Evolving medical treatment for vascular malformation.

IF 1.5
Calver Pang, Rebecca Lee, Rebecca Nisbet, George Hamilton, Jocelyn Brookes, Chung Sim Lim
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Abstract

Vascular malformations are abnormal growth or development of the vascular structure that result from genetic mutations during early vascular development. Traditional invasive treatment for vascular malformations includes embolo-sclerotherapy, cryotherapy, laser therapy and surgery. However, surgical or minimally invasive treatment is rarely optimal due to the risk of treatment complications, and a complete cure is often difficult to achieve. Targeted therapy can be guided by the current understanding of molecular signalling pathways and disease classifications. Existing and novel medical treatments target the major cellular signalling pathways implicated in the pathogenesis of vascular malformations: mTOR inhibitors, phosphatidylinositol-4,5-biphsophate 3-kinase catalytic subunit alpha (PIK3CA) inhibitors, and AKT inhibitors are being developed to target the Phosphoinositide 3-Kinase (PI3K)/AKT/mTOR pathway, while mitogen-activated protein kinase (MEK) inhibitors and BRAF inhibitor are being researched to target the RAS/RAF/MEK/ERK pathway. Angiogenesis inhibitors are also utilised in the treatment of vascular abnormalities. This review aims to discuss the evolving medical therapy available in the treatment of Vascular Malformations.

不断发展的血管畸形医学治疗。
血管畸形是指在早期血管发育过程中由于基因突变导致的血管结构的异常生长或发育。传统的血管畸形侵入性治疗包括栓塞硬化治疗、冷冻治疗、激光治疗和手术治疗。然而,由于治疗并发症的风险,手术或微创治疗很少是最佳的,并且通常难以实现完全治愈。靶向治疗可以根据目前对分子信号通路和疾病分类的理解来指导。现有的和新的药物治疗靶向血管畸形发病机制中涉及的主要细胞信号通路:mTOR抑制剂、磷脂酰肌醇-4,5-双磷酸3-激酶催化亚单位α (PIK3CA)抑制剂和AKT抑制剂正在开发中,以靶向磷酸肌醇3-激酶(PI3K)/AKT/mTOR途径,而丝裂原活化蛋白激酶(MEK)抑制剂和BRAF抑制剂正在研究中,以靶向RAS/RAF/MEK/ERK途径。血管生成抑制剂也用于治疗血管异常。这篇综述的目的是讨论不断发展的医学治疗可用于治疗血管畸形。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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