Riociguat treatment in patients with chronic thromboembolic pulmonary hypertension: Final safety data from the EXPERT registry

Επιστημονική δημοσίευση - Άρθρο Περιοδικού uoadl:3102729 66 Αναγνώσεις

Μονάδα:
Ερευνητικό υλικό ΕΚΠΑ
Τίτλος:
Riociguat treatment in patients with chronic thromboembolic pulmonary hypertension: Final safety data from the EXPERT registry
Γλώσσες Τεκμηρίου:
Αγγλικά
Περίληψη:
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. © 2020 The Authors
Έτος δημοσίευσης:
2021
Συγγραφείς:
Ghofrani, H.-A.
Gomez Sanchez, M.-A.
Humbert, M.
Pittrow, D.
Simonneau, G.
Gall, H.
Grünig, E.
Klose, H.
Halank, M.
Langleben, D.
Snijder, R.J.
Escribano Subias, P.
Mielniczuk, L.M.
Lange, T.J.
Vachiéry, J.-L.
Wirtz, H.
Helmersen, D.S.
Tsangaris, I.
Barberá, J.A.
Pepke-Zaba, J.
Boonstra, A.
Rosenkranz, S.
Ulrich, S.
Steringer-Mascherbauer, R.
Delcroix, M.
Jansa, P.
Šimková, I.
Giannakoulas, G.
Klotsche, J.
Williams, E.
Meier, C.
Hoeper, M.M.
Caneva, J.
Tuhay, G.
Diez, M.
Talavera, M.L.
Acosta, A.
Vulcano, N.
Bosio, M.
Maldonado, L.
Deleo, S.
Melatini, L.
Keogh, A.
Kotlyar, E.
Feenstra, J.
Dwyer, N.
Adams, H.
Stevens, W.
Steele, P.
Proudman, S.
Minson, R.
Reeves, G.
Lavender, M.
Ng, B.
Mackenzie, M.
Barry, L.
Gruenberger, M.
Huber, C.
Lang, I.
Tilea, I.
Sadushi-Kolici, R.
Löffler-Ragg, J.
Feistmantl, L.-T.
Evrard, P.
Louis, R.
Guiot, J.
Naldi, M.
De Pauw, M.
Mehta, S.
Camacho, R.C.
Tovar, P.P.
Londoño, A.
Campo, F.
Garcia, P.
Lema, C.
Orozco-Levi, M.
Martinez, W.
Gomez, J.E.
Nielsen-Kudsk, J.E.
Mellemkjaer, S.
Anton, L.
Altraja, A.
Vihinen, T.
Vasankari, T.
Sitbon, O.
Cottin, V.
Têtu, L.
Noël-Savina, E.
Shearman, N.
Tayler, S.
Olzik, I.
Kulka, C.
Grimminger, J.
Simon, M.
Nolde, A.
Oqueka, T.
Harbaum, L.
Egenlauf, B.
Ewert, R.
Schulz, C.
Regotta, S.
Kramer, T.
Knoop-Busch, S.
Gerhardt, F.
Konstantinides, S.
Pitsiou, G.
Stanopoulos, I.
Sourla, E.
Mouratoglou, S.
Karvounis, H.
Pappas, A.
Georgopoulos, D.
Fanaridis, M.
Mitrouska, I.
Michalis, L.
Pappas, K.
Kotsia, A.
Gaine, S.
Vizza, C.D.
Manzi, G.
Poscia, R.
Badagliacca, R.
Agostoni, P.
Bruno, N.
Farina, S.
D'Alto, M.
Argiento, P.
Correra, A.
Di Marco, G.M.
Cresci, C.
Vannucchi, V.
Torricelli, E.
Garcea, A.
Pesci, A.
Sardella, L.
Paciocco, G.
Pane, F.
D'Armini, A.M.
Pin, M.
Grazioli, V.
Massola, G.
Sciortino, A.
Prediletto, R.
Bauleo, C.
Airò, E.
Ndreu, R.
Pavlickova, I.
Lunardi, C.
Mulè, M.
Farruggio, S.
Costa, S.
Galgano, G.
Petruzzi, M.
De Luca, A.
Lombardi, F.
Roncon, L.
Conte, L.
Picariello, C.
Wirtz, G.
Alexandre, M.
Vonk-Noordegraaf, A.
Boogaard, H.
Mager, J.
Reesink, H.
van den Toorn, L.M.
Boomars, K.
