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DIR Return to: TYSABRI (natalizumab)
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#Post#: 271--------------------------------------------------
MS patient on Tysabri turns out to have Creutzfeldt-Jakob diseas
e, not PML
By: agate Date: April 28, 2014, 3:05 pm
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Reporting a case of an MS patient on Tysabri who converted to
JCV+ during treatment who developed unusual symptoms that were
initially thought to be PML, but the diagnosis turned out to be
Creutzfeldt-Jakob disease.
Extract from the new AAN open-access journal, Neurology,
Neuroimmunology, & Neuroinflammation, April 29, 2014:
[quote]Unusual deterioration in a patient with multiple
sclerosis on natalizumab therapy
Thomas Gattringer, MD, Christian Enzinger, MD, Michael Khalil,
MD, PhD, Petra Schwingenschuh, MD, Alexander Pichler, MD,
Alexander Moser, MD, Winfried Graninger, MD, Christina Ernst,
MSc, Johannes Haybaeck, MD, PhD and Franz Fazekas, MD
From the Department of Neurology (T.G., C. Enzinger, M.K., P.S.,
A.P., F.F.), Division of Neuroradiology, Department of Radiology
(C. Enzinger), Division of Rheumatology and Immunology,
Department of Internal Medicine (W.G.), and Department of
Neuropathology, Institute of Pathology (C. Ernst, J.H.), Medical
University of Graz, Graz, Austria; and Neurorehabilitation
Clinic Kapfenberg (A.M.), Kapfenberg, Austria.
Correspondence to Dr. Gattringer:
thomas.gattringer@medunigraz.at
doi: 10.1212/NXI.0000000000000001
Natalizumab is an effective treatment in patients with highly
active relapsing-remitting multiple sclerosis (RRMS). However,
its positive therapeutic effects have to be weighed against the
potential serious adverse event of progressive multifocal
leukoencephalopathy (PML). Thus, whenever patients with MS on
natalizumab develop uncommon and progressive neurologic
symptoms, the suspicion of PML has to be raised. The risk of PML
becomes higher with increasing duration of natalizumab
treatment, prior immunosuppressive treatment, and JC virus (JCV)
antibody seropositivity. We here report a case of MS in which
unusual symptoms in the context of 5 years of natalizumab
treatment and seroconversion to JCV antibody positivity led to
the initial suspicion of PML and a final diagnosis of
Creutzfeldt-Jakob disease (CJD).
Study funding:
No targeted funding reported.
Disclosure: T. Gattinger reports no disclosures. C. Enzinger has
served on the advisory boards for Biogen Idec, Bayer-Schering,
Merck-Serono, Novartis, and Teva Ratiopharm; has received travel
grants and speaking honoraria from Biogen Idec, Teva-Aventis,
Merck-Serono, Bayer-Schering, and Novartis; is on the editorial
advisory board for PlosOne; is a consultant for Biogen Idec,
Merck-Serono, and Bayer-Schering; and has received unrestricted
research grants from Teva-Aventis, Biogen Idec, and
Merck-Serono. M. Khalil has received honoraria from
Bayer-Schering Pharma. P. Schwingenschuh served on national
advisory boards for UCB and Novartis Austria; received funding
from Boehringer-Ingelheim, Ipsen, Allergan, UCB, and Merz
Pharma; and received speaker honoraria from UCB, Lundbeck, and
Ipsen. A. Pichler, A. Moser, W. Graninger, C. Ernst, and J.
Haybaeck report no disclosures. F. Fazekas has been an advisor
for Bayer-Schering, Biogen Idec, Bristol-Myers Squibb, Genzyme,
Merck-Serono, Novartis, Perceptive Informatics, Pfizer,
Teva-Aventis, Teva Pharmceuticals LTD, and D-Pharm LTD; has been
a member of DSMB; has received honoraria from Bayer-Schering,
Biogen Idec, Merck-Serono, Novartis, Sanofi-Aventis, and Teva
Pharmaceuticals Ltd; is on the editorial board for
Cerebrovascular Diseases, Journal of Neurology, Polish Journal
of Neurology and Neurosurgery, Stroke, Swiss Archives of
Neurology and Psychiatry, and Multiple Sclerosis; and was on the
speakers' bureau for Bayer-Schering and Merck-Serono.[/quote]
The entire article can be seen here
HTML http://nn.neurology.org/content/1/1/e1.full.
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