Toxicities following CAR-T therapy for hematological malignancies

Cancer Treat Rev. 2022 Dec:111:102479. doi: 10.1016/j.ctrv.2022.102479. Epub 2022 Oct 22.

Abstract

Chimeric antigen receptor T-cell (CAR-T) therapy has improved outcomes in patients with relapsed/refractory hematological malignancies. Research is also extending to other diseases, including solid tumors, infections and autoimmune disorders. As living drugs, CAR-T cells are associated with potentially life-threatening immunological toxicities, which frequently require a multidisciplinary team approach. Cytokine-release syndrome, immune effector cell-associated neurotoxicity syndrome, infections and hematotoxicity (including cytopenias, immune reconstitution dysfunction and hypogammaglobulinemia) are associated with significant morbidity and mortality. This review takes a practical approach to summarize current knowledge on CAR-T toxicity, addressing pathogeny, risk factors, and prophylactic and therapeutic strategies.

Keywords: Chimeric antigen receptor T-cell (CAR-T); Cytokine-release syndrome (CRS); Hematotoxicity; Immune effector cell-associated neurotoxicity syndrome (ICANS); Infections.

Publication types

  • Review

MeSH terms

  • Hematologic Neoplasms* / complications
  • Humans
  • Immunotherapy, Adoptive / adverse effects
  • Neoplasm Recurrence, Local / drug therapy
  • Neurotoxicity Syndromes* / etiology
  • Receptors, Antigen, T-Cell
  • Receptors, Chimeric Antigen*

Substances

  • Receptors, Chimeric Antigen
  • Receptors, Antigen, T-Cell