Multiple Myeloma an incurable disease, but I have spent the last 25 years in remission using a blend of conventional oncology and evidence-based nutrition, supplementation, and lifestyle therapies from peer-reviewed studies that your oncologist probably hasn't told you about.
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According to the research linked below cytopenia following CAR-T cell therapy is the most frequent condition listed in the Common Terminology Criteria for Adverse Events of grade 3 or greater associated with CAR T-cell therapy.1-3
Though CAR-T cell therapy holds a great deal of promise for myeloma survivors, as of 2024, this therapy continues to cause serious side effects. As a MM survivor myself who’s spent decades struggling with long-term and late stage side effects, I believe that MM patients must understand their risks thoroughly before undergoing any therapy.
Having said that, I believe that as long as the MM patient understands his/her risks when undergoing a specific therapy, they can choose whatever therapy they please.
There are a number of polyphenols that have been shown to enhance blood health in myeloma patients. However, I have no idea if these polyphenols can help cytopenia following CAR-T cell therapy.
However, if you are interested in learning more about nutritional supplementation that may help cytopenia following CAR-T cell therapy email me at David.PeopleBeatingCancer@gmail.com
thank you,
David Emerson
Cytopenia occurs when one or more of your blood cell types is lower than it should be.
Your blood consists of three main parts. Red blood cells, also called erythrocytes, carry oxygen and nutrients around your body. White blood cells, or leukocytes, fight infection and battle unhealthy bacteria. Platelets are essential for clotting. If any of these elements are below typical levels, you may have cytopenia…”
“Although the extensive study of potentially life-threatening toxicities, such as cytokine release syndrome (CRS) and immune effector cell–associated neurotoxicity syndrome, has informed the iterative development of effective risk evaluation and mitigation strategies over the years, similar advancements have not been achieved for hematological toxicities.
Despite the wealth of pivotal trials and real-world data highlighting the significance of cytopenia following CAR T-cell therapy, this area remains relatively unexplored…2
Cytopenia, which affects 1 or more cell lineages, is the most frequent condition listed in the Common Terminology Criteria for Adverse Events of grade 3 or greater associated with CAR T-cell therapy.1-3
Although the underlying pathophysiology remains to be fully elucidated, cytopenia appears to be a class effect of CAR T-cell therapy, independent of the target antigen or disease entity.3
Furthermore, this effect is characterized by profound and persistent cytopenia, often spanning months to years after CAR T-cell infusion, with periods of intermittent count recovery.4
The management of cytopenia post CAR T-cell therapy is primarily supportive and includes packed red blood cell (PRBC) and/or platelet transfusions, granulocyte colony-stimulating factor (G-CSF), thrombopoietin receptor agonists (TPO-RA), and hematopoietic stem cell boost (HSCB).1,2..
The concept of HSCB has long been utilized in transplantation to restore hematopoiesis.1 This approach can also be applied to patients experiencing persistent or life-threatening cytopenia after CAR T-cell therapy, provided the patient has a source of stored stem cells, typically from a previous transplant.
Three small, retrospective studies have explored the safety and feasibility of HSCBs after CAR T-cell therapy. Overall, HSCBs appear to be highly efficacious, with a majority of patients experiencing a sustained response in neutrophils and platelets within 2 to 3 weeks, and no AEs have been noted. However, there is wide variability in the timing of the boost and the cell dose.16-18…