Impact of Rituximab and Corticosteroids on Late Cytopenias Post-Chimeric Antigen Receptor T Cell Therapy

Transplant Cell Ther. 2022 Oct;28(10):668.e1-668.e6. doi: 10.1016/j.jtct.2022.07.009. Epub 2022 Jul 14.

Abstract

Chimeric antigen receptor (CAR) T cell therapy represents a significant advancement in the treatment of patients with relapsed/refractory B cell lymphoid malignancies. Cytokine release syndrome and immune effector cell-associated neurotoxicity represent the most acute serious adverse events post CAR T cell therapy but the occurrence and persistence of cytopenias post CAR T cell therapy represent a significant adverse event and a management challenge. While most patients typically recover blood counts by 30 days, a significant subset of patients have persistent or late cytopenias beyond 30 days. Patients receiving CAR T cell are heavily pre-treated and the impact of prior therapies on late cytopenias is not well understood. In this study, we found an association between increased number of rituximab infusions and/or cumulative rituximab dose received prior to CAR T cell infusion and persistent anemia and thrombocytopenia at 90 and 180 days afterwards. An overall increased number of prior lines of therapy was also associated with persistent lymphopenia and anemia at 90 days while receiving a prior autologous hematopoietic cell transplant was associated with a greater risk of neutropenia and lymphopenia.

Keywords: Chimeric antigen receptor T cell therapy; Cytopenia; Lymphoma; Rituximab.

MeSH terms

  • Adrenal Cortex Hormones
  • Anemia* / drug therapy
  • Antigens, CD19 / therapeutic use
  • Hematopoietic Stem Cell Transplantation*
  • Humans
  • Immunotherapy, Adoptive / adverse effects
  • Lymphopenia* / chemically induced
  • Neoplasm Recurrence, Local / drug therapy
  • Receptors, Chimeric Antigen*
  • Rituximab / adverse effects
  • Thrombocytopenia* / chemically induced

Substances

  • Adrenal Cortex Hormones
  • Antigens, CD19
  • Receptors, Chimeric Antigen
  • Rituximab