Myelofibrosis (MF) is a rare clonal disease of pluripotent hematopoietic stem and progenitor cells. There have been significant advances in the treatment options for MF in recent years, but anemia remains a major challenge in disease management. This is also reflected in the results of a survey study published in 2024, which was presented at this year’s congress of the European Association of Hematology (EHA).
Autoren
- Mirjam Peter, M.Sc.
Publikation
- HAUSARZT PRAXIS
Related Topics
You May Also Like
- Escitalopram for anxiety disorders
Positive effect, but no immediate improvement in symptoms
- Helicobacter pylori infection
Simplified dual therapy beats quadruple regimen
- Gastric carcinoma
Ways of precision oncology
- Endometrial Cancer
Immunological drivers and new therapeutic pathways
- Exercise for type 1 diabetes
Cyclists and runners with an increased risk of hypoglycemia
- Ozanimod for relapsing-remitting multiple sclerosis
Signs of improved tolerability with prolonged treatment
- When basal cell carcinomas prove difficult to treat
Reaching the goal with innovative therapy strategies
- Irritable Bowel Syndrome