Overview of the Safety Profile of CAR-T Therapy
December 23rd 2024Dr. Mikhael and Dr. Rossi discuss the safety profiles of CAR-T therapies for multiple myeloma, focusing on common and impactful adverse events, comparisons between ide-cel and cilta-cel, alignment with clinical trial data, and how safety considerations influence treatment selection for diverse patient populations.
Recognizing PNH and Initial Challenges
December 19th 2024Panelists discuss how Brandi first noticed symptoms leading to her paroxysmal nocturnal hemoglobinuria (PNH) diagnosis, highlighting the challenges of the initial diagnostic process, and explore the impact of fatigue and brain fog on her daily life. They also address how clinicians assess the severity of these symptoms during consultations and what they indicate about disease progression or treatment needs.
Looking Ahead: The Future of Chronic GVHD Management and Patient Care
October 7th 2024Panelists conclude by discussing the future of graft-versus-host disease management, expressing their hopes for the current treatment landscape and potential advancements that could further improve patient outcomes and quality of life.
Treatment with Axatilimab in Chronic GVHD: How it Works and Insights into Treatment Efficacy
October 7th 2024Panelists discuss how axatilimab, a novel therapy for chronic graft-versus-host disease (cGVHD), functions through a unique mechanism of action compared to other treatments, highlighting its potential role in cGVHD management and presenting key findings from the AGAVE-201 trial that demonstrate its efficacy and safety profile.
Chronic GVHD Treatment Overview: Immunosuppressives, New Agents, and What Patients Need to Know
September 30th 2024Panelists discuss how the current treatment landscape for chronic graft-versus-host disease includes a range of immunosuppressive approaches, from traditional corticosteroids and calcineurin inhibitors to newer approved agents like axatilimab, ruxolitinib, belumosudil, ibrutinib, and abatacept, emphasizing key considerations patients should be aware of when undergoing these therapies.
Patient Communication and Collaborative Care for Symptom Management
September 30th 2024Panelists discuss how physician assistants educate and empower chronic graft-versus-host disease patients and their caregivers to recognize, report, and manage symptoms effectively, detailing strategies for patient communication, developing personalized symptom management plans, addressing challenging symptoms, and collaborating with the broader healthcare team to ensure comprehensive care.
Early Symptom Detection and the Impact on Patient Outcomes in GVHD
September 23rd 2024Panelists discuss how the care team identifies and manages symptoms in chronic graft-versus-host disease patients, particularly those with advanced disease, emphasizing key symptoms to monitor, approaches to symptom identification, and the critical importance of early detection and management for improving patient outcomes.
Managing Severe Symptoms and Disease Progression in the GVHD Journey
September 23rd 2024Panelists discuss how chronic graft-versus-host disease typically progresses in patients requiring third-line treatment and beyond, focusing on severe symptoms, the impact on quality of life, and potential long-term consequences of inadequately managed symptoms.
Comprehensive Patient Education and Symptom Awareness with GVHD
September 16th 2024Panelists discuss how nurse practitioners educate patients about chronic graft-versus-host disease (cGVHD) and its long-term effects, exploring various educational resources and materials such as brochures, apps, websites, and videos that are most effective in supporting patients and their caregivers.
Key Takeaways for Patients With Myelofibrosis
January 31st 2024Patients with myelofibrosis should reflect on their personal priorities and quality of life goals, understand the range of available JAK inhibitor treatment options, and openly communicate with their doctor to arrive at a shared decision for managing their disease.
Dosing JAK Inhibitors in Patients With Myelofibrosis
January 31st 2024For most JAK inhibitors dosing starts at the maximum safe dose, while ruxolitinib often requires lower initial doses and dose reductions over the first 12 weeks when cytopenias typically worsen before partially improving, warranting consideration of earlier switching to alternative JAK inhibitors instead of pushing through transfusions.
Best Approaches to Switching Therapies for a Patient With Myelofibrosis
January 31st 2024Reasons to switch JAK inhibitors include worsening blood counts and insufficient symptom or spleen response at maximum doses, with the goal of avoiding gaps in treatment by stopping one JAK inhibitor when ready to start the next to prevent symptom rebound while still allowing for potential increased efficacy from an alternative mechanism of action.
Assessing Treatment Response in Patients With Myelofibrosis
January 31st 2024Response is assessed in patients starting a JAK inhibitor by monitoring symptoms on a severity scale, spleen size, blood counts, and overall patient impression of change, with the goal being reduction of symptoms and stabilization of blood counts to improve quality of life.