• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
[Research Progress of Small Molecule Anti-angiogenic Drugs 
in Non-small Cell Lung Cancer].[小分子抗血管生成药物在非小细胞肺癌中的研究进展]
Zhongguo Fei Ai Za Zhi. 2021 Jan 20;24(1):56-62. doi: 10.3779/j.issn.1009-3419.2021.102.02.
2
Combining anti-Epidermal Growth Factor Receptor (EGFR) and anti-angiogenic strategies in advanced NSCLC: we should have known better….在晚期非小细胞肺癌中联合抗表皮生长因子受体(EGFR)和抗血管生成策略:我们本应更清楚……
Curr Pharm Des. 2014;20(24):3901-13. doi: 10.2174/13816128113196660762.
3
Epidermal Growth Factor Receptor (EGFR) Pathway, Yes-Associated Protein (YAP) and the Regulation of Programmed Death-Ligand 1 (PD-L1) in Non-Small Cell Lung Cancer (NSCLC).表皮生长因子受体(EGFR)通路、Yes 相关蛋白(YAP)与非小细胞肺癌(NSCLC)中程序性死亡配体 1(PD-L1)的调控。
Int J Mol Sci. 2019 Aug 5;20(15):3821. doi: 10.3390/ijms20153821.
4
Optimizing the sequencing of tyrosine kinase inhibitors (TKIs) in epidermal growth factor receptor (EGFR) mutation-positive non-small cell lung cancer (NSCLC).优化表皮生长因子受体(EGFR)突变阳性非小细胞肺癌(NSCLC)中酪氨酸激酶抑制剂(TKI)的治疗顺序。
Lung Cancer. 2019 Nov;137:113-122. doi: 10.1016/j.lungcan.2019.09.017. Epub 2019 Sep 23.
5
The fibroblast growth factor receptor signaling pathway as a mediator of intrinsic resistance to EGFR-specific tyrosine kinase inhibitors in non-small cell lung cancer.成纤维细胞生长因子受体信号通路作为非小细胞肺癌中表皮生长因子受体特异性酪氨酸激酶抑制剂内在耐药的介质。
Drug Resist Updat. 2009 Aug-Oct;12(4-5):95-102. doi: 10.1016/j.drup.2009.05.001. Epub 2009 Jun 4.
6
Apatinib enhances antitumour activity of EGFR-TKIs in non-small cell lung cancer with EGFR-TKI resistance.阿帕替尼增强了表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKIs)对具有EGFR-TKI耐药性的非小细胞肺癌的抗肿瘤活性。
Eur J Cancer. 2017 Oct;84:184-192. doi: 10.1016/j.ejca.2017.07.037. Epub 2017 Aug 17.
7
MERTK Promotes Resistance to Irreversible EGFR Tyrosine Kinase Inhibitors in Non-small Cell Lung Cancers Expressing Wild-type Family Members.MERTK 促进表达野生型家族成员的非小细胞肺癌对不可逆 EGFR 酪氨酸激酶抑制剂的耐药性。
Clin Cancer Res. 2018 Dec 15;24(24):6523-6535. doi: 10.1158/1078-0432.CCR-18-0040. Epub 2018 Sep 7.
8
The ACTIVE study protocol: apatinib or placebo plus gefitinib as first-line treatment for patients with EGFR-mutant advanced non-small cell lung cancer (CTONG1706).ACTIVE 研究方案:阿帕替尼或安慰剂联合吉非替尼作为表皮生长因子受体突变型晚期非小细胞肺癌(CTONG1706)患者的一线治疗。
Cancer Commun (Lond). 2019 Nov 7;39(1):69. doi: 10.1186/s40880-019-0414-4.
9
Targeting angiogenesis in squamous non-small cell lung cancer.针对鳞状非小细胞肺癌中的血管生成
Drugs. 2014 Mar;74(4):403-13. doi: 10.1007/s40265-014-0182-z.
10
The dual PI3K/mTOR inhibitor BEZ235 restricts the growth of lung cancer tumors regardless of EGFR status, as a potent accompanist in combined therapeutic regimens.双重 PI3K/mTOR 抑制剂 BEZ235 可限制肺癌肿瘤的生长,而与 EGFR 状态无关,是联合治疗方案中的有力辅助药物。
J Exp Clin Cancer Res. 2019 Jul 1;38(1):282. doi: 10.1186/s13046-019-1282-0.

