Albiñana Virginia, Escribano Rosa María Jiménez, Soler Isabel, Padial Luis Rodríguez, Recio-Poveda Lucia, Villar Gómez de Las Heras Karina, Botella Luisa María
Centro de Investigaciones Biológicas, CSIC, Madrid, Spain.
Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Madrid, Spain.
Orphanet J Rare Dis. 2017 Jun 29;12(1):122. doi: 10.1186/s13023-017-0664-7.
Von 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).
7 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.
Propranolol 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.
Although 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.
The 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.
冯·希佩尔-林道(VHL)病是一种罕见的肿瘤疾病,发病率为1:36000,其特征是出现不同类型的肿瘤。中枢神经系统(CNS)和视网膜的血管母细胞瘤、肾癌和嗜铬细胞瘤是最常见的肿瘤。由于缺乏针对VHL病的治疗方法,这些患者唯一的选择就是反复进行手术。迫切需要使用副作用较小的药物来靶向治疗VHL衍生的肿瘤,以避免反复进行中枢神经系统手术。最近的报告表明,普萘洛尔(一种用于治疗高血压及其他心脏和神经疾病的β受体阻滞剂)是治疗婴儿血管瘤(IH)的最佳选择。鉴于我们最近证明的抗血管生成作用,普萘洛尔可能是控制VHL病中血管母细胞瘤生长的有效治疗方法。本研究的主要目的是评估普萘洛尔治疗冯·希佩尔-林道病(VHL)视网膜血管母细胞瘤的疗效和安全性。
来自西班牙不同地区、患有视乳头旁或周边血管母细胞瘤的7例VHL患者,每天服用120毫克普萘洛尔。在托莱多的比拉尔·德拉·萨尔ud医院,每3个月对患者进行一次为期12个月的评估。这些患者患有视乳头旁或周边血管母细胞瘤,但拒绝了标准治疗。
开始使用普萘洛尔时剂量逐渐增加,最终达到每日120毫克。所有肿瘤均保持稳定,且未出现新的肿瘤。在有渗出液的两名患者中,观察到视网膜渗出液的吸收。未记录到不良反应。监测患者血浆中的VEGF和miRNA 210水平,作为VHL可能的生物标志物。从治疗的第一个月起,所有病例中的这些水平均下降。
尽管还需要更多研究,但本研究结果表明,普萘洛尔是治疗患有视网膜血管母细胞瘤的VHL患者时应考虑使用的药物。VEGF和miRNA 210可作为VHL病活动的生物标志物。
该研究采用临床试验设计,已在欧盟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。于2014年9月2日注册。