Induction Versus Escalation in Multiple Sclerosis: A 10-Year Real World Study.


Journal

Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics
ISSN: 1878-7479
Titre abrégé: Neurotherapeutics
Pays: United States
ID NLM: 101290381

Informations de publication

Date de publication:
07 2020
Historique:
pubmed: 3 4 2020
medline: 2 9 2021
entrez: 3 4 2020
Statut: ppublish

Résumé

In this independent, multicenter, post-marketing study, we directly compare induction immunosuppression versus escalation strategies on the risk of reaching the disability milestone of Expanded Disability Status Scale (EDSS) ≥ 6.0 over 10 years in previously untreated patients with relapsing-remitting multiple sclerosis. We collected data of patients who started interferon beta (escalation) versus mitoxantrone or cyclophosphamide (induction) as initial treatment. Main eligibility criteria included an EDSS score ≤ 4.0 at treatment start and either ≥ 2 relapses or 1 disabling relapse with evidence of ≥ 1 gadolinium-enhancing lesion at magnetic resonance imaging scan in the pre-treatment year. Since patients were not randomized to treatment group, we performed a propensity score (PS)-based matching procedure to select individuals with homogeneous baseline characteristics. Comparisons were then conducted using Cox models stratified by matched pairs. Overall, 75 and 738 patients started with induction and escalation, respectively. Patients in the induction group were older and more disabled than those in the escalation group (p < 0.05). The PS-matching procedure retained 75 patients per group. In the re-sampled population, a lower proportion of patients reached the outcome after induction (21/75, 28.0%) than escalation (29/75, 38.7%) (hazard ratio = 0.48; p = 0.024). Considering the whole sample, serious adverse events occurred more frequently after induction (8/75, 10.7%) than escalation (18/738, 2.4%) (odds ratio = 3.36, p = 0.015). These findings suggest that, in patients with poor prognostic factors, induction was more effective than escalation in reducing the risk of reaching the disability milestone, albeit with a worse safety profile. Future studies are warranted to explore if newer induction agents may provide a more advantageous long-lasting risk:benefit profile.

Identifiants

pubmed: 32236822
doi: 10.1007/s13311-020-00847-0
pii: 10.1007/s13311-020-00847-0
pmc: PMC7609676
doi:

Substances chimiques

Immunosuppressive Agents 0

Types de publication

Comparative Study Journal Article Multicenter Study Pragmatic Clinical Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

