马昔腾坦与他达拉非联合治疗肺动脉高压合并心血管疾病患者:来自OPUS和OrPHeUS的真实世界证据

Macitentan and Tadalafil Combination Therapy in Patients with Pulmonary Arterial Hypertension and Cardiovascular Comorbidities: Real-World Evidence from OPUS and OrPHeUS.

作者信息

Kim Nick H, Chin Kelly M, McLaughlin Vallerie V, Ong Rose, MacDonald Gwen, Martin Nicolas, Senatore Assunta, Channick Richard

机构信息

Pulmonary Vascular Medicine, University of California San Diego, 9300 Campus Point Dr., La Jolla, CA, MC7381, USA.

UT Southwestern Medical Center, Dallas, TX, USA.

出版信息

Adv Ther. 2025 May 19. doi: 10.1007/s12325-025-03180-0.

Abstract

INTRODUCTION

Patients diagnosed with pulmonary arterial hypertension (PAH) often present with risk factors associated with cardiovascular disease, including diabetes mellitus (DM), hypertension (HTN), and obesity. The 2022 ESC/ERS pulmonary hypertension treatment guidelines recommend initial monotherapy with an endothelin receptor antagonist (ERA) or phosphodiesterase-5 inhibitor (PDE5i) for patients with PAH and cardiopulmonary comorbidities, with treatment escalation to be considered on an individual basis. Data on safety, tolerability, and effectiveness of combination therapy in these patients are lacking.

METHODS

OPUS (prospective, observational drug registry) and OrPHeUS (retrospective, medical chart review) were multicenter US studies of patients newly initiating the ERA macitentan (2013-2020). Patients in the combined OPUS/OrPHeUS dataset with PAH receiving combination therapy with macitentan and the PDE5i tadalafil were identified. Descriptive analyses were performed for patients with ≥ 1 of DM/HTN/obesity and those without these comorbidities.

RESULTS

In OPUS/OrPHeUS, 1336 patients with PAH received macitentan plus tadalafil during the observation period. Of these, 820 (61.4%) had ≥ 1 of DM/HTN/obesity and 516 (38.6%) had none of these comorbidities at or before enrollment. Median (Q1, Q3) exposure to macitentan and tadalafil combination therapy was similar at 13.7 (3.5, 28.0) and 14.8 (5.4, 27.4) months, respectively. For patients with ≥ 1 of DM/HTN/obesity versus those without, 1-year Kaplan-Meier estimates (95% confidence limits) for survival were 92.3% (89.9, 94.1) and 91.9% (88.8, 94.1), for patients free from hospitalization were 63.6% (59.6, 67.2) and 60.0% (55.1, 64.5), and for patients persisting on combination therapy were 66.5% (63.1, 69.8) and 68.5% (64.1, 72.4). Adverse events (AE; OPUS only) were reported in 78.4% and 80.0%, respectively, with no unexpected AEs observed. There was a trend towards higher AE incidence with increasing comorbidity number and in patients with cardiovascular comorbidities who were treatment-naïve.

CONCLUSION

Patients with PAH and ≥ 1 of diabetes mellitus, hypertension, or obesity treated with macitentan and tadalafil combination therapy had similar hospitalization, survival, and safety profiles as those without these comorbidities, though patients with comorbidities initiated on combination therapy and those with multiple comorbidities may require closer monitoring. These real-world data suggest that combination therapy may be considered for patients with PAH and cardiovascular comorbidities.

TRIAL REGISTRATION

OPsumit Users Registry (OPUS): NCT02126943; Opsumit Historical Users cohort (OrPHeUS): NCT03197688; URL https://www.

CLINICALTRIALS

gov/.

摘要

引言

被诊断为肺动脉高压(PAH)的患者常常伴有与心血管疾病相关的风险因素,包括糖尿病(DM)、高血压(HTN)和肥胖症。2022年欧洲心脏病学会/欧洲呼吸学会肺动脉高压治疗指南建议,对于患有PAH和心肺合并症的患者,初始采用内皮素受体拮抗剂(ERA)或磷酸二酯酶-5抑制剂(PDE5i)进行单药治疗,并根据个体情况考虑升级治疗。目前缺乏关于这些患者联合治疗的安全性、耐受性和有效性的数据。

方法

OPUS(前瞻性观察性药物登记)和OrPHeUS(回顾性病历审查)是在美国进行的多中心研究,研究对象为新开始使用ERA马昔腾坦(2013 - 2020年)的患者。在OPUS/OrPHeUS合并数据集中,确定接受马昔腾坦和PDE5i他达拉非联合治疗的PAH患者。对患有≥1种DM/HTN/肥胖症的患者和没有这些合并症的患者进行描述性分析。

结果

在OPUS/OrPHeUS中,1336例PAH患者在观察期内接受了马昔腾坦加他达拉非治疗。其中,820例(61.4%)在入组时或入组前患有≥1种DM/HTN/肥胖症,516例(38.6%)没有这些合并症。马昔腾坦和他达拉非联合治疗的中位(Q1,Q3)暴露时间相似,分别为13.7(3.5,28.0)个月和14.8(5.4,27.4)个月。对于患有≥1种DM/HTN/肥胖症的患者与没有这些合并症的患者,1年的Kaplan-Meier生存估计值(95%置信区间)分别为92.3%(89.9,94.1)和91.9%(88.8,94.1);无住院患者的估计值分别为63.6%(5

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