引用本文的文献

1
Factors Contributing to the High Malignancy Level of Cholangiocarcinoma and Its Epidemiology: Literature Review and Data.胆管癌高恶性程度的相关因素及其流行病学:文献综述与数据
Biology (Basel). 2025 Mar 28;14(4):351. doi: 10.3390/biology14040351.
2
A single-center, retrospective study-spring-evaluating the efficacy and safety of recombinant human vascular endothelial inhibitor combined with anti-PD-1 in elderly patients aged 80 and above with NSCLC.一项单中心、回顾性研究——评估重组人血管内皮抑制素联合抗 PD-1 治疗 80 岁及以上老年 NSCLC 患者的疗效和安全性。
Front Immunol. 2024 Jun 24;15:1402018. doi: 10.3389/fimmu.2024.1402018. eCollection 2024.

本文引用的文献

1
The impact of previous therapy strategy on the efficiency of anlotinib hydrochloride as a third-line treatment on patients with advanced non-small cell lung cancer (NSCLC): a subgroup analysis of ALTER0303 trial.既往治疗策略对盐酸安罗替尼作为晚期非小细胞肺癌(NSCLC)三线治疗方案疗效的影响:ALTER0303试验的亚组分析
Transl Lung Cancer Res. 2019 Oct;8(5):575-583. doi: 10.21037/tlcr.2019.09.21.
2
Circulating DNA-Based Sequencing Guided Anlotinib Therapy in Non-Small Cell Lung Cancer.循环DNA测序指导安罗替尼治疗非小细胞肺癌
Adv Sci (Weinh). 2019 Aug 19;6(19):1900721. doi: 10.1002/advs.201900721. eCollection 2019 Oct 2.
3
MicroRNA-6077 enhances the sensitivity of patients-derived lung adenocarcinoma cells to anlotinib by repressing the activation of glucose transporter 1 pathway.微小 RNA-6077 通过抑制葡萄糖转运蛋白 1 通路的激活增强患者来源的肺腺癌细胞对安罗替尼的敏感性。
Cell Signal. 2019 Dec;64:109391. doi: 10.1016/j.cellsig.2019.109391. Epub 2019 Aug 14.
4
Apatinib monotherapy for advanced non-small cell lung cancer after the failure of chemotherapy or other targeted therapy.阿帕替尼单药治疗化疗或其他靶向治疗失败后的晚期非小细胞肺癌。
Thorac Cancer. 2018 Oct;9(10):1285-1290. doi: 10.1111/1759-7714.12836. Epub 2018 Aug 20.
5
Effect of Anlotinib as a Third-Line or Further Treatment on Overall Survival of Patients With Advanced Non-Small Cell Lung Cancer: The ALTER 0303 Phase 3 Randomized Clinical Trial.安罗替尼作为三线或后线治疗对晚期非小细胞肺癌患者总生存的影响:ALTER 0303 期随机临床试验。
JAMA Oncol. 2018 Nov 1;4(11):1569-1575. doi: 10.1001/jamaoncol.2018.3039.
6
Apatinib reverses alectinib resistance by targeting vascular endothelial growth factor receptor 2 and attenuating the oncogenic signaling pathway in echinoderm microtubule-associated protein-like 4-anaplastic lymphoma kinase fusion gene-positive lung cancer cell lines.阿帕替尼通过靶向血管内皮生长因子受体 2 和抑制棘皮动物微管相关蛋白样 4-间变性淋巴瘤激酶融合基因阳性肺癌细胞系中的致癌信号通路逆转艾乐替尼耐药。
Anticancer Drugs. 2018 Nov;29(10):935-943. doi: 10.1097/CAD.0000000000000667.
7
Randomized, Double-Blind, Placebo-Controlled, Multicenter Phase II Study of Fruquintinib After Two Prior Chemotherapy Regimens in Chinese Patients With Advanced Nonsquamous Non‒Small-Cell Lung Cancer.随机、双盲、安慰剂对照、多中心 II 期研究:氟喹替尼在两种先前化疗方案后用于中国晚期非鳞状非小细胞肺癌患者。
J Clin Oncol. 2018 Apr 20;36(12):1207-1217. doi: 10.1200/JCO.2017.76.7145. Epub 2018 Mar 12.
8
Anlotinib as a third-line therapy in patients with refractory advanced non-small-cell lung cancer: a multicentre, randomised phase II trial (ALTER0302).安罗替尼三线治疗晚期难治性非小细胞肺癌的多中心、随机、II 期临床研究(ALTER0302)。
Br J Cancer. 2018 Mar 6;118(5):654-661. doi: 10.1038/bjc.2017.478. Epub 2018 Feb 13.
9
Loss of HIF-1α in natural killer cells inhibits tumour growth by stimulating non-productive angiogenesis.自然杀伤细胞中 HIF-1α 的缺失通过刺激非生产性血管生成抑制肿瘤生长。
Nat Commun. 2017 Nov 17;8(1):1597. doi: 10.1038/s41467-017-01599-w.
10
Apatinib in the treatment of advanced lung adenocarcinoma with KRAS mutation.阿帕替尼治疗KRAS突变的晚期肺腺癌
Onco Targets Ther. 2017 Aug 28;10:4269-4272. doi: 10.2147/OTT.S139520. eCollection 2017.

