Regulators of angiogenesis in chemotherapy-induced peripheral neuropathy

V. Bazarnyi, O. Kovtun, O. Koryakina, M. Kopenkin, L. Fechina
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Abstract

Background: Chemotherapy-induced peripheral polyneuropathy is a major neurotoxicity of treatment for acute lymphoblastic leukemia (ALL) in children. Pathophysiological mechanisms of the injury of peripheral neural system are not fully investigated; however, some studies have shown the involvement of vascular endothelial growth factors. Aim: To evaluate plasma levels of angiogenic growth factors in children with ALL and to identify their association with the development of vincristine-induced peripheral polyneuropathy. Materials and methods: This single center prospective study included 41 patients with ALL aged 3 to 17 years. All patients were given the ALL-MB 2015 chemotherapy regimen. Depending on the vincristine-induced peripheral polyneuropathy, the patients were divided into two groups: the main group (n = 22) comprised of the patients with neurological signs and symptoms of peripheral neuropathy and the control group (n = 19), those without clinical signs of the peripheral nervous system involvement. The levels of angiogenic growth factors (VEGF-A, VEGF-D, PlGF-1, and PDGF-BB) were measured in plasma by multiparameter immunofluorescent analysis. Results: During 3 months of the follow up the chemotherapy-induced signs of peripheral polyneuropathy developed in 53.6% (n = 22) of the children. In 72.7% (n = 16) of the patients the chemotherapy-induced peripheral polyneuropathy was characterized by a combination of neurologic abnormalities with prevailing motor symptoms. The comparative analysis of plasma angiogenic growth factors in children with ALL depending on the presence or absence of the vincristine-induced peripheral polyneuropathy showed that there was a significant decrease of the VEGF-A in those with chemotherapy-induced peripheral polyneuropathy, compared to those without (Me [Q1; Q3]: 178.20 [138.40; 228.45] and 558.50 [160.10; 650.0], respectively, p 0.017). This parameter had diagnostic sensitivity of 77.7% and specificity of 76.9%. Conclusion: We have shown a high clinical value of plasma vascular endothelial growth factor (VEGF-A) level, which makes it possible to consider it as a significant biological marker of neurotoxicity in vincristine-induced peripheral polyneuropathy.
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化疗诱导的周围神经病变血管生成的调节因子
背景:化疗诱导的周围多神经病变是儿童急性淋巴细胞白血病(ALL)治疗的主要神经毒性。外周神经系统损伤的病理生理机制尚不清楚;然而,一些研究表明血管内皮生长因子参与其中。目的:评价ALL患儿血浆血管生成生长因子水平,并确定其与长春新碱诱导的周围多发性神经病变的关系。材料和方法:本单中心前瞻性研究纳入41例3 - 17岁ALL患者。所有患者均给予All - mb 2015化疗方案。根据长春新碱引起的周围多神经病变的不同,将患者分为两组:主组(n = 22)为有神经体征和周围神经病变症状的患者,对照组(n = 19)为无周围神经系统受累临床体征的患者。采用多参数免疫荧光法测定血浆中血管生成生长因子(VEGF-A、VEGF-D、PlGF-1和PDGF-BB)的水平。结果:在3个月的随访中,53.6% (n = 22)的儿童出现了化疗引起的周围多发性神经病变迹象。在72.7% (n = 16)的患者中,化疗引起的周围多神经病变的特征是神经系统异常与主要运动症状的结合。根据长春新碱诱导的周围多发性神经病变存在与否对ALL患儿血浆血管生成生长因子的比较分析显示,化疗诱导的周围多发性神经病变患者的VEGF-A明显低于无化疗诱导的周围多发性神经病变患者(Me [Q1;[3]: 178.20 [138.40;228.45]和558.50 [160.10;650.0], p 0.017)。该参数诊断敏感性为77.7%,特异性为76.9%。结论:血浆血管内皮生长因子(VEGF-A)水平具有较高的临床价值,可作为长春新碱诱导的周围多发性神经病神经毒性的重要生物学标志物。
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