PMID- 34319626 OWN - NLM STAT- MEDLINE DCOM- 20220304 LR - 20220304 IS - 1365-2710 (Electronic) IS - 0269-4727 (Linking) VI - 47 IP - 2 DP - 2022 Feb TI - Comparative assessment of efficacy and safety of ambrisentan and bosentan in patients with pulmonary arterial hypertension: A meta-analysis. PG - 146-156 LID - 10.1111/jcpt.13481 [doi] AB - WHAT IS KNOWN AND OBJECTIVE: Two endothelin receptor antagonists, ambrisentan and bosentan, have been demonstrated to be effective individually compared with placebo in the treatment of patients with pulmonary arterial hypertension (PAH). This network meta-analysis compared the efficacy and safety of ambrisentan and bosentan in patients with PAH. METHODS: Clinical trials were identified from the Cochrane Central Register of Controlled Trials (CENTRAL/CCTR), EMBASE and PubMed databases. Weighted mean differences (MD) with 95% confidence intervals (CI) were calculated for continuous outcomes (6-min walk distance [6MWD] and Borg dyspnoea index [BDI]). Hazard ratio (HR) was calculated for binary outcomes, including clinical worsening, discontinuation due to adverse events (AEs) and liver dysfunction. Surface under cumulative ranking curve (SUCRA) was used to rank the treatments in each index. RESULTS: Five clinical trials from four published studies (total patients: n = 920) were included. Ambrisentan and bosentan showed no significant difference in 6MWD (MD: -1.32; 95% CI: -27.87, 25.31, SUCRA score: ambrisentan 0.73, bosentan 0.77), BDI (MD: -0.16; 95% CI: -0.98, 0.65, SUCRA score: ambrisentan 0.83, bosentan 0.66), clinical worsening (HR: 0.99; 95% CI: 0.33, 2.94, SUCRA score: ambrisentan 0.75, bosentan 0.74) and discontinuation due to AEs (HR: 0.84; 95% CI: 0.11, 5.86, SUCRA score: ambrisentan 0.47, bosentan 0.57). However, ambrisentan was significantly better than bosentan with respect to abnormal liver function (HR: 23.18; 95% CI: 2.24, 377.20, SUCRA score: ambrisentan 0.99, bosentan 0.02). WHAT IS NEW AND CONCLUSION: The results of this network meta-analysis suggest that ambrisentan was similar to bosentan in efficacy, while it exhibited better tolerability with respect to abnormal liver function in comparison with bosentan, in patients with PAH. CI - (c) 2021 John Wiley & Sons Ltd. FAU - Zhao, Qinhua AU - Zhao Q AD - Department of Pulmonary Circulation, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai, China. FAU - Guo, Na AU - Guo N AD - GlaxoSmithKline, Beijing, China. FAU - Chen, Jun AU - Chen J AD - GlaxoSmithKline, Beijing, China. FAU - Parks, Daniel AU - Parks D AD - GlaxoSmithKline, Collegeville, PA, USA. FAU - Tian, Zhuang AU - Tian Z AUID- ORCID: 0000-0003-1140-4062 AD - Department of Cardiology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China. LA - eng GR - GlaxoSmithKline (China) R&D Company Limited/ PT - Journal Article PT - Meta-Analysis PT - Review DEP - 20210728 PL - England TA - J Clin Pharm Ther JT - Journal of clinical pharmacy and therapeutics JID - 8704308 RN - 0 (Antihypertensive Agents) RN - 0 (Endothelin Receptor Antagonists) RN - 0 (Phenylpropionates) RN - 0 (Pyridazines) RN - HW6NV07QEC (ambrisentan) RN - Q326023R30 (Bosentan) SB - IM MH - Antihypertensive Agents/administration & dosage/adverse effects/*therapeutic use MH - Bosentan/administration & dosage/adverse effects/*therapeutic use MH - Endothelin Receptor Antagonists/administration & dosage/adverse effects/*therapeutic use MH - Humans MH - Liver Function Tests MH - Network Meta-Analysis MH - Phenylpropionates/administration & dosage/adverse effects/*therapeutic use MH - Pulmonary Arterial Hypertension/*drug therapy MH - Pyridazines/administration & dosage/adverse effects/*therapeutic use MH - Randomized Controlled Trials as Topic MH - Walk Test OTO - NOTNLM OT - 6-min walk distance OT - Borg dyspnoea index OT - liver dysfunction OT - network meta-analysis OT - randomized controlled trials EDAT- 2021/07/29 06:00 MHDA- 2022/03/05 06:00 CRDT- 2021/07/28 12:59 PHST- 2021/06/17 00:00 [revised] PHST- 2021/05/07 00:00 [received] PHST- 2021/06/29 00:00 [accepted] PHST- 2021/07/29 06:00 [pubmed] PHST- 2022/03/05 06:00 [medline] PHST- 2021/07/28 12:59 [entrez] AID - 10.1111/jcpt.13481 [doi] PST - ppublish SO - J Clin Pharm Ther. 2022 Feb;47(2):146-156. doi: 10.1111/jcpt.13481. Epub 2021 Jul 28.