Long-Term Clinical Outcomes of Sotatercept in Pulmonary Hypertension: A Retrospective Cohort Analysis

医学 狼牙棒 倾向得分匹配 内科学 危险系数 回顾性队列研究 比例危险模型 肺动脉高压 队列研究 心脏病学 置信区间 经皮冠状动脉介入治疗 心肌梗塞
作者
Azka Naeem,Olayiwola Bolaji,George G. Kidess,Joud Fahed,Sultana Jahan,Muhammad Hashim Khan,Shaunak Mangeshkar,Steven Sorci,Hayah Kassis George,Sourbha S. Dani,M. Chadi Alraies
出处
期刊: [Cold Spring Harbor Laboratory]
标识
DOI:10.1101/2025.08.05.25333015
摘要

Abstract Background Sotatercept, an activin receptor ligand trap, has demonstrated significant short-term hemodynamic improvements in pulmonary hypertension (PH) based on clinical trials. However, evidence regarding long-term outcomes in real-world settings remains limited. Methods Using data from the TriNetX global federated health research network covering 102 healthcare organizations, we conducted a retrospective cohort study comparing 185 patients with PH receiving sotatercept to 212,349 PH patients not receiving sotatercept. After 1:1 propensity score matching to balance baseline characteristics, we assessed outcomes at 6 months, 1 year, 3 years, and 5 years post-initiation and cox proportional hazards was used. Primary outcomes included all-cause mortality, rehospitalization rates, major adverse cardiovascular events (MACE), and BNP elevation (≥100 pg/mL). Results Over 5 years of follow-up, sotatercept treatment was associated with significantly lower all-cause mortality (5.4% vs. 27.3%; risk difference, -21.9 percentage points [95% CI, -29.1 to -14.7]; p<0.001; hazard ratio [HR], 0.40 [95% CI, 0.16-0.99]). Rehospitalization rates were also substantially reduced in the sotatercept group (15.4% vs. 38.1%; risk difference, -22.8 percentage points [95% CI, - 35.8 to -9.7]; p=0.002; HR, 0.12 [95% CI, 0.03-0.49]). MACE occurrence was significantly lower with sotatercept (6.4% vs. 15.5%; risk difference, -9.1 percentage points [95% CI, -16.2 to -2.0]; p=0.011; HR, 0.45 [95% CI, 0.14-1.41]), while BNP elevation showed no significant difference (12.8% vs. 10.6%; p=0.626). Treatment benefits were observed as early as 6 months post-initiation, progressively increasing magnitude through 5 years of follow-up. Sensitivity analyses using alternative matching methods and instrumental variable approaches confirmed the robustness of these findings. Conclusions In this large real-world cohort study with long-term follow-up, sotatercept was associated with substantial reductions in mortality, rehospitalization, and cardiovascular events in patients with pulmonary hypertension. These benefits increased over time, suggesting potential disease-modifying effects beyond acute hemodynamic improvements. These findings complement data from randomized controlled trials and support the role of sotatercept in improving long-term outcomes in pulmonary hypertension.
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