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Bispecific Antibody Emicizumab for Haemophilia A: A Breakthrough for Patients with Inhibitors

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Abstract

Current unmet needs in haemophilia A patients with inhibitors include the need for intravenous infusion of replacement therapy and the high burden of treatment associated with prophylaxis. Emicizumab is a humanised bispecific monoclonal antibody designed to address these unmet needs and has completed phase III clinical trials in adolescents/adults (HAVEN 1) and paediatric (HAVEN 2) inhibitor populations. In HAVEN 1, there was an 80% bleed reduction across all bleeds, 89% reduction in treated joint bleeds, 92% reduction in treated spontaneous bleeds, and 95% reduction in treated target joint bleeds on emicizumab compared with no prophylaxis. In HAVEN 2, there was a 63% reduction in all bleeds, 94.7% reduction in treated bleeds, 94.7% reduction in treated spontaneous bleeds, 100% reduction in treated joint bleeds, and 100% reduction in treated target joint bleeds on emicizumab prophylaxis when compared with no prophylaxis. For patients on bypassing agent prophylaxis, emicizumab resulted in a 68% reduction in bleeds in HAVEN 1 and a 100% reduction in bleed rates in HAVEN 2. In HAVEN 1, three patients developed thrombotic microangiopathy (TMA) and two developed thrombosis when emicizumab was used together with an activated prothrombin complex concentrate (aPCC) at high or frequent doses. When the combination was avoided in HAVEN 2, no patient developed TMA or thrombosis. In both studies, no anti-emicizumab antibodies developed and the pharmacokinetic profile of emicizumab was similar. Emicizumab use is currently being explored in haemophilia A patients without inhibitors as well as in combination with other haemophilia A replacement therapies. The role of emicizumab in combination with current factor VIII replacement therapies and evolving non-replacement therapies remains to be established.

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References

  1. Srivastava A, Brewer AK, Mauser-Bunschoten EP, Key NS, Kitchen S, Llinas A, et al. Guidelines for the management of hemophilia. Haemophilia. 2012;19(1):e1–47.

    Article  CAS  PubMed  Google Scholar 

  2. Iorio A, Krishnan S, Myrén K-J, Lethagen S, McCormick N, Yermakov S, et al. Continuous prophylaxis with recombinant factor IX Fc fusion protein and conventional recombinant factor IX products: comparisons of efficacy and weekly factor consumption. J Med Econ. 2017;20(4):337–44.

    Article  PubMed  Google Scholar 

  3. Ljung R, Fischer K, Carcao M, Santagostino E, Manco-Johnson MJ, Mathew P, et al. Practical considerations in choosing a factor VIII prophylaxis regimen: Role of clinical phenotype and trough levels. Thromb Haemost. 2016;115(5):913–20.

    Article  PubMed  Google Scholar 

  4. Carcao M. Changing paradigm of prophylaxis with longer acting factor concentrates. Haemophilia. 2014;20(Suppl 4):99–105.

    Article  CAS  PubMed  Google Scholar 

  5. Makris M. Prophylaxis in haemophilia should be life-long. Blood Transfus. 2012;10(2):165–8.

    PubMed  PubMed Central  Google Scholar 

  6. Manco-Johnson M. Comparing prophylaxis with episodic treatment in haemophilia A: implications for clinical practice. Haemophilia. 2007;13(Suppl 2):4–9.

    CAS  PubMed  Google Scholar 

  7. Ota S, McLimont M, Carcao MD, Blanchette VS, Graham N, Paradis E, et al. Definitions for haemophilia prophylaxis and its outcomes: the Canadian consensus study. Haemophilia. 2007;13(1):12–20.

    Article  CAS  PubMed  Google Scholar 

  8. Wyrwich KW, Krishnan S, Auguste P, Maltzahn R, Yu R, Bozkaya D, et al. Health-related quality of life data changes from baseline using HAEM-A-QOL scores in the A-LONG clinical study of recombinant factor VIII Fc fusion protein. Haemophilia. 2014;20:169.

