Prophylaxis in children with haemophilia in an evolving treatment landscape

被引:14
作者
Mancuso, Maria Elisa [1 ]
Male, Christoph [2 ]
Kenet, Gili [3 ]
Kavakli, Kaan [4 ]
Koenigs, Christoph [5 ]
Blatny, Jan [6 ,7 ]
Fijnvandraat, Karin [8 ]
机构
[1] IRCCS Humanitas Res Hosp, Ctr Thrombosis & Haemorrhag Dis, Milan, Italy
[2] Med Univ Vienna, Dept Paediat, Thrombosis Haemostasis Unit, Vienna, Austria
[3] Tel Aviv Univ, Sheba Med Ctr, Amalia Biron Thrombosis Res Inst, Natl Haemophilia Ctr, Tel Hashomer, Israel
[4] Ege Univ, Childrens Hosp, Dept Haematol, Fac Med, Izmir, Turkey
[5] Goethe Univ, Univ Hosp Frankfurt, Dept Paediat & Adolescent Med, Clin & Mol Haemostasis, Frankfurt, Germany
[6] Univ Hosp Brno, Dept Paediat Haematol & Biochem, Brno, Czech Republic
[7] Masaryk Univ, Brno, Czech Republic
[8] Univ Amsterdam, Amsterdam UMC, Emma Childrens Hosp, Dept Paediat Haematol, Amsterdam, Netherlands
关键词
arthropathy; children; EHL factor concentrate; haemophilia; non-replacement therapy; prophylaxis; RECOMBINANT FACTOR-VIII; INHERITED BLEEDING DISORDERS; COAGULATION-FACTOR IX; INTRACRANIAL HEMORRHAGE; INHIBITOR DEVELOPMENT; RIX-FP; COMMUNICATION; OUTCOMES; SAFETY; ADULTS;
D O I
10.1111/hae.14412
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction For children with haemophilia, early initiation of prophylaxis is crucial to prevent life-threatening bleeds and maintain joint health throughout life. Options for prophylaxis have recently increased from replacement therapy with standard or extended half-life coagulation factor products to include other haemostasis products, such as the non-replacement therapy emicizumab. Aim To review key factors that determine the choice of prophylaxis in young children. Methods Key clinical questions on the implementation of prophylaxis for haemophilia in children were identified and PubMed was searched for evidence supporting guidance on the implementation of prophylaxis. Results The results of the literature search and the practical experience of the authors were used to build consensus on when to start prophylaxis, the pros and cons of the products available to guide the choice of product, and practical aspects of starting prophylaxis to guide the choice of regimen. Conclusions In this era of increasing therapeutic choices, available information about the range of treatment options must be considered when initiating prophylaxis in young children. Parents or care givers must be sufficiently informed to allow informed shared decision making. Although plentiful data and clinical experience have been gathered on prophylaxis with clotting factor replacement therapy, its use in young children brings practical challenges, such as the need for intravenous administration. In contrast, our relatively brief experience and limited data with subcutaneously administered non-replacement therapy (i.e., emicizumab) in this patient group imply that starting emicizumab prophylaxis in young children requires careful consideration, despite the more convenient route of administration.
引用
收藏
页码:889 / 896
页数:8
相关论文
共 60 条
[21]   Tailored frequency-escalated primary prophylaxis for severe haemophilia A: results of the 16-year Canadian Hemophilia Prophylaxis Study longitudinal cohort [J].
Feldman, Brian M. ;
Rivard, Georges E. ;
Babyn, Paul ;
Wu, John K. M. ;
Steele, MacGregor ;
Poon, Man-Chiu ;
Card, Robert T. ;
Israels, Sara J. ;
Laferriere, Nicole ;
Gill, Kulwant ;
Chan, Anthony K. ;
Carcao, Manuel ;
Klaassen, Robert J. ;
Cloutier, Stephanie ;
Price, Victoria E. ;
Dover, Saunya ;
Blanchette, Victor S. .
LANCET HAEMATOLOGY, 2018, 5 (06) :E252-E260
[22]   When and how to start prophylaxis in boys with severe hemophilia without inhibitors: communication from the SSC of the ISTH [J].
