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Progressive Multifocal Leukoencephalopathy in a Patient With Progressive Multiple Sclerosis Treated With Ocrelizumab
Arpan Patel1, James Sul1, Marc L Gordon2,3
1Department of Neurology, North Shore University Hospital, Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, Great Neck, New York.
This case report details the first instance of progressive multifocal leukoencephalopathy (PML) in a patient on ocrelizumab monotherapy. The rare JC virus infection highlights risks associated with this multiple sclerosis treatment.
Area of Science:
- Neuroimmunology
- Infectious Diseases
- Oncology
Background:
- Progressive multifocal leukoencephalopathy (PML) is a rare, fatal opportunistic infection caused by the JC virus, typically seen in immunocompromised individuals.
- While other anti-CD20 therapies have been linked to rare PML cases, none had been reported with ocrelizumab monotherapy.
- Ocrelizumab is a B-cell depleting therapy used for multiple sclerosis.
Observation:
- A 78-year-old male with progressive multiple sclerosis developed PML while on ocrelizumab monotherapy for two years.
- Symptoms included visual disturbances and confusion, with MRI revealing a parietal lesion and CSF confirming JC virus.
- The patient experienced lymphopenia and rapid neurological decline despite treatment cessation and initiation of pembrolizumab.
Findings:
- The first documented case of PML associated with ocrelizumab monotherapy in a patient with no prior immunomodulatory treatment.
- JC virus was detected in cerebrospinal fluid, confirming PML.
- Autopsy confirmed PML, with findings likely linked to ocrelizumab's immunomodulatory effects and age-related immune decline.
Implications:
- This case underscores the potential risk of PML with ocrelizumab, even in the absence of prior immunosuppression.
- Physicians must carefully weigh the risks and benefits of ocrelizumab, particularly in elderly patients or those with other risk factors for infection.
- Enhanced vigilance and patient monitoring are crucial for early detection of opportunistic infections during ocrelizumab therapy.
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