Riociguat treatment in patients with chronic thromboembolic pulmonary hypertension: Final safety data from the EXPERT registry
Šimková Iveta; Tsangaris Iraklis; Wirtz Hubert; Escribano Subias Pilar; Helmersen Douglas S; Giannakoulas George; Delcroix Marion; Meier Christian; Pepke-Zaba Joanna; Humbert Marc; Klotsche Jens; Lange Tobias J; Snijder Repke J; Ulrich Silvia; Simonneau Gérald; Barberá Joan A; Halank Michael; Gall Henning; Mielniczuk Lisa M; Hoeper Marius M; EXPERT new collaborators list; Langleben David; Grünig Ekkehard; Steringer-Mascherbauer Regina; Klose Hans; Ghofrani Hossein-Ardeschir; Boonstra Anco; Pittrow David; Jansa Pavel; Vachiéry Jean-Luc; Williams Evgenia; Gomez Sanchez Miguel-Angel; Rosenkranz Stephan
Riociguat treatment in patients with chronic thromboembolic pulmonary hypertension: Final safety data from the EXPERT registry
Šimková Iveta
Tsangaris Iraklis
Wirtz Hubert
Escribano Subias Pilar
Helmersen Douglas S
Giannakoulas George
Delcroix Marion
Meier Christian
Pepke-Zaba Joanna
Humbert Marc
Klotsche Jens
Lange Tobias J
Snijder Repke J
Ulrich Silvia
Simonneau Gérald
Barberá Joan A
Halank Michael
Gall Henning
Mielniczuk Lisa M
Hoeper Marius M; EXPERT new collaborators list
Langleben David
Grünig Ekkehard
Steringer-Mascherbauer Regina
Klose Hans
Ghofrani Hossein-Ardeschir
Boonstra Anco
Pittrow David
Jansa Pavel
Vachiéry Jean-Luc
Williams Evgenia
Gomez Sanchez Miguel-Angel
Rosenkranz Stephan
Elsevier
Julkaisun pysyvä osoite on:
https://urn.fi/URN:NBN:fi-fe2021042821812
https://urn.fi/URN:NBN:fi-fe2021042821812
Tiivistelmä
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 (CTEPH) 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 and collated via case report forms.
Results
In total, 956 patients with CTEPH were included in the analysis. The most common AEs in these patients were peripheral edema/edema (11.7%), dizziness (7.5%), right ventricular (RV)/cardiac failure (7.7%), and pneumonia (5.0%). The most common SAEs were RV/cardiac failure (7.4%), pneumonia (4.1%), dyspnea (3.6%), and syncope (2.5%). Exposure-adjusted rates of hemoptysis/pulmonary hemorrhage and hypotension were low and comparable to those in the long-term extension study of riociguat (Chronic Thromboembolic Pulmonary Hypertension Soluble Guanylate Cyclase–Stimulator Trial [CHEST-2]).
Conclusion
Data from EXPERT show that in patients with CTEPH, the safety of riociguat in routine practice was consistent with the known safety profile of the drug, and no new safety concerns were identified.
Kokoelmat
- Rinnakkaistallenteet [19207]