Improved joint health in subjects with severe haemophilia A treated prophylactically with recombinant factor VIII Fc fusion protein

Introduction Joint arthropathy is the long‐term consequence of joint bleeding in people with severe haemophilia. Aim This study assessed change in joint health over time in subjects receiving recombinant factor VIII Fc fusion protein (rFVIIIFc) prophylaxis. Methods ALONG is the phase 3 pivotal study...

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Published inHaemophilia : the official journal of the World Federation of Hemophilia Vol. 24; no. 1; pp. 77 - 84
Main Authors Oldenburg, J., Kulkarni, R., Srivastava, A., Mahlangu, J. N., Blanchette, V. S., Tsao, E., Winding, B., Dumont, J., Jain, N.
Format Journal Article
LanguageEnglish
Published England Wiley Subscription Services, Inc 01.01.2018
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Abstract Introduction Joint arthropathy is the long‐term consequence of joint bleeding in people with severe haemophilia. Aim This study assessed change in joint health over time in subjects receiving recombinant factor VIII Fc fusion protein (rFVIIIFc) prophylaxis. Methods ALONG is the phase 3 pivotal study in which the benefit of rFVIIIFc as a prophylactic treatment for bleeding control was shown in previously treated severe haemophilia patients ≥12 years of age (arm 1: 25‐65 IU/kg every 3‐5 days, arm 2: 65 IU/kg weekly and arm 3: episodic). After completing ALONG, subjects had the option to enrol into the extension study (ASPIRE). This interim, post hoc analysis assessed changes in joint health over ~2.8 years in these patients. Results Forty‐seven subjects had modified Haemophilia Joint Health Score (mHJHS) data at A‐LONG baseline, ASPIRE baseline and ASPIRE Year 1 and Year 2. Compared with A‐LONG baseline (23.4), mean improvement at ASPIRE Year 2 was −4.1 (95% confidence interval [CI], −6.5, −1.8; P = .001). Regardless of prestudy treatment regimen, subjects showed continuous improvement in mHJHS from A‐LONG baseline through ASPIRE Year 2 (prestudy prophylaxis: −2.4, P = .09; prestudy episodic treatment: −7.2, P = .003). Benefits were seen in subjects with target joints (−5.6, P = .005) as well as those with severe arthropathy (−8.8, P = .02). The mHJHS components with the greatest improvement at ASPIRE Year 2 were swelling (−1.4, P = .008), range of motion (−1.1, P = .03) and strength (−0.8, P = .04). Conclusions Prophylaxis with rFVIIIFc may improve joint health over time regardless of prestudy prophylaxis or episodic treatment regimens.
AbstractList Introduction Joint arthropathy is the long‐term consequence of joint bleeding in people with severe haemophilia. Aim This study assessed change in joint health over time in subjects receiving recombinant factor VIII Fc fusion protein (rFVIIIFc) prophylaxis. Methods ALONG is the phase 3 pivotal study in which the benefit of rFVIIIFc as a prophylactic treatment for bleeding control was shown in previously treated severe haemophilia patients ≥12 years of age (arm 1: 25‐65 IU/kg every 3‐5 days, arm 2: 65 IU/kg weekly and arm 3: episodic). After completing ALONG, subjects had the option to enrol into the extension study (ASPIRE). This interim, post hoc analysis assessed changes in joint health over ~2.8 years in these patients. Results Forty‐seven subjects had modified Haemophilia Joint Health Score (mHJHS) data at A‐LONG baseline, ASPIRE baseline and ASPIRE Year 1 and Year 2. Compared with A‐LONG baseline (23.4), mean improvement at ASPIRE Year 2 was −4.1 (95% confidence interval [CI], −6.5, −1.8; P = .001). Regardless of prestudy treatment regimen, subjects showed continuous improvement in mHJHS from A‐LONG baseline through ASPIRE Year 2 (prestudy prophylaxis: −2.4, P = .09; prestudy episodic treatment: −7.2, P = .003). Benefits were seen in subjects with target joints (−5.6, P = .005) as well as those with severe arthropathy (−8.8, P = .02). The mHJHS components with the greatest improvement at ASPIRE Year 2 were swelling (−1.4, P = .008), range of motion (−1.1, P = .03) and strength (−0.8, P = .04). Conclusions Prophylaxis with rFVIIIFc may improve joint health over time regardless of prestudy prophylaxis or episodic treatment regimens.
