Khan Khurum, Cunningham David, Chau Ian
Consultant in Medical Oncology, Department of Medicine, GI and Lymphoma Unit, The Royal Marsden NHS Foundation Trust, Sutton SM2 5PT, UK.
Curr Drug Targets. 2017;18(1):56-71. doi: 10.2174/1389450116666150325231555.
Colorectal cancer (CRC) is one of the commonest cancers in the world. During the last decade, the development of targeted therapies has given cancer treatment a novel direction in management of metastatic CRC (mCRC) and has enriched the therapeutic armamentarium in the management of this disease. In mCRC, targeting angiogenesis via the vascular endothelial growth factor (VEGF) pathway has been of particular interest based on the favourable survival benefit demonstrated by bevacizumab in clinical trials. More recently, large phase III studies have shown clinical efficacy for the new antiangiogenic agents aflibercept and regorafenib. However, the results of pre-clinical and clinical studies of other anti-angiogenic agents have been disappointing. Furthermore, the benefits from angiogenic inhibitors (AIs) in an unselected patient population are modest. Research into predictive biomarkers is therefore essential, but has, to date, been unsuccessful. Nevertheless, aflibercept and regorafenib have been shown to benefit both bevacizumab naive and refractory patients, suggesting that acquired resistance to AIs can be potentially reversed. This review describes the most recent advances in development of AIs in mCRC with particular focus on aflibercept and regorafenib, the existing challenges for the evaluation of these agents in clinical practice and potential strategies in designing clinical trials that could lead to the discovery of clinically meaningful biomarkers.
结直肠癌(CRC)是全球最常见的癌症之一。在过去十年中,靶向治疗的发展为转移性结直肠癌(mCRC)的治疗带来了新方向,并丰富了该疾病治疗的手段。在mCRC中,基于贝伐单抗在临床试验中显示出的良好生存获益,通过血管内皮生长因子(VEGF)途径靶向血管生成受到了特别关注。最近,大型III期研究显示新型抗血管生成药物阿柏西普和瑞戈非尼具有临床疗效。然而,其他抗血管生成药物的临床前和临床研究结果却令人失望。此外,血管生成抑制剂(AIs)在未经过筛选的患者群体中的获益并不显著。因此,对预测性生物标志物的研究至关重要,但迄今为止尚未成功。尽管如此,阿柏西普和瑞戈非尼已被证明对初治和难治性贝伐单抗患者均有益,这表明对AIs的获得性耐药可能被逆转。本综述描述了mCRC中AIs开发的最新进展,特别关注阿柏西普和瑞戈非尼,评估这些药物在临床实践中存在的挑战,以及设计临床试验的潜在策略,这些策略可能会导致发现具有临床意义的生物标志物。