Univ. Paris-Sud, Faculté de Médecine, Université Paris-Saclay, Le Kremlin-Bicêtre, France AP-HP, Service de Pneumologie, Hôpital Bicêtre, Le Kremlin-Bicêtre, France INSERM UMR_S 999, Hôpital Marie-Lannelongue, Le Plessis-Robinson, France
Univ. Paris-Sud, Faculté de Médecine, Université Paris-Saclay, Le Kremlin-Bicêtre, France AP-HP, Service de Pneumologie, Hôpital Bicêtre, Le Kremlin-Bicêtre, France INSERM UMR_S 999, Hôpital Marie-Lannelongue, Le Plessis-Robinson, France.
Eur Respir J. 2016 Jun;47(6):1727-36. doi: 10.1183/13993003.02043-2015. Epub 2016 Mar 17.
Treatment for pulmonary arterial hypertension (PAH) has been underpinned by single-agent therapy to which concomitant drugs are added sequentially when pre-defined treatment goals are not met.This retrospective analysis of real-world clinical data in 97 patients with newly diagnosed PAH (86% in New York Heart Association functional class III-IV) explored initial dual oral combination treatment with bosentan plus sildenafil (n=61), bosentan plus tadalafil (n=17), ambrisentan plus tadalafil (n=11) or ambrisentan plus sildenafil (n=8).All regimens were associated with significant improvements in functional class, exercise capacity, dyspnoea and haemodynamic indices after 4 months of therapy. Over a median follow-up period of 30 months, 75 (82%) patients were still alive, 53 (71%) of whom received only dual oral combination therapy. Overall survival rates were 97%, 94% and 83% at 1, 2 and 3 years, respectively, and 96%, 94% and 84%, respectively, for the patients with idiopathic PAH, heritable PAH and anorexigen-induced PAH. Expected survival rates calculated from the French equation for the latter were 86%, 75% and 66% at 1, 2 and 3 years, respectively.Initial combination of oral PAH-targeted medications may offer clinical benefits, especially in PAH patients with severe haemodynamic impairment.
肺动脉高压(PAH)的治疗一直以单一药物治疗为基础,如果未达到预定的治疗目标,则会序贯添加联合药物。本回顾性分析了 97 例新诊断的 PAH 患者(86%为纽约心脏协会功能分类 III-IV 级)的真实临床数据,这些患者接受了初始的双联口服联合治疗,包括波生坦联合西地那非(n=61)、波生坦联合他达拉非(n=17)、安立生坦联合他达拉非(n=11)或安立生坦联合西地那非(n=8)。所有方案在治疗 4 个月后,均能显著改善患者的功能分级、运动能力、呼吸困难和血液动力学指标。中位随访 30 个月期间,75 例(82%)患者存活,其中 53 例(71%)仅接受了双联口服联合治疗。1、2 和 3 年的总体生存率分别为 97%、94%和 83%,特发性 PAH、遗传性 PAH 和食欲抑制剂诱导的 PAH 患者的生存率分别为 96%、94%和 84%。根据法国方程计算,后两者的预期生存率分别为 1、2 和 3 年的 86%、75%和 66%。PAH 靶向药物的初始联合治疗可能具有临床获益,尤其是对血流动力学严重受损的 PAH 患者。