Pediatric Cardiology Department, Hospital de Pediatría Garrahan, Buenos Aires, Argentina.
Radiology Department, D'Or Institute for Research and Education, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
Cardiol Young. 2020 Mar;30(3):337-345. doi: 10.1017/S1047951119003147. Epub 2020 Jan 27.
Tuberous sclerosis complex is a rare genetic disorder leading to the growth of hamartomas in multiple organs, including cardiac rhabdomyomas. Children with symptomatic cardiac rhabdomyoma require frequent admissions to intensive care units, have major complications, namely, arrhythmias, cardiac outflow tract obstruction and heart failure, affecting the quality of life and taking on high healthcare cost. Currently, there is no standard pharmacological treatment for this condition, and the management includes a conservative approach and supportive care. Everolimus has shown positive effects on subependymal giant cell astrocytomas, renal angiomyolipoma and refractory seizures associated with tuberous sclerosis complex. However, evidence supporting efficacy in symptomatic cardiac rhabdomyoma is limited to case reports. The ORACLE trial is the first randomised clinical trial assessing the efficacy of everolimus as a specific therapy for symptomatic cardiac rhabdomyoma.
ORACLE is a phase II, prospective, randomised, placebo-controlled, double-blind, multicentre protocol trial. A total of 40 children with symptomatic cardiac rhabdomyoma secondary to tuberous sclerosis complex will be randomised to receive oral everolimus or placebo for 3 months. The primary outcome is 50% or more reduction in the tumour size related to baseline. As secondary outcomes we include the presence of arrhythmias, pericardial effusion, intracardiac obstruction, adverse events, progression of tumour reduction and effect on heart failure.
ORACLE protocol addresses a relevant unmet need in children with tuberous sclerosis complex and cardiac rhabdomyoma. The results of the trial will potentially support the first evidence-based therapy for this condition.
结节性硬化症是一种罕见的遗传性疾病,可导致多个器官的错构瘤生长,包括心脏横纹肌瘤。有症状的心脏横纹肌瘤患儿需要频繁入住重症监护病房,存在重大并发症,即心律失常、心流出道梗阻和心力衰竭,影响生活质量并带来高昂的医疗保健费用。目前,这种疾病没有标准的药物治疗方法,治疗包括保守方法和支持性护理。依维莫司已显示出对室管膜下巨细胞星形细胞瘤、肾血管平滑肌脂肪瘤和结节性硬化症相关的难治性癫痫发作的积极影响。然而,支持依维莫司对有症状的心脏横纹肌瘤疗效的证据仅限于病例报告。ORACLE 试验是第一项评估依维莫司作为有症状的心脏横纹肌瘤的特异性治疗的疗效的随机临床试验。
ORACLE 是一项 II 期、前瞻性、随机、安慰剂对照、双盲、多中心方案试验。共有 40 名因结节性硬化症而患有症状性心脏横纹肌瘤的儿童将被随机分为口服依维莫司或安慰剂组,疗程为 3 个月。主要终点是肿瘤大小相对于基线减少 50%或更多。次要终点包括心律失常、心包积液、心内梗阻、不良事件、肿瘤缩小的进展和对心力衰竭的影响。
ORACLE 方案解决了结节性硬化症伴心脏横纹肌瘤儿童的一个相关未满足的需求。试验结果可能为该疾病提供首个基于证据的治疗方法。