    Google Scholar 

  9. Angelini D, Konkle BA, Sood SL. Aging among persons with hemophilia: contemporary concerns. Semin Hematol. 2016;53(1):35–9.

    Article  PubMed  Google Scholar 

  10. Di Minno G, Cerbone AM, Coppola A, Cimino E, Di Capua M, Pamparana F, et al. Longer-acting factor VIII to overcome limitations in haemophilia management: the PEGylated liposomes formulation issue. Haemophilia. 2010;16(Suppl 1):2–6.

    Article  PubMed  Google Scholar 

  11. Plug I, Van Der Bom JG, Peters M, Mauser-Bunschoten EP, De Goede-Bolder A, Heijnen L, et al. Mortality and causes of death in patients with hemophilia, 1992–2001: a prospective cohort study. J Thromb Haemost. 2006;4(3):510–6.

    Article  CAS  PubMed  Google Scholar 

  12. Oldenburg J, Kulkarni R, Srivastava A, Mahlangu JN, Blanchette VS, Tsao E, et al. Improved joint health in subjects with severe haemophilia A treated prophylactically with recombinant factor VIII Fc fusion protein. Haemophilia. 2018;24(1):77–84.

    Article  CAS  PubMed  Google Scholar 

  13. Carcao M, Hilliard P, Escobar MA, Solimeno L, Mahlangu J, Santagostino E. Optimising musculoskeletal care for patients with haemophilia. Eur J Haematol. 2015;95(Suppl 81):11–21.

    Article  CAS  PubMed  Google Scholar 

  14. DeKoven M, Karkare S, Lee WC, Kelley LA, Cooper DL, Pham H, et al. Impact of haemophilia with inhibitors on caregiver burden in the United States. Haemophilia. 2014;20(6):822–30.

    Article  CAS  PubMed  Google Scholar 

  15. Weatherall J, Barnes N, Brown C, Preaud E. Future characteristics of bypassing agents to improve care of hemophilia inhibitor patients: an economic and health-related quality of life perspective. Expert Rev Pharmacoecon Outcomes Res. 2011;11(4):411–4.

    Article  PubMed  Google Scholar 

  16. Kavakli K, Yesilipek A, Antmen B, Aksu S, Balkan C, Yilmaz D, et al. The value of early treatment in patients with haemophilia and inhibitors. Haemophilia. 2010;16(3):487–94.

    CAS  PubMed  Google Scholar 

  17. Hemophilia Goudemand J. Treatment of patients with inhibitors: cost issues. Haemophilia. 1999;5(6):397–401.

    Article  Google Scholar 

  18. Astermark J, Donfield SM, DiMichele DM, Gringeri A, Gilbert SA, Waters J, et al. A randomized comparison of bypassing agents in hemophilia complicated by an inhibitor: the FEIBA NovoSeven Comparative (FENOC) Study. Blood. 2007;109(2):546–51.

    Article  CAS  PubMed  Google Scholar 

  19. Wight J, Paisley S. The epidemiology of inhibitors in haemophilia A: a systematic review. Haemophilia. 2003;9(4):418–35.

    Article  CAS  PubMed  Google Scholar 

  20. Collins PW, Chalmers E, Hart DP, Liesner R, Rangarajan S, Talks K, et al. Diagnosis and treatment of factor VIII and IX inhibitors in congenital haemophilia: (4th edition). UK Haemophilia Centre Doctors Organization. Br J Haematol. 2013;160(2):153–70.

    Article  CAS  PubMed  Google Scholar 

  21. Bardi E, Astermark J. Genetic risk factors for inhibitors in haemophilia A. Eur J Haematol. 2015;94(Suppl 77):7–10.

    Article  CAS  PubMed  Google Scholar 

  22. Lochan A, Macaulay S, Chen WC, Mahlangu JN, Krause A. Genetic factors influencing inhibitor development in a cohort of South African haemophilia A patients. Haemophilia. 2014;20(5):687–92.

    Article  CAS  PubMed  Google Scholar 

  23. Lacroix-Desmazes S, Scott DW, Goudemand J, Van Den Berg M, Makris M, Van Velzen AS, et al. Summary report of the First International Conference on inhibitors in haemophilia A. Blood Transfus. 2017;15(6):568–76.

