首页> 外文期刊>Orphanet journal of rare diseases >Repurposing propranolol as a drug for the treatment of retinal haemangioblastomas in von Hippel-Lindau disease
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Repurposing propranolol as a drug for the treatment of retinal haemangioblastomas in von Hippel-Lindau disease

机译:重新使用普萘洛尔作为治疗von Hippel-Lindau病的视网膜血管母细胞瘤的药物

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BackgroundVon Hippel-Lindau (VHL) disease is a rare oncological disease with an incidence of 1:36,000, and is characterized by the growth of different types of tumours. Haemangioblastomas in the central nervous system (CNS) and retina, renal carcinoma and pheochromocytomas are the most common tumours. The absence of treatment for VHL leads to the need of repeated surgeries as the only option for these patients. Targeting VHL-derived tumours with drugs with reduced side effects is urgent to avoid repeated CNS surgeries. Recent reports have demonstrated that propranolol, a β-blocker used for the treatment of hypertension and other cardiac and neurological diseases, is the best option for infantile hemangioma (IH). Propranolol could be an efficient treatment to control haemangioblastoma growth in VHL disease given its antiangiogenic effects that were recently demonstrated by us. The main objective of the present study was the assessment of the efficacy and safety of propranolol on retinal haemangioblastoma in von Hippel-Lindau disease (VHL). Methods7 VHL patients, from different regions of Spain, affected from juxtapapillary or peripheral haemangioblastomas were administered 120?mg propranolol daily. Patients were evaluated every 3?months for 12?months, at Virgen de la Salud Hospital (Toledo). The patients had juxtapapillary or peripheral haemangioblastomas but had refused standard treatments. ResultsPropranolol was initiated with a progressive increase up to a final dose of 120?mg daily. All tumours remained stable, and no new tumours appeared. The reabsorption of retinal exudation was noted in the two patients having exudates. No adverse effects were recorded. VEGF and miRNA 210 levels were monitored in the plasma of patients as possible biomarkers of VHL. These levels decreased in all cases from the first month of treatment. ConclusionsAlthough more studies are necessary, the results of this work suggest that propranolol is a drug to be considered in the treatment of VHL patients with retinal haemangioblastomas. VEGF and miRNA 210 could be used as biomarkers of the VHL disease activity. Trial registrationThe study has a clinical trial design and was registered at EU Clinical Trials Register and Spanish Clinical Studies Registry, EudraCT Number: 2014–003671-30 . Registered 2 September 2014.
机译:背景冯·希佩尔-林道(VHL)病是一种罕见的肿瘤病,发病率为1:36,000,其特征是不同类型肿瘤的生长。中枢神经系统(CNS)和视网膜的肾母细胞母细胞瘤,肾癌和嗜铬细胞瘤是最常见的肿瘤。缺乏VHL的治疗方法导致需要重复手术作为这些患者的唯一选择。迫切需要用副作用减少的药物靶向VHL衍生的肿瘤,以避免重复进行中枢神经系统手术。最近的报道表明,普萘洛尔是一种用于治疗高血压以及其他心脏和神经系统疾病的β受体阻滞剂,是婴儿血管瘤(IH)的最佳选择。鉴于我们最近证实了普萘洛尔的抗血管生成作用,它可能是控制VHL疾病中血管母细胞瘤生长的有效方法。本研究的主要目的是评估普萘洛尔对von Hippel-Lindau病(VHL)视网膜血管母细胞瘤的疗效和安全性。方法7例来自西班牙不同地区的VHL患者,因近乳头状或外周血成血管母细胞瘤而受到了每日120 mg普萘洛尔的治疗。在Virgen de la Salud医院(托莱多),每3个月对患者进行12个月的评估。这些患者患有近乳头状或周围血管母细胞瘤,但拒绝了标准治疗。结果普萘洛尔开始逐渐增加剂量,直至最终剂量为每天120?mg。所有肿瘤均保持稳定,并且没有新肿瘤出现。在两名有渗出液的患者中注意到视网膜渗出液的重吸收。没有不良反应的记录。监测患者血浆中VEGF和miRNA 210的水平,将其作为VHL的可能生物标记。从治疗的第一个月起,这些水平在所有情况下均下降。结论尽管还需要进行更多的研究,但这项工作的结果表明,普萘洛尔是治疗VHL视网膜血管母细胞瘤患者的一种药物。 VEGF和miRNA 210可用作VHL疾病活性的生物标志物。试验注册该研究具有临床试验设计,并已在EU临床试验注册中心和西班牙临床研究注册中心注册,EudraCT编号:2014–003671-30。 2014年9月2日注册。

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