欢迎来到OAJRC平台!
登录 | 注册 | English
期刊目次
加入编委
添加您的邮件地址以接收即将发行期刊数据:
Open Access Article
International Medical Research Frontier. 2020; 4: (1) ; 1-6 ; DOI: 10.12208/j.imrf.20200001.
云南省第一人民医院 云南昆明
*通讯作者: 孙志为,单位:云南省第一人民医院 云南昆明;
发布时间: 2020-12-30 总浏览量: 1354
PDF 全文下载 引用本文 收录截图(CNKI-Scholar)
甲磺酸阿帕替尼为中国研发的抗血管生成靶向药,抑制VEGFR-2,破坏了其与酪氨酸激酶ATP间的结合,导致酪氨酸激酶无法被激活,达到阻止恶性肿瘤血管形成的功效。此文总体概述与阿帕替尼治疗末期肝癌相关的基本和临床科学研究工作的现况与发展,使之后的研究有所参照。
Apatinib Mesylate, an anti-angiogenic target drug developed inChina, inhibits VEGFR-2 and destroys its binding to tyrosine kinase AT-P, thus preventing tyrosine kinase from being activated and preventing malignant tumor angiogenesis. This article gives a general overview of the current status and development of basic and clinical research relat-ed to the treatment of advanced liver cancer with Apatinib, so as to provide references for future studies.
[1] Wu H, Ding ZH, Hu DQ, et al. Central role of lactic acidosis in cancer cell resistance to glucose deprivation-induced cell death[J].J Pathol,2012 227 (2) : 189-199.
[2] 金鑫荔, 卢伟. TACE 联合阿帕替尼治疗中晚期肝细胞癌[J].中国介入影像与治疗学,2017 14 (4) : 200-204.
[3] 李威, 满文玲, 郭欢庆, 等. TACE联合甲磺酸阿帕替尼治疗中晚期肝癌的临床研究[J].肿瘤药学,2017 7 (1) : 74-78.
[4] 杨 庆, 潘松松, 施昌盛, 等. 甲磺酸阿帕替尼联合 TACE 治疗中晚期肝癌的效果及对患者血清VEGF和MMP-9的影响[J/CD].中华介入放射学电子杂志,2019 7 (2) : 111-116.
[5] Chen P, Iruela Arispe L, Lou L, et al. VEGFR inhibitorYN968D1 xenograftdose dose response studies against human colon cancer Ls174t and HT29[J].Proc Amer Assoc Cancer Res,2006 47 (9) : 1764-1769.
[6] Ding JF, Chen XY, Gao ZW. Metabolism and pharmaeokinetics of novel selective vascular endothelial growth factor receptor-2 in-hibitor apatinib in humans[J].Drug Metab Dispos,2013 41 (6) : 1195-1120.
[7] 丁珏芳, 陈笑艳, 谢 岑, 等. UPLC/Q-TOFMS法检测和鉴定阿帕替尼在肿瘤患者血浆和尿中代谢产物[C/OL].北京: 2011年中国药学大会暨第11届中国药师周,2011 .
[8] 冯久桓, 秦叔逵, 王琳. 甲磺酸阿帕替尼的研究现状与进展[A].临床肿瘤学杂志,2017 22 (4) : 345-356.
[9] TianS, QuanHT, XieCY, et al. YN968D1 is a novel and seletive inhibitor of vascular endothelial growth factor receptor-2tyro-Sine kinase with potent activity in vitroand invivo[J].Cancer Sci,102 (7) : 1374-1380.
[10] 姜增凯, 叶晓歌, 陈琴华. 阿帕替尼对肝癌细胞增殖和迁移能力的影响研究 [J].中国临床药理学杂志,2016 32 (15) : 1422-1424.
[11] 杨朝旭, 孙飘扬, 秦叔逵. 小分子VEGFR-2酪氨酸激酶抑制剂阿帕替尼对肝癌细胞的抑制作用及其机制的研究[C/OL].北京 : 第十五届全国临床肿瘤学大会暨 2012CSCO学术年,2012 .
[12] PengS, ZhangYY , Peng H, et al. Intracellular autocrine VEGF signaling promotes EBDC cell proliferation, which can be inhibited by Apatinib[J].CancerLetters,2016 373 (2) : 193-202.
[13] 梁树, 童秀珍, 符立悟. 小分子酪氨酸激酶抑制剂 Apatinib对白血病HL-60细胞株抑制增殖作用及机制 [J].南方医科大学学报,2011 31 (5) : 871-874.
