Article (Scientific journals)
Riociguat treatment in patients with pulmonary arterial hypertension: Final safety data from the EXPERT registry.
Hoeper, Marius M.; Gomez Sanchez, Miguel-Angel; Humbert, Marc et al.
2020In Respiratory Medicine, 177, p. 106241
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Keywords :
Clinical practice; Pulmonary arterial hypertension; Pulmonary hypertension; Registry; Riociguat; Safety
Abstract :
[en] OBJECTIVE: The soluble guanylate cyclase stimulator riociguat is approved for the treatment of adult patients with pulmonary arterial hypertension (PAH) and inoperable or persistent/recurrent chronic thromboembolic pulmonary hypertension following Phase 3 randomized trials. The EXPosurE Registry RiociguaT in patients with pulmonary hypertension (EXPERT) study was designed to monitor the long-term safety of riociguat in clinical practice. METHODS: EXPERT was an international, multicenter, prospective, uncontrolled, non-interventional cohort study of patients treated with riociguat. Patients were followed for at least 1 year and up to 4 years from enrollment or until 30 days after stopping riociguat treatment. Primary safety outcomes were adverse events (AEs) and serious adverse events (SAEs) coded using Medical Dictionary for Regulatory Activities preferred terms and System Organ Classes version 21.0, collected during routine clinic visits (usually every 3-6 months) and collated via case report forms. RESULTS: In total, 326 patients with PAH were included in the analysis. The most common AEs in these patients were dizziness (11.7%), right ventricular (RV)/cardiac failure (10.7%), edema/peripheral edema (10.7%), diarrhea (8.6%), dyspnea (8.0%), and cough (7.7%). The most common SAEs were RV/cardiac failure (10.1%), pneumonia (6.1%), dyspnea (4.0%), and syncope (3.4%). The exposure-adjusted rate of hemoptysis/pulmonary hemorrhage was 2.5 events per 100 patient-years. CONCLUSION: Final data from EXPERT show that in patients with PAH, the safety of riociguat in clinical practice was consistent with clinical trials, with no new safety concerns identified and a lower exposure-adjusted rate of hemoptysis/pulmonary hemorrhage than in the long-term extension of the Phase 3 trial in PAH.
Disciplines :
Cardiovascular & respiratory systems
Author, co-author :
Hoeper, Marius M.
Gomez Sanchez, Miguel-Angel
Humbert, Marc
Pittrow, David
Simonneau, Gérald
Gall, Henning
Grünig, Ekkehard
Klose, Hans
Halank, Michael
Langleben, David
Snijder, Repke J.
Escribano Subias, Pilar
Mielniczuk, Lisa M.
Lange, Tobias J.
Vachiéry, Jean-Luc
Wirtz, Hubert
Helmersen, Douglas S.
Tsangaris, Iraklis
Barberà, Joan A.
Pepke-Zaba, Joanna
Boonstra, Anco
Rosenkranz, Stephan
Ulrich, Silvia
Steringer-Mascherbauer, Regina
Delcroix, Marion
Jansa, Pavel
Šimková, Iveta
Giannakoulas, George
Klotsche, Jens
Williams, Evgenia
Meier, Christian
Ghofrani, Hossein-Ardeschir
More authors (22 more) Less
Other collaborator :
Louis, Renaud ;  Université de Liège - ULiège > Département des sciences cliniques > Pneumologie - Allergologie
Language :
English
Title :
Riociguat treatment in patients with pulmonary arterial hypertension: Final safety data from the EXPERT registry.
Publication date :
03 December 2020
Journal title :
Respiratory Medicine
ISSN :
0954-6111
eISSN :
1532-3064
Publisher :
Elsevier, Oxford, United Kingdom
Volume :
177
Pages :
106241
Peer reviewed :
Peer Reviewed verified by ORBi
Commentary :
Copyright © 2020 The Author(s). Published by Elsevier Ltd.. All rights reserved.
Available on ORBi :
since 04 May 2021

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