TY - JOUR
T1 - Oral treprostinil improves pulmonary vascular compliance in pulmonary arterial hypertension
AU - Khan, Akram
AU - White, R. James
AU - Meyer, Gisela
AU - Pulido Zamudio, Tomas R.
AU - Jerjes-Sanchez, Carlos
AU - Johnson, Dana
AU - Grover, Rob
AU - Broderick, Meredith
AU - Ousmanou, Aliou
AU - Holdstock, Louis
AU - Michelakis, Evangelos
N1 - Funding Information:
The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: RJW has received research support and travel support for associated research presentations from United Therapeutics, and consulting fees from Bayer and Merck. TRPZ has research grants from Janssen, Bayer, and United Therapeutics, is on the advisory board of Janssen, Bayer, and Ferrer, and received lecture honoraria for Actelion/Janssen, Bayer, Pfizer, and Ferrer. DJ, RG, MB, AO, and LH are employees of United Therapeutics. Akram Khan has recieved research support from United Theraputics, Johnson & Johnson, Ely Lilly, 4D Medical.
Publisher Copyright:
© 2022 The Authors
PY - 2022/3
Y1 - 2022/3
N2 - Oral treprostinil has been shown to improve exercise capacity and delay disease progression in patients with pulmonary arterial hypertension (PAH), but its effects on hemodynamics are not well-characterized. The FREEDOM-EV trial was a Phase III, international, placebo-controlled, double-blind, event-driven study in 690 participants with PAH who were taking a single oral PAH therapy. FREEDOM-EV demonstrated a significantly reduced risk for clinical worsening with oral treprostinil taken three times daily and did not uncover new safety signals in PAH patients. Sixty-one participants in the FREEDOM-EV trial volunteered for a hemodynamics sub-study. Pulmonary artery compliance (PAC), a ratio of stroke volume to pulmonary pulse pressure, significantly increased from Baseline to Week 24 in the oral treprostinil group compared with the placebo group (geometric mean 26.4% active vs. -6.0% placebo; ANCOVA p=0.007). There was a significant increase in cardiac output in the oral treprostinil group compared to the placebo group (geometric mean 11.3% active vs. -6.4% placebo; ANCOVA p=0.005) and a corresponding significant reduction in pulmonary vascular resistance (PVR) (geometric mean -21.5 active vs. -1.8% placebo; ANCOVA p=0.02) from Baseline to Week 24. These data suggest that increased compliance contributes to the physiological mechanism by which oral treprostinil improves exercise capacity and delays clinical worsening for patients with PAH.
AB - Oral treprostinil has been shown to improve exercise capacity and delay disease progression in patients with pulmonary arterial hypertension (PAH), but its effects on hemodynamics are not well-characterized. The FREEDOM-EV trial was a Phase III, international, placebo-controlled, double-blind, event-driven study in 690 participants with PAH who were taking a single oral PAH therapy. FREEDOM-EV demonstrated a significantly reduced risk for clinical worsening with oral treprostinil taken three times daily and did not uncover new safety signals in PAH patients. Sixty-one participants in the FREEDOM-EV trial volunteered for a hemodynamics sub-study. Pulmonary artery compliance (PAC), a ratio of stroke volume to pulmonary pulse pressure, significantly increased from Baseline to Week 24 in the oral treprostinil group compared with the placebo group (geometric mean 26.4% active vs. -6.0% placebo; ANCOVA p=0.007). There was a significant increase in cardiac output in the oral treprostinil group compared to the placebo group (geometric mean 11.3% active vs. -6.4% placebo; ANCOVA p=0.005) and a corresponding significant reduction in pulmonary vascular resistance (PVR) (geometric mean -21.5 active vs. -1.8% placebo; ANCOVA p=0.02) from Baseline to Week 24. These data suggest that increased compliance contributes to the physiological mechanism by which oral treprostinil improves exercise capacity and delays clinical worsening for patients with PAH.
KW - Cardiac output
KW - FREEDOM-EV
KW - Hemodynamics
KW - PVR
KW - Right-heart catherization
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UR - http://www.scopus.com/inward/citedby.url?scp=85123992182&partnerID=8YFLogxK
U2 - 10.1016/j.rmed.2022.106744
DO - 10.1016/j.rmed.2022.106744
M3 - Article
C2 - 35134631
AN - SCOPUS:85123992182
SN - 0954-6111
VL - 193
JO - Respiratory Medicine
JF - Respiratory Medicine
M1 - 106744
ER -