  24. van den Berg HM, Hashemi SM, Fischer K, Petrini P, Ljung R, Rafowicz A, et al. Increased inhibitor incidence in severe haemophilia A since 1990 attributable to more low titre inhibitors. Thromb Haemost. 2016;115(4):729–37.

    Article  PubMed  Google Scholar 

  25. Fischer K, van der Bom JG, Mauser-Bunschoten EP, Roosendaal G, Prejs R, Grobbee DE, et al. Changes in treatment strategies for severe haemophilia over the last 3 decades: effects on clotting factor consumption and arthropathy. Haemophilia. 2001;7(5):446–52.

    Article  CAS  PubMed  Google Scholar 

  26. Gringeri A, Ewenstein B, Reininger A. The burden of bleeding in haemophilia: is one bleed too many? Haemophilia. 2014;20(4):459–63.

    Article  CAS  PubMed  Google Scholar 

  27. Gater A, Thomson TA, Strandberg-Larsen M. Haemophilia B: impact on patients and economic burden of disease. Thromb Haemost. 2011;106(3):398–404.

    CAS  PubMed  Google Scholar 

  28. Darby SC, Kan SW, Spooner RJ, Giangrande PL, Hill FG, Hay CR, et al. Mortality rates, life expectancy, and causes of death in people with hemophilia A or B in the United Kingdom who were not infected with HIV. Blood. 2007;110(3):815–25.

    Article  CAS  PubMed  Google Scholar 

  29. Szeto CC, Kwan BC, Chow KM, Pang WF, Kwong VW, Leung CB, et al. Life expectancy of Chinese patients with chronic kidney disease without dialysis. Nephrology (Carlton). 2011;16(8):715–9.

    Article  PubMed  Google Scholar 

  30. Witmer CM. Low mortality from intracranial haemorrhage in paediatric patients with haemophilia. Haemophilia. 2015;21(5):e359–63.

    Article  CAS  PubMed  Google Scholar 

  31. Ljung RC. Intracranial haemorrhage in haemophilia A and B. Br J Haematol. 2008;140(4):378–84.

    Article  PubMed  Google Scholar 

  32. Traivaree C, Blanchette V, Armstrong D, Floros G, Stain AM, Carcao MD. Intracranial bleeding in haemophilia beyond the neonatal period–the role of CT imaging in suspected intracranial bleeding. Haemophilia. 2007;13(5):552–9.

    Article  CAS  PubMed  Google Scholar 

  33. Tarantino MD, Gupta SL, Brusky RM. The incidence and outcome of intracranial haemorrhage in newborns with haemophilia: analysis of the Nationwide Inpatient Sample database. Haemophilia. 2007;13(4):380–2.

    Article  CAS  PubMed  Google Scholar 

  34. Zanon E, Milan M, Brandolin B, Barbar S, Spiezia L, Saggiorato G, et al. High dose of human plasma-derived FVIII-VWF as first-line therapy in patients affected by acquired haemophilia A and concomitant cardiovascular disease: four case reports and a literature review. Haemophilia. 2013;19(1):e50–3.

    Article  CAS  PubMed  Google Scholar 

  35. Morfini M, Haya S, Tagariello G, Pollmann H, Quintana M, Siegmund B, et al. European study on orthopaedic status of haemophilia patients with inhibitors. Haemophilia. 2007;13(5):606–12.

    Article  CAS  PubMed  Google Scholar 

  36. McCarthy A, Moore A, Redhead L, McLaughlin P, Iorio A, Chowdary P. Development of haemophilic arthropathy of the ankle: results of a Delphi consensus survey on potential contributory factors. Haemophilia. 2015;21(1):116–23.

    Article  CAS  PubMed  Google Scholar 

  37. Teitel JM, Carcao M, Lillicrap D, Mulder K, Rivard GE, St-Louis J, et al. Orthopaedic surgery in haemophilia patients with inhibitors: a practical guide to haemostatic, surgical and rehabilitative care. Haemophilia. 2009;15(1):227–39.

    Article  CAS  PubMed  Google Scholar 

  38. Santagostino E, Mancuso ME, Novembrino C, Anzoletti Boscolo M, Clerici M, Pasta G, et al. Management of Joint Replacement in Hemophilia a with Inhibitors during Emicizumab Prophylaxis. Blood. 2017;130(Suppl 1):2360.

    Google Scholar 

  39. Iorio A, Barbara AM, Makris M, Fischer K, Castaman G, Catarino C, et al. Natural history and clinical characteristics of inhibitors in previously treated haemophilia A patients: a case series. Haemophilia. 2017;23(2):255–63.

    Article  CAS  PubMed  Google Scholar 

  40. Escobar M, Colberg T, Karim F, Caliskan U, Chowdary P, Giangrande P, et al. Perioperative hemostatic management of major surgery in hemophilia B with long-acting recombinant glycopegylated factor IX: results from the paradigm (TM) 3 clinical trial. J Thromb Haemost. 2015;13:229.

    Google Scholar 

  41. Guideline for the management of haemophilia in Australia. Australian Haemophilia Centre Directors’ Organisation, 2016.

  42. von Mackensen S, Seifert W. Health-related quality of life in pediatric hemophilia B patients treated with rIX-FP. Res Pract Thromb Haemost. 2017;1(1 Supp 1):767.

  43. Carcao M, Kearney S, Santagostino E, Oyesiku JOO, Young NL, Meunier J, et al. Insight into health-related quality of life of young children with haemophilia B treated with long-acting nonacog beta pegol recombinant factor IX. Haemophilia. 2017;23(3):e222–4.

    Article  CAS  PubMed  Google Scholar 

  44. Young J, Grabell J, Rydz N, Hopman W, Good D, Mahlangu J, et al. Relationship between quality of life and coagulation factor level in hemophilia carriers: preliminary results. J Thromb Haemost. 2015;13:590.

    Article  CAS  Google Scholar 

  45. Witt CM, Ausserer O, Baier S, Heidegger H, Icke K, Mayr O, et al. Effectiveness of an additional individualized multi-component complementary medicine treatment on health-related quality of life in breast cancer patients: a pragmatic randomized trial. Breast Cancer Res Treat. 2015;149(2):449–60.

    Article  PubMed  Google Scholar 

  46. Mishra SI, Scherer RW, Snyder C, Geigle P, Gotay C. The effectiveness of exercise interventions for improving health-related quality of life from diagnosis through active cancer treatment. Oncol Nurs Forum. 2015;42(1):E33–53.

    Article  PubMed  Google Scholar 

  47. Kobiela J, Kaska L, Pindel M, Szarmach A, Janiak M, Proczko-Markuszewska M, et al. Dynamics of quality of life improvement after floppy Nissen fundoplication for gastroesophageal reflux disease. Wideochir Inne Tech Maloinwazyjne. 2015;10(3):389–97.

    PubMed  PubMed Central  Google Scholar 

  48. Hajek A, Brettschneider C, Ernst A, Lange C, Wiese B, Prokein J, et al. Complex coevolution of depression and health-related quality of life in old age. Qual Life Res. 2015;24(11):2713–22.

    Article  PubMed  Google Scholar 

  49. Gray WN, Boyle SL, Graef DM, Janicke DM, Jolley CD, Denson LA, et al. Health-related quality of life in youth with Crohn disease: role of disease activity and parenting stress. J Pediatr Gastroenterol Nutr. 2015;60(6):749–53.

    Article  PubMed  PubMed Central  Google Scholar 

  50. Granstrom T, Forsman H, Leksell J, Jani S, Raghib AM, Granstam E. Visual functioning and health-related quality of life in diabetic patients about to undergo anti-vascular endothelial growth factor treatment for sight-threatening macular edema. J Diabetes Complications. 2015;29(8):1183–90.