994-1004

Commentaires et corrections

Type : CommentIn

Références

Rotstein D, Montalban X. Reaching an evidence-based prognosis for personalized treatment of multiple sclerosis. Nat. Rev. Neurol. 2019:15(5):287-300.
doi: 10.1038/s41582-019-0170-8
Naismith RT. Multiple sclerosis therapeutic strategies: Start safe and effective, reassess early, and escalate if necessary. Neurol. Clin. Pract. 2011; 1(1):69–72.
doi: 10.1212/CPJ.0b013e31823cc2b0
Gasperini C, Prosperini L, Tintoré M, et al. Unraveling treatment response in multiple sclerosis: A clinical and MRI challenge. Neurology. 2019; 92(4):180–192.
doi: 10.1212/WNL.0000000000006810
Ransohoff RM, Hafler DA, Lucchinetti CF. Multiple sclerosis-a quiet revolution. Nat. Rev. Neurol. 2015; 11(3):134–142.
doi: 10.1038/nrneurol.2015.14
Ontaneda D, Tallantyre E, Kalincik T, et al. Early highly effective versus escalation treatment approaches in relapsing multiple sclerosis. Lancet. Neurol. 2019; 18(10):973-980.
Prosperini L, Kinkel RP, Miravalle AA, Iaffaldano P, Fantaccini S. Post-natalizumab disease reactivation in multiple sclerosis: systematic review and meta-analysis. Ther. Adv. Neurol. Disord. 2019; 12:1756286419837809.
Giovannoni G. Disease-modifying treatments for early and advanced multiple sclerosis: a new treatment paradigm. Curr. Opin. Neurol.. 2018; 31(3):233–243.
Le Page E, Edan G. Induction or escalation therapy for patients with multiple sclerosis? Rev. Neurol. (Paris). 2018; 174(6):449–457.
Lebrun C, Rocher F. Cancer Risk in Patients with Multiple Sclerosis: Potential Impact of Disease-Modifying Drugs. CNS Drugs. 2018; 32(10):939–949.
doi: 10.1007/s40263-018-0564-y
Martinelli V, Cocco E, Capra R, et al. Acute myeloid leukemia in Italian patients with multiple sclerosis treated with mitoxantrone. Neurology. 2011; 77(21):1887–1895.
Grebenciucova E, Pruitt A. Infections in Patients Receiving Multiple Sclerosis Disease-Modifying Therapies. Curr. Neurol. Neurosci. Rep. 2017; 17(11):88.
Rush CA, MacLean HJ, Freedman MS. Aggressive multiple sclerosis: proposed definition and treatment algorithm. Nat. Rev. Neurol. 2015; 11(7):379–389.
doi: 10.1038/nrneurol.2015.85
Harding K, Williams O, Willis M, et al. Clinical Outcomes of Escalation vs Early Intensive Disease-Modifying Therapy in Patients With Multiple Sclerosis. JAMA Neurol. 2019;76(5):536-541
doi: 10.1001/jamaneurol.2018.4905
Merkel B, Butzkueven H, Traboulsee AL, Havrdova E, Kalincik T. Timing of high-efficacy therapy in relapsing-remitting multiple sclerosis: A systematic review. Autoimmun. Rev. 2017; 16(6):658–665.
doi: 10.1016/j.autrev.2017.04.010
Lublin FD, Reingold SC, Cohen JA, et al. Defining the clinical course of multiple sclerosis: the 2013 revisions. Neurology. 2014; 83(3):278–286.
doi: 10.1212/WNL.0000000000000560
Fisniku LK, Brex PA, Altmann DR, et al. Disability and T2 MRI lesions: a 20-year follow-up of patients with relapse onset of multiple sclerosis. Brain 2008; 131(Pt 3):808–817.
Degenhardt A, Ramagopalan SV, Scalfari A, Ebers GC. Clinical prognostic factors in multiple sclerosis: a natural history review. Nat. Rev. Neurol. 2009; 5(12):672–682.
doi: 10.1038/nrneurol.2009.178
Brown JWL, Coles A, Horakova D, et al. Association of Initial Disease-Modifying Therapy With Later Conversion to Secondary Progressive Multiple Sclerosis. JAMA. 2019; 321(2):175–187.
doi: 10.1001/jama.2018.20588
Kurtzke JF. Rating neurologic impairment in multiple sclerosis: an expanded disability status scale (EDSS). Neurology. 1983; 33(11):1444–1452.
doi: 10.1212/WNL.33.11.1444
Confavreux C, Vukusic S, Adeleine P. Early clinical predictors and progression of irreversible disability in multiple sclerosis: an amnesic process. Brain 2003; 126(Pt 4):770–782.
Le Page E, Leray E, Taurin G, et al. Mitoxantrone as induction treatment in aggressive relapsing remitting multiple sclerosis: treatment response factors in a 5 year follow-up observational study of 100 consecutive patients. J. Neurol. Neurosurg. Psychiatry. 2008; 79(1):52–56.
doi: 10.1136/jnnp.2007.124958
Río J, Nos C, Tintoré M, et al. Defining the response to interferon-beta in relapsing-remitting multiple sclerosis patients. Ann. Neurol. 2006; 59(2):344–352.
