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Abstract Details

Effectiveness of Natalizumab Treatment Inpatients With Early Relapsing-Remitting Multiple Sclerosis (RRMS) who were Treatment-Naive Versus Those Who Had Prior Disease-Modifying Therapy (DMT) Use
Multiple Sclerosis
P6 - Poster Session 6 (5:30 PM-6:30 PM)
12-006

STRIVE was a 4-year observational study of natalizumab-treated anti–JC virus antibody negative patients with early RRMS (disease duration ≤3 years).

To describe the real-world effectiveness of natalizumab in patients with early RRMS who were treatment-naive versus those who had prior DMT use at natalizumab initiation.

No evidence of disease activity (NEDA) included attainment of both Clinical NEDA (no relapses and no 24-week CDW) and MRI NEDA (no gadolinium-enhancing lesions and no new or newly enlarging T2 lesions). Confirmed disability worsening (CDW) was defined as an Expanded Disability Status Scale score increase ≥0.5 from a baseline score ≥6.0, an increase ≥1.0 from a baseline score of 1.0 to <6.0, or an increase ≥1.5 from a baseline score of 0.0, confirmed after 24 weeks.

The STRIVE intent-to-treat population included 222 patients (treatment-naive, n=119; prior-DMT, n=103). Baseline characteristics were similar in treatment-naive and prior-DMT patients except for mean time since MS diagnosis (1.2 vs 2.1 years; P<0.0001) and mean number of relapses in the prior year (1.2 vs 1.7; P=0.0002). Similar proportions of treatment-naive and prior-DMT patients achieved NEDA except at year 2 (80.9% vs 63.8%; P=0.0192). Significantly more treatment-naive patients achieved Clinical NEDA compared to prior-DMT patients in years 1 (89.1% vs 71.1%; P=0.0018) and 2 (92.0% vs 75.7%; P=0.0045); however, similar proportions were seen between groups in years 3 and 4. MRI NEDA achievement did not differ by group. While both groups demonstrated significant on-natalizumab reductions in annualized relapse rate (ARR), treatment-naive patients had significantly lower on-natalizumab ARR (P<0.05 for all years). At 4 years, the cumulative probability of CDW was lower in treatment-naive than prior-DMT patients (11.5% vs 29.0%; P=0.0015).

Results confirm natalizumab’s effectiveness regardless of prior DMT use. However, treatment-naïve patients receiving natalizumab early in their disease course had improved clinical outcomes over the long term. 

Authors/Disclosures
Robin L. Avila, PhD (Biogen)
PRESENTER
Mrs. Avila has received personal compensation for serving as an employee of Biogen. Mrs. Avila has stock in Biogen.
Jai Perumal, MD Dr. Perumal has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Genentech. Dr. Perumal has received personal compensation in the range of $500-$4,999 for serving as a Consultant for T G therapeutics. Dr. Perumal has received personal compensation in the range of $500-$4,999 for serving as a Consultant for EMD Serono.
Roumen D. Balabanov, MD (Northwestern University) Dr. Balabanov has received personal compensation in the range of $5,000-$9,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Biogen. Dr. Balabanov 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. Balabanov has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Genentech. Dr. Balabanov has received personal compensation in the range of $10,000-$49,999 for serving on a Speakers Bureau for Biogen. The institution of Dr. Balabanov has received research support from NextCure. The institution of Dr. Balabanov has received research support from Biogen. The institution of Dr. Balabanov has received research support from NINDS.
No disclosure on file
Laura J. Balcer, MD, MSCE, FAAN (NYU Grossman School of Medicine) An immediate family member of Dr. Balcer has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for Children's Hospital of Philadelphia. Dr. Balcer has received personal compensation in the range of $50,000-$99,999 for serving as an Editor, Associate Editor, or Editorial Advisory Board Member for North American Neuro-Ophthalmology Society.
Steven Galetta, MD, FAAN (NYU Langone Medical Center) Dr. Galetta has nothing to disclose.
Danette J. Rutledge Ms. Rutledge has received personal compensation for serving as an employee of Biogen. Ms. Rutledge has received stock or an ownership interest from Biogen.
Robert J. Fox, MD, FAAN (Cleveland Clinic) Dr. Fox has received personal compensation in the range of $500-$4,999 for serving as a Consultant for AB Science. Dr. Fox has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for Janssen. Dr. Fox has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for Biogen. Dr. Fox has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for BMS. Dr. Fox has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for EMD Serono. Dr. Fox has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for Genentech. Dr. Fox has received personal compensation in the range of $10,000-$49,999 for serving as a Consultant for Immunic. Dr. Fox has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for Novartis. Dr. Fox has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for Sanofi. Dr. Fox has received personal compensation in the range of $500-$4,999 for serving as a Consultant for TG Therapeutics. Dr. Fox has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for Genzyme. Dr. Fox has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Siemens. Dr. Fox has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for INmune Bio. Dr. Fox has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Lily. Dr. Fox has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Greenwich Biosciences. Dr. Fox has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for Roche. Dr. Fox has received personal compensation in the range of $5,000-$9,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Biogen. Dr. Fox has received personal compensation in the range of $5,000-$9,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Immunic. Dr. Fox has received personal compensation in the range of $5,000-$9,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Novartis. Dr. Fox has received personal compensation in the range of $5,000-$9,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Janssen. Dr. Fox has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for AB Science. Dr. Fox has received personal compensation in the range of $5,000-$9,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Sanofi. Dr. Fox has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for BMS. The institution of Dr. Fox has received research support from National Institutes of Health. The institution of Dr. Fox has received research support from National MS Society. Dr. Fox has received publishing royalties from a publication relating to health care.