好色先生

好色先生

Explore the latest content from across our publications

Log In

Forgot Password?
Create New Account

Loading... please wait

Abstract Details

Progressive Multifocal Leukoencephalopathy and Sphingosine 1-Phosphate Receptor Modulators Used in Multiple Sclerosis: An Updated Review of Literature
Infectious Disease
P1 - Poster Session 1 (9:00 AM-5:00 PM)
221
The objective of this review was to investigate the characteristics of progressive multifocal leukoencephalopathy in multiple sclerosis patients associated with drugs of the sphingosine 1-phosphate receptor modulator class of disease modifying therapies.

Progressive multifocal leukoencephalopathy (PML) is a serious viral infection associated with therapies for multiple sclerosis (MS) including sphingosine 1-phosphate (S1PR) receptor modulators.

We conducted a literature review and analysis of 24 patients from 12 publications in PubMed, SCOPUS and EMBASE. This was a descriptive analysis and study of characteristics of PML associated fingolimod and related S1PR modulator group of medications including siponimod, ozanimod and ponesimod.

A total of 24 cases of PML in MS patients treated with fingolimod were identified from 12 articles. Of these, 21 patients had data about changes in the expanded disability status scale (EDSS). One case of PML in association with treatment with ozanimod in a clinical trial was also identified. In PML cases associated with fingolimod, the mean age at the time of PML diagnosis was 50.91 ± 11.5 years with youngest 27 years to oldest 75 years old. All patients were treated with fingolimod for more than 24 months. Compared to patients who improved or were stable in terms of EDSS after symptomatic management of PML, the non-improving group were significantly older, but no difference was seen in gender distribution. The only management modality for PML which significantly differed between the two groups was mefloquine which was used more often in the non-improving group. There were no fatalities in either group during the reported follow-up period.

The incidence of PML appears to be extremely low in MS patients treated with S1PR modulators. Risk of PML increases with increase in duration of treatment with S1PR modulators like fingolimod and increased age at the time of diagnosis of PML is associated with worse prognosis.
Authors/Disclosures
Durgesh Chaudhary, MBBS (Penn State U, Milton S Hershey Medical Center)
PRESENTER
Dr. Chaudhary has nothing to disclose.
Samiksha Srivastava, MD (Wayne State University) Dr. Srivastava has nothing to disclose.
Katherine E. Beard, MD (Thomas Jefferson University Hospital) Miss Beard has nothing to disclose.
No disclosure on file
No disclosure on file
Syed Hassan Khalid, MD, MBBS (Loma Linda University, Department of Neurology) Dr. Khalid has nothing to disclose.
Shitiz K. Sriwastava, MBBS (UT Health Houston) Dr. Sriwastava has nothing to disclose.
Robert P. Lisak, MD, FAAN (Wayne State Univ Sch of Med, Dept of Neuro) Dr. Lisak has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Argnex. Dr. Lisak has received personal compensation in the range of $500-$4,999 for serving as a Consultant for GLG Consulting. Dr. Lisak has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Third Bridge Consulting. Dr. Lisak has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Clearview Consulting. Dr. Lisak has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Takeda. Dr. Lisak has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Alivar Therapeutics. Dr. Lisak has received personal compensation in the range of $500-$4,999 for serving as a Consultant for ANI Pharmaceuticals. Dr. Lisak has received personal compensation in the range of $0-$499 for serving as a Consultant for Coleman Research. Dr. Lisak has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Horizon. Dr. Lisak has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Immunic. Dr. Lisak has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Guidepoint Consulting. Dr. Lisak has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Tedus Consulting. Dr. Lisak has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for COUR Pharma. The institution of Dr. Lisak has received research support from NINDS. The institution of Dr. Lisak has received research support from Argenx. The institution of Dr. Lisak has received research support from Ra Pharmaceuticals. Dr. Lisak has received publishing royalties from a publication relating to health care. Dr. Lisak has received publishing royalties from a publication relating to health care.