메뉴 건너뛰기




Volumn 124, Issue 23, 2014, Pages 3398-3408

Recombinant factor VIII products and inhibitor development in previously untreated boys with severe hemophilia A

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD CLOTTING FACTOR 8; F8 PROTEIN, HUMAN; RECOMBINANT PROTEIN;

EID: 84914140043     PISSN: 00064971     EISSN: 15280020     Source Type: Journal    
DOI: 10.1182/blood-2014-07-586347     Document Type: Article
Times cited : (140)

References (46)
  • 2
    • 84859596442 scopus 로고    scopus 로고
    • Modern haemophilia care
    • Berntorp E, Shapiro AD. Modern haemophilia care. Lancet. 2012;379(9824):1447-1456.
    • (2012) Lancet , vol.379 , Issue.9824 , pp. 1447-1456
    • Berntorp, E.1    Shapiro, A.D.2
  • 3
    • 9144271883 scopus 로고    scopus 로고
    • The incidence of factor VIII and factor IX inhibitors in the hemophilia population of the UK and their effect on subsequent mortality 1977-99
    • Darby SC, Keeling DM, Spooner RJD, et al; UK Haemophilia Centre Doctors' Organisation. The incidence of factor VIII and factor IX inhibitors in the hemophilia population of the UK and their effect on subsequent mortality, 1977-99. J Thromb Haemost. 2004;2(7):1047-1054.
    • (2004) J Thromb Haemost , vol.2 , Issue.7 , pp. 1047-1054
    • Darby, S.C.1    Keeling, D.M.2    Spooner, R.J.D.3
  • 4
    • 0033768130 scopus 로고    scopus 로고
    • The diagnosis and management of factor viii and ix inhibitors: A guideline from the uk haemophilia centre doctors' organization (ukhcdo)
    • Hay CR, Baglin TP, Collins PW, Hill FG, Keeling DM. The diagnosis and management of factor VIII and IX inhibitors: a guideline from the UK Haemophilia Centre Doctors' Organization (UKHCDO). Br J Haematol. 2000;111(1):78-90.
    • (2000) Br J Haematol , vol.111 , Issue.1 , pp. 78-90
    • Hay, C.R.1    Baglin, T.P.2    Collins, P.W.3    Hill, F.G.4    Keeling, D.M.5
  • 5
    • 84875258603 scopus 로고    scopus 로고
    • Current status and future prospects for the prophylactic management of hemophilia patients with inhibitor antibodies
    • Teitel JM, Sholzberg M. Current status and future prospects for the prophylactic management of hemophilia patients with inhibitor antibodies. Blood Rev. 2013;27(2):103-109.
    • (2013) Blood Rev , vol.27 , Issue.2 , pp. 103-109
    • Teitel, J.M.1    Sholzberg, M.2
  • 7
    • 77954506432 scopus 로고    scopus 로고
    • Rate of inhibitor development in previously untreated hemophilia A patients treated with plasma-derived or recombinant factor VIII concentrates: A systematic review
    • Iorio A, Halimeh S, Holzhauer S, et al. Rate of inhibitor development in previously untreated hemophilia A patients treated with plasma-derived or recombinant factor VIII concentrates: a systematic review. J Thromb Haemost. 2010; 8(6):1256-1265.
    • (2010) J Thromb Haemost , vol.8 , Issue.6 , pp. 1256-1265
    • Iorio, A.1    Halimeh, S.2    Holzhauer, S.3
  • 8
    • 84855912746 scopus 로고    scopus 로고
    • Cumulative inhibitor incidence in previously untreated patients with severe hemophilia A treated with plasma-derived versus recombinant factor VIII concentrates: A critical systematic review
    • Franchini M, Tagliaferri A, Mengoli C, Cruciani M. Cumulative inhibitor incidence in previously untreated patients with severe hemophilia A treated with plasma-derived versus recombinant factor VIII concentrates: a critical systematic review. Crit Rev Oncol Hematol. 2012;81(1): 82-93.
