2024
Real-world effectiveness of cladribine as an escalation strategy for MS: Insights from the Czech nationwide ReMuS registry
POTUZNIK, Pavel, Jiri DRAHOTA, Dana HORAKOVA, Marek PETERKA, Aneta MAZOUCHOVA et. al.Základní údaje
Originální název
Real-world effectiveness of cladribine as an escalation strategy for MS: Insights from the Czech nationwide ReMuS registry
Autoři
POTUZNIK, Pavel (203 Česká republika), Jiri DRAHOTA (203 Česká republika), Dana HORAKOVA (203 Česká republika), Marek PETERKA (203 Česká republika), Aneta MAZOUCHOVA (203 Česká republika), David MATYAS (203 Česká republika), Zbysek PAVELEK (203 Česká republika), Marta VACHOVA (203 Česká republika), Eva RECMANOVA (203 Česká republika), Ivana STETKAROVA (203 Česká republika), Jana LIBERTINOVA (203 Česká republika), Jan MARES (203 Česká republika), Pavel ŠTOURAČ (203 Česká republika, domácí), Marketa GRUNERMELOVA (203 Česká republika), Alena MARTINKOVA (203 Česká republika), Jana ADAMKOVA (203 Česká republika), Pavel HRADILEK (203 Česká republika), Radek AMPAPA, Michal DUFEK (203 Česká republika, domácí), Eva HAVRDOVA KUBALA (203 Česká republika) a Dominika STASTNA (203 Česká republika)
Vydání
JOURNAL OF CENTRAL NERVOUS SYSTEM DISEASE, LONDON, SAGE PUBLICATIONS LTD, 2024, 1179-5735
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30210 Clinical neurology
Stát vydavatele
Velká Británie a Severní Irsko
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 4.800 v roce 2022
Organizační jednotka
Lékařská fakulta
UT WoS
001275614400001
Klíčová slova anglicky
Cladribine; high-efficacy disease-modifying therapy; multiple sclerosis; annualised relapse rate; expanded disability status scale; adherence
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 15. 8. 2024 12:13, Mgr. Tereza Miškechová
Anotace
V originále
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.