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

被引:5
作者
Ebbert, Patrick T. [1 ,2 ]
Xavier, Frederico [1 ,2 ,3 ]
Malec, Lynn M. [4 ,5 ]
Seaman, Craig D. [1 ,2 ]
Ragni, Margaret, V [1 ,2 ]
机构
[1] Univ Pittsburgh, Dept Med, Pittsburgh, PA USA
[2] Hemophilia Ctr Western PA, 3636 Blvd Allies, Pittsburgh, PA 15213 USA
[3] Univ Pittsburgh, Chilrens Hosp Pittsburgh, Pittsburgh, PA USA
[4] BloodCtr Wisconsin, Dept Pediat, Milwaukee, WI USA
[5] Med Coll Wisconsin, Milwaukee, WI 53226 USA
关键词
Hemophilia A; Eloctate; Immune tolerance; Inhibitor formation; rFVIIIFc; IMMUNE TOLERANCE INDUCTION; REGULATORY T-CELLS; FUSION PROTEIN; INHIBITOR DEVELOPMENT; HALF-LIFE; THERAPY; PROPHYLAXIS; CHILDREN; IMPACT; SAFETY;
D O I
10.1016/j.thromres.2020.07.004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: 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-naive. Methods: 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. Results: 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-naive 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. Discussion: rFVIIIFc was immunogenic in HA PUPs and in HA-I PTPs persistently ITI-naive or ITI-refractory, with inhibitor resolution in the majority. rFVIIIFc immunogenicity appears to be similar to other FVIII products.
引用
收藏
页码:51 / 54
页数:4
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