Department of Medical Oncology, University General Hospital of Heraklion, Heraklion, Crete, Greece ;
Department of Medical Oncology, University General Hospital of Heraklion, Heraklion, Crete, Greece;; Hellenic Oncology Research Group (HORG), Athens, Greece;
Transl Lung Cancer Res. 2016 Aug;5(4):389-400. doi: 10.21037/tlcr.2016.08.04.
Small cell lung cancer (SCLC) is a highly aggressive and lethal malignancy. Despite high initial response rates to systemic chemotherapy, the disease eventually relapses; further treatment only modestly improves outcomes and overall survival (OS) for patients with extensive stage disease is less than one year. Little progress has been made during the past decades, with no new drugs approved. Consequently, the development of novel strategies is an unmet need. The inhibition of angiogenesis, a defining characteristic of cancer, has demonstrated modest efficacy in several human malignancies, including non-small cell lung cancer (NSCLC). However, results from clinical trials in SCLC have been disappointing, and no anti-angiogenic agent has received regulatory approval due to lack of clinical efficacy. The elucidation of underlying mechanisms responsible for tumor resistance to angiogenic therapy and the simultaneous blockade of multiple elements that play a role in angiogenesis need to be further explored.
小细胞肺癌(SCLC)是一种侵袭性强、致死率高的恶性肿瘤。尽管全身性化疗初始反应率高,但疾病最终会复发;对于广泛期疾病患者,进一步的治疗只能适度改善预后,总生存期(OS)不到一年。在过去几十年中几乎没有取得进展,没有新的药物获得批准。因此,开发新的策略是一个未满足的需求。抑制血管生成,这是癌症的一个决定性特征,在包括非小细胞肺癌(NSCLC)在内的几种人类恶性肿瘤中已经显示出一定的疗效。然而,SCLC 的临床试验结果令人失望,由于缺乏临床疗效,没有一种抗血管生成药物获得监管部门的批准。阐明肿瘤对血管生成治疗产生耐药性的潜在机制,并同时阻断在血管生成中起作用的多个元素,这需要进一步研究。
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