Fischer, K. ;
Collins, P. W. ;
Ozelo, M. C. ;
Srivastava, A. ;
Young, G. ;
Blanchette, V. S. .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2016, 14 (05) :1105-1109
[23]  
Franchini M, 2010, BLOOD TRANSFUS-ITALY, V8, P292, DOI [10.2450/2010.0067-10, 10.2450/2010.0067.10]
[24]   Intensity of factor VIII treatment and inhibitor development in children with severe hemophilia A: the RODIN study [J].
Gouw, Samantha C. ;
van den Berg, H. Marijke ;
Fischer, Kathelijn ;
Auerswald, Guenter ;
Carcao, Manuel ;
Chalmers, Elizabeth ;
Chambost, Herve ;
Kurnik, Karin ;
Liesner, Ri ;
Petrini, Pia ;
Platokouki, Helen ;
Altisent, Carmen ;
Oldenburg, Johannes ;
Nolan, Beatrice ;
Perez Garrido, Rosario ;
Mancuso, M. Elisa ;
Rafowicz, Anne ;
Williams, Mike ;
Clausen, Niels ;
Middelburg, Rutger A. ;
Ljung, Rolf ;
van der Bom, Johanna G. .
BLOOD, 2013, 121 (20) :4046-4055
[25]   Factor VIII Products and Inhibitor Development in Severe Hemophilia A [J].
Gouw, Samantha C. ;
van der Bom, Johanna G. ;
Ljung, Rolf ;
Escuriola, Carmen ;
Cid, Ana R. ;
Claeyssens-Donadel, Segolene ;
van Geet, Christel ;
Kenet, Gili ;
Makipernaa, Anne ;
Molinari, Angelo Claudio ;
Muntean, Wolfgang ;
Kobelt, Rainer ;
Rivard, George ;
Santagostino, Elena ;
Thomas, Angela ;
van den Berg, H. Marijke .
NEW ENGLAND JOURNAL OF MEDICINE, 2013, 368 (03) :231-239
[26]   Factor VIII safety: plasma-derived versus recombinant products [J].
Gringeri, Alessandro .
BLOOD TRANSFUSION, 2011, 9 (04) :366-370
[27]   Long-Term Safety and Efficacy of Recombinant Coagulation Factor IX Albumin Fusion Protein (rIX-FP) in Previously Treated Pediatric Patients with Hemophilia B: Results from a Phase 3b Extension Study [J].
Kenet, Gili ;
Chambost, Herve ;
Male, Christoph ;
Halimeh, Susan ;
Lambert, Thierry ;
Li, Yanyan ;
Seifert, Wilfried ;
Santagostino, Elena .
THROMBOSIS AND HAEMOSTASIS, 2020, 120 (04) :599-606
[28]   Long-acting recombinant fusion protein linking coagulation factor IX with albumin (rIX-FP) in children Results of a phase 3 trial [J].
Kenet, Gili ;
Chambost, Herve ;
Male, Christoph ;
Lambert, Thierry ;
Halimeh, Susan ;
Chernova, Tatiana ;
Mancuso, Maria Elisa ;
Curtin, Julie ;
Voigt, Christine ;
Li, Yanyan ;
Jacobs, Iris ;
Santagostino, Elena .
THROMBOSIS AND HAEMOSTASIS, 2016, 116 (04) :659-668
[29]   HOw Patients view Extended half-life products: Impressions from real-world experience (The HOPE study) [J].
Khair, Kate ;
Pollard, Debra ;
Harrison, Catherine ;
Hook, Susan ;
O'Driscoll, Mike ;
Holland, Michael .
HAEMOPHILIA, 2019, 25 (05) :814-820
[30]   BIVV001 Fusion Protein as Factor VIII Replacement Therapy for Hemophilia A [J].
Konkle, Barbara A. ;
Shapiro, Amy D. ;
Quon, Doris V. ;
Staber, Janice M. ;
Kulkarni, Roshni ;
Ragni, Margaret V. ;
Chhabra, Ekta S. ;
Poloskey, Stacey ;
Rice, Kara ;
Katragadda, Suresh ;
Fruebis, Joachim ;
Benson, Craig C. .
NEW ENGLAND JOURNAL OF MEDICINE, 2020, 383 (11) :1018-1027