Department of Respiratory Medicine, Shanghai Chest Hospital, Jiaotong University, Huaihai West Road No. 241, Shanghai, 200030, People's Republic of China.
J Cancer Res Clin Oncol. 2020 Mar;146(3):631-645. doi: 10.1007/s00432-020-03129-6. Epub 2020 Feb 17.
Tumor growth relies on the sufficient blood supply and continuously requires new blood vessels to maintain, which lead to vascular abnormalities (Folkman, N Engl J Med 285:1182-1186, 1971). Antiangiogenic therapy has emerged with the goal of normalizing vasculature and tumor microenvironment (TME). Some antiangiogenic therapies combined with chemotherapy, targeted therapy or immunotherapy have been approved for clinical application. In this review, we summarize the recent advances of antiangiogenic combination therapeutic strategies in advanced NSCLC.
References of this review are searched through PubMed and EMBASE and the abstracts of cancer conferences. The ClinicalTrials.gov database was used for relative trials.
Based on different mechanisms, antiangiogenic agents can be divided into monoclonal antibodies (mAbs), which mainly include bevacizumab and ramucirumab, and multi-target antiangiogenic tyrosine kinase inhibitors (TKIs) which include sunitinib, sorafenib, nintedanib, apatinib, anlotinib, fruquintinib, etc. In recent years, a number of large clinical studies have shown that antiangiogenic agents have conferred a significant overall survival (OS) benefit to patients with advanced non-small cell lung cancer (NSCLC). More and more evidences confirm that the combination of antiangiogenic agents with chemotherapy, targeted therapy and immunotherapy can improve the effect and prolong the survival of NSCLC patients. However, many problems about the application of antiangiogenic agents on advanced NSCLC patients still need to be explored. For example, the combination therapy of multi-target antiangiogenic agents is just beginning, and the biomarkers are not clear.
Antiangiogenic agents can achieve therapeutic benefit in advanced NSCLC patients and the combination of chemotherapy, targeted therapy or immunotherapy can lead to synergistic effect. However, exploring the best combination therapy and efficacy-related biomarkers needs further study.
肿瘤的生长依赖于充足的血液供应,并不断需要新的血管来维持,这导致了血管异常(Folkman,N Engl J Med 285:1182-1186,1971)。抗血管生成治疗的出现旨在使血管和肿瘤微环境(TME)正常化。一些抗血管生成疗法与化疗、靶向治疗或免疫疗法联合已被批准用于临床应用。在这篇综述中,我们总结了晚期 NSCLC 中抗血管生成联合治疗策略的最新进展。
通过 PubMed 和 EMBASE 搜索本综述的参考文献,并检索癌症会议的摘要。使用 ClinicalTrials.gov 数据库查找相关试验。
根据不同的机制,抗血管生成药物可分为单克隆抗体(mAbs),主要包括贝伐珠单抗和雷莫芦单抗,以及多靶点抗血管生成酪氨酸激酶抑制剂(TKIs),包括舒尼替尼、索拉非尼、尼达尼布、阿帕替尼、安罗替尼、呋喹替尼等。近年来,许多大型临床研究表明,抗血管生成药物为晚期非小细胞肺癌(NSCLC)患者带来了显著的总生存(OS)获益。越来越多的证据证实,抗血管生成药物与化疗、靶向治疗和免疫治疗的联合应用可以提高 NSCLC 患者的疗效并延长其生存时间。然而,关于抗血管生成药物在晚期 NSCLC 患者中的应用仍有许多问题需要探索。例如,多靶点抗血管生成药物的联合治疗才刚刚开始,生物标志物也不明确。
抗血管生成药物可使晚期 NSCLC 患者获得治疗益处,化疗、靶向治疗或免疫治疗的联合应用可产生协同作用。然而,探索最佳的联合治疗方案和疗效相关的生物标志物需要进一步研究。