Granulocyte colony-stimulating factor for stem cell mobilisation in acute myocardial infarction: a randomised controlled trial.

IF 5.1 2区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Heart Pub Date : 2024-10-28 DOI:10.1136/heartjnl-2024-323926
Felice Achilli, Stefano Maggiolini, Fabiana Madotto, Beatrice Bassetti, Francesco Gentile, Aldo Pietro Maggioni, Gualtiero I Colombo, Giulio Pompilio
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引用次数: 0

Abstract

Background: To determine whether granulocyte colony-stimulating factor (G-CSF) improves clinical outcomes after large ST-elevation myocardial infarction (STEMI) when administered early in patients with left ventricular (LV) dysfunction after successful percutaneous coronary intervention (PCI).

Methods: STEM-AMI OUTCOME was designed as a prospective, multicentre, nationwide, randomised, open-label, phase III trial (ClinicalTrials.gov ID: NCT01969890) to demonstrate the efficacy and safety of early G-CSF administration in reducing 2-year cardiac mortality and morbidity in patients with STEMI with LV ejection fraction ≤45% after PCI. The primary outcome was a composite of all-cause death, recurrence of myocardial infarction and hospitalisation for heart failure. Due to low recruitment and event rates, the study was discontinued and did not achieve adequate statistical power to verify the hypothesis.

Results: Patients were randomly allocated to G-CSF (n=260) or standard of care (SOC; n=261). No difference was found in the composite primary outcome between study groups (HR 1.20; 95% CI 0.63 to 2.28). The 2-year mortality was 2.31% in the G-CSF and 2.68% in the control group (HR 0.88; 95% CI 0.29 to 2.60). Adverse events did not differ between the G-CSF (n=65) and SOC groups (n=58; OR 1.17; 95% CI 0.78 to 1.75). In post hoc analyses on the intervention group, we observed a trend towards fewer composite primary outcomes in patients with low bone marrow (BM) cell mobilisation (n=108) versus those with high mobilisation (n=152, with peak leucocyte count >50×109/L; HR 2.86; 95% CI 0.96 to 8.56). Primary outcomes were lower in patients with severe LV systolic dysfunction at discharge treated with G-CSF than in controls (interaction β±SE, -0.08±0.04; p=0.034).

Conclusions: Although inconclusive, this is the largest trial in the field of cell-based cardiac repair after STEMI providing evidence of the tolerability and long-term safety of G-CSF treatment. The results prompt further studies to understand which patient can benefit most from BM cell mobilisation.

Trial registration number: NCT01969890.

用于急性心肌梗死干细胞动员的粒细胞集落刺激因子:随机对照试验。
研究背景目的:确定经皮冠状动脉介入治疗(PCI)成功后左心室(LV)功能障碍患者早期使用粒细胞集落刺激因子(G-CSF)能否改善大面积ST段抬高型心肌梗死(STEMI)后的临床预后:STEM-AMI OUTCOME是一项前瞻性、多中心、全国性、随机、开放标签的III期试验(ClinicalTrials.gov ID:NCT01969890),旨在证明早期给予G-CSF对降低PCI后左心室射血分数≤45%的STEMI患者2年心脏死亡率和发病率的有效性和安全性。主要结果是全因死亡、心肌梗死复发和心力衰竭住院的综合结果。由于招募率和事件发生率较低,该研究被终止,并且没有达到验证假设的足够统计能力:患者被随机分配至G-CSF(260人)或标准护理(261人)。研究组之间的综合主要结果无差异(HR 1.20;95% CI 0.63 至 2.28)。G-CSF组的2年死亡率为2.31%,对照组为2.68%(HR为0.88;95% CI为0.29至2.60)。G-CSF组(n=65)和SOC组(n=58;OR 1.17;95% CI 0.78至1.75)的不良事件没有差异。在对干预组进行的事后分析中,我们观察到骨髓细胞动员率低的患者(108人)与动员率高的患者(152人,白细胞计数峰值>50×109/L;HR 2.86;95% CI 0.96至8.56)相比,综合主要结局有减少的趋势。接受G-CSF治疗的出院时左心室收缩功能严重障碍患者的主要结局低于对照组(交互作用β±SE,-0.08±0.04;P=0.034):尽管尚无定论,但这是 STEMI 后基于细胞的心脏修复领域最大规模的试验,为 G-CSF 治疗的耐受性和长期安全性提供了证据。试验注册号:NCT01969890:NCT01969890.
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Heart
Heart 医学-心血管系统
CiteScore
10.30
自引率
5.30%
发文量
320
审稿时长
3-6 weeks
期刊介绍: Heart is an international peer reviewed journal that keeps cardiologists up to date with important research advances in cardiovascular disease. New scientific developments are highlighted in editorials and put in context with concise review articles. There is one free Editor’s Choice article in each issue, with open access options available to authors for all articles. Education in Heart articles provide a comprehensive, continuously updated, cardiology curriculum.
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