[14] Ozben T. Mechanisms and strategies to overcome multiple drug resistance in cancer[J].FEBSLett,2006 580 (12) : 2903-2909.
[15] Percz-Tomas R. Muhidrugre sistance: retrospect and prospectsin anti-cancer drug treatment[J].CurrMedChem,2006 13 (16) : 1859-1876.
[16] SzakacsG, Paterson JK, Ludwig JA, et al. Targeting nmhidrug resistanceincancer[J].NatRevDrugDiscov,2006 5 (3) : 219-234.
[17] 林岩. 榄香烯注射液联合甲磺酸阿帕替尼抗肝癌的实验研究[D].南京: 南京中医药大学,2014 .
[18] 秦叔逵, 白玉贤, 欧阳学农, 等. 阿帕替尼一线治疗晚期肝细胞癌的前瞻性、随机、开放、全国多中心Ⅱ期临床试验[A].南京 南京中医药大学附属八一医院全军肿瘤中心 中山大学学报,2017 .
[19] Abou-Alfa GK, Schwartz L, Ricci S, et al. PhaseⅡ study of Sorafenib in patients with advanced hepatocellular carcinoma[J].J Clin Oncol,2006 24 (26) : 4293-4300.
[20] kudo M, Imanaka K, Chida N, et al. Phase Ⅲ study of sorafenib after transarterial chemoembolisation in Japanese and Korean patients with unresectable hepatocellular carcinoma [J].Eur J Cancer,2011 47 (14) : 2117-2127.
[21] Sui P, Zhang Y, Hong P, et al. Intracellular autocrine VEGF singaling promotes EBDC cell proliferation, which can be inhibited by Apatinib [J].Cancer Letters,2016 373 (2) : 193-202.
[22] KouBS, ZhangY, ShaoWB, et al. Signifcant efcacy and well safety of apatinib in an advanced liver cancer patient: a case Report and literature review [J/OL].Oncotarget,2017 .
[23] 黎启菊. 肝动脉灌注吉西他滨后栓塞联合甲磺酸阿帕替尼治疗晚期肝癌的疗效及生存质量分析[A].四川 凉山彝族自治州第一人民医院肿瘤科 医学前沿,2018 .
[24] 万源, 陈斌, 李楠, 等. 载药微球栓塞联合甲磺酸阿帕替尼治疗中晚期原发性肝癌的近期疗效[A].广州 中山大学附属第一医院放射介入科,2019 .
[25] Johannes L, Katarina M, Thomas V, et al. Prospective randomized study of doxorubicin-eluting-bead embolization in the treatment of hepatocellulal carcinoma: results of the PRECISION V study[J].Cardiovasc Intervent Radiol,2010 33 (1) : 41-52.
[26] 马耀凯, 方世明, 陈 舲. 健脾解毒方联合甲磺酸阿帕替尼片治疗晚期原发性肝癌临床疗效[A].河北中医, .
[27] 杨柳青, 陈映霞, 秦叔逵, 等. 肿瘤抗血管生成药物致高血压的临床观察[J].临床肿瘤学杂志,2014 19 (7) : 603-607.
[28] 马兴群, 成 远, 陈映霞. VEGF信号通路抑制剂相关蛋白尿的研究进展[J].临床肿瘤学杂志,2015 20 (4) : 357-362.
[29] McLellan B, Ciardiello F, Lacouture ME, et al. Regorafenib associated hand foot skin reaction: practicaladvice on diagnosis, prevention, and management[J].Ann Oncol,2015 26 (10) : 2017-2026.
[30] 赵成龙, 傅昌芳. 阿帕替尼致消化道出血[J].世界最新医学信息文摘,2015 15 (100) : 221.
[31] 杨晓瑞, 梁明杰, 王伟兰. 从1例溃疡型胃癌患者上消化道出血探讨抗血管生成药物的安全应用[J].中国药物应用与监测,2016 13 (5) : 280-283.
[32] Daniel GR. On-target and off-target-based toxicologic effects[J].Toxieol Pathol,2013 41 (2) : 310-314.
[33] 贾卡. 甲磺酸阿帕替尼疗效预测因子的研究[D].上海: 复旦大学,2009 .
[34] 张宁刚, 王育生. 甲磺酸阿帕替尼片治疗原发性肝癌肺转移1例报道 [J].肿瘤防治研究,2016 43 (10) : 913-915.
[35] 涂艳, 彭枫, 罗德云. 阿帕替尼治疗直肠癌肺转移有效1例报告[J].四川大学学报(医学版),2016 47 (5) : 818.
入驻平台
回到首页
扫一扫,添加我们