Progressive multifocal leukoencephalopathy after CAR T therapy

Int J Hematol. 2020 Jul;112(1):118-121. doi: 10.1007/s12185-020-02840-x. Epub 2020 Mar 3.

Abstract

Progressive multifocal leukoencephalopathy (PML) remains a life-threatening central nervous system infection in immunocompromised patients. Although outcomes have improved in cases that immune reconstitution is feasible with anti-retroviral therapy (ART) in HIV + patients or natalizumab removal in those with multiple sclerosis, in individuals with hematological malignancies, the prognosis is usually dismal. Anti-viral treatments have been largely ineffective, but immunotherapy-based approaches with checkpoint inhibitors and adoptive virus-specific T cells' transfer are currently explored in clinical trials. PML has not been described as a cause of encephalopathy after CAR T therapy. We report the first case of PML 7 months after lymphodepleting chemotherapy with fludarabine/cyclophosphamide and anti-CD19-directed CAR T therapy in a patient with relapsed diffuse large B-cell lymphoma who relapsed fast after a previous autologous hematopoietic stem cell transplant. She remains alive 12 months after diagnosis with stabilization of her symptoms with a combination of therapies targeting viral replication and immunotherapy.

Keywords: Adoptive cell therapy; CAR-T; Immunotherapy; PML.

Publication types

  • Case Reports

MeSH terms

  • Adoptive Transfer / methods*
  • Aged
  • Antigens, CD19 / administration & dosage
  • Antigens, CD19 / therapeutic use*
  • Antineoplastic Agents / therapeutic use
  • Biological Products
  • Female
  • Hematopoietic Stem Cell Transplantation
  • Humans
  • Immunocompromised Host*
  • Immunotherapy, Adoptive / adverse effects*
  • Immunotherapy, Adoptive / methods*
  • Leukoencephalopathy, Progressive Multifocal / etiology*
  • Leukoencephalopathy, Progressive Multifocal / therapy*
  • Lymphoma, Large B-Cell, Diffuse / therapy
  • Receptors, Chimeric Antigen / administration & dosage*
  • Recurrence
  • T-Lymphocytes*
  • Transplantation, Autologous

Substances

  • Antigens, CD19
  • Antineoplastic Agents
  • Biological Products
  • Receptors, Chimeric Antigen
  • axicabtagene ciloleucel