Evaluation of patients treated with natalizumab for progressive multifocal leukoencephalopathy
- PMID: 16510746
- PMCID: PMC1934511
- DOI: 10.1056/NEJMoa054693
Evaluation of patients treated with natalizumab for progressive multifocal leukoencephalopathy
Abstract
Background: Progressive multifocal leukoencephalopathy (PML) was reported to have developed in three patients treated with natalizumab. We conducted an evaluation to determine whether PML had developed in any other treated patients.
Methods: We invited patients who had participated in clinical trials in which they received recent or long-term treatment with natalizumab for multiple sclerosis, Crohn's disease, or rheumatoid arthritis to participate. The clinical history, physical examination, brain magnetic resonance imaging (MRI), and testing of cerebrospinal fluid for JC virus DNA were used by an expert panel to evaluate patients for PML. We estimated the risk of PML in patients who completed at least a clinical examination for PML or had an MRI.
Results: Of 3417 patients who had recently received natalizumab while participating in clinical trials, 3116 (91 percent) who were exposed to a mean of 17.9 monthly doses underwent evaluation for PML. Of these, 44 patients were referred to the expert panel because of clinical findings of possible PML, abnormalities on MRI, or a high plasma viral load of JC virus. No patient had detectable JC virus DNA in the cerebrospinal fluid. PML was ruled out in 43 of the 44 patients, but it could not be ruled out in one patient who had multiple sclerosis and progression of neurologic disease because data on cerebrospinal fluid testing and follow-up MRI were not available. Only the three previously reported cases of PML were confirmed (1.0 per 1000 treated patients; 95 percent confidence interval, 0.2 to 2.8 per 1000).
Conclusions: A detailed review of possible cases of PML in patients exposed to natalizumab found no new cases and suggested a risk of PML of roughly 1 in 1000 patients treated with natalizumab for a mean of 17.9 months. The risk associated with longer treatment is not known.
Copyright 2006 Massachusetts Medical Society.
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Comment in
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Selective treatment of multiple sclerosis.N Engl J Med. 2006 Mar 2;354(9):965-7. doi: 10.1056/NEJMe068002. N Engl J Med. 2006. PMID: 16510751 No abstract available.
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Natalizumab for relapsing multiple sclerosis.N Engl J Med. 2006 Jun 1;354(22):2387-9; author reply 2387-9. doi: 10.1056/NEJMc060894. N Engl J Med. 2006. PMID: 16738278 No abstract available.
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Natalizumab for relapsing multiple sclerosis.N Engl J Med. 2006 Jun 1;354(22):2387-9; author reply 2387-9. N Engl J Med. 2006. PMID: 16742008 No abstract available.
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Natalizumab for relapsing multiple sclerosis.N Engl J Med. 2006 Jun 1;354(22):2387-9; author reply 2387-9. N Engl J Med. 2006. PMID: 16742009 No abstract available.
References
-
- Koralnik IJ. New insights into progressive multifocal leukoencephalopathy. Curr Opin Neurol. 2004;17:365–70. - PubMed
-
- Langer-Gould A, Atlas SW, Green AJ, Bollen AW, Pelletier D. Progressive multi-focal leukoencephalopathy in a patient treated with natalizumab. N Engl J Med. 2005;353:375–81. - PubMed
-
- Kleinschmidt-DeMasters BK, Tyler KL. Progressive multifocal leukoencephalopathy complicating treatment with natalizumab and interferon beta-1a for multiple sclerosis. N Engl J Med. 2005;353:369–74. - PubMed
-
- Van Assche G, Van Ranst M, Sciot R, et al. Progressive multifocal leukoencephalopathy after natalizumab therapy for Crohn's disease. N Engl J Med. 2005;353:362–8. - PubMed
-
- Rice GP, Hartung HP, Calabresi PA. Anti-alpha4 integrin therapy for multiple sclerosis: mechanisms and rationale. Neurology. 2005;64:1336–42. - PubMed
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