Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Observational Study
. 2021 Apr;18(2):1166-1174.
doi: 10.1007/s13311-021-01037-2. Epub 2021 Apr 12.

Exit Strategies in Natalizumab-Treated RRMS at High Risk of Progressive Multifocal Leukoencephalopathy: a Multicentre Comparison Study

Affiliations
Observational Study

Exit Strategies in Natalizumab-Treated RRMS at High Risk of Progressive Multifocal Leukoencephalopathy: a Multicentre Comparison Study

Aurora Zanghì et al. Neurotherapeutics. 2021 Apr.

Abstract

The main aim of the study is to evaluate the efficacy and safety profile of ocrelizumab (OCR), rituximab (RTX), and cladribine (CLA), employed as natalizumab (NTZ) exit strategies in relapsing-remitting multiple sclerosis (RRMS) patients at high-risk for progressive multifocal leukoencephalopathy (PML). This is a multicentre, retrospective, real-world study on consecutive RRMS patients from eleven tertiary Italian MS centres, who switched from NTZ to OCR, RTX, and CLA from January 1st, 2019, to December 31st, 2019. The primary study outcomes were the annualized relapse rate (ARR) and magnetic resonance imaging (MRI) outcome. Treatment effects were estimated by the inverse probability treatment weighting (IPTW), based on propensity-score (PS) approach. Additional endpoint included confirmed disability progression (CDP) as measured by Expanded Disability Status Scale and adverse events (AEs). Patients satisfying predefined inclusion and exclusion criteria were 120; 64 switched to OCR, 36 to RTX, and 20 to CLA. Patients from the 3 groups did not show differences for baseline characteristics, also after post hoc analysis. The IPTW PS-adjusted models revealed that patients on OCR had a lower risk for ARR than patients on CLA (ExpBOCR 0.485, CI 95% 0.264-0.893, p = 0.020). This result was confirmed also for 12-month MRI activity (ExpBOCR 0.248 CI 95% 0.065-0.948, p = 0.042). No differences were found in other pairwise comparisons (OCR vs RTX and RTX vs CLA) for the investigated outcomes. AEs were similar among the 3 groups. Anti-CD20 drugs were revealed to be effective and safe options as NTZ exit strategies. All investigated DMTs showed a good safety profile.

Keywords: Cladribine; Disease activity; Exit strategy; Natalizumab; Ocrelizumab; Rituximab.

PubMed Disclaimer

Figures

Fig. 1
Fig. 1
Patients’ selection flow chart. CLA = cladribine; NTZ = natalizumab; OCR = ocrelizumab; RTX = rituximab
Fig. 2
Fig. 2
ARR endpoint (asterisk). The treatment effects were explored by a propensity-score adjustment in quintiles for age, sex, and EDSS in the year prior to switch to new DMT, number of NTZ infusions, and EID during the NTZ treatment. ARR = annualized relapse rate; CI = confidence interval; CLA = cladribine; NTZ = natalizumab; OCR = ocrelizumab; RTX = rituximab

References

    1. Yin Y, Wang J, Wang X, Gu L, Pei H, Kuai S, et al. Prognostic value of the neutrophil to lymphocyte ratio in lung cancer: a meta-analysis. Clinics (Sao Paulo, Brazil). 2015;70:524–530. doi: 10.6061/clinics/2015(07)10. - DOI - PMC - PubMed
    1. Bloomgren G, Richman S, Hotermans C, Subramanyam M, Goelz S, Natarajan A, et al. Risk of natalizumab-associated progressive multifocal leukoencephalopathy. N Engl J Med. 2012;366:1870–1880. doi: 10.1056/NEJMoa1107829. - DOI - PubMed
    1. D’Amico E, Zanghì A, Leone C, Tumani H, Patti F. Treatment-related progressive multifocal leukoencephalopathy in multiple sclerosis: a comprehensive review of current evidence and future needs. Drug Safety. 2016;39:1163–1174. doi: 10.1007/s40264-016-0461-6. - DOI - PubMed
    1. Fragoso YD, Arruda NM, Arruda WO, Brooks JB, Correa EC, Damasceno A, et al. We know how to prescribe natalizumab for multiple sclerosis, but do we know how to withdraw it? Expert review of neurotherapeutics. 2014;14:127–130. doi: 10.1586/14737175.2014.874947. - DOI - PubMed
    1. Ryerson LZ, Foley J, Chang I, Kister I, Cutter G, Metzger RR, et al. Risk of natalizumab-associated PML in patients with MS is reduced with extended interval dosing. Neurology. 2019;93:e1452–e1462. - PMC - PubMed

MeSH terms