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Long‐term follow‐up of patients treated with caplacizumab and safety and efficacy of repeat caplacizumab use: Post‐HERCULES study

INTRODUCTION: Caplacizumab demonstrated efficacy and safety in patients with immune‐mediated thrombotic thrombocytopenic purpura (iTTP) in the phase 3 HERCULES trial. However, data on long‐term outcomes following caplacizumab treatment are limited. OBJECTIVES: The post‐HERCULES trial (NCT02878603) e...

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Autores principales: Scully, Marie, de la Rubia, Javier, Pavenski, Katerina, Metjian, Ara, Knöbl, Paul, Peyvandi, Flora, Cataland, Spero, Coppo, Paul, Kremer Hovinga, Johanna A., Minkue Mi Edou, Jessica, De Passos Sousa, Rui, Callewaert, Filip, Gunawardena, Sriya, Lin, Julie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9827931/
https://www.ncbi.nlm.nih.gov/pubmed/36138517
http://dx.doi.org/10.1111/jth.15892
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author Scully, Marie
de la Rubia, Javier
Pavenski, Katerina
Metjian, Ara
Knöbl, Paul
Peyvandi, Flora
Cataland, Spero
Coppo, Paul
Kremer Hovinga, Johanna A.
Minkue Mi Edou, Jessica
De Passos Sousa, Rui
Callewaert, Filip
Gunawardena, Sriya
Lin, Julie
author_facet Scully, Marie
de la Rubia, Javier
Pavenski, Katerina
Metjian, Ara
Knöbl, Paul
Peyvandi, Flora
Cataland, Spero
Coppo, Paul
Kremer Hovinga, Johanna A.
Minkue Mi Edou, Jessica
De Passos Sousa, Rui
Callewaert, Filip
Gunawardena, Sriya
Lin, Julie
author_sort Scully, Marie
collection PubMed
description INTRODUCTION: Caplacizumab demonstrated efficacy and safety in patients with immune‐mediated thrombotic thrombocytopenic purpura (iTTP) in the phase 3 HERCULES trial. However, data on long‐term outcomes following caplacizumab treatment are limited. OBJECTIVES: The post‐HERCULES trial (NCT02878603) evaluated long‐term outcomes of patients with iTTP treated with caplacizumab in HERCULES and safety and efficacy of repeated caplacizumab use. PATIENTS/METHODS: Over 3 years of follow‐up, patients could receive open‐label caplacizumab with therapeutic plasma exchange (TPE) and immunosuppressive therapy (IST) in case of recurrence. Adverse events (AEs) were assessed during the overall study period (intention‐to‐observe [ITO] population) and during recurrences (recurrence population). TTP‐related events (TTP‐related death, recurrence, major thromboembolic events) were assessed in the efficacy ITO population (patients without recurrence during HERCULES or before post‐HERCULES). RESULTS: Among 104 enrolled patients, incidences of AEs and serious AEs were similar between patients who had received caplacizumab + TPE + IST during HERCULES (n = 75) and those treated with placebo + TPE + IST (placebo; n = 29). TTP‐related events occurred in 8% of patients (4/49) randomized to caplacizumab during HERCULES versus 38% (11/29) randomized to placebo. Nineteen patients had ≥1 recurrence; 13 of these were treated with caplacizumab. The first recurrence episode was resolved or resolving for all patients treated with caplacizumab, including nine patients with repeat caplacizumab use. All second recurrences (6/6) were resolved. Safety profile of caplacizumab for treatment of recurrence was consistent with HERCULES; most bleeding events were nonserious. No major cases of organ dysfunction were observed. CONCLUSIONS: Long‐term follow‐up supports the safety and efficacy of caplacizumab for iTTP and its repeated use for recurrences.