Joint arthropathy is the long-term consequence of joint bleeding in people with severe haemophilia. This study assessed change in joint health over time in subjects receiving recombinant factor VIII Fc fusion protein (rFVIIIFc) prophylaxis. ALONG is the phase 3 pivotal study in which the benefit of rFVIIIFc as a prophylactic treatment for bleeding control was shown in previously treated severe haemophilia patients ≥12 years of age (arm 1: 25-65 IU/kg every 3-5 days, arm 2: 65 IU/kg weekly and arm 3: episodic). After completing ALONG, subjects had the option to enrol into the extension study (ASPIRE). This interim, post hoc analysis assessed changes in joint health over ~2.8 years in these patients. Forty-seven subjects had modified Haemophilia Joint Health Score (mHJHS) data at A-LONG baseline, ASPIRE baseline and ASPIRE Year 1 and Year 2. Compared with A-LONG baseline (23.4), mean improvement at ASPIRE Year 2 was -4.1 (95% confidence interval [CI], -6.5, -1.8; P = .001). Regardless of prestudy treatment regimen, subjects showed continuous improvement in mHJHS from A-LONG baseline through ASPIRE Year 2 (prestudy prophylaxis: -2.4, P = .09; prestudy episodic treatment: -7.2, P = .003). Benefits were seen in subjects with target joints (-5.6, P = .005) as well as those with severe arthropathy (-8.8, P = .02). The mHJHS components with the greatest improvement at ASPIRE Year 2 were swelling (-1.4, P = .008), range of motion (-1.1, P = .03) and strength (-0.8, P = .04). Prophylaxis with rFVIIIFc may improve joint health over time regardless of prestudy prophylaxis or episodic treatment regimens.
Joint arthropathy is the long-term consequence of joint bleeding in people with severe haemophilia.INTRODUCTIONJoint arthropathy is the long-term consequence of joint bleeding in people with severe haemophilia.This study assessed change in joint health over time in subjects receiving recombinant factor VIII Fc fusion protein (rFVIIIFc) prophylaxis.AIMThis study assessed change in joint health over time in subjects receiving recombinant factor VIII Fc fusion protein (rFVIIIFc) prophylaxis.ALONG is the phase 3 pivotal study in which the benefit of rFVIIIFc as a prophylactic treatment for bleeding control was shown in previously treated severe haemophilia patients ≥12 years of age (arm 1: 25-65 IU/kg every 3-5 days, arm 2: 65 IU/kg weekly and arm 3: episodic). After completing ALONG, subjects had the option to enrol into the extension study (ASPIRE). This interim, post hoc analysis assessed changes in joint health over ~2.8 years in these patients.METHODSALONG is the phase 3 pivotal study in which the benefit of rFVIIIFc as a prophylactic treatment for bleeding control was shown in previously treated severe haemophilia patients ≥12 years of age (arm 1: 25-65 IU/kg every 3-5 days, arm 2: 65 IU/kg weekly and arm 3: episodic). After completing ALONG, subjects had the option to enrol into the extension study (ASPIRE). This interim, post hoc analysis assessed changes in joint health over ~2.8 years in these patients.Forty-seven subjects had modified Haemophilia Joint Health Score (mHJHS) data at A-LONG baseline, ASPIRE baseline and ASPIRE Year 1 and Year 2. Compared with A-LONG baseline (23.4), mean improvement at ASPIRE Year 2 was -4.1 (95% confidence interval [CI], -6.5, -1.8; P = .001). Regardless