TY - JOUR
T1 - Positive Predictors for Response to Ambrisentan Combination Therapy in Pulmonary Arterial Hypertension
AU - Hatano, Masaru
AU - Abe, Kohtaro
AU - Koike, George
AU - Takahashi, Tomohiko
AU - Tunmer, Grant
AU - Kiely, David G.
N1 - Funding Information:
Conflicts of interest: MH works in a department endowed by Actelion Pharmaceuticals Japan, Nippon Shinyaku Co. Ltd, and Mochida Pharmaceutical Co. Ltd, and has received personal fees from Bayer Yakuhin Ltd, Actelion Pharmaceuticals Japan, Pfizer Japan Inc., and Nippon Shinyaku Co. Ltd. KA has received consulting fees from Actelion Pharmaceuticals Japan and a research grant from Mochida Pharmaceutical Co. Ltd. GK declares no competing interests. TT is a former employee of GSK. GT is an employee of GSK and holds GSK stocks/shares. DGK has received consulting fees and funding to attend educational meetings from Actelion, Bayer, GSK, and MSD, and his department has received grant funding from Actelion and GSK. Author contributions: MH, GT, and TT conceived of the analysis. MH, KA, GK, and DGK were involved in data acquisition in the AMBITION study. TT and GK performed the current analysis. All authors contributed to data interpretation. All authors revised the manuscript critically for important intellectual content, approved the final version for publication, and agreed to be listed as authors. Declarations: Ethics approval and informed consent to participate. The protocol was approved by the Institutional Review Boards and/or Independent Ethics Committees at each center. Details have been described previously.6,9,11) Trial registration: NCT01178073; A Study of First-Line Ambrisentan and Tadalafil Combination Therapy in Subjects With Pulmonary Arterial Hypertension (PAH) (AMBITION); https://www.clinicaltrials.gov/ct2/show/NCT011 78073?term=NCT01178073&draw=2&rank=1 Data availability: Anonymized individual participant data and study documents can be requested for further research from www.clinicalstudydatarequest.com or should be directed to the corresponding author.
Funding Information:
From the 1Department of Therapeutic Strategy for Heart Failure, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan, 2Department of Cardiovascular Medicine, Kyushu University Hospital, Fukuoka, Japan, 3Department of Internal Medicine, Fukuoka University Nishijin Hospital, Fukuoka, Japan, 4GSK K.K, Medical Division, Tokyo, Japan, 5GSK, Brentford, London, UK and 6Department of Infection, Immunity and Cardiovascular Disease, University of Sheffield, UK. The AMBITION study was funded by GlaxoSmithKline (GSK; study number 112565; trial registration number: NCT01178073) and Gilead Sciences, Inc. Address for correspondence: Masaru Hatano, MD, Department of Therapeutic Strategy for Heart Failure, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-Ku, Tokyo 113-8655 Japan. E-mail: hatanoma@pg8.so-net.ne.jp Received for publication August 6, 2021. Revised and accepted November 8, 2021. doi: 10.1536/ihj.21-497 All rights reserved by the International Heart Journal Association.
Funding Information:
GlaxoSmithKline (GSK) funded this post hoc analysis. Trademarks are owned by or licensed to the GSK group of companies and Gilead Sciences, Inc. The results of this analysis were presented in part as a poster presentation at the European Society of Cardiology congress, 2020 (abstract supplement of the European Heart Journal-Volume 41, October 2020). This submission was supported by Yasuo Nakajima MPharm (GSK). Editorial support, including submission of the manuscript, was provided by Liz Morgan, PhD, at Fishawack Indicia Ltd of Fishawack Health, UK, and was funded by GSK. The listed authors have authorized the submission of their manuscript via Fishawack Indicia Ltd of Fishawack Health, UK, and approved the declaration of funding, conflicting interests, and data availability.
Publisher Copyright:
© All rights reserved by the International Heart Journal Association.
PY - 2022
Y1 - 2022
N2 - The AMBITION study (NCT01178073) provided the first long-term clinical evidence for initial combination therapy with ambrisentan and tadalafil in patients with pulmonary arterial hypertension (PAH). Nevertheless, predictors of treatment response were not assessed. To identify predictors for response to initial combination therapy, we examined pdata from 302 patients with PAH (World Health Organization Functional Class II or III) who received initial combination therapy from the modified intention-to-treat population of the AMBITION study (n = 605). A responder was defined as not having undergone a clinical failure event. Univariate and multivariate analyses were performed. Multivariate logistic regression with interactive backward selection was used to assess the independent association of potential predictors with response. Treatment responders were younger, more often female, and less likely to have comorbidities or a requirement for oxygen therapy, compared with nonresponders. At multivariate analysis, female sex (odds ratio [OR] 2.67; 95% confidence interval [CI] 1.29, 5.52; P = 0.0081), longer 6-minute walk distance (OR 1.01; 95% CI 1.00, 1.01; P = 0.0039), lower baseline log N-terminal-prohormone of brain natriuretic peptide (OR 0.70; 95% CI 0.52, 0.94; P = 0.0190), and aldosterone antagonist use (OR 2.54; 95% CI 1.03, 6.26; P = 0.0436) independently predicted response to initial combination therapy. Besides demographic factors, the absence of comorbidities and less severe disease state, and the use of aldosterone antagonist therapy identified patients with PAH most likely to respond to initial combination therapy with ambrisentan and tadalafil. Further study to evaluate the role of aldosterone antagonist therapy in PAH is warranted.
AB - The AMBITION study (NCT01178073) provided the first long-term clinical evidence for initial combination therapy with ambrisentan and tadalafil in patients with pulmonary arterial hypertension (PAH). Nevertheless, predictors of treatment response were not assessed. To identify predictors for response to initial combination therapy, we examined pdata from 302 patients with PAH (World Health Organization Functional Class II or III) who received initial combination therapy from the modified intention-to-treat population of the AMBITION study (n = 605). A responder was defined as not having undergone a clinical failure event. Univariate and multivariate analyses were performed. Multivariate logistic regression with interactive backward selection was used to assess the independent association of potential predictors with response. Treatment responders were younger, more often female, and less likely to have comorbidities or a requirement for oxygen therapy, compared with nonresponders. At multivariate analysis, female sex (odds ratio [OR] 2.67; 95% confidence interval [CI] 1.29, 5.52; P = 0.0081), longer 6-minute walk distance (OR 1.01; 95% CI 1.00, 1.01; P = 0.0039), lower baseline log N-terminal-prohormone of brain natriuretic peptide (OR 0.70; 95% CI 0.52, 0.94; P = 0.0190), and aldosterone antagonist use (OR 2.54; 95% CI 1.03, 6.26; P = 0.0436) independently predicted response to initial combination therapy. Besides demographic factors, the absence of comorbidities and less severe disease state, and the use of aldosterone antagonist therapy identified patients with PAH most likely to respond to initial combination therapy with ambrisentan and tadalafil. Further study to evaluate the role of aldosterone antagonist therapy in PAH is warranted.
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U2 - 10.1536/ihj.21-497
DO - 10.1536/ihj.21-497
M3 - Article
C2 - 35095084
AN - SCOPUS:85123904931
SN - 1349-2365
VL - 63
SP - 99
EP - 105
JO - International heart journal
JF - International heart journal
IS - 1
ER -