心脏横纹肌瘤:依维莫司治疗的临床进展、疗效和安全性。

IF 0.8 4区 医学 Q4 PEDIATRICS
Saygın Yıldırım, Ebru Aypar, Burça Aydın, Canan Akyüz, Hayrettin Hakan Aykan, İlker Ertuğrul, Tevfik Karagöz, Dursun Alehan
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引用次数: 0

摘要

背景:原发性心脏肿瘤极为罕见。心脏横纹肌瘤是最常见的原发性心脏肿瘤。50-80%的单纯性横纹肌瘤和所有多发性横纹肌瘤与结节性硬化症有关。由于自发性消退,只有在严重的血流动力学损害和持续性心律失常时才需要手术。依维莫司是雷帕霉素(mTOR)抑制剂的一种机制靶点,可用于治疗结节性硬化症中出现的横纹肌瘤。本研究旨在评价2014-2019年在本中心随访的横纹肌瘤的临床进展情况,评价依维莫司治疗肿瘤消退的疗效和安全性。方法:回顾性评价患者的临床特点、产前诊断、临床表现、结节性硬化症是否存在、治疗及随访结果。结果:56例原发性心脏肿瘤患儿中,47例确诊为横纹肌瘤,产前诊断28/47(59.6%),1岁前确诊85.1%,无症状42/47(89.3%)。多发性横纹肌瘤占51%,肿瘤中位直径为16mm (4.5 ~ 52 mm)。47例患者中29例(61.7%)不需要药物或手术治疗,其中34%的患者自发消退。6/47例(12.7%)患者需要手术。47例患者中有14例(29.8%)使用依维莫司。适应症为癫痫(2例)和心功能障碍(12例)。10/12例(83%)患者横纹肌瘤的大小有所缩小。虽然从长期来看,接受依维莫司治疗的患者与未接受治疗的患者肿瘤体积缩小量没有显著差异(p=0.139),但接受依维莫司治疗的患者肿瘤体积缩小率高出12.4倍。未见白细胞减少,3/14(21.4%)患者有高脂血症。结论:依维莫司可以促进肿瘤的体积缩小,但不能促进肿瘤的体积缩小。依维莫司可被考虑用于横纹肌瘤的治疗,这些横纹肌瘤会导致血流动力学损害或危及生命的心律失常。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cardiac rhabdomyomas: clinical progression, efficacy and safety of everolimus treatment.

Background: Primary cardiac tumors are extremely rare. Cardiac rhabdomyoma is the most common primary cardiac tumor. 50-80% of solitary rhabdomyomas and all multiple rhabdomyomas are associated with tuberous sclerosis complex. Due to spontaneous regression, surgery is necessary only in severe hemodynamic compromise and persistent arrhythmias. Everolimus, a mechanistic target of rapamycin (mTOR) inhibitor, can be used in the treatment of rhabdomyomas seen in tuberous sclerosis complex. We aimed to evaluate the clinical progression of rhabdomyomas followed-up in our center between the years 2014-2019 and evaluate the efficacy and safety of everolimus treatment on tumor regression.

Methods: Clinical features, prenatal diagnosis, clinical findings, tuberous sclerosis complex presence, treatment and follow-up results were evaluated retrospectively.

Results: Among 56 children with primary cardiac tumors, 47 were diagnosed as rhabdomyomas, 28/47 patients (59.6%) had prenatal diagnosis, 85.1% were diagnosed before one year of age and 42/47 patients (89.3%) were asymptomatic. Multiple rhabdomyomas were present in 51% and median diameter of tumors was 16mm (4.5 - 52 mm). In 29/47 patients (61.7%) no medical or surgical treatment were necessary while 34% of these had spontaneous regression. Surgery was necessary in 6/47 patients (12.7%). Everolimus was used in 14/47 patients (29.8%). Indications were seizures (2 patients) and cardiac dysfunction (12 patients). Regression in size of rhabdomyomas was achieved in 10/12 patients (83%). Although, in the long-term, the amount of tumor mass shrinkage was not significantly different between patients who received everolimus and untreated patients (p=0.139), the rate of mass reduction was 12.4 times higher in patients who received everolimus. Leukopenia was not detected in any of the patients, but, hyperlipidemia was noted in 3/14 patients (21.4%).

Conclusions: According to our results, everolimus accelerates tumor mass reduction, but not amount of mass regression in the long term. Everolimus may be considered for treatment of rhabdomyomas which cause hemodynamic compromise or life-threatening arrhythmias before surgical intervention.

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来源期刊
CiteScore
1.40
自引率
0.00%
发文量
122
审稿时长
6-12 weeks
期刊介绍: The Turkish Journal of Pediatrics is a multidisciplinary, peer reviewed, open access journal that seeks to publish research to advance the field of Pediatrics. The Journal publishes original articles, case reports, review of the literature, short communications, clinicopathological exercises and letter to the editor in the field of pediatrics. Articles published in this journal are evaluated in an independent and unbiased, double blinded peer-reviewed fashion by an advisory committee.
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