From the Department of Cardiology, Minneapolis Heart Institute Foundation, Abbott Northwestern Hospital, MN (J.H.T., T.D.H.); Department of Medicine, University of Minnesota School of Medicine, Minneapolis (J.H.T., G.R.); Department of Medicine, Cedars Sinai Medical Center, Los Angeles, CA (T.D.H.); Department of Medicine, College of Medicine, University of Florida, Gainesville (C.J.P., J.R.F.); Stem Cell Center (J.T.W., E.C.P.), and Regenerative Medicine Research (D.A.T.), Texas Heart Institute, CHI St. Luke's Health Baylor College of Medicine Medical Center, Houston; Franciscan Saint Francis Health, Indianapolis, IN (A.C.); Department of Cardiovascular Medicine, Stanford University School of Medicine, CA (P.C.Y.); Department of Cardiology, Wake Forest University School of Medicine, Winston-Salem, NC (D.X.M.Z.); Department of Cardiovascular Medicine, Cleveland Clinic Foundation, OH (S.G.E.); Summa Health Heart and Vascular Institute, Akron, OH (M.S.P.); Department of Cell and Developmental Biology, Vanderbilt University School of Medicine, Nashville, TN (A.K.H.); Metropolitan Heart and Vascular Institute, Mercy Hospital, Coon Rapids, MN (J.C.C.); United Heart and Vascular Clinic (K.W.B.); Center for Cell and Gene Therapy, Baylor College of Medicine, Houston, TX (A.P.G.); Coordinating Center for Clinical Trials, UTHealth School of Public Health, Houston, TX (L.M.); National Heart Lung, and Blood Institute, Bethesda, MD (R.F.E.); and University of Kansas School of Medicine (R.D.S.).
Circ Res. 2018 Feb 2;122(3):479-488. doi: 10.1161/CIRCRESAHA.117.311466. Epub 2017 Dec 5.
The TIME trial (Timing in Myocardial Infarction Evaluation) was the first cell therapy trial sufficiently powered to determine if timing of cell delivery after ST-segment-elevation myocardial infarction affects recovery of left ventricular (LV) function.
To report the 2-year clinical and cardiac magnetic resonance imaging results and their modification by microvascular obstruction.
TIME was a randomized, double-blind, placebo-controlled trial comparing 150 million bone marrow mononuclear cells versus placebo in 120 patients with anterior ST-segment-elevation myocardial infarctions resulting in LV dysfunction. Primary end points included changes in global (LV ejection fraction) and regional (infarct and border zone) function. Secondary end points included changes in LV volumes, infarct size, and major adverse cardiac events. Here, we analyzed the continued trajectory of these measures out to 2 years and the influence of microvascular obstruction present at baseline on these long-term outcomes. At 2 years (n=85), LV ejection fraction was similar in the bone marrow mononuclear cells (48.7%) and placebo groups (51.6%) with no difference in regional LV function. Infarct size and LV mass decreased ≥30% in each group at 6 months and declined gradually to 2 years. LV volumes increased ≈10% at 6 months and remained stable to 2 years. Microvascular obstruction was present in 48 patients at baseline and was associated with significantly larger infarct size (56.5 versus 36.2 g), greater adverse LV remodeling, and marked reduction in LV ejection fraction recovery (0.2% versus 6.2%).
In one of the longest serial cardiac magnetic resonance imaging analyses of patients with large anterior ST-segment-elevation myocardial infarctions, bone marrow mononuclear cells administration did not improve recovery of LV function over 2 years. Microvascular obstruction was associated with reduced recovery of LV function, greater adverse LV remodeling, and more device implantations. The use of cardiac magnetic resonance imaging leads to greater dropout of patients over time because of device implantation in patients with more severe LV dysfunction resulting in overestimation of clinical stability of the cohort.
URL: http://www.clinicaltrials.gov. Unique identifier: NCT00684021.
TIME 试验(心肌梗死评估中的时间)是第一个有足够效力确定 ST 段抬高型心肌梗死患者细胞输送时间是否影响左心室(LV)功能恢复的细胞治疗试验。
报告 2 年临床和心脏磁共振成像结果及其受微血管阻塞的影响。
TIME 是一项随机、双盲、安慰剂对照试验,比较了 1.5 亿个骨髓单核细胞与安慰剂在 120 例导致 LV 功能障碍的前壁 ST 段抬高型心肌梗死患者中的疗效。主要终点包括整体(LV 射血分数)和局部(梗死和交界区)功能的变化。次要终点包括 LV 容积、梗死面积和主要不良心脏事件的变化。在这里,我们分析了这些指标在 2 年时的持续变化轨迹,以及基线时存在的微血管阻塞对这些长期结局的影响。在 2 年时(n=85),骨髓单核细胞组(48.7%)和安慰剂组(51.6%)的 LV 射血分数相似,局部 LV 功能无差异。两组的梗死面积和 LV 质量在 6 个月时均下降≥30%,并逐渐下降至 2 年。LV 容积在 6 个月时增加约 10%,并保持稳定至 2 年。48 例患者在基线时存在微血管阻塞,与更大的梗死面积(56.5 比 36.2 克)、更严重的 LV 重构和 LV 射血分数恢复明显减少(0.2%比 6.2%)显著相关。
在前壁 ST 段抬高型心肌梗死患者最长的一系列心脏磁共振成像分析之一中,骨髓单核细胞治疗在 2 年内并未改善 LV 功能恢复。微血管阻塞与 LV 功能恢复减少、更严重的 LV 重构和更多的器械植入相关。随着时间的推移,由于更多严重 LV 功能障碍患者需要植入器械,心脏磁共振成像的使用导致患者脱落率增加,从而高估了队列的临床稳定性。