Publication:
Matching-Adjusted Indirect Comparison of Efficacy and Consumption of rVIII-SingleChain Versus Two Recombinant FVIII Products Used for Prophylactic Treatment of Adults/Adolescents with Severe Haemophilia A.

dc.contributor.authorBonanad, Santiago
dc.contributor.authorNúñez, Ramiro
dc.contributor.authorPoveda, Jose Luis
dc.contributor.authorKurnik, Karin
dc.contributor.authorGoldmann, Georg
dc.contributor.authorAndreozzi, Valeska
dc.contributor.authorVandewalle, Björn
dc.contributor.authorSantos, Sandra
dc.date.accessioned2023-02-09T11:46:08Z
dc.date.available2023-02-09T11:46:08Z
dc.date.issued2021-08-08
dc.description.abstractGiven the relatively small number of patients with haemophilia A, head-to-head comparisons between recombinant FVIII (rFVIII) products are difficult to conduct. This study compared the efficacy and consumption of rVIII-SingleChain (lonoctocog alfa, AFSTYLA®) with rAHF-PFM (octocog alfa, Advate®) and rFVIIIFc (efmoroctocog alfa, Elocta®), for the prophylaxis and treatment of bleeding episodes in previously treated adolescents/adults with severe haemophilia A, through a matching-adjusted indirect comparison (MAIC). A systematic literature review identified published clinical trials for rAHF-PFM and rFVIIIFc. Individual patient data for rVIII-SingleChain were used to match baseline patient characteristics to those from published trials, using an approach similar to propensity score weighting. After matching, annualized bleeding rates (ABR), percentage of patients with zero bleeds, and rFVIII consumption were compared across trial populations. Published data were identified from two rAHF-PFM trials and one rFVIIIFc trial. rVIII-SingleChain had similar ABR (risk ratio [RR]: 0.74 [0.16; 3.48]; RR: 1.18 [0.85; 1.65]) and percentage of patients with zero bleeds (odds ratio [OR]: 1.34 [0.56; 3.22]; OR: 0.78 [0.47; 1.31]) versus rAHF-PFM and rFVIIIFc, respectively. Annual rVIII-SingleChain consumption was significantly lower than rAHF-PFM (mean difference: - 1507.66 IU/kg/year [- 2011.71; - 1003.61]) and equivalent to rFVIIIFc (RR: 0.96 [0.62; 1.49]). Although limited to published information for comparator trials, these results suggest that with an annualized rFVIII consumption comparable to rFVIIIFc, but significantly lower than rAHF-PFM, routine prophylaxis with rVIII-SingleChain is able to maintain a similar ABR and percentage of patients with zero bleeds, attesting to the long-acting nature of rVIII-SingleChain.
dc.identifier.doi10.1007/s12325-021-01853-0
dc.identifier.essn1865-8652
dc.identifier.pmcPMC8408075
dc.identifier.pmid34368918
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8408075/pdf
dc.identifier.unpaywallURLhttps://link.springer.com/content/pdf/10.1007/s12325-021-01853-0.pdf
dc.identifier.urihttp://hdl.handle.net/10668/18343
dc.issue.number9
dc.journal.titleAdvances in therapy
dc.journal.titleabbreviationAdv Ther
dc.language.isoen
dc.organizationHospital Universitario Virgen del Rocío
dc.organizationHospital Universitario Virgen del Rocío
dc.page.number4872-4884
dc.pubmedtypeJournal Article
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.pubmedtypeSystematic Review
dc.rightsAttribution-NonCommercial 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.subjectAnnualized bleeding rate
dc.subjectEfmoroctocog alfa
dc.subjectFVIII consumption
dc.subjectHaemophilia A
dc.subjectLonoctocog alfa
dc.subjectMAIC
dc.subjectMatching-adjusted indirect comparison
dc.subjectOctocog alfa
dc.subjectrVIII-SingleChain
dc.subject.meshAdolescent
dc.subject.meshAdult
dc.subject.meshFactor VIII
dc.subject.meshHemophilia A
dc.subject.meshHemorrhage
dc.subject.meshHumans
dc.subject.meshImmunotherapy, Adoptive
dc.subject.meshPropensity Score
dc.subject.meshRecombinant Proteins
dc.titleMatching-Adjusted Indirect Comparison of Efficacy and Consumption of rVIII-SingleChain Versus Two Recombinant FVIII Products Used for Prophylactic Treatment of Adults/Adolescents with Severe Haemophilia A.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number38
dspace.entity.typePublication

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