Andreassen, A.K.
Castro, G.
Tania, G.
Baptista, R.
Marinho, A.
Shiang, T.
Oliveira, A.
Coutinho, D.
Sousa, J.
Loureiro, M.J.
Repolho, D.
Martins Jesus, S.M.
Capinha, M.
Agostinho, J.
Cardoso, T.
Rocha, A.
Espinha, M.
Ivanov, K.I.
Alexeeva, D.E.
Batalina, M.V.
Hegya, D.V.
Zvereva, T.N.
Avdeev, S.N.
Tsareva, N.A.
Galyavich, A.S.
Nikolaevich, B.A.
Filippov, E.V.
Yakovleva, O.E.
Pavlova, O.B.
Skripkina, E.S.
Martynyuk, T.V.
Bukatova, I.F.
Tregubova, A.V.
Platonov, D.Y.
Kolomeytseva, T.M.
Al Dalaan, A.
Abdelsayed, A.A.
Weheba, I.
Saleemi, S.
Sakkijha, H.
Bohacekova, M.
Valkovicova, T.
Farkasova, I.
Quezada, C.A.
Piccari, L.
Blanco, I.
Sebastian, L.
Roman, A.
Lopez, M.
Otero, R.
Elias, T.
Jara, L.
Asencio, I.
Arjona, J.J.
Almagro, R.M.
Cárdenas, S.L.
García, S.A.
Rodríguez, P.V.
Lopez, R.
Garcia, A.
Avilés, F.F.
De La Pava, S.
Yotti, R.
Peñate, G.P.
Marrero, F.L.
Cifrián Martínez, J.M.
Martinez-Meñaca, A.
Alonso, L.P.
Rozas, S.F.
Fernandez, D.I.
Cuesta, V.M.
Söderberg, S.
Bartfay, S.-E.
Rundqvist, B.
Alfetlawi, M.
Wodlin, P.
Schwarz, E.I.
Speich, R.
Lador, F.
Rochat, T.
Gasche-Soccal, P.
Hsu, C.-H.
Lin, T.-H.
Su, H.-M.
Lai, W.-T.
Chu, C.Y.
Hsu, P.-C.
Voon, W.-C.
Yen, H.-W.
Yih-Jer Wu, J.
Wu, S.-H.
Huang, W.-P.
Fong, M.-C.
Huang, C.-L.
Kuo, P.-H.
Lin, Y.-H.
Lin, J.-L.
Hung, C.-S.
Wu, C.-K.
Sung, S.-H.
Huang, W.-C.
Cheng, C.-C.
Kuo, S.-H.
Wang, W.-H.
Ho, W.-J.
Hsu, T.-S.
Mutlu, B.
Atas, H.
Ongen, G.
Un, Z.
Okumus, G.
Hanta, I.
Corris, P.
Peacock, A.
Church, C.
Toshner, M.
Newnham, M.
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Περιοδικό:
Advances in Respiratory Medicine
Εκδότης:
W.B. Saunders Ltd
Τόμος:
178
Λέξεις-κλειδιά:
ambrisentan; bosentan; guanylate cyclase; iloprost; macitentan; prostacyclin; prostanoid; riociguat; treprostinil; pyrazole derivative; pyrimidine derivative; riociguat, adverse event; aged; Article; chronic thromboembolic pulmonary hypertension; clinical practice; clinical trial; cohort analysis; combination drug therapy; disease registry; dizziness; drug safety; dyspnea; faintness; female; heart right ventricle failure; hemoptysis; human; hypotension; lung hemorrhage; major clinical study; male; Medical Dictionary for Regulatory Activities; monotherapy; multicenter study; peripheral edema; phase 3 clinical trial; pneumonia; priority journal; prospective study; pulmonary hypertension; randomized controlled trial; chronic disease; complication; data analysis; lung embolism; middle aged; multicenter study (topic); pulmonary hypertension; randomized controlled trial (topic); recurrent disease; register; safety; time factor; treatment outcome, Aged; Chronic Disease; Data Analysis; Female; Humans; Hypertension, Pulmonary; Male; Middle Aged; Multicenter Studies as Topic; Prospective Studies; Pulmonary Embolism; Pyrazoles; Pyrimidines; Randomized Controlled Trials as Topic; Recurrence; Registries; Safety; Time Factors; Treatment Outcome
Επίσημο URL (Εκδότης):
DOI:
10.1016/j.rmed.2020.106220
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