Literature DB >> 32634237

ADAMTS13 and VWF activities guide individualized caplacizumab treatment in patients with aTTP.

Linus A Völker1,2, Jessica Kaufeld3, Wolfgang Miesbach4, Sebastian Brähler1,2, Martin Reinhardt3, Lucas Kühne1,2, Anja Mühlfeld5, Adrian Schreiber6,7, Jens Gaedeke6,7, Markus Tölle8,9, Wolfram J Jabs10, Fedai Özcan11, Silke Markau12, Matthias Girndt12, Frederic Bauer13, Timm H Westhoff13, Helmut Felten14, Martin Hausberg14, Marcus Brand15, Jens Gerth16, Markus Bieringer17, Martin Bommer18, Stefan Zschiedrich19, Johanna Schneider19, Saban Elitok20, Alexander Gawlik20, Anja Gäckler21, Andreas Kribben21, Vedat Schwenger22, Ulf Schoenermarck23, Maximilian Roeder24, Jörg Radermacher25, Jörn Bramstedt26, Anke Morgner27, Regina Herbst27, Ana Harth28, Sebastian A Potthoff27,29, Charis von Auer30, Ralph Wendt31, Hildegard Christ32, Paul T Brinkkoetter1,2, Jan Menne3.   

Abstract

Introduction of the nanobody caplacizumab was shown to be effective in the treatment of acquired thrombotic thrombocytopenic purpura (aTTP) in the acute setting. The official recommendations include plasma exchange (PEX), immunosuppression, and the use of caplacizumab for a minimum of 30 days after stopping daily PEX. This study was a retrospective, observational analysis of the use of caplacizumab in 60 patients from 29 medical centers in Germany. Immunosuppressive treatment led to a rapid normalization of ADAMTS13 activities (calculated median, 21 days). In 35 of 60 patients, ADAMTS13 activities started to normalize before day 30 after PEX; in 11 of 60 patients, the treatment was extended beyond day 30; and in 5 patients, it was extended even beyond day 58 due to persistent autoimmune activity. In 34 of 60 instances, caplacizumab was stopped before day 30 with a favorable outcome whenever ADAMTS13 activities were >10%. In contrast, 11 of 34 patients with ADAMTS13 activities <10% at the time of stopping caplacizumab treatment developed a nonfavorable outcome (disease exacerbation or relapse). In some cases, prolongation of the treatment interval to every other day was feasible and resulted in a sustained reduction of von Willebrand factor activity. ADAMTS13 activity measurements are central for a rapid diagnosis in the acute setting but also to tailor disease management. An ADAMTS13 activity-guided approach seems safe for identifying the individual time point when to stop caplacizumab to prevent overtreatment and undertreatment; this approach will result in significant cost savings without jeopardizing the well-being of patients. In addition, von Willebrand factor activity may serve as a biomarker for drug monitoring.
© 2020 by The American Society of Hematology.

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Year:  2020        PMID: 32634237      PMCID: PMC7362349          DOI: 10.1182/bloodadvances.2020001987

Source DB:  PubMed          Journal:  Blood Adv        ISSN: 2473-9529


  18 in total

1.  ADAMTS13: what it does, how it works, and why it's important.

Authors:  James N George
Journal:  Transfusion       Date:  2009-02       Impact factor: 3.157

2.  Caplacizumab Treatment for Acquired Thrombotic Thrombocytopenic Purpura.

Authors:  Marie Scully; Spero R Cataland; Flora Peyvandi; Paul Coppo; Paul Knöbl; Johanna A Kremer Hovinga; Ara Metjian; Javier de la Rubia; Katerina Pavenski; Filip Callewaert; Debjit Biswas; Hilde De Winter; Robert K Zeldin
Journal:  N Engl J Med       Date:  2019-01-09       Impact factor: 91.245

3.  Caplacizumab Therapy without Plasma Exchange for Acquired Thrombotic Thrombocytopenic Purpura.

Authors:  Deepak P Chander; Michelle M Loch; Spero R Cataland; James N George
Journal:  N Engl J Med       Date:  2019-07-04       Impact factor: 91.245

4.  Role of ADAMTS13 in the management of thrombotic microangiopathies including thrombotic thrombocytopenic purpura (TTP).

Authors:  Neil Shah; Cynthia Rutherford; Karen Matevosyan; Yu-Min Shen; Ravi Sarode
Journal:  Br J Haematol       Date:  2013-09-20       Impact factor: 6.998

5.  Consensus on the standardization of terminology in thrombotic thrombocytopenic purpura and related thrombotic microangiopathies.

