Thrombin generation to predict breakthrough bleeding in patients with acquired hemophilia A under emicizumab prophylaxis

Acquired hemophilia A (AHA) is a serious bleeding disorder due to neutralizing autoantibodies against factor VIII (FVIII). Emicizumab mimics the activity of FVIIIa restoring thrombin generation. It was shown to protect patients with AHA from bleeding, but some patients experience clinically relevant breakthrough bleeding. Therefore, monitoring the efficacy of emicizumab might be useful, potentially through thrombin generation assay (TGA). The aims of this study were to assess (i) how TGA is related to emicizumab levels, residual FVIII activity, and antigen concentration of other coagulation factors, and (ii) whether it can predict breakthrough bleeding during emicizumab prophylaxis. We used samples from patients enrolled into the GTH-AHAEMI study that prospectively assessed the risk of bleeding in AHA patients receiving emicizumab for 12 weeks. Calibrated automated thrombogram assay was used with minute amounts of tissue factor (TF-TGA) or factor XIa (FXIa-TGA) to initiate coagulation. We observed that FXIa-TGA peak thrombin generation increased with emicizumab levels and FVIII activity. Higher peak thrombin values were associated with lower rates of bleeding as indicated by incident rate ratios below 1 (IRR 0.40 [0.17-0.84], p.

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Publication Details

Journal
Haematologica
Published
2025-11-13
DOI
https://doi.org/10.3324/haematol.2025.288115
Primary Topic
Hemophilia Treatment and Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Thrombin generation to predict breakthrough bleeding in patients with acquired hemophilia A under emicizumab prophylaxis

Ella Ertekin, Ulrich J. Sachs, Hermann Eichler, Richard Greil et al.
Haematologica
Hemophilia Treatment and Research
article

Thrombin generation to predict breakthrough bleeding in patients with acquired hemophilia A under emicizumab prophylaxis

Ella Ertekin, Ulrich J. Sachs, Hermann Eichler, Richard Greil, Christian Pfrepper, Sonja Werwitzke, Wolfgang Miesbach, Patrick Möhnle, Katharina Holstein, Robert Klamroth, Johannes Oldenburg, Annika Klingberg, Andreas Tiede, Olga Oleshko, Fabius J. Pelzer, Christina Hart, Paul Knöbl, Karolin Trautmann-Grill
article en

Abstract

Acquired hemophilia A (AHA) is a serious bleeding disorder due to neutralizing autoantibodies against factor VIII (FVIII). Emicizumab mimics the activity of FVIIIa restoring thrombin generation. It was shown to protect patients with AHA from bleeding, but some patients experience clinically relevant breakthrough bleeding. Therefore, monitoring the efficacy of emicizumab might be useful, potentially through thrombin generation assay (TGA). The aims of this study were to assess (i) how TGA is related to emicizumab levels, residual FVIII activity, and antigen concentration of other coagulation factors, and (ii) whether it can predict breakthrough bleeding during emicizumab prophylaxis. We used samples from patients enrolled into the GTH-AHAEMI study that prospectively assessed the risk of bleeding in AHA patients receiving emicizumab for 12 weeks. Calibrated automated thrombogram assay was used with minute amounts of tissue factor (TF-TGA) or factor XIa (FXIa-TGA) to initiate coagulation. We observed that FXIa-TGA peak thrombin generation increased with emicizumab levels and FVIII activity. Higher peak thrombin values were associated with lower rates of bleeding as indicated by incident rate ratios below 1 (IRR 0.40 [0.17-0.84], p.

Haematologica
Goethe University Frankfurt (DE), Goethe-Institute United Kingdom (GB), Universität Hamburg (DE), Justus-Liebig-Universität Gießen (DE), Paracelsus Medical University (AT), University Hospital Regensburg (DE), Medizinische Hochschule Hannover (DE), Institute for Transfusion Medicine (US), University Medical Center Hamburg-Eppendorf (DE), University Hospital Leipzig (DE), Cellular Therapeutics (United Kingdom) (GB), Klinikum im Friedrichshain (DE), University Hospital Carl Gustav Carus (DE), Hannover Re (Germany) (DE), Medical University of Vienna (AT), Ludwig-Maximilians-Universität München (DE), Saarland University (DE)
American Heart Association, Pfizer, AstraZeneca, Sanofi, Alexion Pharmaceuticals, Celgene, CSL Behring, Ablynx, Novo Nordisk, Swedish Orphan Biovitrum, Chugai Pharmaceutical
Openalex Percentile: Top 55%
Hemophilia Treatment and Research
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