[小分子抗血管生成药物在非小细胞肺癌中的研究进展]

[Research Progress of Small Molecule Anti-angiogenic Drugs 
in Non-small Cell Lung Cancer].

作者信息

Dou Yan, Jiang Da

机构信息

Department of Oncology, The Fourth Hospital of Hebei Medical University, Shijiazhuang 050011, China.

出版信息

Zhongguo Fei Ai Za Zhi. 2021 Jan 20;24(1):56-62. doi: 10.3779/j.issn.1009-3419.2021.102.02.

DOI:10.3779/j.issn.1009-3419.2021.102.02
PMID:33478192
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7849040/
Abstract

Lung cancer is one of the cancers with the highest incidence in the world, and there is no standard treatment plan after second-line progression. Tumor angiogenesis has now been identified as an important therapeutic target for malignant tumors. Small molecule multi-target vascular kinase inhibitors can inhibit tumor angiogenesis by inhibiting angiogenesis-related signal pathways. At present, a lot of clinical trials of small molecule anti-angiogenic drugs for the treatment of non-small cell lung cancer (NSCLC) have been carried out, and some vascular endothelial growth factor receptor-tyrosine kinase inhibitors (VEGFR-TKIs) have been approved for the treatment of advanced NSCLC. Based on the development status of multiple small molecule anti-angiogenic drugs at home and abroad for the treatment of NSCLC, this article summarizes the efficacy and safety studies of multiple VEGFR-TKIs and fibroblast growth factor receptor (FGFR)-TKI single agents or combination treatments [including combined with chemotherapy, epidermal growth factor receptor (EGFR)-TKIs, immunotherapy, and radiotherapy, etc.] for NSCLC, and at the same time discussed the possible existence of VEGFR-TKIs drug resistance mechanisms and efficacy predictors, etc., and prospect the future development trend and potential problems of anti-vascular treatment of NSCLC, and provide new ideas for the follow-up precision and individualized treatment of lung cancer.
.

摘要

肺癌是全球发病率最高的癌症之一,二线进展后尚无标准治疗方案。肿瘤血管生成现已被确定为恶性肿瘤的重要治疗靶点。小分子多靶点血管激酶抑制剂可通过抑制血管生成相关信号通路来抑制肿瘤血管生成。目前,已开展了许多小分子抗血管生成药物治疗非小细胞肺癌(NSCLC)的临床试验,一些血管内皮生长因子受体酪氨酸激酶抑制剂(VEGFR-TKIs)已被批准用于治疗晚期NSCLC。基于国内外多种小分子抗血管生成药物治疗NSCLC的发展现状,本文总结了多种VEGFR-TKIs和成纤维细胞生长因子受体(FGFR)-TKI单药或联合治疗(包括联合化疗、表皮生长因子受体(EGFR)-TKIs、免疫治疗和放疗等)治疗NSCLC的疗效和安全性研究,同时探讨了VEGFR-TKIs可能存在的耐药机制和疗效预测指标等,并对NSCLC抗血管治疗的未来发展趋势和潜在问题进行了展望,为肺癌后续的精准和个体化治疗提供新思路。