The effect of oral immunomodulatory therapy on treatment uptake and persistence in multiple sclerosis

被引:30
|
作者
Warrender-Sparkes, Matthew [1 ]
Spelman, Tim [2 ]
Izquierdo, Guillermo [3 ]
Trojano, Maria [4 ]
Lugaresi, Alessandra [5 ]
Grand'Maison, Francois [6 ]
Havrdova, Eva [7 ,8 ,9 ]
Horakova, Dana [7 ,8 ,9 ]
Boz, Cavit [10 ]
Oreja-Guevara, Celia [11 ]
Alroughani, Raed [12 ]
Iuliano, Gerardo [13 ]
Duquette, Pierre [14 ]
Girard, Marc [14 ]
Terzi, Murat [15 ]
Hupperts, Raymond [16 ]
Grammond, Pierre [17 ]
Petersen, Thor [18 ]
Fernandez-Bolanos, Ricardo [19 ]
Fiol, Marcela [20 ]
Pucci, Eugenio [21 ]
Lechner-Scott, Jeannette [22 ]
Verheul, Freek [23 ]
Cristiano, Edgardo [24 ]
Van Pesch, Vincent [25 ]
Petkovska-Boskova, Tatjana [26 ]
Moore, Fraser [27 ]
Kister, Ilya [28 ]
Bergamaschi, Roberto [29 ]
Laura Saladino, Maria [30 ]
Slee, Mark [31 ]
Barnett, Michael [32 ]
Amato, Maria Pia [33 ]
Shaw, Cameron [34 ]
Shuey, Neil [35 ]
Young, Carolyn [36 ]
Gray, Orla [37 ]
Kappos, Ludwig [38 ,39 ,40 ]
Butzkueven, Helmut [1 ,41 ]
Kalincik, Tomas [1 ,2 ]
Jokubaitis, Vilija [1 ]
机构
[1] Univ Melbourne, Dept Med, Melbourne, Vic, Australia
[2] Royal Melbourne Hosp, Dept Nephrol, Melbourne, Vic 3050, Australia
[3] Hosp Univ Virgen Macarena, Seville, Spain
[4] Univ Bari, Dept Basic Med Sci Neurosci & Sense Organs, I-70121 Bari, Italy
[5] Univ G DAnnunzio, Dept Neurosci Imaging & Clin Sci, MS Ctr, Chieti, Italy
[6] Hop Charles LeMoyne, Neuro Rive Sud, Quebec City, PQ, Canada
[7] Gen Univ Hosp, Dept Neurol, Prague, Czech Republic
[8] Gen Univ Hosp, Fac Med 1, Ctr Clin Neurosci, Prague, Czech Republic
[9] Charles Univ Prague, Prague, Czech Republic
[10] Karadeniz Tech Univ, Trabzon, Turkey
[11] Univ Hosp San Carlos, IdISSC, Madrid, Spain
[12] Amiri Hosp, Kuwait, Kuwait
[13] Osped Riuniti Salerno, Salerno, Italy
[14] Hop Notre Dame de Bon Secours, Montreal, PQ H2L 4K8, Canada
[15] Ondokuz Mayis Univ, Samsun, Turkey
[16] Orbis Medicle Ctr, Sittard, Netherlands
[17] Hotel Dieu Levis, Quebec City, PQ, Canada
[18] Aarhus Univ Hosp, DK-8000 Aarhus C, Denmark
[19] Hosp Univ Virgen Valme, Seville, Spain
[20] FLENI, Buenos Aires, DF, Argentina
[21] Osped Macerata, Macerata, Italy
[22] John Hunter Hosp, Newcastle, NSW, Australia
[23] Groen Hart Ziekenhuis, Gouda, Netherlands
[24] Hosp Italiano Buenos Aires, Buenos Aires, DF, Argentina
[25] Clin Univ St Luc, B-1200 Brussels, Belgium
[26] Neurol Clin Ctr, Skopje, Macedonia
[27] McGill Univ, Jewish Gen Hosp, Montreal, PQ H3T 1E2, Canada
[28] NYU, Langone Med Ctr, New York, NY USA
[29] Natl Neurol Inst C Mondino, Pavia, Italy
[30] INEBA, Buenos Aires, DF, Argentina
[31] Flinders Univ & Med Ctr, Adelaide, SA, Australia
[32] Brain & Mind Res Inst, Sydney, NSW, Australia
[33] Univ Florence, Sect Neurosci, Dept NEUROFARBA, Florence, Italy
[34] Geelong Hosp, Geelong, Vic, Australia
[35] St Vincents Hosp, Melbourne, Vic, Australia
[36] Walton Ctr Neurol & Neurosurg, Liverpool, Merseyside, England
[37] Craigavon Area Hosp, Portadown, Vic, Australia
[38] Univ Basel Hosp, Neurol, Dept Med, CH-4031 Basel, Switzerland
[39] Univ Basel Hosp, Neurol, Dept Clin Res, CH-4031 Basel, Switzerland
[40] Univ Basel Hosp, Neurol, Dept Biomed, CH-4031 Basel, Switzerland
[41] Monash Univ, Box Hill Hosp, Dept Neurol, Box Hill, Vic, Australia
基金
澳大利亚国家健康与医学研究理事会; 英国医学研究理事会;
关键词
Multiple sclerosis; disease-modifying therapy; fingolimod; medication persistence; MSBase; DISEASE-MODIFYING THERAPIES; INTERFERON-BETA THERAPY; TREATMENT PATTERNS; ADHERENCE; FINGOLIMOD; NATALIZUMAB;
D O I
10.1177/1352458515594041
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: We aimed to analyse the effect of the introduction of fingolimod, the first oral disease-modifying therapy, on treatment utilisation and persistence in an international cohort of patients with multiple sclerosis (MS). Methods: MSBASIS, a prospective, observational sub-study of the MSBase registry, collects demographic, clinical and paraclinical data on patients followed from MS onset (n=4718). We conducted a multivariable conditional risk set survival analysis to identify predictors of treatment discontinuation, and to assess if the introduction of fingolimod has altered treatment persistence. Results: A total of 2640 patients commenced immunomodulatory therapy. Following the introduction of fingolimod, patients were more likely to discontinue all other treatments (hazard ratio 1.64, p<0.001) while more patients switched to fingolimod than any other therapy (42.3% of switches). Patients switched to fingolimod due to convenience. Patients treated with fingolimod were less likely to discontinue treatment compared with other therapies (p<0.001). Female sex, country of residence, younger age, a high Expanded Disability Status Scale score and relapse activity were all independently associated with higher rates of treatment discontinuation. Conclusion: Following the availability of fingolimod, patients were more likely to discontinue injectable treatments. Those who switched to fingolimod were more likely to do so for convenience. Persistence was improved on fingolimod compared to other medications.
引用
收藏
页码:520 / 532
页数:13
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