Acute and delayed cytopenias following CAR T-cell therapy: an investigation of risk factors and mechanisms

Leuk Lymphoma. 2022 Aug;63(8):1849-1860. doi: 10.1080/10428194.2022.2056172. Epub 2022 Apr 7.

Abstract

Prolonged myelosuppression after chimeric antigen receptor (CAR) T-cell therapy is common and poorly understood. A retrospective analysis of 43 patients was conducted to investigate factors contributing to CAR T-cell-related cytopenias. Thirty-five patients were evaluable for analysis of delayed cytopenias occurring after initial hematologic recovery. Time to hematologic recovery (TTHR) was defined as number of days after CAR T-cell infusion for recovery to hemoglobin ≥8.0 g/dL, platelets ≥50.0 k/µL, and neutrophil count ≥1.0 k/µL without transfusions or growth factors for 7 days. Baseline percent bone marrow (BM) malignancy involvement correlated with TTHR (p = .0047). Patients with grades 3-4 cytokine-release syndrome (CRS) had longer TTHR than those with grades 0-2 CRS (p = .0479). Patients who developed prolonged or delayed cytopenias after anti-BCMA CAR T cells had a higher percentage of BM aspirate CAR+ cells at 2 months (n = 10; p = .0159).

Keywords: CAR T-cell; Chimeric antigen receptor; bone marrow suppression; cytopenia; hematologic malignancies.

Publication types

  • Research Support, N.I.H., Intramural

MeSH terms

  • Anemia* / etiology
  • Humans
  • Immunotherapy, Adoptive / adverse effects
  • Leukopenia*
  • Retrospective Studies
  • Risk Factors
  • T-Lymphocytes
  • Thrombocytopenia* / etiology