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首页> 外文期刊>Critical reviews in oncology/hematology >Pazopanib a tyrosine kinase inhibitor with strong anti-angiogenetic activity: A new treatment for metastatic soft tissue sarcoma
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Pazopanib a tyrosine kinase inhibitor with strong anti-angiogenetic activity: A new treatment for metastatic soft tissue sarcoma

机译:Pazopanib是一种具有强抗血管生成活性的酪氨酸激酶抑制剂:一种治疗转移性软组织肉瘤的新方法

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摘要

Soft tissue sarcomas (STS) are rare tumors with mesenchymal origin, accounting for 1% of all human cancer. Local control of STS can be obtained through the use of surgery and radiotherapy. In about 40% of these patients, disease will recur at distant sites, and of these more than 90% will die because of this aggressive malignancy. In advanced and/or metastatic STS patients treated with anthracycline-based regimen the median overall survival is about 12 months, and it has remained unchanged during the last 20 years. Clearly, this strongly suggests the need for discover more active compounds in STS, such as imatinib in GIST or dermatofibrosarcoma patients. In this paper we describe the crucial role of angiogenesis mechanisms in sarcomas development and progression. Consequentially, we focus on pazopanib, a novel multitargeted tyrosine kinase inhibitor with anti-angiogenic activity, mainly due to VEGFR2 pathway interference. We also analyze principal completed trials leading pazopanib approval in sarcomas pretreated patients.
机译:软组织肉瘤(STS)是间充质起源的罕见肿瘤,占所有人类癌症的1%。 STS的局部控制可通过手术和放疗获得。在大约40%的患者中,疾病会在远处复发,其中90%以上的患者会因恶性恶性肿瘤而死亡。在以蒽环类为基础的方案治疗的晚期和/或转移性STS患者中,平均总生存期约为12个月,并且在最近20年中保持不变。显然,这强烈表明需要在STS中发现更多活性化合物,例如GIST或皮肤纤维肉瘤患者中的伊马替尼。在本文中,我们描述了血管生成机制在肉瘤发展和进展中的关键作用。因此,我们专注于pazopanib,一种具有抗血管生成活性的新型多靶点酪氨酸激酶抑制剂,主要是由于VEGFR2途径的干扰。我们还分析了主要的完成试验,这些试验在肉瘤预处理的患者中导致帕唑帕尼的批准。

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