Determinants of therapy switch in multiple sclerosis treatment-naïve patients: A real-life study. (August 2019)
- Record Type:
- Journal Article
- Title:
- Determinants of therapy switch in multiple sclerosis treatment-naïve patients: A real-life study. (August 2019)
- Main Title:
- Determinants of therapy switch in multiple sclerosis treatment-naïve patients: A real-life study
- Authors:
- Saccà, Francesco
Lanzillo, Roberta
Signori, Alessio
Maniscalco, Giorgia T
Signoriello, Elisabetta
Lo Fermo, Salvatore
Repice, Annamaria
Annovazzi, Pietro
Baroncini, Damiano
Clerico, Marinella
Binello, Eleonora
Cerqua, Raffaella
Mataluni, Giorgia
Bonavita, Simona
Lavorgna, Luigi
Zarbo, Ignazio Roberto
Laroni, Alice
Rossi, Silvia
Pareja Gutierrez, Lorena
La Gioia, Sara
Frigeni, Barbara
Barcella, Valeria
Frau, Jessica
Cocco, Eleonora
Fenu, Giuseppe
Torri Clerici, Valentina
Sartori, Arianna
Rasia, Sarah
Cordioli, Cinzia
Di Sapio, Alessia
Pontecorvo, Simona
Grasso, Roberta
Barrilà, Caterina
Russo, Cinzia Valeria
Esposito, Sabrina
Ippolito, Domenico
Bovis, Francesca
Gallo, Fabio
Sormani, Maria Pia
… (more) - Abstract:
- Background: With many options now available, first therapy choice is challenging in multiple sclerosis (MS) and depends mainly on neurologist and patient preferences. Objectives: To identify prognostic factors for early switch after first therapy choice. Methods: Newly diagnosed relapsing–remitting MS patients from 24 Italian centers were included. We evaluated the association of baseline demographics, clinical, and magnetic resonance imaging (MRI) data to the switch probability for lack of efficacy or intolerance/safety with a multivariate Cox analysis and estimated switch rates by competing risks models. Results: We enrolled 3025 patients. The overall switch frequency was 48% after 3 years. Switch risk for lack of efficacy was lower with fingolimod (hazard ratio (HR) = 0.50; p = 0.009), natalizumab (HR = 0.13; p < 0.001), dimethyl-fumarate (HR = 0.60; p = 0.037), teriflunomide (HR = 0.21; p = 0.031) as compared to interferons. Younger age (HR = 0.96; p < 0.001), diagnosis delay (HR = 1.23; p = 0.021), higher baseline Expanded Disability Status Scale (HR = 1.17; p = 0.001), and spinal cord lesions (HR = 1.46; p = 0.001) were independently associated with higher inefficacy switch rates. We found lower switch for intolerance/safety with glatiramer acetate (HR = 0.61; p = 0.001), fingolimod (HR = 0.35; p = 0.002), and dimethyl-fumarate (HR = 0.57; p = 0.022) as compared to interferons, while it increased with natalizumab (HR = 1.43; p = 0.022). Comorbidities wereBackground: With many options now available, first therapy choice is challenging in multiple sclerosis (MS) and depends mainly on neurologist and patient preferences. Objectives: To identify prognostic factors for early switch after first therapy choice. Methods: Newly diagnosed relapsing–remitting MS patients from 24 Italian centers were included. We evaluated the association of baseline demographics, clinical, and magnetic resonance imaging (MRI) data to the switch probability for lack of efficacy or intolerance/safety with a multivariate Cox analysis and estimated switch rates by competing risks models. Results: We enrolled 3025 patients. The overall switch frequency was 48% after 3 years. Switch risk for lack of efficacy was lower with fingolimod (hazard ratio (HR) = 0.50; p = 0.009), natalizumab (HR = 0.13; p < 0.001), dimethyl-fumarate (HR = 0.60; p = 0.037), teriflunomide (HR = 0.21; p = 0.031) as compared to interferons. Younger age (HR = 0.96; p < 0.001), diagnosis delay (HR = 1.23; p = 0.021), higher baseline Expanded Disability Status Scale (HR = 1.17; p = 0.001), and spinal cord lesions (HR = 1.46; p = 0.001) were independently associated with higher inefficacy switch rates. We found lower switch for intolerance/safety with glatiramer acetate (HR = 0.61; p = 0.001), fingolimod (HR = 0.35; p = 0.002), and dimethyl-fumarate (HR = 0.57; p = 0.022) as compared to interferons, while it increased with natalizumab (HR = 1.43; p = 0.022). Comorbidities were associated with intolerance switch (HR = 1.28; p = 0.047). Conclusion: Several factors are associated with higher switch risk in patients starting a first-line therapy and could be integrated in the decision-making process of first treatment choice. … (more)
- Is Part Of:
- Multiple sclerosis. Volume 25:Number 9(2019)
- Journal:
- Multiple sclerosis
- Issue:
- Volume 25:Number 9(2019)
- Issue Display:
- Volume 25, Issue 9 (2019)
- Year:
- 2019
- Volume:
- 25
- Issue:
- 9
- Issue Sort Value:
- 2019-0025-0009-0000
- Page Start:
- 1263
- Page End:
- 1272
- Publication Date:
- 2019-08
- Subjects:
- Switch -- naïve -- persistence -- disease modifying therapies -- relapsing–remitting -- real-life
Central nervous system -- Diseases -- Periodicals
Myelin sheath -- Diseases -- Periodicals
Inflammation -- Periodicals
Multiple sclerosis -- Periodicals
Central Nervous System Diseases -- Periodicals
Demyelinating Diseases -- Periodicals
Inflammation -- Periodicals
Multiple Sclerosis -- Periodicals
Système nerveux central -- Maladies -- Périodiques
Gaine de myéline -- Maladies -- Périodiques
Inflammation (Pathologie) -- Périodiques
Sclérose en plaques -- Périodiques
Electronic journals
616.834005 - Journal URLs:
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http://firstsearch.oclc.org/journal=1352-4585;screen=info;ECOIP ↗
http://www.arnoldpublishers.com/journals/pages/mul_scl/13524585.htm ↗ - DOI:
- 10.1177/1352458518790390 ↗
- Languages:
- English
- ISSNs:
- 1352-4585
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