Division of Cardiovascular Medicine, University of California at San Diego, San Diego, California.
AY Statistical Consulting, San Andreas, California.
JACC Heart Fail. 2014 Feb;2(1):84-92. doi: 10.1016/j.jchf.2013.09.008. Epub 2014 Jan 25.
Impaired cardiac isoform of sarco(endo)plasmic reticulum Ca(2+) ATPase (SERCA2a) activity is a key abnormality in heart failure patients with reduced ejection fraction. The CUPID 2 (Calcium Up-Regulation by Percutaneous Administration of Gene Therapy in Cardiac Disease Phase 2b) trial is designed to evaluate whether increasing SERCA2a activity via gene therapy improves clinical outcome in these patients.
Intracoronary delivery of recombinant adeno-associated virus serotype 1 (AAV1)/SERCA2a improves intracellular Ca(2+) handling by increasing SERCA2a protein levels and, as a consequence, restores systolic and diastolic function. In a previous phase 2a trial, this therapy improved symptoms, functional status, biomarkers, and left ventricular function, and reduced cardiovascular events in advanced heart failure patients.
CUPID 2 is a phase 2b, double-blind, placebo-controlled, multinational, multicenter, randomized event-driven study in up to 250 patients with moderate-to-severe heart failure with reduced ejection fraction and New York Heart Association functional class II to IV symptoms despite optimal therapy. Enrolled patients will be at high risk for recurrent heart-failure hospitalizations by virtue of having elevated N-terminal pro-B-type natriuretic peptide/BNP (>1,200 pg/ml, or >1,600 pg/ml if atrial fibrillation is present) and/or recent heart failure hospitalization. The primary endpoint of time-to-recurrent event (heart failure-related hospitalizations in the presence of terminal events [all-cause death, heart transplant, left ventricular assist device implantation or ambulatory worsening heart failure]) will be assessed using the joint frailty model. This ongoing trial is expected to complete recruitment in 2014, with the required number of 186 recurrent events estimated to occur by mid 2015.
Available data indicate that calcium up-regulation by AAV1/SERCA2a gene therapy is safe and of potential benefit in advanced heart failure patients.
The CUPID 2 trial is designed to study the effects of this therapy on clinical outcome in these patients. (Calcium Up-Regulation by Percutaneous Administration of Gene Therapy in Cardiac Disease Phase 2b [CUPID-2b]; NCT01643330).
心肌肌浆网钙转运 ATP 酶(SERCA2a)的心脏同工型活性受损是射血分数降低的心力衰竭患者的一个关键异常。CUPID 2(经皮基因治疗增加心脏疾病中的钙调控 2b 期)试验旨在评估通过基因治疗增加 SERCA2a 活性是否能改善这些患者的临床预后。
经冠状动脉给予重组腺相关病毒血清型 1(AAV1)/SERCA2a 可通过增加 SERCA2a 蛋白水平来改善细胞内 Ca2+处理,从而恢复收缩和舒张功能。在一项先前的 2a 期试验中,该治疗方法改善了晚期心力衰竭患者的症状、功能状态、生物标志物和左心室功能,并减少了心血管事件。
CUPID 2 是一项 2b 期、双盲、安慰剂对照、多中心、多国、随机、事件驱动的研究,纳入了 250 名射血分数降低的中重度心力衰竭且伴有纽约心脏协会心功能 II 至 IV 级症状的患者,这些患者尽管接受了最佳治疗,但仍存在心力衰竭反复发作的风险。由于 N 端脑利钠肽前体/B 型利钠肽(NT-proBNP)升高(>1200 pg/ml,如果存在心房颤动,则>1600 pg/ml)和/或最近发生心力衰竭住院,这些患者将具有较高的心力衰竭住院反复发作风险。主要终点是通过联合脆弱性模型评估的复发性事件(心力衰竭相关住院,伴有终末事件[全因死亡、心脏移植、左心室辅助装置植入或可走动的心力衰竭恶化])。这项正在进行的试验预计将于 2014 年完成招募,预计到 2015 年年中会发生 186 次所需的复发性事件。
现有数据表明,AAV1/SERCA2a 基因治疗的钙上调是安全的,对晚期心力衰竭患者具有潜在益处。
CUPID 2 试验旨在研究该治疗方法对这些患者临床结局的影响。(经皮基因治疗增加心脏疾病中的钙调控 2b 期[CUPID-2b];NCT01643330)。