doi: 10.1002/ana.20740
Austin PC. Balance diagnostics for comparing the distribution of baseline covariates between treatment groups in propensity-score matched samples. Stat. Med. 2009; 28(25):3083–3107.
doi: 10.1002/sim.3697
Cummings P, McKnight B, Greenland S. Matched cohort methods for injury research. Epidemiol. Rev. 2003; 25:43–50.
doi: 10.1093/epirev/mxg002
Péron J, Buyse M, Ozenne B, Roche L, Roy P. An extension of generalized pairwise comparisons for prioritized outcomes in the presence of censoring. Stat. Methods Med. Res. 2018; 27(4):1230–1239.
doi: 10.1177/0962280216658320
Rassen JA, Shelat AA, Myers J, et al. One-to-many propensity score matching in cohort studies. Pharmacoepidemiol. Drug Saf. 2012; 21 Suppl 2:69–80.
doi: 10.1002/pds.3263
Confavreux C, Vukusic S. The clinical course of multiple sclerosis. Handb. Clin. Neurol. 2014; 122:343–369.
doi: 10.1016/B978-0-444-52001-2.00014-5
Pardo G, Jones DE. The sequence of disease-modifying therapies in relapsing multiple sclerosis: safety and immunologic considerations. J. Neurol. 2017; 264(12):2351–2374.
doi: 10.1007/s00415-017-8594-9
Döhner H, Estey EH, Amadori S, et al. Diagnosis and management of acute myeloid leukemia in adults: recommendations from an international expert panel, on behalf of the European LeukemiaNet. Blood. 2010; 115(3):453–474.
doi: 10.1182/blood-2009-07-235358
Verhoeven MMA, Welsing PMJ, Bijlsma JWJ, et al. Effectiveness of Remission Induction Strategies for Early Rheumatoid Arthritis: a Systematic Literature Review. Curr. Rheumatol. Rep. 2019; 21(6):24. Available at: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6478774/ [Accessed July 26, 2019].
doi: 10.1007/s11926-019-0821-1
Vollmer T, Panitch H, Bar-Or A, et al. Glatiramer acetate after induction therapy with mitoxantrone in relapsing multiple sclerosis. Mult. Scler. 2008; 14(5):663–670.
Edan G, Comi G, Le Page E, et al. Mitoxantrone prior to interferon beta-1b in aggressive relapsing multiple sclerosis: a 3-year randomised trial. J. Neurol. Neurosurg. Psychiatry. 2011; 82(12):1344–1350.
doi: 10.1136/jnnp.2010.229724
Harrison DM, Gladstone DE, Hammond E, et al. Treatment of relapsing-remitting multiple sclerosis with high-dose cyclophosphamide induction followed by glatiramer acetate maintenance. Mult. Scler. 2012; 18(2):202–209.
CAMMS223 Trial Investigators, Coles AJ, Compston DAS, et al. Alemtuzumab vs. interferon beta-1a in early multiple sclerosis. N. Engl. J. Med. 2008; 359(17):1786–1801.
doi: 10.1056/NEJMoa0802670
Cohen JA, Coles AJ, Arnold DL, et al. Alemtuzumab versus interferon beta 1a as first-line treatment for patients with relapsing-remitting multiple sclerosis: a randomised controlled phase 3 trial. Lancet 2012; 380(9856):1819–1828.
Leist TP, Comi G, Cree BAC, et al. Effect of oral cladribine on time to conversion to clinically definite multiple sclerosis in patients with a first demyelinating event (ORACLE MS): a phase 3 randomised trial. Lancet Neurol. 2014; 13(3):257–267.
doi: 10.1016/S1474-4422(14)70005-5
Marriott JJ, Miyasaki JM, Gronseth G, O’Connor PW, Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology. Evidence Report: The efficacy and safety of mitoxantrone (Novantrone) in the treatment of multiple sclerosis: Report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology. Neurology. 2010; 74(18):1463–1470.
De Ridder D, van Poppel H, Demonty L, et al. Bladder cancer in patients with multiple sclerosis treated with cyclophosphamide. J. Urol. 1998; 159(6):1881–1884.
Hasan SK, Buttari F, Ottone T, et al. Risk of acute promyelocytic leukemia in multiple sclerosis: coding variants of DNA repair genes. Neurology.. 2011; 76(12):1059–1065.
doi: 10.1212/WNL.0b013e318211c3c8
Trojano M, Pellegrini F, Paolicelli D, Fuiani A, Di Renzo V. Observational studies: propensity score analysis of non-randomized data. Int. MS J. 2009; 16(3):90–97.
Kalincik T, Sormani MP. Reporting treatment outcomes in observational data: A fine balance. Mult. Scler. 2017; 23(1):21–22.
Austin PC. Double propensity-score adjustment: A solution to design bias or bias due to incomplete matching. Stat Methods Med. Res.. 2017; 26(1):201–222.