    • (2012) Crit Rev Oncol Hematol , vol.81 , Issue.1 , pp. 82-93
    • Franchini, M.1    Tagliaferri, A.2    Mengoli, C.3    Cruciani, M.4
  • 9
    • 77955928309 scopus 로고    scopus 로고
    • Non-genetic risk factors and the development of inhibitors in haemophilia: A comprehensive review and consensus report
    • Astermark J, Altisent C, Batorova A, et al; European Haemophilia Therapy Standardisation Board. Non-genetic risk factors and the development of inhibitors in haemophilia: a comprehensive review and consensus report. Haemophilia. 2010;16(5):747-766.
    • (2010) Haemophilia , vol.16 , Issue.5 , pp. 747-766
    • Astermark, J.1    Altisent, C.2    Batorova, A.3
  • 10
    • 84885081117 scopus 로고    scopus 로고
    • Identifying nongenetic risk factors for inhibitor development in severe hemophilia a
    • Gouw SC, Fijnvandraat K. Identifying nongenetic risk factors for inhibitor development in severe hemophilia a. Semin Thromb Hemost. 2013;39(7): 740-751.
    • (2013) Semin Thromb Hemost , vol.39 , Issue.7 , pp. 740-751
    • Gouw, S.C.1    Fijnvandraat, K.2
  • 11
    • 84881014770 scopus 로고    scopus 로고
    • Intensity of factor viii treatment and inhibitor development in children with severe hemophilia a: The rodin study
    • Gouw SC, van den Berg HM, Fischer K, et al; PedNet and Research of Determinants of INhibitor development (RODIN) Study Group. Intensity of factor VIII treatment and inhibitor development in children with severe hemophilia A: the RODIN study. Blood. 2013;121(20): 4046-4055.
    • (2013) Blood , vol.121 , Issue.20 , pp. 4046-4055
    • Gouw, S.C.1    Van Den Berg, H.M.2    Fischer, K.3
  • 12
    • 34249711370 scopus 로고    scopus 로고
    • Recombinant versus plasma-derived factor VIII products and the development of inhibitors in previously untreated patients with severe hemophilia A: The CANAL cohort study
    • Gouw SC, van der Bom JG, Auerswald G, Ettinghausen CE, Tedgård U, van den Berg HM. Recombinant versus plasma-derived factor VIII products and the development of inhibitors in previously untreated patients with severe hemophilia A: the CANAL cohort study. Blood. 2007;109(11):4693-4697.
    • (2007) Blood , vol.109 , Issue.11 , pp. 4693-4697
    • Gouw, S.C.1    Van Der Bom, J.G.2    Auerswald, G.3    Ettinghausen, C.E.4    Tedgård, U.5    Van Den Berg, H.M.6
  • 13
    • 84860447633 scopus 로고    scopus 로고
    • Source and purity of factor viii products as risk factors for inhibitor development in patients with hemophilia a
    • Mancuso ME, Mannucci PM, Rocino A, Garagiola I, Tagliaferri A, Santagostino E. Source and purity of factor VIII products as risk factors for inhibitor development in patients with hemophilia A. J Thromb Haemost. 2012;10(5):781-790.
    • (2012) J Thromb Haemost , vol.10 , Issue.5 , pp. 781-790
    • Mancuso, M.E.1    Mannucci, P.M.2    Rocino, A.3    Garagiola, I.4    Tagliaferri, A.5    Santagostino, E.6
  • 14
    • 84872450786 scopus 로고    scopus 로고
    • Factor VIII products and inhibitor development in severe hemophilia A
    • Gouw SC, van der Bom JG, Ljung R, et al; PedNet and RODIN Study Group. Factor VIII products and inhibitor development in severe hemophilia A. N Engl J Med. 2013;368(3): 231-239.
    • (2013) N Engl J Med , vol.368 , Issue.3 , pp. 231-239
    • Gouw, S.C.1    Van Der Bom, J.G.2    Ljung, R.3
  • 15
    • 84875912773 scopus 로고    scopus 로고
    • Factor VIII products and inhibitors in severe hemophilia A
    • Iorio A, Skinner MW, Makris M. Factor VIII products and inhibitors in severe hemophilia A. N Engl J Med. 2013;368(15):1456.