    Article  PubMed  Google Scholar 

  51. Eisele M, Kaduszkiewicz H, Konig HH, Lange C, Wiese B, Prokein J, et al. Determinants of health-related quality of life in older primary care patients: results of the longitudinal observational AgeCoDe Study. Br J Gen Pract. 2015;65(640):e716–23.

    Article  PubMed  PubMed Central  Google Scholar 

  52. Srivastava A, Brewer AK, Mauser-Bunschoten EP, Key NS, Kitchen S, Llinas A, et al. Guidelines for the management of hemophilia. Haemophilia. 2013;19(1):e1–47.

    Article  CAS  PubMed  Google Scholar 

  53. Shulman R, McKenzie CA, Landa J, Bourne RS, Jones A, Borthwick M, et al. Pharmacist’s review and outcomes: Treatment-enhancing contributions tallied, evaluated, and documented (PROTECTED-UK). J Crit Care. 2015;30(4):808–13.

    Article  CAS  PubMed  Google Scholar 

  54. Santagostino E, Escobar M, Ozelo M, Solimeno L, Arkhammar P, Lee HY, et al. Recombinant activated factor VII in the treatment of bleeds and for the prevention of surgery-related bleeding in congenital haemophilia with inhibitors. Blood Rev. 2015;29(Suppl 1):S9–18.

    Article  CAS  PubMed  Google Scholar 

  55. Blanchette VS, O’Mahony B, McJames L, Mahlangu JN. Assessment of outcomes. Haemophilia. 2014;20(Suppl 4):114–20.

    Article  PubMed  Google Scholar 

  56. Kempton CL, Meeks SL. Toward optimal therapy for inhibitors in hemophilia. Hematology Am Soc Hematol Educ Program. 2014;2014(1):364–71.

    Article  PubMed  Google Scholar 

  57. Jimenez-Yuste V, Oldenburg J, Rangarajan S, Peiro-Jordan R, Santagostino E. Long-term outcome of haemophilia A patients after successful immune tolerance induction therapy using a single plasma-derived FVIII/VWF product: the long-term ITI study. Haemophilia. 2016;22(6):859–65.

    Article  CAS  PubMed  Google Scholar 

  58. Jimenez-Yuste V, Oldenburg J, Rangarajan S, Kurth MH, Bozzo J, Santagostino E. Clinical overview of Fanhdi/Alphanate (plasma-derived, VWF-containing FVIII concentrate) in immune tolerance induction in haemophilia A patients with inhibitors. Haemophilia. 2016;22(1):e71–4.

    Article  CAS  PubMed  Google Scholar 

  59. Barnes C, Brown SA, Curtin J, Dunkley S. When is enough…enough? Developing consensus of definition of failure of immune tolerance induction in patients with haemophilia and inhibitors. Haemophilia. 2014;20(4):e275–9.

  60. Athale AH, Marcucci M, Iorio A. Immune tolerance induction for treating inhibitors in people with congenital haemophilia A or B. Cochrane Database Syst Rev. 2014;4:CD010561.

  61. Walsh CE, Jimenez-Yuste V, Auerswald G, Grancha S. The burden of inhibitors in haemophilia patients. Thromb Haemost. 2016;31(116 Suppl 1):S10–7.

    Article  Google Scholar 

  62. Uchida N, Sambe T, Yoneyama K, Fukazawa N, Kawanishi T, Kobayashi S, et al. A first-in-human phase 1 study of ACE910, a novel factor VIII-mimetic bispecific antibody, in healthy subjects. Blood. 2016;127(13):1633–41.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  63. Nogami K. Bispecific antibody mimicking factor VIII. Thromb Res. 2016;141(Suppl 2):S34–5.

    Article  CAS  PubMed  Google Scholar 

  64. Shima M, Hermans C, de Moerloose P. Novel products for haemostasis. Haemophilia. 2014;20(Suppl 4):29–35.

    Article  CAS  PubMed  Google Scholar 

  65. Muto A, Yoshihashi K, Takeda M, Kitazawa T, Soeda T, Igawa T, et al. Anti-factor IXa/X bispecific antibody (ACE910): hemostatic potency against ongoing bleeds in a hemophilia A model and the possibility of routine supplementation. J Thromb Haemost. 2014;12(2):206–13.

