Chimeric antigen receptor (CAR) T cell therapy is a vital tool in the treatment of cancer, and it has revolutionized the landscape of relapsed or refractory DLBCL. However, retrospective reviews have shown that CAR-T therapy is associated with adverse effects such as the development of myelodysplastic syndromes (MDS) and clonal cytopenias of undetermined significance (CCUS).
“Clonal cytopenia of unknown significance (CCUS) is characterized by a low blood count without an apparent cause, as well as a portion of blood cells that carry an acquired genetic mutation. Individuals with these genetic mutations have a 75% chance of developing myelodysplastic syndromes (MDS) or a related condition within four to five years, and low blood counts alone can have negative consequences.”
A recent study of 4 patients with diffuse large B-cell lymphoma (DLBCL) who had received CAR-T therapy, showed the following:
Each patient had a complete response after the initial completion of the CAR-T therapy.
This study indicated several risk factors for developing CCUS or MDS after CAR-T therapy:
Treatment for CCUS is not required, and close follow-up is recommended for patients who develop MDS. “Recognizing patients with MDS/CCUS mutations before CAR-T cell therapy can aid in the prediction of the development of these disorders post-CAR-T cell therapy.” CCUS patients have a higher risk of developing MDS.
Despite the risk of developing CCUS or MDS, CAR-T therapy remains a promising and highly effective treatment for relapsed or refractory DLBCL patients. This therapy can help achieve a sustained and positive response. “Emergence of this form of adoptive immunotherapy has resulted in improved response rates in relapsed and refractory B-cell malignancies.”
Monitoring and follow-up care needs to be a priority. Side effects after CAR-T therapy are common, although most effects will be brief and respond well to treatment. Watch for any long-lasting conditions of CCUS or MDS, such as: fatigue, shortness of breath, very low white blood cell counts, bruising or bleeding and bone pain.
“Long-term follow-up of patients receiving CAR-T cell therapy is necessary to monitor for incidence of MDS/CCUS, especially in prolonged cytopenic patients. Further investigations need to be undertaken to establish a connection between CAR-T cell therapy and MDS/CCUS to allow timely management of these patients before they progress to AML.”
Chimeric antigen receptor (CAR) T cell therapy is a vital tool in the treatment of cancer, and it has revolutionized the landscape of relapsed or refractory DLBCL. However, retrospective reviews have shown that CAR-T therapy is associated with adverse effects such as the development of myelodysplastic syndromes (MDS) and clonal cytopenias of undetermined significance (CCUS).
“Clonal cytopenia of unknown significance (CCUS) is characterized by a low blood count without an apparent cause, as well as a portion of blood cells that carry an acquired genetic mutation. Individuals with these genetic mutations have a 75% chance of developing myelodysplastic syndromes (MDS) or a related condition within four to five years, and low blood counts alone can have negative consequences.”
A recent study of 4 patients with diffuse large B-cell lymphoma (DLBCL) who had received CAR-T therapy, showed the following:
Each patient had a complete response after the initial completion of the CAR-T therapy.
This study indicated several risk factors for developing CCUS or MDS after CAR-T therapy:
Treatment for CCUS is not required, and close follow-up is recommended for patients who develop MDS. “Recognizing patients with MDS/CCUS mutations before CAR-T cell therapy can aid in the prediction of the development of these disorders post-CAR-T cell therapy.” CCUS patients have a higher risk of developing MDS.
Despite the risk of developing CCUS or MDS, CAR-T therapy remains a promising and highly effective treatment for relapsed or refractory DLBCL patients. This therapy can help achieve a sustained and positive response. “Emergence of this form of adoptive immunotherapy has resulted in improved response rates in relapsed and refractory B-cell malignancies.”
Monitoring and follow-up care needs to be a priority. Side effects after CAR-T therapy are common, although most effects will be brief and respond well to treatment. Watch for any long-lasting conditions of CCUS or MDS, such as: fatigue, shortness of breath, very low white blood cell counts, bruising or bleeding and bone pain.
“Long-term follow-up of patients receiving CAR-T cell therapy is necessary to monitor for incidence of MDS/CCUS, especially in prolonged cytopenic patients. Further investigations need to be undertaken to establish a connection between CAR-T cell therapy and MDS/CCUS to allow timely management of these patients before they progress to AML.”
about the author
Lisa Foster
Lisa Foster is a mom of 3 daughters, a puzzle lover, a writer, and a HealthTree advocate. She believes in the mission of the foundation and the team that builds it forward. She calls Houston, Texas home.
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