Management and monitoring recommendations for the use of eliglustat in adults with type 1 Gaucher disease in Europe

被引:56
作者
Belmatoug, Nadia [1 ]
Di Rocco, Maja [2 ]
Fraga, Cristina [3 ]
Giraldo, Pilar [4 ]
Hughes, Derralynn [5 ]
Lukina, Elena [6 ]
Maison-Blanche, Pierre [7 ]
Merkel, Martin [8 ]
Niederau, Claus [9 ]
Plockinger, Ursula [10 ]
Richter, Johan [11 ]
Stulnig, Thomas M. [12 ]
Dahl, Stephan vom [13 ]
Cox, Timothy M. [14 ]
机构
[1] Univ Beaujon Hosp Paris Nord Val de Seine, AP HP, Dept Internal Med, Referral Ctr Lysosomal Dis, 100 Blvd Gen Leclerc, F-92110 Clichy, France
[2] Gaslini Inst, Dept Pediat, Unit Rare Dis, Largo Gaslini 3, I-16147 Genoa, Italy
[3] HDES Hosp, Dept Haematol, PDL, Av D Manuel 1, Ponta Delgada, Acores, Portugal
[4] CIBER Enfermedades Raras CIBERER, Inst Invest Sanitaria Aragon, Translat Res Unit, Zaragoza, Spain
[5] UCL, Royal Free London NHS Fdn Trust, Dept Haematol, Pond St, London NW1 2QG, England
[6] Hematol Res Ctr, Dept Orphan Dis, 4 Novy Zykovsky Lane, Moscow 125167, Russia
[7] Hop Xavier Bichat, Cardiol Unit, 46 Rue Henri Huchard, F-75018 Paris, France
[8] Asklepios Klin St Georg, Dept Internal Med, Lohmuhlenstr 5, D-20099 Hamburg, Germany
[9] Univ Duisburg Essen, Katholisches Klinikum Oberhausen GmbH, St Josef Hosp, Dept Med,Acad Teaching Hosp, Mulheimer Str 83, D-46045 Oberhausen, Germany
[10] Charite, Interdisziplinares Stoffwechsel Ctr Diabet Endokr, Campus Virchow Klinikum, Augustenburger Pl 1, D-13352 Berlin, Germany
[11] Skane Univ Hosp, Dept Hematol & Vasc Dis, S-22185 Lund, Sweden
[12] Med Univ Vienna, Dept Med 3, Clin Div Endocrinol & Metab, Waehringer Guertel 18-20, A-1090 Vienna, Austria
[13] Univ Dusseldorf, Univ Hosp, Dept Gastroenterol Hepatol & Infect Dis, Moorenstr 5, D-40225 Dusseldorf, Germany
[14] Univ Cambridge, Addenbrookes Hosp, Dept Med, Box 157,Level 5, Cambridge CB2 0QQ, England
关键词
Type 1 Gaucher disease; Eliglustat; Substrate reduction therapy; Enzyme replacement/augmentation therapy; Drug metabolism; Drug interactions; ENZYME REPLACEMENT THERAPY; NON-INFERIORITY; OPEN-LABEL; IMIGLUCERASE; MIGLUSTAT; DIAGNOSIS; SAFETY; INVOLVEMENT; REDUCTION; INHIBITOR;
D O I
10.1016/j.ejim.2016.07.011
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose: In Gaucher disease, diminished activity of the lysosomal enzyme, acid beta-glucosidase, leads to accumulation of glucosylceramides and related substrates, primarily in the spleen, liver, and bone marrow. Eliglustat is an oral substrate reduction therapy approved in the European Union and the United States as a first-line treatment for adults with type 1 Gaucher disease who have compatible CYP2D6 metabolism phenotypes. A European Advisory Council of experts in Gaucher disease describes the characteristics of eliglustat that are distinct from enzyme augmentation therapy (the standard of care) and miglustat (the other approved substrate reduction therapy) and recommends investigations and monitoring for patients on eliglustat therapy within the context of current recommendations for Gaucher disease management. Results: Eliglustat is a selective, potent inhibitor of glucosylceramide synthase, the enzyme responsible for biosynthesis of glucosylceramides which accumulate in Gaucher disease. Extensive metabolism of eliglustat by CYP2D6, and, to a lesser extent, CYP3A of the cytochrome P450 pathway, necessitates careful consideration of the patient's CYP2D6 metaboliser status and use of concomitant medications which share metabolism by these pathways. Guidance on specific assessments and monitoring required for eliglustat therapy, including an algorithm to determine eligibility for eliglustat, are provided. Conclusions: As a first-line therapy for type 1 Gaucher disease, eliglustat offers eligible patients a daily oral therapy alternative to biweekly infusions of enzyme therapy. Physicians will need to carefully assess individual Gaucher patients to determine their appropriateness for eliglustat therapy. The therapeutic response to eliglustat and use of concomitant medications will require long-term monitoring. (C) 2016 The Authors. Published by Elsevier B.V. on behalf of European Federation of Internal Medicine.
