Case report: Treatment of parkinsonism secondary to ciltacabtagene autoleucel using a combination dopaminergic regimen

Front Immunol. 2024 Sep 20:15:1444010. doi: 10.3389/fimmu.2024.1444010. eCollection 2024.

Abstract

We report on a patient with ciltacabtagene autoleucel-induced movement and neurocognitive toxicity, which was refractory to immunosuppression but responsive to combination dopaminergic therapy (carbidopa/levodopa, ropinirole, amantadine). Response was seen upon both initial treatment and rechallenge after unintended withdrawal. This is the first report of a successful symptomatic treatment of this well-described neurotoxic syndrome.

Keywords: CAR-T; ciltacabtagene autoleucel; movement and neurocognitive toxicity; multiple myeloma; parkinsonism.

Publication types

  • Case Reports

MeSH terms

  • Amantadine / administration & dosage
  • Amantadine / therapeutic use
  • Antiparkinson Agents / administration & dosage
  • Antiparkinson Agents / adverse effects
  • Biological Products / administration & dosage
  • Biological Products / adverse effects
  • Biological Products / therapeutic use
  • Carbidopa* / administration & dosage
  • Dopamine Agents / administration & dosage
  • Dopamine Agents / adverse effects
  • Dopamine Agonists / administration & dosage
  • Dopamine Agonists / adverse effects
  • Dopamine Agonists / therapeutic use
  • Drug Combinations
  • Drug Therapy, Combination
  • Female
  • Humans
  • Immunotherapy, Adoptive* / adverse effects
  • Immunotherapy, Adoptive* / methods
  • Indoles / administration & dosage
  • Indoles / adverse effects
  • Levodopa* / administration & dosage
  • Levodopa* / adverse effects
  • Male
  • Middle Aged
  • Parkinsonian Disorders / chemically induced
  • Parkinsonian Disorders / drug therapy
  • Receptors, Chimeric Antigen / immunology
  • Treatment Outcome

Substances

  • Carbidopa
  • Levodopa
  • carbidopa, levodopa drug combination
  • Drug Combinations
  • ropinirole
  • Amantadine
  • axicabtagene ciloleucel
  • Dopamine Agents
  • Indoles
  • Dopamine Agonists
  • Antiparkinson Agents
  • Biological Products
  • Receptors, Chimeric Antigen

Grants and funding

The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.