Observational study of recombinant factor VIII-Fc, rFVIIIFc, in hemophilia A.


Journal

Thrombosis research
ISSN: 1879-2472
Titre abrégé: Thromb Res
Pays: United States
ID NLM: 0326377

Informations de publication

Date de publication:
11 2020
Historique:
received: 12 12 2019
revised: 03 06 2020
accepted: 03 07 2020
pubmed: 13 7 2020
medline: 22 6 2021
entrez: 13 7 2020
Statut: ppublish

Résumé

rFVIIIFc (Eloctate) is an extended-half-life recombinant factor VIII-Fc fusion protein that may promote factor VIII (FVIII) tolerance through Fc immunoregulatory properties. Yet, little is known regarding its immunogenicity in patients with hemophilia A (HA) or in HA with inhibitors (HA-I), including tolerized, immune tolerance induction (ITI)-refractory, or ITI-naïve. We reviewed medical records of 60 patients, including 2 previously-untreated patients (PUPs) and 58 previously-treated patients (PTPs), cared for between 01/01/06 and 06/01/17, on whom anti-FVIII antibody data were available before and after initiating rFVIIIFc. Continuous data were analyzed by student's t-test, and discrete data by chi square or Fisher's exact test. After initiating rFVIIIFc, one of two HA PUPs developed a low-responding (LR) inhibitor after 10 exposures, which resolved (anti-VIII<0.6 B.U.) within 8 additional exposures, while none of 41 HA PTPS developed an inhibitor. Among 19 HA-I PTPs with detectable inhibitors prior to rFVIIIFc, 5 developed an anamnestic response to rFVIIIFc, including 1 of 8 (12.5%) low-responding (LR), and 4 of 9 (44.9%) high-responding (HR), of whom 3 were ITI-naïve and 1 ITI-refractory. Inhibitors resolved in 4 HR within 2 months of continuing rFVIIIFc (median) but persisted in 1 LR at low titer. The remaining 11 HA-I PTPs, including 4 HR and seven LR, had no detectable inhibitor at the time of or after initiating rFVIIIFc. rFVIIIFc was immunogenic in HA PUPs and in HA-I PTPs persistently ITI-naïve or ITI-refractory, with inhibitor resolution in the majority. rFVIIIFc immunogenicity appears to be similar to other FVIII products.

Identifiants

pubmed: 32653601
pii: S0049-3848(20)30295-4
doi: 10.1016/j.thromres.2020.07.004
pii:
doi:

Substances chimiques

Factor VIII 9001-27-8

Types de publication

Journal Article Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

51-54

Informations de copyright

Copyright © 2020 Elsevier Ltd. All rights reserved.

Auteurs

Patrick T Ebbert (PT)

University of Pittsburgh Department of Medicine and Hemophilia Center of Western PA, Pittsburgh, PA, United States of America.

Frederico Xavier (F)

University of Pittsburgh Department of Medicine and Hemophilia Center of Western PA, Pittsburgh, PA, United States of America; Chilren's Hospital of Pittsburgh, University of Pittsburgh, Pittsburgh, PA, United States of America.

Lynn M Malec (LM)

BloodCenter of Wisconsin Department of Pediatrics and Medical College of Wisconsin, Milwaukee, WI, United States of America.

Craig D Seaman (CD)

University of Pittsburgh Department of Medicine and Hemophilia Center of Western PA, Pittsburgh, PA, United States of America.

Margaret V Ragni (MV)

University of Pittsburgh Department of Medicine and Hemophilia Center of Western PA, Pittsburgh, PA, United States of America. Electronic address: ragni@pitt.edu.

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Classifications MeSH