Relapse recovery The forgotten variable in multiple sclerosis clinical trials

被引:16
|
作者
Kantarci, Orhun H. [1 ]
Zeydan, Burcu [1 ,3 ]
Atkinson, Elizabeth J. [2 ]
Conway, Brittani L. [1 ,4 ]
Castrillo-Viguera, Carmen [5 ]
Rodriguez, Moses [1 ]
机构
[1] Mayo Clin, Coll Med, Dept Neurol, Ctr Multiple Sclerosis & CNS Demyelinating Dis, Rochester, MN USA
[2] Mayo Clin, Coll Med, Dept Hlth Sci Res, Rochester, MN USA
[3] Mayo Clin, Coll Med, Dept Radiol, Rochester, MN USA
[4] HealthPartners Neurosci Ctr, St Paul, MN USA
[5] Biogen Inc, US Med, Boston, MA USA
来源
关键词
NATURAL-HISTORY; DISABILITY; PROGRESSION; PREDICTORS; SEVERITY; ONSET;
D O I
10.1212/NXI.0000000000000653
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective To determine whether basing the decision to initiate immediate vs delayed disease-modifying therapy (DMT) on extent of recovery after initial relapse affects long-term disability accumulation in a multiple sclerosis (MS) evidence-based setting. Methods We analyzed the double-blind, placebo-controlled interferon beta-1a 30 mc once a week in clinically isolated syndrome and 10-year-follow-up extension trial. Good recovery after presenting relapse was defined as (1) full early recovery within 28 days of symptom onset (Expanded Disability Status Scale [EDSS] score of 0 at enrollment maintained >= 6 months) and (2) delayed good recovery (EDSS score > 0 at enrollment and improvement from peak deficit to 6th-month or 1-year visit >= median). Time from recovery assignment to future disability (EDSS score >= 2.5 or >= 4.0) was studied on a relapse-recovery-stratified age axis and immediate vs 3-year delayed treatment initiation with Kaplan-Meier statistics and hazard ratios (HRs). Results One hundred seventy-five/328 patients had good recovery (94 immediate and 81 delayed treatment); 153 did not have good recovery (77 immediate and 76 delayed treatment). HRs for EDSS score >= 2.5 outcome were: delayed treatment without good recovery as reference (HR = 1.0), delayed treatment with good recovery (HR6th-month: 0.67, p = 0.207; HR1st-year: 0.40, p = 0.027), immediate treatment without good recovery (HR6th-month: 0.56, p = 0.061; HR1st-year: 0.40, p = 0.011), and immediate treatment with good recovery (HR6th-month: 0.43, p = 0.014; HR1st-year: 0.48, p = 0.034). Placebo patients were switched to long-term treatment after 3 years, and insufficient EDSS score >= 4.0 outcome events were available to study. Conclusions In patients with MS presenting without good recovery after the initial relapse, immediate DMT initiation favorably influences the likelihood of more ambulatory-benign disease akin to patients with good recovery after the initial relapse. Classification of evidence This study provides Class III evidence that for patients with MS without good recovery after the initial relapse, immediate DMT initiation increases the likelihood of a benign disease course.
引用
收藏
页数:9
相关论文
共 50 条
  • [1] Time to first relapse as an endpoint in multiple sclerosis clinical trials
    Sormani, M. P.
    Signori, A.
    Siri, P.
    De Stefano, N.
    [J]. MULTIPLE SCLEROSIS JOURNAL, 2013, 19 (04) : 466 - 474
  • [2] Statistical properties of time to first relapse as an endpoint in multiple sclerosis clinical trials
    Signori, A.
    Siri, P.
    Sormani, M. P.
    [J]. MULTIPLE SCLEROSIS JOURNAL, 2012, 18 : 29 - 30
  • [3] Acute relapse recovery in pediatric multiple sclerosis
    Gurevich, M.
    Khavkin, Y.
    Menascu, S.
    Zilkha-Falb, R.
    Magalashvili, D.
    Dolev, M.
    Achiron, A.
    [J]. MULTIPLE SCLEROSIS JOURNAL, 2018, 24 : 611 - 611
  • [4] Efficacy of combination therapy with erythropoietin and methylprednisolone in clinical recovery of severe relapse in multiple sclerosis
    Fatemeh Najmi Varzaneh
    Farnaz Najmi Varzaneh
    Amir Reza Azimi
    Nima Rezaei
    Mohammad Ali Sahraian
    [J]. Acta Neurologica Belgica, 2014, 114 : 273 - 278
  • [5] Efficacy of combination therapy with erythropoietin and methylprednisolone in clinical recovery of severe relapse in multiple sclerosis
    Varzaneh, Fatemeh Najmi
    Varzaneh, Farnaz Najmi
    Azimi, Amir Reza
    Rezaei, Nima
    Sahraian, Mohammad Ali
    [J]. ACTA NEUROLOGICA BELGICA, 2014, 114 (04) : 273 - 278
  • [6] Relapse severity and recovery in early pediatric multiple sclerosis
    Fay, Alex J.
    Mowry, Ellen M.
    Strober, Jonathan
    Waubant, Emmanuelle
    [J]. MULTIPLE SCLEROSIS JOURNAL, 2012, 18 (07) : 1008 - 1012
  • [7] Recovery of cognitive function after relapse in multiple sclerosis
    Benedict, Ralph H. B.
    Pol, Jeta
    Yasin, Faizan
    Hojnacki, David
    Kolb, Channa
    Eckert, Svetlana
    Tacca, Beth
    Drake, Allison
    Wojcik, Curtis
    Morrow, Sarah A.
    Jakimovski, Dejan
    Fuchs, Tom A.
    Dwyer, Michael G.
    Zivadinov, Robert
    Weinstock-Guttman, Bianca
    [J]. MULTIPLE SCLEROSIS JOURNAL, 2021, 27 (01) : 71 - 78
  • [8] Clinical trials in multiple sclerosis: milestones
    Zhang, Yinan
    Salter, Amber
    Cutter, Gary
    Stuve, Olaf
    [J]. THERAPEUTIC ADVANCES IN NEUROLOGICAL DISORDERS, 2018, 11
  • [9] Methodology of clinical trials in multiple sclerosis
    Mitsikostas, D. D.
    [J]. NEUROLOGICAL SCIENCES, 2006, 27 (Suppl 5) : S362 - S364
  • [10] Methodology of clinical trials in multiple sclerosis
    D. D. Mitsikostas
    [J]. Neurological Sciences, 2006, 27 : s362 - s364