Publication details

Real-world effectiveness of cladribine as an escalation strategy for MS: Insights from the Czech nationwide ReMuS registry

Authors

POTUZNIK Pavel DRAHOTA Jiri HORAKOVA Dana PETERKA Marek MAZOUCHOVA Aneta MATYAS David PAVELEK Zbysek VACHOVA Marta RECMANOVA Eva STETKAROVA Ivana LIBERTINOVA Jana MARES Jan ŠTOURAČ Pavel GRUNERMELOVA Marketa MARTINKOVA Alena ADAMKOVA Jana HRADILEK Pavel AMPAPA Radek DUFEK Michal HAVRDOVA KUBALA Eva STASTNA Dominika

Year of publication 2024
Type Article in Periodical
Magazine / Source JOURNAL OF CENTRAL NERVOUS SYSTEM DISEASE
MU Faculty or unit

Faculty of Medicine

Citation
web https://journals.sagepub.com/doi/10.1177/11795735241262743
Doi http://dx.doi.org/10.1177/11795735241262743
Keywords Cladribine; high-efficacy disease-modifying therapy; multiple sclerosis; annualised relapse rate; expanded disability status scale; adherence
Description BackgroundCladribine, a selective immune reconstitution therapy, is approved for the treatment of adult patients with highly active multiple sclerosis (MS).ObjectivesProvide experience with cladribine therapy in a real-world setting.MethodsThis is a registry-based retrospective observational cohort study. First, using data from the Czech nationwide registry ReMuS, we analysed patients who initiated cladribine from September 1, 2018 to December 31, 2021. Second, we analysed a subgroup of patients who initiated cladribine between September 1, 2018 to June 30, 2020, thus possessing a follow-up period of at least 2 years. We evaluated demographic and MS characteristics including disease-modifying therapies (DMTs) before and after cladribine administration, relapses, Expanded Disability Status Scale (EDSS), and adherence.ResultsIn total, 617 patients (335 with follow-up of at least 2 years) started cladribine therapy in the study period (mean age 37.0, mean disease duration 8.4 years, 74.1% females). In most cases, cladribine was administered as a second-line drug, a total of 80.7% had been escalated from a platform DMT. During 2 years before cladribine initiation, the average annualised relapse rate (ARR) was .67. Following cladribine initiation, the ARR decreased to .28 in the first year and .22 in the second year. Overall, across the entire two-year treatment period, 69.0% of patients were relapse-free and the average ARR was .25. As for EDSS development, the median baseline EDSS was 2.5 and remained stable even after 24 months. The adherence to treatment ranged of around 90%.ConclusionThis nationwide study confirms the efficacy of cladribine in real-world settings, especially in patients who are not treatment-na & iuml;ve. In addition, the study shows an exceptionally high adherence rate, a finding that underscores the invaluable role of cladribine, but also the value of registry-based studies in capturing real-world clinical practice.

You are running an old browser version. We recommend updating your browser to its latest version.

More info