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Abstract Details

Increased John Cunningham Virus Seroconversion Rates Seen in a Southern Hemisphere International Cohort of Natalizumab Treated Patients
Multiple Sclerosis
P5 - Poster Session 5 (8:00 AM-9:00 AM)
9-018

To assess factors associated with John Cunningham virus (JCV) seroconversion in natalizumab-treated patients.

Natalizumab is a highly effective treatment for relapsing-remitting multiple sclerosis (RRMS), but its use is complicated by JCV co-infection. This virus can result in progressive multifocal leukoencephalopathy (PML), a devastating infection of the central nervous system. Serial assessment of JCV serostatus is therefore mandated during natalizumab treatment

Patients treated with natalizumab for RRMS at six tertiary hospitals in Melbourne, Australia (n=869) and eleven MS treatment centres in Brazil (n=137) were assessed for change in JCV serostatus, duration of natalizumab exposure and prior immunosuppression. Sensitivity analyses examined whether sex, age, hospital, prior immunosuppression or number of JCV tests affected time to seroconversion.

From a cohort of 1001 natalizumab-treated patients (510 with multiple measures of JCV serostatus), durable positive seroconversion was observed in 83 of 345 initially JCV negative patients (24.1%; 7.3% per year). Conversely, 16 of 165 initially JCV positive patients experienced durable negative seroconversion (9.7%; 3.8% per year). Forty (3.9%) patients had fluctuating serostatus. Time-to-event analysis did not identify a relationship between JCV seroconversion and duration of natalizumab exposure or prior immunosuppressive use. Male sex was associated with a greater risk of JCV seroconversion (adjusted hazard ratio 2.09 (95% CI 1.17-3.71) p=0.012).

In this large cohort of natalizumab-treated patients we observed durable positive seroconversion at an annualised rate of 7.3%. This rate exceeds that noted in registration and post-marketing studies for natalizumab and is consistent with increased rates of seroconversion reported recently by European centres. This rate also greatly exceeds that predicted by epidemiological studies of JCV seroconversion in healthy populations. Taken together, our finding supports emerging evidence that natalizumab causes off-target immune system changes that may be trophic for JCV seroconversion. In addition, male sex may be associated with an increased risk of positive JCV seroconversion
Authors/Disclosures
Chris Dwyer, MBBS (Royal Melbourne Hospital)
PRESENTER
No disclosure on file
No disclosure on file
No disclosure on file
No disclosure on file
John T. Carey, MD No disclosure on file
Trevor J. Kilpatrick, MBBS, PhD (Melbourne Neuroscience Institute, University of Melbourne) Dr. Kilpatrick has received stock or an ownership interest from Mx3 diagnostics. The institution of Dr. Kilpatrick has received research support from NHMRC. The institution of Dr. Kilpatrick has received research support from NMSS. The institution of Dr. Kilpatrick has received research support from MSRA. Dr. Kilpatrick has received intellectual property interests from a discovery or technology relating to health care. Dr. Kilpatrick has received publishing royalties from a publication relating to health care.
No disclosure on file
Ernest G. Butler, MD, PhD, FRACP Dr. Butler has nothing to disclose.
Jodi Haartsen (Eastern Health) No disclosure on file
Helmut Butzkueven, MD, MBBS Dr. Butzkueven has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Oxford Health Policy Forum. The institution of Dr. Butzkueven has received personal compensation in the range of $10,000-$49,999 for serving as a Consultant for Biogen. The institution of Dr. Butzkueven has received personal compensation in the range of $10,000-$49,999 for serving as a Consultant for Merck. The institution of Dr. Butzkueven has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for Novartis. The institution of Dr. Butzkueven has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for Roche. Dr. Butzkueven has received personal compensation in the range of $10,000-$49,999 for serving as an officer or member of the Board of Directors for MSBase . The institution of Dr. Butzkueven has received research support from NHMRC. The institution of Dr. Butzkueven has received research support from Biogen. The institution of Dr. Butzkueven has received research support from Roche. The institution of Dr. Butzkueven has received research support from Novartis.
No disclosure on file
Neil Shuey, MD (St Vincent'S Hospital) No disclosure on file
No disclosure on file
Richard A. Macdonell, MD, FÂé¶¹´«Ã½Ó³»­ (Austin Health) Dr. Macdonell has nothing to disclose.
No disclosure on file
Yara D. Fragoso Yara D. Fragoso has nothing to disclose.
Anneke Van Der Walt, MD (Alfred Health) Dr. Van Der Walt has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Merck. Dr. Van Der Walt has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Alexion. Dr. Van Der Walt has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Novartis. Dr. Van Der Walt has received personal compensation in the range of $500-$4,999 for serving on a Speakers Bureau for Novartis. Dr. Van Der Walt has received personal compensation in the range of $500-$4,999 for serving on a Speakers Bureau for Biogen. The institution of Dr. Van Der Walt has received research support from NHMRC Australia. The institution of Dr. Van Der Walt has received research support from MSRA. The institution of Dr. Van Der Walt has received research support from Roche.