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Eur J Haematol ; 112(4): 538-546, 2024 Apr.
Article in English | MEDLINE | ID: mdl-38044594

ABSTRACT

BACKGROUND: While chimeric antigen receptor (CAR) T-cell therapy has revolutionized the treatment outcomes of relapsed/refractory hematological malignancies, this therapy is associated with post-treatment cytopenias, which can pose a challenge to its safe administration. This study describes the management of post-CAR T cytopenias using the thrombopoietin mimetic eltrombopag. METHODS: This retrospective analysis included adult patients with lymphoma or myeloma who received CAR T-cell therapy at two academic medical centers. Eltrombopag was initiated for patients who had persistent high-grade leukopenia and/or thrombocytopenia beyond 21 days post-CAR T infusion. Risk factors and outcomes were assessed and compared for patients who did or did not receive eltrombopag. RESULTS: Among the 185 patients analyzed, a majority (88%) experienced thrombocytopenia or leukopenia at day +30 post-CAR T infusion. A total of 42 patients met the criteria for eltrombopag treatment and initiated therapy. Patients who received eltrombopag were more likely to have pre-existing cytopenias at lymphodepletion, receive bridging therapy, experience an infection, or require intensive care. Recovery from cytopenias occurred within 180 days for a majority (94%) of patients. CONCLUSIONS: The use of eltrombopag for post-CAR T leukopenia and thrombocytopenia was considered safe without any significant toxicities. The use of eltrombopag for post-CAR T cytopenias might be effective in a high-risk patient population but requires further study.


Subject(s)
Anemia , Benzoates , Cytopenia , Hematologic Neoplasms , Hydrazines , Leukopenia , Pyrazoles , Receptors, Chimeric Antigen , Thrombocytopenia , Adult , Humans , Retrospective Studies , Neoplasm Recurrence, Local , Thrombocytopenia/drug therapy , Thrombocytopenia/etiology , Immunotherapy, Adoptive/adverse effects , Anemia/etiology , Hematologic Neoplasms/complications , Hematologic Neoplasms/therapy
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