Long-term efficacy and safety of alemtuzumab in participants with highly active MS: TOPAZ clinical trial and interim analysis of TREAT-MS real-world study

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Tjalf Ziemssen - , Department of Neurology, University Hospital Carl Gustav Carus Dresden (Author)
  • Ann D Bass - , Neurology Center of San Antonio (Author)
  • Bart Van Wijmeersch - , Noorderhart Hospitals (Author)
  • Sara Eichau - , Hospital Universitario Virgen Macarena (Author)
  • Stephan Richter - , Mind MVZ Neurology Center Stuttgart (Author)
  • Frank Hoffmann - , Hospital Martha-Maria Halle-Dölau (Author)
  • Nicole M Armstrong - , Sanofi US (Author)
  • Magdalena Chirieac - , Sanofi US (Author)
  • Janete Cunha-Santos - , Sanofi S.A. (Author)
  • Barry A Singer - , Missouri Baptist Medical Center (Author)

Abstract

BACKGROUND: Alemtuzumab is a disease-modifying therapy for highly active relapsing-remitting multiple sclerosis (RRMS). Sustained efficacy up to 9 years was observed in the phase IIIb/IV open-label TOPAZ clinical trial and assessed in the real-world retrospective and prospective study, TREAT-MS.

OBJECTIVES: To examine long-term efficacy and safety of alemtuzumab in participants with multiple sclerosis (MS) and highly active disease (HAD) by combining up to 13 years of TOPAZ data and TREAT-MS interim data.

DESIGN: TOPAZ: Randomized participants completing core CARE-MS I and II could receive additional alemtuzumab (12 mg/day, 3 consecutive days; ⩾12 months apart) for 11-13 years after initiating treatment. TREAT-MS: Participants from German MS clinics were observed for 4 years after last alemtuzumab treatment phase.

METHODS: Efficacy outcomes (annualized relapse rate (ARR), change in Expanded Disability Status Scale (EDSS), 6-month confirmed disability worsening/improvement, magnetic resonance imaging), and adverse events (AEs) were examined. Primary HAD definition (⩾2 relapses in the year prior to baseline and ⩾1 gadolinium-enhancing lesion at baseline), and two alternative HAD definitions were assessed.

RESULTS: More participants from CARE-MS I (28%) and II (24%) met primary HAD criteria than TREAT-MS (~14%). Mean ARR for alemtuzumab-treated HAD participants was significantly reduced in CARE-MS I and II (0.14 and 0.15, respectively, Years 3-13) and in TREAT-MS (0.24, >2 years). Stable/improved EDSS scores were achieved by 74% of HAD participants in CARE-MS I, 67% in CARE-MS II (both Year 11), and 79% in TREAT-MS (Year 3.6), with 6-month CDI achieved by about half at Year 11 (CARE-MS I, II). Annual treatment-emergent AE incidences declined in TOPAZ and were lower in TREAT-MS.

CONCLUSION: Sustained efficacy of alemtuzumab was observed for clinical and radiological outcomes in participants with HAD in the TOPAZ clinical trial and real-world TREAT-MS study with no new safety signals.

TRIAL REGISTRATION: ClinicalTrials.gov (CARE-MS I, NCT00530348; CARE-MS II, NCT00548405; CARE-MS Extension Study, NCT00930553; TOPAZ, NCT02255656). Paul-Ehrlich-Institut (TREAT-MS, NIS 281).

Details

Original languageEnglish
Number of pages24
JournalTherapeutic advances in neurological disorders
Volume18 (2025)
Early online date10 Feb 2025
Publication statusPublished - 2025
Peer-reviewedYes

External IDs

PubMedCentral PMC11811979
ORCID /0000-0001-8799-8202/work/178384633
unpaywall 10.1177/17562864241306575
Mendeley d4c27cf4-749d-316b-9635-51368ad352ac
Scopus 85217839452

Keywords

Keywords

  • RRMS, CARE-MS, TREAT-MS, alemtuzumab, multiple sclerosis, TOPAZ, highly active disease