    • (2013) N Engl J Med , vol.368 , Issue.15 , pp. 1456
    • Iorio, A.1    Skinner, M.W.2    Makris, M.3
  • 16
    • 84876794924 scopus 로고    scopus 로고
    • The rodin (research of determinants of inhibitor development among pups with haemophilia) study: The clinical conundrum from the perspective of haemophilia treaters
    • Kessler CM, Iorio A. The Rodin (Research Of Determinants of INhibitor Development among PUPs with haemophilia) study: the clinical conundrum from the perspective of haemophilia treaters. Haemophilia. 2013;19(3):351-354.
    • (2013) Haemophilia , vol.19 , Issue.3 , pp. 351-354
    • Kessler, C.M.1    Iorio, A.2
  • 17
    • 84914174456 scopus 로고    scopus 로고
    • Accessed July 1, 2014
    • European Medicines Agency. Kogenate Bayer and Helixate NexGen. http://www.ema.europa.eu/ema/index.jsp?curl5pages/medicines/human/referrals/Kogenate-Bayer-and-Helixate-NexGen/human-referral-prac-000022.jsp.Accessed July 1, 2014.
    • Kogenate Bayer and Helixate NexGen
    • European Medicines Agency1
  • 18
    • 0035134654 scopus 로고    scopus 로고
    • The French haemophilia cohort: Rationale and organization of a long-term national pharmacosurveillance system
    • Calvez T, Biou M, Costagliola D, et al; Suivi Thérapeutique National des Hémophiles Group. The French haemophilia cohort: rationale and organization of a long-term national pharmacosurveillance system. Haemophilia. 2001;7(1):82-88.
    • (2001) Haemophilia , vol.7 , Issue.1 , pp. 82-88
    • Calvez, T.1    Biou, M.2    Costagliola, D.3
  • 19
    • 59449097322 scopus 로고    scopus 로고
    • How we treat a hemophilia A patient with a factor VIII inhibitor
    • Kempton CL, White GC II. How we treat a hemophilia A patient with a factor VIII inhibitor. Blood. 2009;113(1):11-17.
    • (2009) Blood , vol.113 , Issue.1 , pp. 11-17
    • Kempton, C.L.1    White, G.C.I.I.2
  • 20
    • 0025695593 scopus 로고
    • Relation of pooled logistic regression to time dependent cox regression analysis: The framingham heart study
    • D'Agostino RB, Lee ML, Belanger AJ, Cupples LA, Anderson K, Kannel WB. Relation of pooled logistic regression to time dependent Cox regression analysis: the Framingham Heart Study. Stat Med. 1990;9(12):1501-1515.
    • (1990) Stat Med , vol.9 , Issue.12 , pp. 1501-1515
    • D'agostino, R.B.1    Lee, M.L.2    Belanger, A.J.3    Cupples, L.A.4    Anderson, K.5    Kannel, W.B.6
  • 21
    • 0032583387 scopus 로고    scopus 로고
    • Extracting summary statistics to perform meta-analyses of the published literature for survival endpoints
    • Parmar MK, Torri V, Stewart L. Extracting summary statistics to perform meta-analyses of the published literature for survival endpoints. Stat Med. 1998;17(24):2815-2834.
    • (1998) Stat Med , vol.17 , Issue.24 , pp. 2815-2834
    • Parmar, M.K.1    Torri, V.2    Stewart, L.3
  • 23
    • 17944404210 scopus 로고    scopus 로고
    • Safety and efficacy of KOGENATE Bayer in previously untreated patients (PUPs) and minimally treated patients (MTPs)
    • Giangrande PLF; KOGENATE Bayer Study Group. Safety and efficacy of KOGENATE Bayer in previously untreated patients (PUPs) and minimally treated patients (MTPs). Haemophilia. 2002;8(Suppl 2):19-22.
    • (2002) Haemophilia , vol.8 , pp. 19-22
    • Plf, G.1
  • 24
    • 15344351616 scopus 로고    scopus 로고
    • Full-length sucrose-formulated recombinant factor VIII for treatment of previously untreated or minimally treated young children with severe haemophilia A: Results of an international clinical investigation
    • Kreuz W, Gill JC, Rothschild C, et al; International Kogenate-FS Study Group. Full-length sucrose-formulated recombinant factor VIII for treatment of previously untreated or minimally treated young children with severe haemophilia A: results of an international clinical investigation. Thromb Haemost. 2005;93(3):457-467.