of prestudy treatment regimen, subjects showed continuous improvement in mHJHS from A-LONG baseline through ASPIRE Year 2 (prestudy prophylaxis: -2.4, P = .09; prestudy episodic treatment: -7.2, P = .003). Benefits were seen in subjects with target joints (-5.6, P = .005) as well as those with severe arthropathy (-8.8, P = .02). The mHJHS components with the greatest improvement at ASPIRE Year 2 were swelling (-1.4, P = .008), range of motion (-1.1, P = .03) and strength (-0.8, P = .04).RESULTSForty-seven subjects had modified Haemophilia Joint Health Score (mHJHS) data at A-LONG baseline, ASPIRE baseline and ASPIRE Year 1 and Year 2. Compared with A-LONG baseline (23.4), mean improvement at ASPIRE Year 2 was -4.1 (95% confidence interval [CI], -6.5, -1.8; P = .001). Regardless of prestudy treatment regimen, subjects showed continuous improvement in mHJHS from A-LONG baseline through ASPIRE Year 2 (prestudy prophylaxis: -2.4, P = .09; prestudy episodic treatment: -7.2, P = .003). Benefits were seen in subjects with target joints (-5.6, P = .005) as well as those with severe arthropathy (-8.8, P = .02). The mHJHS components with the greatest improvement at ASPIRE Year 2 were swelling (-1.4, P = .008), range of motion (-1.1, P = .03) and strength (-0.8, P = .04).Prophylaxis with rFVIIIFc may improve joint health over time regardless of prestudy prophylaxis or episodic treatment regimens.CONCLUSIONSProphylaxis with rFVIIIFc may improve joint health over time regardless of prestudy prophylaxis or episodic treatment regimens.
Introduction Joint arthropathy is the long-term consequence of joint bleeding in people with severe haemophilia. Aim This study assessed change in joint health over time in subjects receiving recombinant factor VIII Fc fusion protein (rFVIIIFc) prophylaxis. Methods ALONG is the phase 3 pivotal study in which the benefit of rFVIIIFc as a prophylactic treatment for bleeding control was shown in previously treated severe haemophilia patients ≥12 years of age (arm 1: 25-65 IU/kg every 3-5 days, arm 2: 65 IU/kg weekly and arm 3: episodic). After completing ALONG, subjects had the option to enrol into the extension study (ASPIRE). This interim, post hoc analysis assessed changes in joint health over ~2.8 years in these patients. Results Forty-seven subjects had modified Haemophilia Joint Health Score (mHJHS) data at A-LONG baseline, ASPIRE baseline and ASPIRE Year 1 and Year 2. Compared with A-LONG baseline (23.4), mean improvement at ASPIRE Year 2 was -4.1 (95% confidence interval [CI], -6.5, -1.8; P = .001). Regardless of prestudy treatment regimen, subjects showed continuous improvement in mHJHS from A-LONG baseline through ASPIRE Year 2 (prestudy prophylaxis: -2.4, P = .09; prestudy episodic treatment: -7.2, P = .003). Benefits were seen in subjects with target joints (-5.6, P = .005) as well as those with severe arthropathy (-8.8, P = .02). The mHJHS components with the greatest improvement at ASPIRE Year 2 were swelling (-1.4, P = .008), range of motion (-1.1, P = .03) and strength (-0.8, P = .04). Conclusions Prophylaxis with rFVIIIFc may improve joint health over time regardless of prestudy prophylaxis or episodic treatment regimens.
Author Srivastava, A.
Winding, B.
Jain, N.
Kulkarni, R.
Mahlangu, J. N.
Blanchette, V. S.
Dumont, J.
Oldenburg, J.
Tsao, E.
