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首页> 外文期刊>Critical reviews in oncology/hematology >Challenges in the current antiangiogenic treatment paradigm for patients with non-small cell lung cancer
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Challenges in the current antiangiogenic treatment paradigm for patients with non-small cell lung cancer

机译:当前非小细胞肺癌患者抗血管生成治疗模式的挑战

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摘要

Patients with non-small cell lung cancer (NSCLC) often present with advanced disease and cure rates are dismal with currently available treatment. Novel therapies including small molecule tyrosine kinase inhibitors and monoclonal antibodies are being developed to target angiogenesis, an essential step in tumorigenesis and metastasis. The only antiangiogenic agent currently approved for treatment of NSCLC is bevacizumab, although numerous other antiangiogenic inhibitors (e.g., sorafenib, sunitinib, cediranib, motesanib, BIBF 1120) are in clinical trials. Individualized treatment algorithms may improve patient outcomes and new evidence suggests that biomarkers may guide treatment decisions. We present an overview of the molecular pathways involved in angiogenesis, discuss clinical trials of bevacizumab and developmental antiangiogenic agents, and address the challenges of developing individualized treatment paradigms for NSCLC, particularly the use of biomarkers.
机译:非小细胞肺癌(NSCLC)患者通常表现为晚期疾病,治愈率因目前可用的治疗而令人沮丧。正在开发包括小分子酪氨酸激酶抑制剂和单克隆抗体在内的新型疗法来靶向血管生成,这是肿瘤发生和转移的关键步骤。尽管许多其他抗血管生成抑制剂(例如索拉非尼,舒尼替尼,西地那尼,莫替沙尼,BIBF 1120)正在临床试验中,但目前被批准用于治疗NSCLC的唯一抗血管生成剂是贝伐单抗。个性化的治疗算法可能会改善患者的预后,新的证据表明生物标志物可以指导治疗决策。我们提供了涉及血管生成的分子途径的概述,讨论了贝伐单抗和发展性抗血管生成剂的临床试验,并解决了开发针对NSCLC的个体化治疗范例的挑战,尤其是生物标志物的使用。

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