    • (2005) Thromb Haemost , vol.93 , Issue.3 , pp. 457-467
    • Kreuz, W.1    Gill, J.C.2    Rothschild, C.3
  • 25
    • 38349109840 scopus 로고    scopus 로고
    • Safety and efficacy of sucrose-formulated full-length recombinant factor VIII: Experience in the standard clinical setting
    • Musso R, Santagostino E, Faradji A, et al; KOGENATE Bayer European PMS Study Group. Safety and efficacy of sucrose-formulated full-length recombinant factor VIII: experience in the standard clinical setting. Thromb Haemost. 2008;99(1):52-58.
    • (2008) Thromb Haemost , vol.99 , Issue.1 , pp. 52-58
    • Musso, R.1    Santagostino, E.2    Faradji, A.3
  • 26
    • 46849093433 scopus 로고    scopus 로고
    • An observational study of sucrose-formulated recombinant factor VIII for Japanese patients with haemophilia A
    • Delumeau J-C, Ikegawa C, Yokoyama C, Haupt V. An observational study of sucrose-formulated recombinant factor VIII for Japanese patients with haemophilia A. Thromb Haemost. 2008; 100(1):32-37.
    • (2008) Thromb Haemost , vol.100 , Issue.1 , pp. 32-37
    • Delumeau, J.-C.1    Ikegawa, C.2    Yokoyama, C.3    Haupt, V.4
  • 28
    • 33845773426 scopus 로고    scopus 로고
    • Prevalence of sporadic and familial haemophilia
    • Kasper CK, Lin JC. Prevalence of sporadic and familial haemophilia. Haemophilia. 2007;13(1): 90-92.
    • (2007) Haemophilia , vol.13 , Issue.1 , pp. 90-92
    • Kasper, C.K.1    Lin, J.C.2
  • 29
    • 84863419863 scopus 로고    scopus 로고
    • F8 gene mutation type and inhibitor development in patients with severe hemophilia A: Systematic review and meta-analysis
    • Gouw SC, van den Berg HM, Oldenburg J, et al. F8 gene mutation type and inhibitor development in patients with severe hemophilia A: systematic review and meta-analysis. Blood. 2012;119(12): 2922-2934.
    • (2012) Blood , vol.119 , Issue.12 , pp. 2922-2934
    • Gouw, S.C.1    Van Den Berg, H.M.2    Oldenburg, J.3
  • 30
    • 0031057651 scopus 로고    scopus 로고
    • HLA class II profile: A weak determinant of factor VIII inhibitor development in severe haemophilia A
    • Hay CR, Ollier W, Pepper L, et al; UKHCDO Inhibitor Working Party. HLA class II profile: a weak determinant of factor VIII inhibitor development in severe haemophilia A. Thromb Haemost. 1997;77(2):234-237.
    • (1997) Thromb Haemost , vol.77 , Issue.2 , pp. 234-237
    • Hay, C.R.1    Ollier, W.2    Pepper, L.3
  • 31
    • 0031045680 scopus 로고    scopus 로고
    • HLA genotype of patients with severe haemophilia A due to intron 22 inversion with and without inhibitors of factor VIII
    • Oldenburg J, Picard JK, Schwaab R, Brackmann HH, Tuddenham EG, Simpson E. HLA genotype of patients with severe haemophilia A due to intron 22 inversion with and without inhibitors of factor VIII. Thromb Haemost. 1997;77(2): 238-242.
    • (1997) Thromb Haemost , vol.77 , Issue.2 , pp. 238-242
    • Oldenburg, J.1    Picard, J.K.2    Schwaab, R.3    Brackmann, H.H.4    Tuddenham, E.G.5    Simpson, E.6
  • 32
    • 77449101167 scopus 로고    scopus 로고
    • Impact of polymorphisms of the major histocompatibility complex class II, interleukin-10, tumor necrosis factor-alpha and cytotoxic T-lymphocyte antigen-4 genes on inhibitor development in severe hemophilia A
    • Pavlova A, Delev D, Lacroix-Desmazes S, et al. Impact of polymorphisms of the major histocompatibility complex class II, interleukin-10, tumor necrosis factor-alpha and cytotoxic T-lymphocyte antigen-4 genes on inhibitor development in severe hemophilia A. J Thromb Haemost. 2009;7(12):2006-2015.