Auteurs

Luca Prosperini (L)

Department of Neurosciences, S. Camillo-Forlanini Hospital, C.ne Gianicolense 87, 00152, Rome, Italy. luca.prosperini@gmail.com.

Chiara Rosa Mancinelli (CR)

Multiple Sclerosis Centre, ASST Spedali Civili di Brescia, P.O. Montichiari, Via Ciotti 154, 25018, Montichiari, BS, Italy.

Claudio Marcello Solaro (CM)

Rehabilitation Unit 'Mons. L. Novarese' Hospital, Loc. Trompone, 13040, Moncrivello, VC, Italy.

Viviana Nociti (V)

Fondazione Policlinico Universitario 'A. Gemelli' IRCCS, L.go A. Gemelli 8, 00168, Rome, Italy.
Università Cattolica del Sacro Cuore, L.go A. Gemelli 8, 00168, Rome, Italy.

Shalom Haggiag (S)

Department of Neurosciences, S. Camillo-Forlanini Hospital, C.ne Gianicolense 87, 00152, Rome, Italy.

Cinzia Cordioli (C)

Multiple Sclerosis Centre, ASST Spedali Civili di Brescia, P.O. Montichiari, Via Ciotti 154, 25018, Montichiari, BS, Italy.

Laura De Giglio (L)

Neurology Unit, S. Filippo Neri Hospital, Via G. Martinotti 20, 00135, Rome, Italy.
Multiple Sclerosis Centre, S. Andrea Hospital, Via di Grottarossa 1035, 00189, Rome, Italy.

Nicola De Rossi (N)

Multiple Sclerosis Centre, ASST Spedali Civili di Brescia, P.O. Montichiari, Via Ciotti 154, 25018, Montichiari, BS, Italy.

Simonetta Galgani (S)

Department of Neurosciences, S. Camillo-Forlanini Hospital, C.ne Gianicolense 87, 00152, Rome, Italy.

Sarah Rasia (S)

Multiple Sclerosis Centre, ASST Spedali Civili di Brescia, P.O. Montichiari, Via Ciotti 154, 25018, Montichiari, BS, Italy.

Serena Ruggieri (S)

Department of Neurosciences, S. Camillo-Forlanini Hospital, C.ne Gianicolense 87, 00152, Rome, Italy.
Multiple Sclerosis Centre, S. Andrea Hospital, Via di Grottarossa 1035, 00189, Rome, Italy.

Carla Tortorella (C)

Department of Neurosciences, S. Camillo-Forlanini Hospital, C.ne Gianicolense 87, 00152, Rome, Italy.

Ruggero Capra (R)

Multiple Sclerosis Centre, ASST Spedali Civili di Brescia, P.O. Montichiari, Via Ciotti 154, 25018, Montichiari, BS, Italy.

Massimiliano Mirabella (M)

Fondazione Policlinico Universitario 'A. Gemelli' IRCCS, L.go A. Gemelli 8, 00168, Rome, Italy.
Università Cattolica del Sacro Cuore, L.go A. Gemelli 8, 00168, Rome, Italy.

Claudio Gasperini (C)

Department of Neurosciences, S. Camillo-Forlanini Hospital, C.ne Gianicolense 87, 00152, Rome, Italy.

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