[A case of progressive multifocal leukoencephalopathy associated with daratumumab, bortezomib, and dexamethasone for

Kojiro Usui1, Yuki Kitazaki1, Soichi Enomoto1

  • 1Department of Neurology, University of Fukui Hospital.

Insights

Progressive multifocal leukoencephalopathy (PML) is a rare brain infection that can occur in multiple myeloma (MM) patients treated with daratumumab, bortezomib, and dexamethasone (DBd). Early consideration of PML is crucial in MM patients with low CD4+ T-lymphocyte counts.

Area of Science:

  • Neurology
  • Oncology
  • Infectious Diseases

Background:

  • Multiple myeloma (MM) is a hematologic malignancy.
  • Daratumumab, bortezomib, and dexamethasone (DBd) is a common treatment regimen for MM.
  • Immunosuppression is a known risk factor for opportunistic infections.

Observation:

  • An 83-year-old male with MM presented with visual disturbance and hemiparalysis one month post-DBd therapy.
  • Laboratory tests revealed a CD4+ T-lymphocyte count of 132/μl.
  • Cerebrospinal fluid (CSF) analysis detected JC virus (JCV) DNA via PCR.

Findings:

  • Magnetic resonance imaging (MRI) showed characteristic high-intensity signals in the occipital lobes and left precentral gyrus.
  • The patient was diagnosed with progressive multifocal leukoencephalopathy (PML).
  • Despite treatment with mefloquine and mirtazapine, CSF JCV-DNA PCR levels did not decrease, and the patient died six months after symptom onset.

Implications:

  • This case highlights the potential for PML in MM patients receiving DBd therapy, particularly those with iatrogenic immunosuppression (low CD4+ counts).
  • Clinicians should consider PML in the differential diagnosis of neurological symptoms in MM patients undergoing immunosuppressive therapy.
  • Further research is needed to explore preventative strategies and optimize treatment for PML in this vulnerable patient population.