    • (2009) J Thromb Haemost , vol.7 , Issue.12 , pp. 2006-2015
    • Pavlova, A.1    Delev, D.2    Lacroix-Desmazes, S.3
  • 33
    • 79959494195 scopus 로고    scopus 로고
    • A case-control study reveals immunoregulatory gene haplotypes that influence inhibitor risk in severe haemophilia A
    • Lozier JN, Rosenberg PS, Goedert JJ, Menashe I. A case-control study reveals immunoregulatory gene haplotypes that influence inhibitor risk in severe haemophilia A. Haemophilia. 2011;17(4): 641-649.
    • (2011) Haemophilia , vol.17 , Issue.4 , pp. 641-649
    • Lozier, J.N.1    Rosenberg, P.S.2    Goedert, J.J.3    Menashe, I.4
  • 34
    • 84874393543 scopus 로고    scopus 로고
    • The polygenic nature of inhibitors in hemophilia a: Results from the hemophilia inhibitor genetics study (higs) combined cohort
    • Astermark J, Donfield SM, Gomperts ED, et al; Hemophilia Inhibitor Genetics Study (HIGS) Combined Cohort. The polygenic nature of inhibitors in hemophilia A: results from the Hemophilia Inhibitor Genetics Study (HIGS) Combined Cohort. Blood. 2013;121(8): 1446-1454.
    • (2013) Blood , vol.121 , Issue.8 , pp. 1446-1454
    • Astermark, J.1    Donfield, S.M.2    Gomperts, E.D.3
  • 35
    • 34249690732 scopus 로고    scopus 로고
    • Treatment-related risk factors of inhibitor development in previously untreated patients with hemophilia A: The CANAL cohort study
    • Gouw SC, van der Bom JG, Marijke van den Berg H. Treatment-related risk factors of inhibitor development in previously untreated patients with hemophilia A: the CANAL cohort study. Blood. 2007;109(11):4648-4654.
    • (2007) Blood , vol.109 , Issue.11 , pp. 4648-4654
    • Gouw, S.C.1    Van Der Bom, J.G.2    Marijke Van Den Berg, H.3
  • 36
    • 73449109462 scopus 로고    scopus 로고
    • Evolution of recombinant factor VIII safety: KOGENATE and Kogenate FS/Bayer
    • Lusher JM, Scharrer I. Evolution of recombinant factor VIII safety: KOGENATE and Kogenate FS/Bayer. Int J Hematol. 2009;90(4):446-454.
    • (2009) Int J Hematol , vol.90 , Issue.4 , pp. 446-454
    • Lusher, J.M.1    Scharrer, I.2
  • 37
    • 84880464142 scopus 로고    scopus 로고
    • Elucidating the role of carbohydrate determinants in regulating hemostasis: Insights and opportunities
    • Preston RJS, Rawley O, Gleeson EM, O'Donnell JS. Elucidating the role of carbohydrate determinants in regulating hemostasis: insights and opportunities. Blood. 2013;121(19): 3801-3810.
    • (2013) Blood , vol.121 , Issue.19 , pp. 3801-3810
    • Preston, R.J.S.1    Rawley, O.2    Gleeson, E.M.3    O'donnell, J.S.4
  • 38
    • 34547430130 scopus 로고    scopus 로고
    • A role for exposed mannosylations in presentation of human therapeutic self-proteins to CD4+ T lymphocytes
    • Dasgupta S, Navarrete A-M, Bayry J, et al. A role for exposed mannosylations in presentation of human therapeutic self-proteins to CD4+ T lymphocytes. Proc Natl Acad Sci USA. 2007;104(21): 8965-8970.
    • (2007) Proc Natl Acad Sci USA , vol.104 , Issue.21 , pp. 8965-8970
    • Dasgupta, S.1    Navarrete, A.-M.2    Bayry, J.3
  • 39
    • 64749096663 scopus 로고    scopus 로고
    • Inhibitors of factor VIII in black patients with hemophilia
    • Viel KR, Ameri A, Abshire TC, et al. Inhibitors of factor VIII in black patients with hemophilia. N Engl J Med. 2009;360(16):1618-1627.
