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

Disease-modifying Therapy Discontinuation and Outcomes of Older People with Multiple Sclerosis (MS) at a Large Academic MS Center in Toronto, Canada
Multiple Sclerosis
S3 - Multiple Sclerosis: Clinical Trials (1:48 PM-2:00 PM)
005
MS typically presents between ages 20 and 40, and DMT use is the standard of care in most pwMS. Prior studies indicate that MS disease activity decreases with age, suggesting that DMTs in older pwMS may not be necessary. Most phase 3 clinical trials exclude older pwMS (>55 years), so the risks and benefits of DMT use in this population remain unclear.

To describe the clinical characteristics of older people with multiple sclerosis (pwMS), proportion and reasons for older pwMS to discontinue disease-modifying therapy (DMT), and rates of clinical and MRI disease activity after discontinuation.

Older pwMS were identified from the St. Michael’s Hospital MS Clinic Registry from 06/2015-04/2024. Demographics, clinical characteristics, DMT discontinuation data, and clinical (relapses, disability progression) and radiographical (new/enlarging T2 lesions on sequential MRIs) activity after DMT discontinuation were extracted.

Of 1828 pwMS, 14% (n=253) discontinued a DMT after age 55 at mean age of 61.3 (SD=5) years and were then followed for 7.9 (SD=4) years. The most common DMTs discontinued among older pwMS were interferon beta agents (n=104, 41%) and glatiramer acetate (n=54, 21%). The most common reasons for discontinuation were transition to secondary progressive MS (n=58, 23%), choice/convenience (n=41, 16%), and tolerability concerns (n=36, 14%). Following discontinuation, 14% (n=35) pwMS had a clinical relapse, and 31% (n=49/160) had MRI disease activity.

At our center, a small proportion of older pwMS discontinued DMTs after age 55, mainly due to transition to progressive disease, preference, and tolerability concerns. Few relapses and new/enlarging lesions on MRI were reported after discontinuation. Our real-world findings suggest that DMT discontinuation in older pwMS may be a reasonable strategy, potentially impacting future MS management in older patients. Future studies of older pwMS at diverse geographic regions are needed to assess the risk and benefits of discontinuing a wider range of DMTs.

Authors/Disclosures
Chia-Chen Tsai
PRESENTER
Ms. Tsai has received research support from Foundation of the Consortium of Multiple Sclerosis Centers. Ms. Tsai has received research support from UBC Multiple Sclerosis Connect Program.
Fasna Raufdeen Ms. Raufdeen has nothing to disclose.
Raphael Schneider, MD (St. Michael'S Hospital) Dr. Schneider has nothing to disclose.
James Marriott, MD, BSc (University of Toronto / BARLO MS Centre) Dr. Marriott has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Novartis. Dr. Marriott has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Roche. The institution of Dr. Marriott has received personal compensation in the range of $500-$4,999 for serving as a Consultant for EMD Serono. Dr. Marriott has received personal compensation in the range of $500-$4,999 for serving on a Speakers Bureau for Novartis. The institution of Dr. Marriott has received research support from Sanofi. The institution of Dr. Marriott has received research support from Roche. The institution of Dr. Marriott has received research support from Novartis.
Jiwon Oh, MD, FAAN (St Michael's Hospital) Dr. Oh has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for Roche. The institution of Dr. Oh has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Biogen-Idec. Dr. Oh has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for EMD-Serono. Dr. Oh has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for Sanofi-Genzyme. Dr. Oh has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Novartis. Dr. Oh has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Eli Lilly. Dr. Oh has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Amgen. Dr. Oh has received personal compensation in the range of $0-$499 for serving on a Scientific Advisory or Data Safety Monitoring board for Roche. Dr. Oh has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Biogen-Idec. Dr. Oh has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Sanofi-Genzyme. The institution of Dr. Oh has received research support from Biogen-Idec. The institution of Dr. Oh has received research support from Roche.