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Diabetes insipidus and Guillain-Barré-like syndrome following CAR-T cell therapy: a case report.
Koch, Christian; Fleischer, Juliane; Popov, Todor; Frontzek, Karl; Schreiner, Bettina; Roth, Patrick; Manz, Markus G; Unseld, Simone; Müller, Antonia M S; Russkamp, Norman F.
Affiliation
  • Koch C; Department of Medical Oncology and Hematology, University Hospital Zurich and University of Zurich, Zurich, Switzerland.
  • Fleischer J; Institute of Intensive Care Medicine, University Hospital Zurich, Zurich, Switzerland.
  • Popov T; Department of Neurology, University Hospital and University of Zurich, Zurich, Switzerland.
  • Frontzek K; Institute of Neuropathology, University Hospital and University of Zurich, Zurich, Switzerland.
  • Schreiner B; Department of Neurology, University Hospital and University of Zurich, Zurich, Switzerland.
  • Roth P; Department of Neurology, University Hospital and University of Zurich, Zurich, Switzerland.
  • Manz MG; Department of Medical Oncology and Hematology, University Hospital Zurich and University of Zurich, Zurich, Switzerland.
  • Unseld S; Institute of Intensive Care Medicine, University Hospital Zurich, Zurich, Switzerland.
  • Müller AMS; Department of Transfusion Medicine and Cell Therapy, Medical University Vienna, Vienna, Austria.
  • Russkamp NF; Department of Medical Oncology and Hematology, University Hospital Zurich and University of Zurich, Zurich, Switzerland norman.russkamp@usz.ch.
J Immunother Cancer ; 11(1)2023 01.
Article in En | MEDLINE | ID: mdl-36690387
ABSTRACT

BACKGROUND:

Immune effector cell-associated neurotoxicity syndrome (ICANS) is a common adverse event of CD19-directed chimeric antigen receptor (CAR) T cell therapy. Other neurological adverse events, however, have not methodically been described and studied. Furthermore, safety data on CAR-T cell therapy in patients with central nervous system (CNS) lymphoma remain limited. MAIN BODY We here report occurrence of a Guillain-Barré-like syndrome (GBS) and central diabetes insipidus (cDI) following tisagenlecleucel therapy for relapsed high-grade lymphoma with CNS involvement. Both complications were refractory to standard treatment of ICANS. Weakness of respiratory muscles required mechanical ventilation and tracheostomy while cDI was treated with desmopressin substitution for several weeks. Muscle-nerve biopsy and nerve conduction studies confirmed an axonal pattern of nerve damage. T cell-rich infiltrates and detection of the CAR transgene in muscle-nerve sections imply a direct or indirect role of CAR-T cell-mediated inflammation. In line with current treatment guidelines for GBS, intravenous immunoglobulin was administered and gradual but incomplete recovery was observed over the course of several months.

CONCLUSIONS:

This case report highlights the risk of rare but severe neurological adverse events, such as acute GBS or cDI, in patients treated with CAR-T cells. It further underlines the importance of appropriate patient surveillance and systematic reporting of rare complications to eventually improve treatment.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Lymphoma, Non-Hodgkin / Central Nervous System Neoplasms / Diabetes Insipidus / Diabetes Mellitus / Receptors, Chimeric Antigen Type of study: Etiology_studies / Guideline Limits: Humans Language: En Journal: J Immunother Cancer Year: 2023 Document type: Article Affiliation country: Switzerland

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Lymphoma, Non-Hodgkin / Central Nervous System Neoplasms / Diabetes Insipidus / Diabetes Mellitus / Receptors, Chimeric Antigen Type of study: Etiology_studies / Guideline Limits: Humans Language: En Journal: J Immunother Cancer Year: 2023 Document type: Article Affiliation country: Switzerland