    • (2009) N Engl J Med , vol.360 , Issue.16 , pp. 1618-1627
    • Viel, K.R.1    Ameri, A.2    Abshire, T.C.3
  • 40
    • 84871015816 scopus 로고    scopus 로고
    • F8 haplotype and inhibitor risk: Results from the hemophilia inhibitor genetics study (higs) combined cohort
    • Schwarz J, Astermark J, Menius ED, et al; Hemophilia Inhibitor Genetics Study Combined Cohort. F8 haplotype and inhibitor risk: results from the Hemophilia Inhibitor Genetics Study (HIGS) Combined Cohort. Haemophilia. 2013; 19(1):113-118.
    • (2013) Haemophilia , vol.19 , Issue.1 , pp. 113-118
    • Schwarz, J.1    Astermark, J.2    Menius, E.D.3
  • 41
    • 84876785042 scopus 로고    scopus 로고
    • In vitro characterization of recombinant factor VIII concentrates reveals significant differences in protein content, activity and thrombin activation profile
    • Pahl S, Pavlova A, Driesen J, Müller J, Pötzsch B, Oldenburg J. In vitro characterization of recombinant factor VIII concentrates reveals significant differences in protein content, activity and thrombin activation profile. Haemophilia. 2013;19(3):392-398.
    • (2013) Haemophilia , vol.19 , Issue.3 , pp. 392-398
    • Pahl, S.1    Pavlova, A.2    Driesen, J.3    Müller, J.4    Pötzsch, B.5    Oldenburg, J.6
  • 42
    • 84894045169 scopus 로고    scopus 로고
    • Second-generation recombinant factor VIII and inhibitor risk: Interpretation of RODIN study findings and implications for patients with haemophilia A
    • van der Bom JG, Gouw SC, Rosendaal FR. Second-generation recombinant factor VIII and inhibitor risk: interpretation of RODIN study findings and implications for patients with haemophilia A. Haemophilia. 2014;20(2): e171-e174.
    • (2014) Haemophilia , vol.20 , Issue.2 , pp. e171-e174
    • Van Der Bom, J.G.1    Gouw, S.C.2    Rosendaal, F.R.3
  • 43
    • 37149022850 scopus 로고    scopus 로고
    • Factor VIII products and inhibitor development: The SIPPET study (survey of inhibitors in plasma-product exposed toddlers)
    • Mannucci PM, Gringeri A, Peyvandi F, Santagostino E. Factor VIII products and inhibitor development: the SIPPET study (survey of inhibitors in plasma-product exposed toddlers). Haemophilia. 2007;13(Suppl 5):65-68.
    • (2007) Haemophilia , vol.13 , pp. 65-68
    • Mannucci, P.M.1    Gringeri, A.2    Peyvandi, F.3    Santagostino, E.4
  • 44
    • 84894261803 scopus 로고    scopus 로고
    • A study of prospective surveillance for inhibitors among persons with haemophilia in the united states
    • Soucie JM, Miller CH, Kelly FM, et al; Haemophilia Inhibitor Research Study Investigators. A study of prospective surveillance for inhibitors among persons with haemophilia in the United States. Haemophilia. 2014;20(2):230-237.
    • (2014) Haemophilia , vol.20 , Issue.2 , pp. 230-237
    • Soucie, J.M.1    Miller, C.H.2    Kelly, F.M.3
  • 45
    • 78650784094 scopus 로고    scopus 로고
    • EUHASS: The european haemophilia safety surveillance system
    • Makris M, Calizzani G, Fischer K, et al. EUHASS: The European Haemophilia Safety Surveillance system. Thromb Res. 2011;127(Suppl 2):S22-S25.
    • (2011) Thromb Res , vol.127 , pp. S22-S25
    • Makris, M.1    Calizzani, G.2    Fischer, K.3
  • 46
    • 84860320467 scopus 로고    scopus 로고
    • Validity of assessing inhibitor development in haemophilia PUPs using registry data: The EUHASS project
    • Fischer K, Lewandowski D, Marijke van den Berg H, Janssen MP. Validity of assessing inhibitor development in haemophilia PUPs using registry data: the EUHASS project. Haemophilia. 2012; 18(3):e241-e246.
    • (2012) Haemophilia , vol.18 , Issue.3 , pp. e241-e246
    • Fischer, K.1    Lewandowski, D.2    Marijke Van Den Berg, H.3    Janssen, M.P.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.