    Article  CAS  PubMed  Google Scholar 

  66. Lenting PJ, Denis CV, Christophe OD. Emicizumab, a bispecific antibody recognizing coagulation factors IX and X: how does it actually compare to factor VIII? Blood. 2017;130(23):2463–8.

    Article  CAS  PubMed  Google Scholar 

  67. Kitazawa T, Esaki K, Tachibana T, Ishii S, Soeda T, Muto A, et al. Factor VIIIa-mimetic cofactor activity of a bispecific antibody to factors IX/IXa and X/Xa, emicizumab, depends on its ability to bridge the antigens. Thromb Haemost. 2017;117(7):1348–57.

    Article  PubMed  Google Scholar 

  68. Sampei Z, Igawa T, Soeda T, Okuyama-Nishida Y, Moriyama C, Wakabayashi T, et al. Identification and multidimensional optimization of an asymmetric bispecific IgG antibody mimicking the function of factor VIII cofactor activity. PLoS One. 2013;8(2):e574–79.

    Article  CAS  Google Scholar 

  69. Oldenburg J, Mahlangu JN, Kim B, Schmitt C, Callaghan MU, Young G, et al. Emicizumab prophylaxis in hemophilia A with inhibitors. N Engl J Med. 2017;377(9):809–18.

    Article  CAS  PubMed  Google Scholar 

  70. Young G, Sidonio RF, Liesner R, Oldenburg J, Chang T, Uguen M, et al. HAVEN 2 updated analysis: multicenter, open-label, phase 3 study to evaluate efficacy, safety and pharmacokinetics of subcutaneous administration of emicizumab prophylaxis in pediatric patients with hemophilia A with inhibitors. Blood. 2017;130(Suppl 1):85.

    Google Scholar 

  71. Pipe SJ, Shapiro A, et al. . Emicizumab subcutaneous dosing every 4 weeks is safe and efficacious in the control of bleeding in persons with haemophilia A with and without inhibitors- results from the phase 3 HAVEN 4 study. In: Kessler M, editor. 2018 world congress of the World Federation Hemophilia. Glasgow, United Kingdom; 2018.

  72. Mahlangu J, Oldenburg J, Paz-Priel I, Negrier C, Niggli M, Mancuso ME, et al. Emicizumab prophylaxis in patients who have hemophilia A without inhibitors. N Engl J Med. 2018;379(9):811–22.

    Article  CAS  PubMed  Google Scholar 

  73. Hartmann R, Feenstra T, Valentino L, Dockal M, Scheiflinger F. In vitro studies show synergistic effects of a procoagulant bispecific antibody and bypassing agents. J Thromb Haemost. 2018. https://doi.org/10.1111/jth.14203.

    Article  PubMed  Google Scholar 

  74. Rebecca Kruse-Jarres MUC, Stacy E. Croteau, Victor Jimenez-Yuste, Liane Khoo, Ri Liesner, Tadashi Matsushita, Michael Recht, Guy Young, Tiffany Chang, Christophe Dhalluin, Yunming Mu, Jin Xu, Jenny Devenport, Richard H. Ko, Paul Solari and Johannes Oldenburg. Surgical Experience in Two Multicenter, Open-Label Phase 3 Studies of Emicizumab in Persons with Hemophilia A with Inhibitors (HAVEN 1 and HAVEN 2). Blood. 2017;130:89.

  75. Collins PW, Liesner R, Makris M, Talks K, Chowdary P, Chalmers E, et al. Treatment of bleeding episodes in haemophilia A complicated by a factor VIII inhibitor in patients receiving Emicizumab. Interim guidance from UKHCDO Inhibitor Working Party and Executive Committee. Haemophilia. 2018;24(3):344–7.

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Mahlangu, J.N. Bispecific Antibody Emicizumab for Haemophilia A: A Breakthrough for Patients with Inhibitors. BioDrugs 32, 561–570 (2018). https://doi.org/10.1007/s40259-018-0315-0

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