期刊文献+

肿瘤免疫治疗超进展的研究和展望 被引量:6

Research progress and prospect of tumor immunotherapy
下载PDF
导出
摘要 近年来,免疫治疗成为肿瘤治疗的热点并在多个瘤种中广泛应用。然而免疫治疗为肿瘤患者带来益处的同时,有时会出现肿瘤生长速度加快或者肿瘤负荷快速增大并产生新病灶的情况,临床上将其称为“超进展(HPD)”。目前关于HPD的争议很多,包括HPD的定义和评估标准,以及生物标志物和发生机制等相关问题未完全明确。因此,本文对目前国内外关于HPD的定义及评估标准、高危因素预测、鉴别等进行系统综述,以期对未来HPD的研究及今后临床实践优化提供帮助。 In recent years, tumor immunotherapy has become a hot spot in tumor therapy and has been widely used in many tumor species. However, while immunotherapy has brought significant benefits to tumor patients, a number of clinical trials have shown that sometimes after immunotherapy, tumor growth rate or tumor load increases rapidly and new lesions are generated, which is clinically referred to as “hyperprogressive disease(HPD)”. At present, there are many controversies about HPD, including the definition and evaluation criteria of HPD, as well as the related issues such as biomarkers and occurrence mechanism, which are not completely clear. Therefore, this paper systematically reviewed the definition, assessment criteria, risk factor prediction and identification of HPD at home and abroad, with a view to providing help for future research on HPD and optimization of clinical practice in the future.
作者 杨宏 李皓静 罗丹阳 何敏 陈速研 王相成 杨昊 YANG Hong;LI Haojing;LUO Danyang;HE Min;CHEN Suyan;WANG Xiangcheng;YANG Hao(Department of Oncology,Inner Mongolia People's Hospital,Hohhot,Inner Mongolia 010017,China;Affiliated Hos-pital of Inner Mongolia Medical University,Hohhot,Inner Mongolia 010050,China;Tumor Hospital of Inner Mongolia Autonomous Region,Hohhot,Inner Mongolia 010020,China)
出处 《中南医学科学杂志》 CAS 2022年第2期297-301,共5页 Medical Science Journal of Central South China
基金 国家自然科学基金(81860534) 北京医学奖励基金会(YXJL-20200785-0315) 第二届三生TCP中青年科研基金(8) 内蒙古自治区科技计划项目(2019GG086,2019GG039,2021GG0167)。
关键词 肿瘤 免疫检查点抑制剂 超进展 鉴别 预测指标 tumor immune checkpoint inhibitors super progress identification forecast index
  • 相关文献

参考文献3

二级参考文献8

  • 1Bronte V, Apolloni E, Ronca R, et al. Genetic vaccination with "self' tyrosinase-related protein 2 causes melanoma eradication but not vitiligo[J]. Cancer Research, 2000, 60:253~258.
  • 2Tuting V, Gambotto A, DeLeo A, et al. Induction of tumor antigen specific immunity using plasmid DNA immunization in mice[J]. Cancer Gene Therapy, 1999, 6:73~80.
  • 3Conry RM, LoBuglio AF, Loechel F, et al. A carcinoembryonic antigen polynucleotide vaccine for human clinical use[J]. Cancer Gene Therapy, 1995, 2:33~38.
  • 4Petra Hanke, Matthias Serwe, Frank Dombrowski, et al. DNA vaccination with AFP-encoding plasmid DNA prevents growth of subcutaneous AFP-expressing tumors and does not interfere with liver regeneration in mice[J]. Cancer Gene Therapy, 2002,9:346~355.
  • 5Axel Heiser, Margaret A, Maurice, et al. Induction of polyclonal prostate cancer-specific CTL using dendritic cells transfected with amplified tumor RNA[J]. Immunol, 2001, 166: 2953~2960.
  • 6Axel Heiser, Doris Coleman, Jens Dannull, et al. Autologous dendritic cells transfected with prostate-specific antigen RNA stimulate CTL responses against metastatic prostate tumors[J]. Clin Invest ,2002 , 109(3):409~417.
  • 7Gong J, Chen I, Chen D, et al. Induction of antigen- specific antitumour immunity with adenovirus tranduced dendritic cells[J]. Gene Therapy, 1997, 4(10):1023~1028.
  • 8隋延仿,李增山.肿瘤疫苗研究进展[J].现代肿瘤医学,2003,11(4):241-244. 被引量:5

共引文献26

同被引文献49

引证文献6

二级引证文献4

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部