Aaron Gerds, MD, MS, compares myelofibrosis with other myeloproliferative neoplasms, explores its prevalence in the US, and reviews the diverse clinical presentations and the impact on patients’ quality of life.
This is a video synopsis/summary of a Guidelines featuring Aaron Gerds, MD, MS.
Gerds sheds light on myelofibrosis (MF), a clonal myeloid disorder categorized under myeloproliferative neoplasms. He draws comparisons between MF, polycythemia vera (PV), and essential thrombocythemia (ET), emphasizing the shared pathobiologic factor of constitutive activation of the JAK-STAT pathway. MF clinically manifests with diverse symptoms, including elevated blood counts, constitutional symptoms like night sweats and weight loss, and splenomegaly, affecting the patient's quality of life significantly.
Gerds discusses the prevalence of MF, estimating approximately 300,000 people in the United States living with myeloproliferative neoplasms. He notes that while MF may have a higher incidence, the shortened life expectancy compared with PV and ET results in lower prevalence. The clinical presentation of MF varies, often diagnosed through routine blood work, symptom manifestation, or as a progression from ET or PV.
Exploring the burdens of MF, Gerds addresses cytokine-mediated symptoms, anemia challenges, and the overarching impact of having a chronic illness. Anemia, affecting around 40% of patients at diagnosis, presents a significant burden on patients' lives, particularly when transfusion-dependent. Furthermore, the chronic nature of MF, unless treated with stem cell transplant, adds an emotional burden often underrepresented in disease analyses. The conversation provides a comprehensive understanding of MF and its multifaceted effects on patients.
Video synopsis is AI-generated and reviewed by AJMC® editorial staff.
DMD Guidance Could Benefit From Update, Experts Say
January 24th 2024MEDLINE, the Turning Research Into Practice database, Google Scholar, and organization guidelines were searched for their ongoing applicability to the management of Duchenne muscular dystrophy (DMD) and to determine if there is a need to develop new treatment recommendations.
Read More
NCCN Guidelines Update Adds Momelotinib Below Ruxolitinib for High-, Low-Risk Myelofibrosis
January 23rd 2024Momelotinib was given category 2A and 2B status for patients with high- and low-risk myelofibrosis (MF) and MF with anemia. However, ruxolitinib retains a higher category of recommendation as a treatment for patients with MF.
Read More
NCCN Guidelines Update Recommends Ropeginterferon Alfa-2b for Polycythemia Vera
July 7th 2023Ropeginterferon alfa-2b was moved to preferred status for patients with high- and low-risk polycythemia vera in a recent update to the National Comprehensive Cancer Network (NCCN) Clinical Practice Guidelines in Oncology.
Read More
NCCN Adds Epcoritamab to Clinical Practice Guidelines in Oncology for DLBCL
June 23rd 2023Epcoritamab has been added to the National Comprehensive Cancer Network Clinical Practice Guidelines in Oncology for B-cell Lymphomas in the third- or later-line setting for the treatment of patients with diffuse large B-cell lymphoma.
Read More
Review Finds EORTC QLQ-MY20 Useful, Robust 25 Years After Development
June 16th 2023The treatment landscape for multiple myeloma has shifted since European Organisation for Research and Treatment of Cancer Quality of Life Multiple Myeloma Questionnaire (EORTC QLQ-MY20) was first developed in 1996.
Read More
ASTRO, ESTRO Release First Guideline for Definitive Local Therapy in Oligometastatic NSCLC
April 27th 2023The American Society for Radiation Oncology (ASTRO) and European Society for Radiotherapy and Oncology (ESTRO) jointly released a clinical guideline on the use of definitive local therapy for the treatment of oligometastatic non–small cell lung cancer (NSCLC).
Read More