引用
收藏
页码:25 / 32
页数:8
相关论文
共 46 条
  • [1] [Anonymous], 2013, ZAV MIGL SUMM PROD C
  • [2] Balwani M, 2015, MOL GENET METAB
  • [3] Results from a 9-year Intensive Safety Surveillance Scheme (IS3) in miglustat (Zavesca®)-treated patients
    Brand, Monika
    Muller, Audrey
    Alsop, Jonathan
    van Schaik, Ivo N.
    Bembi, Bruno
    Hughes, Derralynn
    [J]. PHARMACOEPIDEMIOLOGY AND DRUG SAFETY, 2015, 24 (03) : 329 - 333
  • [4] CERDELGA&TRADE, 2014, SUMMARY PRODUCT CHAR
  • [5] Gaucher disease - Recommendations on diagnosis, evaluation, and monitoring
    Charrow, J
    Esplin, JA
    Gribble, TJ
    Kaplan, P
    Kolodny, EH
    Pastores, GM
    Scot, CR
    Wappner, RS
    Weinreb, NJ
    Wisch, JS
    [J]. ARCHIVES OF INTERNAL MEDICINE, 1998, 158 (16) : 1754 - 1760
  • [6] Eliglustat compared with imiglucerase in patients with Gaucher's disease type 1 stabilised on enzyme replacement therapy: a phase 3, randomised, open-label, non-inferiority trial
    Cox, Timothy M.
    Drelichman, Guillermo
    Cravo, Renata
    Balwani, Manisha
    Burrow, Thomas Andrew
    Martins, Ana Maria
    Lukina, Elena
    Rosenbloom, Barry
    Ross, Leorah
    Angell, Jennifer
    Puga, Ana Cristina
    [J]. LANCET, 2015, 385 (9985) : 2355 - 2362
  • [7] ENCORE, a randomized, controlled, open-label non-inferiority study comparing eliglustat to imiglucerase in Gaucher disease type 1 patients stabilized on enzyme replacement therapy: 24-month results
    Cox, Timothy M.
    Drelichman, Guillermo I.
    Cravo, Renata
    Balwani, Manisha
    Burrow, Thomas Andrew
    Martins, Ana Maria
    Lukinag, Elena
    Rosenbloom, Barry E.
    Ross, Leorah H.
    Angell, Jennifer
    Peterschmitt, M. Judith
    [J]. MOLECULAR GENETICS AND METABOLISM, 2015, 114 (02) : S33 - S34
  • [8] Cox TM, 2010, CURR OPIN INVEST DR, V11, P1169
  • [9] The role of the iminosugar N-butyldeoxynojirimycin (miglustat) in the management of type I (non-neuronopathic) Gaucher disease:: A position statement
    Cox, TM
    Aerts, JMFG
    Andria, G
    Beck, M
    Belmatoug, N
    Bembi, B
    Chertkoff, R
    Vom Dahl, S
    Elstein, D
    Erikson, A
    Giralt, M
    Heitner, R
    Hollak, C
    Hrebicek, M
    Lewis, S
    Mehta, A
    Pastores, GM
    Rolfs, A
    Miranda, MCS
    Zimran, A
    [J]. JOURNAL OF INHERITED METABOLIC DISEASE, 2003, 26 (06) : 513 - 526
  • [10] Superior effects of high-dose enzyme replacement therapy in type 1 Gaucher disease on bone marrow involvement and chitotriosidase levels:: a 2-center retrospective analysis
    de Fost, Maaike
    Hollak, Carla E. M.
    Greener, Johanna E. M.
    Aerts, Johannes M. F. G.
    Maas, Mario
    Poll, Ludger W.
    Wiersma, Maaike G.
    Haeussinger, Dieter
    Brett, Sarah
    Brill, Nicole
    vom Dahl, Stephan
    [J]. BLOOD, 2006, 108 (03) : 830 - 835