| Literature DB >> 29549468 |
Roberta Lanzillo1, Luca Prosperini2,3, Claudio Gasperini4, Marcello Moccia5, Roberta Fantozzi6, Carla Tortorella4, Viviana Nociti7, Pietro Annovazzi8, Paola Cavalla9, Marta Radaelli10, Simona Malucchi11, Valentina Torri Clerici12, Laura Boffa13, Fabio Buttari6,13, Paolo Ragonese14, Giorgia Teresa Maniscalco15, Massimiliano Di Filippo16, Maria Chiara Buscarinu17, Federica Pinardi18, Antonio Gallo19, Giancarlo Coghe20, Ilaria Pesci21, Alice Laroni22, Alberto Gajofatto23, Massimiliano Calabrese23, Valentina Tomassini24, Eleonora Cocco20, Claudio Solaro25.
Abstract
In this independent, multicenter, retrospective study, we investigated the short-term persistence to treatment with first-line self-injectable or oral disease-modifying treatments (DMTs) in patients with relapsing-remitting multiple sclerosis. Data of patients regularly attending 21 Italian MS Centres who started a self-injectable or an oral DMT in 2015 were collected to: (1) estimate the proportion of patients discontinuing the treatment; (3) explore reasons for discontinuation; (3) identify baseline predictors of treatment discontinuation over a follow-up period of 12 months. We analyzed data of 1832 consecutive patients (1289 women, 543 men); 374 (20.4%) of them discontinued the prescribed DMT after a median time of 6 months (range 3 days to 11.5 months) due to poor tolerability (n = 163; 43.6%), disease activity (n = 95; 25.4%), adverse events (n = 64; 17.1%), convenience (i.e. availability of new drug formulations) and pregnancy planning (n = 21; 1.1%). Although the proportion of discontinuers was higher with self-injectable (n = 107; 22.9%) than with oral DMT (n = 215; 16.4%), the Cox regression model revealed no significant between-group difference (p = 0.12). Female sex [hazard ratio (HR) = 1.39, p = 0.01] and previous exposure to ≥ 3 DMTs (HR = 1.71, p = 0.009) were two independent risk factors for treatment discontinuation, regardless of prescribed DMTs. Our study confirms that persistence to treatment represents a clinical challenge, irrespective of the route of administration.Entities:
Keywords: Disease-modifying therapies; Multiple sclerosis; Outcome measurement; Persistence to treatment; Quality of life
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Year: 2018 PMID: 29549468 DOI: 10.1007/s00415-018-8831-x
Source DB: PubMed Journal: J Neurol ISSN: 0340-5354 Impact factor: 4.849