The ocrelizumab phase II extension trial suggests the potential to improve the risk: Benefit balance in multiple sclerosis

被引:95
作者
Baker, David [1 ]
Pryce, Gareth [1 ]
James, Louisa K. [1 ]
Marta, Monica [1 ,2 ]
Schmierer, Klaus [1 ,2 ]
机构
[1] Queen Mary Univ London, Barts & London Sch Med & Dent, Blizard Inst, 4 Newark St, London E1 2AT, England
[2] Royal London Hosp, Barts Hlth NHS Trust, Clin Board Med Neurosci, London E1 1BB, England
关键词
B cell; CD20; Immunotherapy; Ocrelizumab; Multiple sclerosis; MEMORY B-CELLS; OPEN-LABEL; RITUXIMAB; LYMPHOCYTE; ANTIBODY; THERAPY; MS;
D O I
10.1016/j.msard.2020.102279
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: Ocrelizumab inhibits relapsing multiple sclerosis when administered every six months. Based on potential similar memory B cell depletion mechanisms with cladribine and alemtuzumab, we hypothesised that CD20-depletion of B cells by ocrelizumab may exhibit a duration of response exceeding the current licenced treatment interval. Methods: Internet-located information from regulatory submissions and meeting reports relating to the unpublished open-label, phase II ocrelizumab extension trial (NCT00676715) were reviewed. This followed people (54-55/arm) with MS, who switched from placebo or interferon-beta to ocrelizumab for three 600 mg treatment cycles (week 24, 48, 72) or people treated with ocrelizumab for four 600 mg treatment cycles (week 0-72), followed by an 18 month treatment-free period. Results: CD19+ B cells were rapidly depleted within 2 weeks and slow CD19+ B cell repopulation began about 6 months after the last infusion with median-repletion of over 15 months. The reduced annualized relapse rate during the published efficacy study appeared to be maintained in the extension study and there were no new T1 gadolinium-enhancing or T2 lesions detected in the treatment-free period. Importantly, within these extension cohorts, there appeared to be fewer adverse events and infections events. Conclusions: Ocrelizumab appears to induce durable relapsing disease inhibition, within 3 treatment cycles Therefore, it may be possible to reduce the frequency of dosing to maintain efficacy, whilst limiting infection and other risks associated with continuous immunosuppression and could allow more effective vaccination against new pathogens. Further studies are now clearly required to determine whether this data is robust.
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共 43 条
[1]   Safety and tolerability of inebilizumab (MEDI-551), an anti-CD19 monoclonal antibody, in patients with relapsing forms of multiple sclerosis: Results from a phase 1 randomised, placebo-controlled, escalating intravenous and subcutaneous dose study [J].
Agius, Mark A. ;
Klodowska-Duda, Gabriela ;
Maciejowski, Maciej ;
Potemkowski, Andrzej ;
Li, Jing ;
Patra, Kaushik ;
Wesley, Jacob ;
Madani, Soraya ;
Barron, Gerard ;
Katz, Eliezer ;
Flor, Armando .
MULTIPLE SCLEROSIS JOURNAL, 2019, 25 (02) :235-245
[2]  
[Anonymous], SUMMARY PRODUCT CHAR
[3]  
[Anonymous], 2019, NEUROLOGY, DOI DOI 10.1016/J.CLLC.2018.11.010
[4]  
[Anonymous], 2016, 1062910 RRMS
[5]   Learning from other autoimmunities to understand targeting of B cells to control multiple sclerosis [J].
Baker, David ;
Pryce, Gareth ;
Amor, Sandra ;
Giovannoni, Gavin ;
Schmierer, Klaus .
BRAIN, 2018, 141 :2834-2847
[6]   Interpreting Lymphocyte Reconstitution Data From the Pivotal Phase 3 Trials of Alemtuzumab [J].
Baker, David ;
Herrod, Samuel S. ;
Alvarez-Gonzalez, Cesar ;
Giovannoni, Gavin ;
Schmierer, Klaus .
JAMA NEUROLOGY, 2017, 74 (08) :961-969
[7]   Memory B Cells are Major Targets for Effective Immunotherapy in Relapsing Multiple Sclerosis [J].
Baker, David ;
Marta, Monica ;
Pryce, Gareth ;
Giovannoni, Gavin ;
Schmierer, Klaus .
EBIOMEDICINE, 2017, 16 :41-50
[8]   Rituximab in relapsing-remitting multiple sclerosis: A 72-week, open-label, phase I trial [J].
Bar-Or, Amit ;
Calabresi, Peter A. J. ;
Arnlod, Douglas ;
Markowitz, Clyde ;
Shafer, Stuart ;
Kasper, Lloyd H. ;
Waubant, Ernmanuelle ;
Gazda, Suzanne ;
Fox, Robert J. ;
Panzara, Michael ;
Sarkar, Neena ;
Agarwal, Sunil ;
Smith, Craig H. .
ANNALS OF NEUROLOGY, 2008, 63 (03) :395-400
[9]  
Barkhof Frederik, 2019, Neurology, V93, pe1778, DOI 10.1212/WNL.0000000000008189
[10]  
Barra Megan E, 2016, Mult Scler J Exp Transl Clin, V2, p2055217316672100, DOI 10.1177/2055217316672100