Advances in the Treatment of Myelofibrosis: Clinical Trial Data of Next Generation Therapeutics – Live

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Description

Program Description


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This activity addresses advancements in managing patients with myelofibrosis (MF), including symptom recognition, prognostic risk scoring, and next-generation therapeutics for the treatment of MF.

The program will focus on the following:

MF – Myelofibrosis (MF) is a myeloproliferative neoplasm (MPN) characterized by clonal hematopoietic cell expansion with bone marrow fibrosis.

  • Pathophysiology of MF
  • Symptomology of MF based on myeloproliferative neoplasm symptom assessment (MPN-SAF)
  • Prognostic scoring systems and risk assessment based on IPSS, DIPSS+, MIPSS70, Genetically Inspired IPSS, Myelofibrosis secondary to PV, and ET-prognostic model (MYSEC-PM)
  • Molecular profiling of MF – Molecular profiling, cytogenetic and molecular characteristics.
  • Prognostic scoring systems and risk assessment based on IPSS, DIPSS+, MIPSS70, Genetically Inspired IPSS, Myelofibrosis secondary to PV, and ET-prognostic model (MYSEC-PM)

Treatment Options for MF – NCCN guideline-directed treatment strategies for MF with JAK inhibitors and a first-in-class telomerase inhibitor.

  • JAK Inhibitors
    • Ruxolitinib
    • Fedratinib
    • Pacritinib
  • Newer Therapies – Ongoing Clinical Trials
    • PIM1 Kinase Inhibitor
      • Nuvisertib
    • Telomerase Inhibitor
      • Imetelstat (GRN163L)
    • Bromodomain and extraterminal domain (BET) inhibitor (BETi)
      • Pelabresib

Symptomatic patients with anemia and myelofibrosis

  • Momelotinib, an activin A receptor type 1, and JAK1 and JAK2 have shown symptom, spleen, and anemia benefits in patients with MF
  • Navitoclax (NAV) is an oral, small-molecule inhibitor of BCL-XL and BCL-2 that has a synergistic effect when used in combination with JAK inhibitors

Agenda


Overview of pathophysiology, symptom burden, risk stratification, and molecular profiling of MF
John Mascarenhas, MD

Discuss NCCN treatment guidelines-based treatment options, and next-generation therapeutics for the treatment of MF
Raajit K. Rampal, MD, PhD

Intended Audience


This activity is designed to meet the educational needs of hematologists/oncologists, community oncologists, physician assistants, nurse practitioners, nurses, and pathologists who manage patients with myelofibrosis.

Commercial Supporter


Supported by educational grants from Geron Corporation and Incyte Corporation.

CancerNet

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EVENT Summary

Dates
Saturday, December 13, 2025, 10:00 AM ET/ 9:00 AM CT/ 8:00 AM MT/ 7:00 AM PT

Location
Virtual

Target Audience
Hematologists/oncologists, community oncologists, physician assistants, nurse practitioners, nurses, and pathologists who manage patients with myelofibrosis

Format
Live Webinar

Credits
1.25 / AMA PRA Category 1 CreditsTM
1.25 / CNE Contact Hours

Cost
Free

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