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Time to clinical improvement: an appropriate surrogate endpoint for pulmonary arterial hypertension medication trials
BACKGROUND: Many retrospective studies suggest that risk improvement may be a suitable efficacy surrogate endpoint for pulmonary arterial hypertension (PAH) medication trials. This prospective multicenter study assessed the efficacy of domestic ambrisentan in Chinese PAH patients and observed risk i...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10291317/ https://www.ncbi.nlm.nih.gov/pubmed/37378404 http://dx.doi.org/10.3389/fcvm.2023.1142721 |
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author | Wang, An Chen, Mengqi Zhuang, Qi Guan, Lihua Xie, Weiping Wang, Lan Huang, Wei Cheng, Zhaozhong Yu, Shiyong Zhou, Hongmei Shen, Jieyan |
author_facet | Wang, An Chen, Mengqi Zhuang, Qi Guan, Lihua Xie, Weiping Wang, Lan Huang, Wei Cheng, Zhaozhong Yu, Shiyong Zhou, Hongmei Shen, Jieyan |
author_sort | Wang, An |
collection | PubMed |
description | BACKGROUND: Many retrospective studies suggest that risk improvement may be a suitable efficacy surrogate endpoint for pulmonary arterial hypertension (PAH) medication trials. This prospective multicenter study assessed the efficacy of domestic ambrisentan in Chinese PAH patients and observed risk improvement and time to clinical improvement (TTCI) under ambrisentan treatment. METHODS: Eligible patients with PAH were enrolled for a 24-week treatment with ambrisentan. The primary efficacy endpoint was 6-min walk distance (Δ6MWD). The exploratory endpoints were risk improvement and TTCI, defined as the time from initiation of treatment to the first occurrence of risk improvement. RESULTS: A total of 83 subjects were enrolled. After ambrisentan treatment, Δ6MWD was significantly increased at week 12 (42.2 m, P < 0.0001) and week 24 (53.4 m, P < 0.0001). Within 24 weeks, risk improvement was observed in 53 (64.6%) subjects (P < 0.0001), which is higher than WHO-FC (30.5%) and TAPSE/PASP (32.9%). Kaplan–Meier analysis of TTCI showed a median improvement time of 131 days and a cumulative improvement rate of 75.1%. Also, TTCI is consistent across different baseline risk status populations (log-rank P = 0.51). The naive group had more risk improvement (P = 0.043) and shorter TTCI (log-rank P = 0.008) than the add-on group, while Δ6MWD did not show significant differences between the two groups. CONCLUSIONS: Domestic ambrisentan significantly improved the exercise capacity and risk status of Chinese PAH patients. TTCI has a relatively high positive event rate within 24-week treatment duration. Compared to Δ6MWD, TTCI is not affected by baseline risk status. Additionally, TTCI could identify better improvements in patients, which Δ6MWD does not detect. TTCI is an appropriate composite surrogate endpoint for PAH medication trials. CLINICAL TRIAL REGISTRATION: NCT No. [ClinicalTrials.gov], identifier [NCT05437224]. |
format | Online Article Text |
id | pubmed-10291317 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102913172023-06-27 Time to clinical improvement: an appropriate surrogate endpoint for pulmonary arterial hypertension medication trials Wang, An Chen, Mengqi Zhuang, Qi Guan, Lihua Xie, Weiping Wang, Lan Huang, Wei Cheng, Zhaozhong Yu, Shiyong Zhou, Hongmei Shen, Jieyan Front Cardiovasc Med Cardiovascular Medicine BACKGROUND: Many retrospective studies suggest that risk improvement may be a suitable efficacy surrogate endpoint for pulmonary arterial hypertension (PAH) medication trials. This prospective multicenter study assessed the efficacy of domestic ambrisentan in Chinese PAH patients and observed risk improvement and time to clinical improvement (TTCI) under ambrisentan treatment. METHODS: Eligible patients with PAH were enrolled for a 24-week treatment with ambrisentan. The primary efficacy endpoint was 6-min walk distance (Δ6MWD). The exploratory endpoints were risk improvement and TTCI, defined as the time from initiation of treatment to the first occurrence of risk improvement. RESULTS: A total of 83 subjects were enrolled. After ambrisentan treatment, Δ6MWD was significantly increased at week 12 (42.2 m, P < 0.0001) and week 24 (53.4 m, P < 0.0001). Within 24 weeks, risk improvement was observed in 53 (64.6%) subjects (P < 0.0001), which is higher than WHO-FC (30.5%) and TAPSE/PASP (32.9%). Kaplan–Meier analysis of TTCI showed a median improvement time of 131 days and a cumulative improvement rate of 75.1%. Also, TTCI is consistent across different baseline risk status populations (log-rank P = 0.51). The naive group had more risk improvement (P = 0.043) and shorter TTCI (log-rank P = 0.008) than the add-on group, while Δ6MWD did not show significant differences between the two groups. CONCLUSIONS: Domestic ambrisentan significantly improved the exercise capacity and risk status of Chinese PAH patients. TTCI has a relatively high positive event rate within 24-week treatment duration. Compared to Δ6MWD, TTCI is not affected by baseline risk status. Additionally, TTCI could identify better improvements in patients, which Δ6MWD does not detect. TTCI is an appropriate composite surrogate endpoint for PAH medication trials. CLINICAL TRIAL REGISTRATION: NCT No. [ClinicalTrials.gov], identifier [NCT05437224]. Frontiers Media S.A. 2023-06-12 /pmc/articles/PMC10291317/ /pubmed/37378404 http://dx.doi.org/10.3389/fcvm.2023.1142721 Text en © 2023 Wang, Chen, Zhuang, Guan, Xie, Wang, Huang, Cheng, Yu, Zhou and Shen. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY) (https://creativecommons.org/licenses/by/4.0/) . The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cardiovascular Medicine Wang, An Chen, Mengqi Zhuang, Qi Guan, Lihua Xie, Weiping Wang, Lan Huang, Wei Cheng, Zhaozhong Yu, Shiyong Zhou, Hongmei Shen, Jieyan Time to clinical improvement: an appropriate surrogate endpoint for pulmonary arterial hypertension medication trials |
title | Time to clinical improvement: an appropriate surrogate endpoint for pulmonary arterial hypertension medication trials |
title_full | Time to clinical improvement: an appropriate surrogate endpoint for pulmonary arterial hypertension medication trials |
title_fullStr | Time to clinical improvement: an appropriate surrogate endpoint for pulmonary arterial hypertension medication trials |
title_full_unstemmed | Time to clinical improvement: an appropriate surrogate endpoint for pulmonary arterial hypertension medication trials |
title_short | Time to clinical improvement: an appropriate surrogate endpoint for pulmonary arterial hypertension medication trials |
title_sort | time to clinical improvement: an appropriate surrogate endpoint for pulmonary arterial hypertension medication trials |
topic | Cardiovascular Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10291317/ https://www.ncbi.nlm.nih.gov/pubmed/37378404 http://dx.doi.org/10.3389/fcvm.2023.1142721 |
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