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  surname: Mahlangu
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Cites_doi 10.1016/j.biologicals.2015.05.012
10.1182/blood-2013-10-529974
10.1056/NEJMoa067659
10.1111/j.1365-2516.2006.01312.x
10.1053/j.seminhematol.2015.10.005
10.1182/blood-2015-01-528414
10.1182/blood-2012-12-470898
10.1002/acr.20353
10.1182/blood-2011-08-367813
10.2147/JBM.S50644
10.1038/nri2206
10.1111/hae.12766
10.1111/jth.12672
10.1126/science.291.5503.484
10.1111/jth.12911
10.1111/jth.12076
10.1586/ehm.12.27
10.1111/hae.12539
10.1182/blood-2011-09-382846
10.1016/0140-6736(93)92000-J
10.15256/joc.2011.1.2
10.1111/j.1365-2516.2004.00998.x
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Keywords haemophilia
joint health
haemarthrosis
arthropathy
factor VIII
prophylaxis
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References 2015; 13
2004; 10
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2015; 43
2016; 53
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References_xml – volume: 5
  start-page: 459
  year: 2012
  end-page: 468
  article-title: Management of joint bleeding in hemophilia
  publication-title: Expert Rev Hematol
– volume: 125
  start-page: 2038
  year: 2015
  end-page: 44
  article-title: Optimal treatment strategies for hemophilia: achievements and limitations of current prophylactic regimens
  publication-title: Blood
– volume: 122
  start-page: 1129
  year: 2013
  end-page: 1136
  article-title: Intermediate‐dose versus high‐dose prophylaxis for severe hemophilia: comparing outcome and costs since the 1970s
  publication-title: Blood
– volume: 291
  start-page: 484
  year: 2001
  end-page: 486
  article-title: Anti‐inflammatoryactivity of IVIG mediated through the inhibitory Fc receptor
  publication-title: Science
– volume: 342
  start-page: 945
  year: 1993
  end-page: 949
  article-title: Infusion of Fcgamma fragments for treatment of children with acute immune thrombocytopenic purpura
  publication-title: Lancet
– volume: 43
  start-page: 213
  year: 2015
  end-page: 219
  article-title: Manufacturing process used to produce long‐acting recombinant factor VIII Fc fusion protein
  publication-title: Biologicals
– volume: 1
  start-page: 51
  year: 2011
  end-page: 59
  article-title: Haemophilia and joint disease: pathophysiology, evaluation, and management
  publication-title: J Comorb
– volume: 21
  start-page: 171
  year: 2015
  end-page: 179
  article-title: Controlled, cross‐sectional MRI evaluation of joint status in severe haemophilia A patients treated with prophylaxis vs. on demand
  publication-title: Haemophilia
– volume: 53
  start-page: 10
  year: 2016
  end-page: 19
  article-title: Advances and challenges in hemophilic arthropathy
  publication-title: Semin Hematol
– volume: 11
  start-page: 132
  year: 2013
  end-page: 141
  article-title: Biochemical and functional characterization of a recombinant monomeric factor VIII‐Fc fusion protein
  publication-title: J Thromb Haemost
– volume: 22
  start-page: 72
  year: 2016
  end-page: 80
  article-title: Long‐term safety and efficacy of recombinant factor VIII Fc fusion protein (rFVIIIFc) in subjects with haemophilia A
  publication-title: Haemophilia
– volume: 12
  start-page: 518
  year: 2006
  end-page: 525
  article-title: Hemophilia joint health score reliability study
  publication-title: Haemophilia
– volume: 123
  start-page: 317
  year: 2014
  end-page: 325
  article-title: Phase 3 study of recombinant factor VIII Fc fusion protein in severe hemophilia A
  publication-title: Blood
– volume: 13
  start-page: 967
  year: 2015
  end-page: 977
  article-title: Recombinant factor VIII Fc fusion protein for the prevention and treatment of bleeding in children with severe hemophilia A
  publication-title: J Thromb Haemost
– volume: 5
  start-page: 207
  year: 2014
  end-page: 218
  article-title: Optimal management of hemophilic arthropathy and hematomas
  publication-title: J Blood Med
– volume: 119
  start-page: 3031
  year: 2012
  end-page: 3037
  article-title: Safety and prolonged activity of recombinant factor VIII Fc fusion protein in hemophilia A patients
  publication-title: Blood
– volume: 10
  start-page: 97
  issue: Suppl 4
  year: 2004
  end-page: 104
  article-title: Optimizing factor prophylaxis for the haemophilia population: where do we stand?
