Schweintzger Sabrina, Koestenberger Martin, Schlagenhauf Axel, Grangl Gernot, Burmas Ante, Kurath-Koller Stefan, Pocivalnik Mirjam, Sallmon Hannes, Baumgartner Daniela, Hansmann Georg, Gamillscheg Andreas
Division of Pediatric Cardiology, Department of Pediatrics, Medical University of Graz, Austria.
European Pediatric Pulmonary Vascular Disease Network, Berlin, Germany.
Cardiovasc Diagn Ther. 2020 Oct;10(5):1675-1685. doi: 10.21037/cdt.2020.04.01.
Macitentan, a dual endothelin receptor antagonist (ERA), was approved in 2014 for the treatment of adults with idiopathic pulmonary arterial hypertension (PAH). Once-per-day dosing and low potential hepatic toxicity make macitentan an appealing therapeutic option for children with PAH, but reports on its use in pediatric patients are still lacking.
Prospective observational study of 18 children [10 male; median age: 8.5, minimum (min.): 0.6, maximum (max.): 16.8 years] with pulmonary hypertension (PH). Four of these 18 patients were treatment-naïve and started on a de novo macitentan therapy. The remaining 14/18 children were already on a PH-targeted pharmacotherapy (sildenafil or bosentan as monotherapy or in combination). Nine children who were on bosentan were switched to macitentan. We analyzed the 6-minute walking distance (6MWD), NYHA functional class (FC)/modified ROSS score, invasive hemodynamics, echocardiographic variables and the biomarker N-terminal pro-brain natriuretic peptide (NT-proBNP).
The median follow up was 6 months (min.: 0.5, max.: 30). Macitentan treatment was associated with improvement of invasive hemodynamics, e.g., the ratio of mean pulmonary arterial pressure/mean systemic arterial pressure decreased from a median of 62% (min.: 30%, max.: 87%) to 49% (min.: 30%, max.: 69%), P<0.05; pulmonary vascular resistance index (PVRi) decreased from a median of 7.6 (min.: 3.3, max.: 11.5) to 4.8 Wood units × m body surface area (min.: 2.5, max.: 10), P<0.05. The tricuspid annular plane systolic excursion (TAPSE) increased from a median of 1.4 (min.: 0.8, max.: 2.8) to 1.9 (min.: 0.8, max.: 2.7) cm, (P<0.05). NT-proBNP values decreased from a median of 272 (min.: 27, max.: 2,010) to 229 (min.: 23, max.: 814) pg/mL under macitentan therapy (P<0.05). The 6MWD and NYHA FC/modified ROSS score did not change significantly.
This is the first prospective study of macitentan pharmacotherapy in infants and children with PH <12 years of age. Except in one patient, macitentan treatment was well tolerated and was associated with improvements in invasive hemodynamics, longitudinal systolic RV function (TAPSE) and serum NT-proBNP values.
马西替坦是一种双重内皮素受体拮抗剂(ERA),于2014年被批准用于治疗成人特发性肺动脉高压(PAH)。每日一次给药且肝毒性低,使马西替坦成为PAH儿童患者有吸引力的治疗选择,但关于其在儿科患者中使用的报道仍然缺乏。
对18例肺动脉高压(PH)儿童[10例男性;中位年龄:8.5岁,最小(min.):0.6岁,最大(max.):16.8岁]进行前瞻性观察研究。这18例患者中有4例未接受过治疗,开始接受马西替坦从头治疗。其余14/18例儿童已经在接受针对PH的药物治疗(西地那非或波生坦单药治疗或联合治疗)。9例正在接受波生坦治疗的儿童改用马西替坦。我们分析了6分钟步行距离(6MWD)、纽约心脏协会功能分级(FC)/改良ROSS评分、有创血流动力学、超声心动图变量以及生物标志物N末端脑钠肽前体(NT-proBNP)。
中位随访时间为6个月(min.:0.5个月,max.:30个月)。马西替坦治疗与有创血流动力学改善相关,例如平均肺动脉压/平均体动脉压比值从中位值62%(min.:30%,max.:87%)降至49%(min.:30%,max.:69%),P<0.05;肺血管阻力指数(PVRi)从中位值7.6(min.:3.3,max.:11.5)降至4.8伍德单位×m体表面积(min.:2.5,max.:10),P<0.05。三尖瓣环平面收缩期位移(TAPSE)从中位值1.4(min.:0.8,max.:2.8)cm增至1.9(min.:0.8,max.:2.7)cm,(P<0.05)。在马西替坦治疗下,NT-proBNP值从中位值272(min.:27,max.:2,010)降至229(min.:23,max.:814)pg/mL(P<0.05)。6MWD和纽约心脏协会FC/改良ROSS评分无显著变化。
这是第一项关于马西替坦药物治疗12岁以下婴儿和儿童PH的前瞻性研究。除1例患者外,马西替坦治疗耐受性良好,并与有创血流动力学、纵向右心室收缩功能(TAPSE)和血清NT-proBNP值改善相关。