Pregled bibliografske jedinice broj: 1130876
Effectiveness and safety of alemtuzumab in the treatment of active relapsing-remitting multiple sclerosis: a multicenter, observational study
Effectiveness and safety of alemtuzumab in the treatment of active relapsing-remitting multiple sclerosis: a multicenter, observational study // Neurological sciences, 42 (2021), 11; 4591-4597 doi:10.1007/s10072-021-05145-x (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 1130876 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Effectiveness and safety of alemtuzumab in the
treatment of active relapsing-remitting multiple
sclerosis: a multicenter, observational study
Autori
Brecl Jakob, Gregor ; Barun, Barbara ; Gomezelj, Sarah ; Gabelić, Tereza ; Šega Jazbec, Saša ; Adamec, Ivan ; Horvat Ledinek, Alenka ; Rot, Uroš ; Krbot Skorić, Magdalena ; Habek, Mario
Izvornik
Neurological sciences (1590-1874) 42
(2021), 11;
4591-4597
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
alemtuzumab ; no evidence of disease activity ; relapsing–remitting multiple sclerosis ; safety
Sažetak
Objective: So far, a limited number of real-world evidence studies about the effectiveness and safety of alemtuzumab (ALM) have been published, some of them with a relatively small number of included patients. We aimed to study the efficacy and safety of ALM in real-world clinical practice in two MS centers in Slovenia and Croatia. Methods: This was a retrospective chart review of 71 consecutive patients with relapsing-remitting MS who were treated with ALM from 2015 till 2018. The following data were collected: gender, age at disease onset, disease duration at ALM initiation, previous disease modifying therapy, number of relapses, active MRI lesions, and EDSS in the year prior to ALM initiation and every year of follow- up. Results: All patients completed the standard dosing schedule and were followed for a mean time of 3.2±1.1 years after the initiation of treatment. Complete data for the 2 years after treatment (relapses, EDSS, and MRI) were available for 48 patients, of which 14 (29.2%) achieved NEDA. Clinical NEDA was achieved in 38 out of 63 participants (60.3%). In year 1, 24 out of 57 (42.1%) patients achieved NEDA. In year 2, 26 out of 41 (63.4%) patients achieved NEDA. Lower EDSS prior to starting ALM was the only independent predictor of NEDA in a multivariable model. Adverse events occurred in 58 participants (84.1%), with no new safety signals identified. Conclusion: According to the data from our cohort of early active RRMS patients we conclude ALM efficacy remains high in the real-world clinical practice.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Ustanove:
Fakultet elektrotehnike i računarstva, Zagreb,
Medicinski fakultet, Zagreb,
Klinički bolnički centar Zagreb
Profili:
MAGDALENA KRBOT SKORIĆ
(autor)
Mario Habek
(autor)
Tereza Gabelić
(autor)
Ivan Adamec
(autor)
Barbara Barun
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE