients achieving any molecular response at 24 months, treatment with ropeg will be continued until disease progression.

After obtaining a written informed consent, screening evaluations will be performed. Eligibility will be determined based on the inclusion and exclusion criteria in section 6 of this protocol. Subject visits will be scheduled regularly after recruitment for efficacy evaluations and safety assessments. A safety follow-up will be scheduled 28 days after end-of-treatment visit. Efficacy evaluations, safety assessments and sample collection will be performed according to the schedule laid in section 2 in this protocol.

Efficacy will be evaluated using laboratory assessment of haematological parameters, physical examination for liver and spleen size assessment, quantitative assessment of JAK2V617F, CALR, MPL and other driver mutations, bone marrow examination, and symptom burden assessment by MPN-SAF-TSS. Quantitative assessment of JAK2V617F, CALR, MPL and other driver mutations will be performed using real-time quantitative PCR or ddPCR at the laboratory at the Department of Medicine, the University of Hong Kong, National Taiwan University Hospital and Chang Gung Memorial Hospital Chiayi.

Safety evaluations will be performed using symptoms, physical examination, laboratory studies, Chest X-rays, ophthalmic assessment, ECOG performance status and CTCAE version 5.0.

Eligibility

Inclusion Criteria:

  • Adults ≥ 18 years (or based on the legal age of the territory) Diagnosed of primary myelofibrosis, post-PV and post-ET myelofibrosis according to the WHO 2016 classification Bone marrow reticulin fibrosis grade of 0-1 or low/intermediate-1 risk according to DIPSS Compensated liver function defined as: bilirubin ≤ 1.5 x upper limit normal (ULN); alanine aminotransferase (ALT) ≤ 2 x ULNor aspartate aminotransferase (AST) ≤ 2 x ULN; prothrombin time versus control <3 seconds at screening Glomerular filtration rate ≥ 50 mL/min (by MDRD equation or Cockcroft-Gault formula) Men and women of childbearing potential must agree to perform contraception until 28 days after the last dose of ropeg.
        Women must avoid breast-feeding during the study. Able to give a written informed consent
        and fully comply to the requirements of the study.
        Exclusion Criteria:
          -  Prior or current use of IFNα preparations for PMF or secondary MF. Prior use of IFNα
             for antecedent PV or ET is allowed provided that the time from the last dose of IFNα
             to recruitment is > 4 weeks.
        Patients currently on other investigational therapy (ies) Contraindications or
        hypersensitivity to IFNα preparations History of organ transplantation Pregnant or
        lactating women Documented autoimmune disease at screening Infection with human
        immunodeficiency virus (HIV) Active and uncontrolled infections with hepatitis B virus
        (HBV) and hepatitis C virus (HCV). Please note that patients on antiviral therapy with
        undetectable HBV DNA and HCV RNA may be recruited.
        Evidence of severe retinopathy including but not limited to macular degeneration, diabetic
        retinopathy and hypertensive retinopathy.
        History of clinically significant neuropsychiatric conditions including but not limited to
        depression and epilepsy.
        Clinically significant neuropsychiatric conditions including but not limited to depression
        and epilepsy.
        Presence of other active malignancies within three years prior to the time of recruitment.
        History of malignant disease, including solid tumours and haematological malignancies
        (except basal cell and squamous cell carcinomas of the skin and carcinoma in situ of the
        cervix that have been completely excised and are considered cured) within the last 3 years.
        Evidence of alcohol or drug abuse within 6 months

Study details
    Pre-fibrotic Myelofibrosis

NCT05731245

National Taiwan University Hospital

27 January 2024

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