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Management of immune thrombotic thrombocytopenic purpura without therapeutic plasma exchange.
Kühne, Lucas; Knöbl, Paul; Eller, Kathrin; Thaler, Johannes; Sperr, Wolfgang R; Gleixner, Karoline; Osterholt, Thomas; Kaufeld, Jessica; Menne, Jan; Buxhofer-Ausch, Veronika; Mühlfeld, Anja; Seelow, Evelyn; Schreiber, Adrian; Todorova, Polina; Cukoski, Sadrija; Jabs, Wolfram J; Özcan, Fedai; Gäckler, Anja; Schönfelder, Kristina; Seibert, Felix S; Westhoff, Timm; Schwenger, Vedat; Eichenauer, Dennis A; Völker, Linus A; Brinkkoetter, Paul T.
Affiliation
  • Kühne L; Department II of Internal Medicine and Center for Molecular Medicine Cologne, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.
  • Knöbl P; Division of Hematology and Hemostasis, Department of Medicine 1, Medical University of Vienna, Vienna, Austria.
  • Eller K; Division of Nephrology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
  • Thaler J; Division of Hematology and Hemostasis, Department of Medicine 1, Medical University of Vienna, Vienna, Austria.
  • Sperr WR; Division of Hematology and Hemostasis, Department of Medicine 1, Medical University of Vienna, Vienna, Austria.
  • Gleixner K; Division of Hematology and Hemostasis, Department of Medicine 1, Medical University of Vienna, Vienna, Austria.
  • Osterholt T; Department II of Internal Medicine and Center for Molecular Medicine Cologne, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.
  • Kaufeld J; Department of Nephrology and Hypertension, Medical School Hannover, Hannover, Germany.
  • Menne J; KRH Klinikum Mitte-Location Siloah, Hannover, Germany.
  • Buxhofer-Ausch V; Department of Internal Medicine I with Hematology, Stem Cell Transplantation, Hemostaseology and Medical Oncology, Ordensklinikum Linz Elisabethinnen, Linz, Austria.
  • Mühlfeld A; Medical Faculty, Johannes Kepler University Linz, Linz, Austria.
  • Seelow E; Division of Nephrology, Department of Medicine, Uniklinik RWTH Aachen, Aachen, Germany.
  • Schreiber A; Department of Nephrology and Intensive Care Medicine, Charité-Universitätsmedizin Berlin, Berlin, Germany.
  • Todorova P; Department of Nephrology and Intensive Care Medicine, Charité-Universitätsmedizin Berlin, Berlin, Germany.
  • Cukoski S; Department II of Internal Medicine and Center for Molecular Medicine Cologne, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.
  • Jabs WJ; Department II of Internal Medicine and Center for Molecular Medicine Cologne, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.
  • Özcan F; Department of Nephrology, Vivantes Klinikum im Friedrichshain, Berlin, Germany.
  • Gäckler A; Klinik für Nephrologie, Klinikum Dortmund, Universität Witten-Herdecke, Campus Dortmund, Dortmund, Germany.
  • Schönfelder K; Department of Nephrology, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
  • Seibert FS; Department of Nephrology, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
  • Westhoff T; Medical Department 1, Marien Hospital Herne-Universitätsklinikum der Ruhr-Universität Bochum, Herne, Germany.
  • Schwenger V; Medical Department 1, Marien Hospital Herne-Universitätsklinikum der Ruhr-Universität Bochum, Herne, Germany.
  • Eichenauer DA; Department of Nephrology, Klinikum Stuttgart, Stuttgart, Germany.
  • Völker LA; Department I of Internal Medicine, Center for Integrated Oncology Aachen Bonn Cologne Dusseldorf, University of Cologne, Cologne, Germany.
  • Brinkkoetter PT; Department II of Internal Medicine and Center for Molecular Medicine Cologne, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.
Blood ; 144(14): 1486-1495, 2024 Oct 03.
Article in En | MEDLINE | ID: mdl-38838300
ABSTRACT
ABSTRACT Immune thrombotic thrombocytopenic purpura (iTTP) is a rare, life-threatening autoimmune disorder caused by a disintegrin and metalloproteinase with thrombospondin type 1 motif, member 13 (ADAMTS13) deficiency. Caplacizumab, an anti-von Willebrand factor nanobody, is approved for iTTP treatment, reducing the need for therapeutic plasma exchange (TPE) and improving platelet count recovery and survival. We conducted a retrospective study on 42 acute iTTP cases in Austria and Germany, treated with a modified regimen aimed at avoiding TPE if platelet count increased after the first caplacizumab dose. Baseline characteristics and patient outcomes were compared with a control group of 59 patients with iTTP receiving frontline treatment with TPE, caplacizumab, and immunosuppression. The main outcome was the time to platelet count normalization. Secondary outcomes included clinical response, exacerbation, refractory iTTP, iTTP-related deaths, and the time to platelet count doubling. The median time to platelet count normalization was similar between the 2 cohorts (3 and 4 days; P = .31). There were no significant differences in clinical response, exacerbations, refractoriness, iTTP-related deaths, or time to platelet count doubling, reflecting the short-term treatment response. Four patients did not respond to the first caplacizumab dose, and TPE was subsequently initiated. Cytomegalovirus infection, HIV/hepatitis B virus coinfection, an ovarian teratoma with associated antiplatelet antibodies, and multiple platelet transfusions before the correct diagnosis may have impeded the immediate treatment response in these patients. In conclusion, caplacizumab and immunosuppression alone, without TPE, rapidly controlled thrombotic microangiopathy and achieved a sustained clinical response in iTTP. Our study provides a basis for TPE-free iTTP management in experienced centers via shared decision-making between patients and treating physicians.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Plasma Exchange / Purpura, Thrombotic Thrombocytopenic / Single-Domain Antibodies Limits: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Blood Year: 2024 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Plasma Exchange / Purpura, Thrombotic Thrombocytopenic / Single-Domain Antibodies Limits: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Blood Year: 2024 Document type: Article Affiliation country: Country of publication: