Effect of cladribine tablets on lymphocyte reduction and repopulation dynamics in patients with relapsing multiple sclerosis

被引:102
作者
Comi, Giancarlo [1 ,2 ]
Cook, Stuart [3 ]
Giovannoni, Gavin [4 ]
Rieckmann, Peter [5 ,6 ]
Sorensen, Per Soelberg [7 ]
Vermersch, Patrick [8 ]
Galazka, Andrew [9 ]
Nolting, Axel [10 ]
Hicking, Christine [10 ]
Dangond, Fernando [11 ]
机构
[1] Univ Vita Salute San Raffaele, Dept Neurol, Osped San Raffaele, Milan, Italy
[2] Univ Vita Salute San Raffaele, Inst Expt Neurol, Osped San Raffaele, Milan, Italy
[3] Rutgers State Univ, New Jersey Med Sch, Dept Neurol & Neurosci, MSB, Med Sci Bldg,185 South Orange Ave,H506, Newark, NJ 07101 USA
[4] Queen Mary Univ London, Blizard Inst, Barts & London Sch Med & Dent, London, England
[5] Med Pk Loipl, Dept Neurol, Erlangen, Germany
[6] Univ Erlangen Nurnberg, Erlangen, Germany
[7] Univ Copenhagen, Rigshosp, Danish MS Ctr, Dept Neurol, Copenhagen, Denmark
[8] Univ Lille, FHU Imminent, LIRIC INSERM U995, CHU Lille, Lille, France
[9] Merck, Aubonne, Switzerland
[10] Merck KGaA, Darmstadt, Germany
[11] EMD Serono Res & Dev Inst Inc, Billerica, MA USA
关键词
Cladribine tablets; Safety; Efficacy; Lymphocytes; RECONSTITUTION; 2-CHLORODEOXYADENOSINE; ALEMTUZUMAB; CLARITY; PLACEBO; CANCER;
D O I
10.1016/j.msard.2019.01.038
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Immune reconstitution therapies (IRT) for patients with multiple sclerosis are used for short, intermittent treatment periods to induce immune resetting and allow subsequent treatment-free periods. Cladribine tablets are postulated to be an IRT that causes selective and transient reductions in CD19(+) B cells and T cells, followed by reconstitution of adaptive immune function. Objective: To characterize long-term lymphocyte count changes in pooled data from the 2-year CLARITY and subsequent 2-year CLARITY Extension studies, and the PREMIERE registry (Long-term CLARITY cohort). Methods: Data from patients randomized to placebo (n= 435) or cladribine tablets 10 mg (MAVENCLAD (R); 3.5 mg/kg cumulative dose over 2 years, referred to as cladribine tablets 3.5 mg/kg; n= 685) in CLARITY or CLARITY Extension, including time spent in the PREMIERE registry were pooled to provide long-term follow-up data. The study investigated absolute lymphocyte counts (ALC) up to 312 weeks and B and T cell subsets up to 240 weeks after the first dose, in patients receiving placebo or cladribine tablets 3.5 mg/kg administered as two short (4 or 5 days) weekly treatments at the start of months 1 and 2 in each treatment year, followed by no further active treatment. Results: Treatment with cladribine tablets 3.5 mg/kg resulted in selective reductions in B and T lymphocytes. Lymphocyte recovery began soon after treatment in each of years 1 and 2. Median ALC recovered to the normal range and CD19(+) B cells recovered to threshold values by week 84, approximately 30 weeks after the last dose of cladribine tablets in year 2. Median CD4(+) T cell counts recovered to threshold values by week 96 (approximately 43 weeks after the last dose of cladribine tablets in year 2). Median CD8(+) cell counts never dropped below the threshold value. Conclusion: These results show the dynamics of lymphocyte count changes following treatment with cladribine tablets 3.5 mg/kg. The immune cell repopulation results provide further evidence that cladribine tablets may represent a form of IRT.
引用
收藏
页码:168 / 174
页数:7
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