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Real-World Treatment Outcomes in Black, Hispanic, Asian, and White Patients with Multiple Sclerosis Treated with Natalizumab.

Publication ,  Journal Article
Blitz-Shabbir, K; Banks, AM; Garg, H; Nelson, F; Shah, S; Belviso, N; Mendoza, JP; Avila, RL; Bian, B; Fong, K
Published in: Drugs Real World Outcomes
June 2025

BACKGROUND: Multiple sclerosis (MS) is a heterogeneous disease that may manifest differently among racial/ethnic groups, influencing response to disease-modifying therapy (DMT). Data on natalizumab (NTZ) effectiveness in people with MS (PwMS) based on race/ethnicity are limited. OBJECTIVE: The aim of this study was to evaluate the effectiveness of NTZ on relapse onset and rate, and to assess MS-related healthcare encounters and costs in Black, Hispanic, Asian, and White PwMS. METHODS: This was a retrospective analysis of the Komodo Health Claims Database, including adult patients in the US with one or more MS claim at index date (January 1, 2016-August 31, 2022). Patients were followed from first NTZ exposure through end of study, end of insurance eligibility, gap in index DMT > 45 days, or DMT switch. Annualized relapse rate (ARR), time to first relapse, and MS-related healthcare encounters and costs were compared in the 12 months pre/post NTZ initiation and while on treatment across racial strata. RESULTS: The study included 3244 PwMS (Black, n = 632; Hispanic, n = 382; Asian, n = 49; White, n = 2181). Mean post-index NTZ exposure was 15.5-19.2 months. Post-index ARRs were significantly reduced across racial/ethnic groups (p < 0.001). The adjusted Kaplan-Meier estimated proportion of relapse-free patients at 2 years for all racial/ethnic groups was not significantly different from the White group. Significant differences were observed in annualized MS-related healthcare cost rates but not in annualized MS-related encounter rates before and after NTZ initiation across the racial/ethnic groups. CONCLUSION: NTZ was effective across racial/ethnic groups although not significantly different between groups.

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Published In

Drugs Real World Outcomes

DOI

ISSN

2199-1154

Publication Date

June 2025

Volume

12

Issue

2

Start / End Page

301 / 310

Location

Switzerland

Related Subject Headings

  • 3214 Pharmacology and pharmaceutical sciences
  • 1115 Pharmacology and Pharmaceutical Sciences
 

Citation

APA
Chicago
ICMJE
MLA
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Blitz-Shabbir, K., Banks, A. M., Garg, H., Nelson, F., Shah, S., Belviso, N., … Fong, K. (2025). Real-World Treatment Outcomes in Black, Hispanic, Asian, and White Patients with Multiple Sclerosis Treated with Natalizumab. Drugs Real World Outcomes, 12(2), 301–310. https://doi.org/10.1007/s40801-025-00495-w
Blitz-Shabbir, Karen, Aimee M. Banks, Hina Garg, Flavia Nelson, Suma Shah, Nicholas Belviso, Jason P. Mendoza, Robin L. Avila, Boyang Bian, and Kinyee Fong. “Real-World Treatment Outcomes in Black, Hispanic, Asian, and White Patients with Multiple Sclerosis Treated with Natalizumab.Drugs Real World Outcomes 12, no. 2 (June 2025): 301–10. https://doi.org/10.1007/s40801-025-00495-w.
Blitz-Shabbir K, Banks AM, Garg H, Nelson F, Shah S, Belviso N, et al. Real-World Treatment Outcomes in Black, Hispanic, Asian, and White Patients with Multiple Sclerosis Treated with Natalizumab. Drugs Real World Outcomes. 2025 Jun;12(2):301–10.
Blitz-Shabbir, Karen, et al. “Real-World Treatment Outcomes in Black, Hispanic, Asian, and White Patients with Multiple Sclerosis Treated with Natalizumab.Drugs Real World Outcomes, vol. 12, no. 2, June 2025, pp. 301–10. Pubmed, doi:10.1007/s40801-025-00495-w.
Blitz-Shabbir K, Banks AM, Garg H, Nelson F, Shah S, Belviso N, Mendoza JP, Avila RL, Bian B, Fong K. Real-World Treatment Outcomes in Black, Hispanic, Asian, and White Patients with Multiple Sclerosis Treated with Natalizumab. Drugs Real World Outcomes. 2025 Jun;12(2):301–310.

Published In

Drugs Real World Outcomes

DOI

ISSN

2199-1154

Publication Date

June 2025

Volume

12

Issue

2

Start / End Page

301 / 310

Location

Switzerland

Related Subject Headings

  • 3214 Pharmacology and pharmaceutical sciences
  • 1115 Pharmacology and Pharmaceutical Sciences