Authors:  M Scully; S Cataland; P Coppo; J de la Rubia; K D Friedman; J Kremer Hovinga; B Lämmle; M Matsumoto; K Pavenski; E Sadler; R Sarode; H Wu
Journal:  J Thromb Haemost       Date:  2017-01-30       Impact factor: 5.824

6.  The clinical utility of ADAMTS13 activity, antigen and autoantibody assays in thrombotic thrombocytopenic purpura.

Authors:  Richard Starke; Samuel Machin; Marie Scully; Gordon Purdy; Ian Mackie
Journal:  Br J Haematol       Date:  2007-02       Impact factor: 6.998

7.  Effect of plasma exchange on plasma ADAMTS13 metalloprotease activity, inhibitor level, and clinical outcome in patients with idiopathic and nonidiopathic thrombotic thrombocytopenic purpura.

Authors:  X Long Zheng; Richard M Kaufman; Lawrence T Goodnough; J Evan Sadler
Journal:  Blood       Date:  2004-02-24       Impact factor: 22.113

8.  Incidence of acquired thrombotic thrombocytopenic purpura in Germany: a hospital level study.

Authors:  Wolfgang Miesbach; Jan Menne; Martin Bommer; Ulf Schönermarck; Thorsten Feldkamp; Martin Nitschke; Timm H Westhoff; Felix S Seibert; Rainer Woitas; Rui Sousa; Michael Wolf; Stefan Walzer; Björn Schwander
Journal:  Orphanet J Rare Dis       Date:  2019-11-15       Impact factor: 4.123

9.  A German national prevalence study on the cost of intensive care: an evaluation from 51 intensive care units.

Authors:  Onnen Moerer; Enno Plock; Uchenna Mgbor; Alexandra Schmid; Heinz Schneider; Manfred Bernd Wischnewsky; Hilmar Burchardi
Journal:  Crit Care       Date:  2007       Impact factor: 9.097

Review 10.  Management of thrombotic thrombocytopenic purpura: current perspectives.

Authors:  Piers Blombery; Marie Scully
Journal:  J Blood Med       Date:  2014-02-05
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  9 in total

1.  Counting the cost of caplacizumab.

Authors:  Shruti Chaturvedi
Journal:  Blood       Date:  2021-02-18       Impact factor: 22.113

2.  First diagnosis of thrombotic thrombocytopenic purpura after SARS-CoV-2 vaccine - case report.

Authors:  Bilgin Osmanodja; Adrian Schreiber; Eva Schrezenmeier; Evelyn Seelow
Journal:  BMC Nephrol       Date:  2021-12-11       Impact factor: 2.388

3.  Immune thrombotic thrombocytopenic purpura: Personalized therapy using ADAMTS-13 activity and autoantibodies.

Authors:  Francesca Palandri; Christian Di Pietro; Francesca Ricci; Pier Luigi Tazzari; Vanda Randi; Daniela Bartoletti; Michele Cavo; Nicola Vianelli; Giuseppe Auteri
Journal:  Res Pract Thromb Haemost       Date:  2021-12-09

4.  Daratumumab for immune thrombotic thrombocytopenic purpura.

Authors:  Jana van den Berg; Johanna A Kremer Hovinga; Claudia Pfleger; Inga Hegemann; Gregor Stehle; Andreas Holbro; Jan-Dirk Studt
Journal:  Blood Adv       Date:  2022-02-08

Review 5.  TTP: From empiricism for an enigmatic disease to targeted molecular therapies.

Authors:  Nuno A G Graça; Bérangère S Joly; Jan Voorberg; Karen Vanhoorelbeke; Nicolas Béranger; Agnès Veyradier; Paul Coppo
Journal:  Br J Haematol       Date:  2022-02-10       Impact factor: 8.615

Review 6.  Management of acquired, immune thrombocytopenic purpura (iTTP): beyond the acute phase.

Authors:  John Paul Westwood; Marie Scully
Journal:  Ther Adv Hematol       Date:  2022-07-26

Review 7.  Diagnosis and treatment of thrombotic microangiopathy.

Authors:  Gemma L Thompson; David Kavanagh
Journal:  Int J Lab Hematol       Date:  2022-09       Impact factor: 3.450

8.  Treatment of acquired thrombotic thrombocytopenic purpura without plasma exchange in selected patients under caplacizumab.

Authors:  Linus A Völker; Paul T Brinkkoetter; Paul N Knöbl; Miroslav Krstic; Jessica Kaufeld; Jan Menne; Veronika Buxhofer-Ausch; Wolfgang Miesbach
Journal:  J Thromb Haemost       Date:  2020-09-06       Impact factor: 5.824

Review 9.  COVID-19 and biomarkers of thrombosis: focus on von Willebrand factor and extracellular vesicles.

Authors:  Richard C Becker; Travis Sexton; Susan Smyth
Journal:  J Thromb Thrombolysis       Date:  2021-08-04       Impact factor: 2.300

  9 in total

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