Chimeric antigen receptor T cell therapy can be administered safely under the real-time monitoring of Th1/Th2 cytokine pattern using the cytometric bead array technology for relapsed and refractory acute lymphoblastic leukemia in children

Pediatr Hematol Oncol. 2020 May;37(4):288-299. doi: 10.1080/08880018.2019.1704325. Epub 2020 Feb 12.

Abstract

CD19 chimeric antigen receptor T (CD19CAR-T) cell therapy has shown striking response in treating relapsed and refractory B-lineage acute lymphoblastic leukemia (r/r B-ALL). However, side-effects including cytokine release syndrome (CRS) and neurotoxicity can be fatal to patients. In this report, five patients with r/r B-ALL were treated with CD19CAR-T cells. Cytokine release syndrome experienced by four patients who achieved complete remission (CR) with minimal residual disease (MRD) negative. One patient who did not response to the treatment had no CRS. Acute toxicities including fever, hypotension and other neurological toxicities occurred in responding patients within 2 weeks post infusion and managed properly with tocilizumab and/or steroids according to the "real-time" monitoring of a simple 6 Th1/Th2 cytokine pattern. In conclusion, our study demonstrates that CD19CAR-T cell therapy can be safely administered for patients with relapsed and refractory leukemia under the "real-time" monitoring of a simple 6-cytokine pattern.

Keywords: CD19 CAR-T cell therapy; Th1/Th2 cytokine pattern; cytokine release syndrome; neurotoxicity; relapsed and refractory B-lineage acute lymphoblastic leukemia.

Publication types

  • Video-Audio Media

MeSH terms

  • Adoptive Transfer
  • Child
  • Child, Preschool
  • Cytokines* / blood
  • Cytokines* / immunology
  • Female
  • Flow Cytometry*
  • Humans
  • Infant
  • Male
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma* / blood
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma* / immunology
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma* / pathology
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma* / therapy
  • Th1 Cells* / immunology
  • Th1 Cells* / metabolism
  • Th1 Cells* / pathology
  • Th2 Cells* / immunology
  • Th2 Cells* / metabolism
  • Th2 Cells* / pathology
  • Time Factors

Substances

  • Cytokines