  publication-title: Haemophilia
– volume: 63
  start-page: 223
  year: 2011
  end-page: 230
  article-title: Validation of a new pediatric joint scoring system from the International Hemophilia Prophylaxis Study Group: validity of the hemophilia joint health score
  publication-title: Arthritis Care Res (Hoboken)
– volume: 12
  start-page: 1935
  year: 2014
  end-page: 1939
  article-title: Definitions in hemophilia: communication from the SSC of the ISTH
  publication-title: J Thromb Haemost
– year: 2016
– volume: 35
  start-page: 235
  year: 2013
  end-page: 254
  article-title: Fc‐fusion proteins and FcRn: structural insights for longer lasting and more effective therapeutics
  publication-title: Curr Opin Biotechnol
– volume: 357
  start-page: 535
  year: 2007
  end-page: 544
  article-title: Prophylaxis versus episodic treatment to prevent joint disease in boys with severe hemophilia
  publication-title: N Engl J Med
– volume: 8
  start-page: 34
  year: 2008
  end-page: 47
  article-title: Fc gamma receptors as regulators of immune responses
  publication-title: Nat Rev Immunol
– volume: 119
  start-page: 3024
  year: 2012
  end-page: 3030
  article-title: Prolonged activity of a recombinant factor VIII‐Fc fusion protein in hemophilia A mice and dogs
  publication-title: Blood
– ident: e_1_2_8_12_1
  doi: 10.1016/j.biologicals.2015.05.012
– ident: e_1_2_8_13_1
  doi: 10.1182/blood-2013-10-529974
– ident: e_1_2_8_7_1
  doi: 10.1056/NEJMoa067659
– ident: e_1_2_8_18_1
  doi: 10.1111/j.1365-2516.2006.01312.x
– ident: e_1_2_8_4_1
  doi: 10.1053/j.seminhematol.2015.10.005
– ident: e_1_2_8_5_1
  doi: 10.1182/blood-2015-01-528414
– ident: e_1_2_8_16_1
  doi: 10.1182/blood-2012-12-470898
– ident: e_1_2_8_17_1
  doi: 10.1002/acr.20353
– ident: e_1_2_8_8_1
  doi: 10.1182/blood-2011-08-367813
– ident: e_1_2_8_2_1
  doi: 10.2147/JBM.S50644
– ident: e_1_2_8_24_1
  doi: 10.1038/nri2206
– ident: e_1_2_8_15_1
  doi: 10.1111/hae.12766
– ident: e_1_2_8_20_1
  doi: 10.1111/jth.12672
– ident: e_1_2_8_22_1
  doi: 10.1126/science.291.5503.484
– ident: e_1_2_8_14_1
  doi: 10.1111/jth.12911
– ident: e_1_2_8_10_1
  doi: 10.1111/jth.12076
– ident: e_1_2_8_25_1
  doi: 10.1586/ehm.12.27
– ident: e_1_2_8_6_1
  doi: 10.1111/hae.12539
– volume: 35
  start-page: 235
  year: 2013
  ident: e_1_2_8_9_1
  article-title: Fc‐fusion proteins and FcRn: structural insights for longer lasting and more effective therapeutics
  publication-title: Curr Opin Biotechnol
– ident: e_1_2_8_11_1
  doi: 10.1182/blood-2011-09-382846
– ident: e_1_2_8_21_1
– ident: e_1_2_8_23_1
  doi: 10.1016/0140-6736(93)92000-J
– ident: e_1_2_8_3_1
  doi: 10.15256/joc.2011.1.2
– ident: e_1_2_8_19_1
  doi: 10.1111/j.1365-2516.2004.00998.x
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Snippet Introduction Joint arthropathy is the long‐term consequence of joint bleeding in people with severe haemophilia. Aim This study assessed change in joint health...
Joint arthropathy is the long-term consequence of joint bleeding in people with severe haemophilia. This study assessed change in joint health over time in...
Introduction Joint arthropathy is the long-term consequence of joint bleeding in people with severe haemophilia. Aim This study assessed change in joint health...
Joint arthropathy is the long-term consequence of joint bleeding in people with severe haemophilia.INTRODUCTIONJoint arthropathy is the long-term consequence...
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StartPage 77
SubjectTerms arthropathy
Bleeding
Coagulation factors
factor VIII
Factor VIII deficiency
Fc receptors
Fusion protein
haemarthrosis
haemophilia
Hemophilia
joint health
Prophylaxis
Title Improved joint health in subjects with severe haemophilia A treated prophylactically with recombinant factor VIII Fc fusion protein
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fhae.13353
https://www.ncbi.nlm.nih.gov/pubmed/29082639
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