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spelling pubmed-98279312023-01-10 Long‐term follow‐up of patients treated with caplacizumab and safety and efficacy of repeat caplacizumab use: Post‐HERCULES study Scully, Marie de la Rubia, Javier Pavenski, Katerina Metjian, Ara Knöbl, Paul Peyvandi, Flora Cataland, Spero Coppo, Paul Kremer Hovinga, Johanna A. Minkue Mi Edou, Jessica De Passos Sousa, Rui Callewaert, Filip Gunawardena, Sriya Lin, Julie J Thromb Haemost HAEMOSTASIS INTRODUCTION: Caplacizumab demonstrated efficacy and safety in patients with immune‐mediated thrombotic thrombocytopenic purpura (iTTP) in the phase 3 HERCULES trial. However, data on long‐term outcomes following caplacizumab treatment are limited. OBJECTIVES: The post‐HERCULES trial (NCT02878603) evaluated long‐term outcomes of patients with iTTP treated with caplacizumab in HERCULES and safety and efficacy of repeated caplacizumab use. PATIENTS/METHODS: Over 3 years of follow‐up, patients could receive open‐label caplacizumab with therapeutic plasma exchange (TPE) and immunosuppressive therapy (IST) in case of recurrence. Adverse events (AEs) were assessed during the overall study period (intention‐to‐observe [ITO] population) and during recurrences (recurrence population). TTP‐related events (TTP‐related death, recurrence, major thromboembolic events) were assessed in the efficacy ITO population (patients without recurrence during HERCULES or before post‐HERCULES). RESULTS: Among 104 enrolled patients, incidences of AEs and serious AEs were similar between patients who had received caplacizumab + TPE + IST during HERCULES (n = 75) and those treated with placebo + TPE + IST (placebo; n = 29). TTP‐related events occurred in 8% of patients (4/49) randomized to caplacizumab during HERCULES versus 38% (11/29) randomized to placebo. Nineteen patients had ≥1 recurrence; 13 of these were treated with caplacizumab. The first recurrence episode was resolved or resolving for all patients treated with caplacizumab, including nine patients with repeat caplacizumab use. All second recurrences (6/6) were resolved. Safety profile of caplacizumab for treatment of recurrence was consistent with HERCULES; most bleeding events were nonserious. No major cases of organ dysfunction were observed. CONCLUSIONS: Long‐term follow‐up supports the safety and efficacy of caplacizumab for iTTP and its repeated use for recurrences. John Wiley and Sons Inc. 2022-10-21 2022-12 /pmc/articles/PMC9827931/ /pubmed/36138517 http://dx.doi.org/10.1111/jth.15892 Text en © 2022 Sanofi and The Authors. Journal of Thrombosis and Haemostasis published by Wiley Periodicals LLC on behalf of International Society on Thrombosis and Haemostasis. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle HAEMOSTASIS
Scully, Marie
de la Rubia, Javier
Pavenski, Katerina
Metjian, Ara
Knöbl, Paul
Peyvandi, Flora
Cataland, Spero
Coppo, Paul
Kremer Hovinga, Johanna A.
Minkue Mi Edou, Jessica
De Passos Sousa, Rui
Callewaert, Filip
Gunawardena, Sriya
Lin, Julie
Long‐term follow‐up of patients treated with caplacizumab and safety and efficacy of repeat caplacizumab use: Post‐HERCULES study
title Long‐term follow‐up of patients treated with caplacizumab and safety and efficacy of repeat caplacizumab use: Post‐HERCULES study
title_full Long‐term follow‐up of patients treated with caplacizumab and safety and efficacy of repeat caplacizumab use: Post‐HERCULES study
title_fullStr Long‐term follow‐up of patients treated with caplacizumab and safety and efficacy of repeat caplacizumab use: Post‐HERCULES study
title_full_unstemmed Long‐term follow‐up of patients treated with caplacizumab and safety and efficacy of repeat caplacizumab use: Post‐HERCULES study
title_short Long‐term follow‐up of patients treated with caplacizumab and safety and efficacy of repeat caplacizumab use: Post‐HERCULES study
title_sort long‐term follow‐up of patients treated with caplacizumab and safety and efficacy of repeat caplacizumab use: post‐hercules study
topic HAEMOSTASIS
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9827931/
https://www.ncbi.nlm.nih.gov/pubmed/36138517
http://dx.doi.org/10.1111/jth.15892
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