Subcutaneous immunoglobulin replacement following CD19-specific chimeric antigen receptor T-cell therapy for B-cell acute lymphoblastic leukemia in pediatric patients

Pediatr Blood Cancer. 2020 Mar;67(3):e28092. doi: 10.1002/pbc.28092. Epub 2019 Dec 2.

Abstract

Twenty-eight patients were maintained on subcutaneous immunoglobulin replacement for persistent B-cell aplasia and agammaglobulinemia following CD19-targeted chimeric antigen receptor T-cell therapy for B-cell lymphoblastic leukemia. Patients were transitioned from intravenous to subcutaneous immunoglobulin replacement at a median of 11.5 months (range, 4-20). Increasing serum IgG level was significantly associated with a lower rate of sinopulmonary infection (P = 0.0072). The median serum IgG level during infection-free periods was 1000 mg/dL (range, 720-1430), which was significantly higher than IgG levels in patients with sinopulmonary infections. As such, we recommend maintaining a goal IgG level > 1000 mg/dL to provide optimal protection.

Keywords: B-cell aplasia; chimeric antigen receptor T cell; hypogammaglobulinemia; immunoglobulin replacement; subcutaneous immunoglobulin.

MeSH terms

  • Adolescent
  • Adult
  • Cell- and Tissue-Based Therapy / methods*
  • Child
  • Child, Preschool
  • Female
  • Follow-Up Studies
  • Humans
  • Immunoglobulins / administration & dosage*
  • Injections, Subcutaneous
  • Male
  • Precursor B-Cell Lymphoblastic Leukemia-Lymphoma / immunology
  • Precursor B-Cell Lymphoblastic Leukemia-Lymphoma / pathology
  • Precursor B-Cell Lymphoblastic Leukemia-Lymphoma / therapy*
  • Prognosis
  • Receptors, Antigen, T-Cell / immunology*
  • Retrospective Studies
  • T-Lymphocytes / immunology
  • T-Lymphocytes / transplantation*
  • Young Adult

Substances

  • CD19-specific chimeric antigen receptor
  • Immunoglobulins
  • Receptors, Antigen, T-Cell