期刊文献+

吉非替尼对非小细胞肺癌的疗效与T细胞亚群变化分析 被引量:3

Analysis of the effects of Gefitinib on patients with advanced non-small cell lung cancer and their T lymphocyte subsets
原文传递
导出
摘要 目的观察吉非替尼治疗晚期非小细胞肺癌(NSCLC)临床疗效与外周T淋巴细胞亚群变化的关系。方法对组织或细胞病理证实的35例晚期NSCLC患者口服吉非替尼250 mg/d。采集全部患者治疗前及治疗后外周血标本,三色染色后流式细胞仪分析CD3+、CD4+、CD8+T淋巴细胞亚群变化。结果35例患者中部分缓解13例,稳定13例,进展9例,疾病控制率为74.2%。治疗前后T淋巴细胞亚群无显著差异。结论吉非替尼治疗晚期非小细胞肺癌疗效较好,毒副反应轻微。治疗后T淋巴细胞可以恢复到治疗前水平。 Objective To analyze the effects of Gefitinib on patients with advanced non-small cell lung cancer (NSCLC) and the effect on T lymphocyte subsets. Methods A total of 35 patients with NSCLC confirmed by pathology or cytology administered orally 250 mg of Gefitinib once a day. Three-color fluorescent flow cytometry were used to analyze the percentage of CD3+ , CD4+ , and CD8+ T lymphocyte in peripheral blood before and after the treatment. Results No complete response (CR) was achieved. At the same time, there were 13 cases with partial response (PR), 13 cases with stable disease (SD), and 9 with progressed disease (PD). The disease control rate (CR+PR+SD) was 74.2%. There was not signi- ficant difference in the variations of T lymphocyte subsets before and after the treatment. Conclusion Gefitinib is very effective in the treatment of patients with advanced NSCLC, with minimal side effects. The percentage of CD3+ , CD4+ , and CD8+ T lymphocyte in peripheral blood after the treatment can be returned to that of pre-treatment.
出处 《现代药物与临床》 CAS 2009年第5期298-300,共3页 Drugs & Clinic
关键词 吉非替尼 非小细胞肺癌 T淋巴细胞亚群 Gefitinib non-small cell lung cancer T lymphocyte subsets
  • 相关文献

参考文献5

  • 1Parra H S, Cavina R, Latteri F, et al. Analysis of epidermal growth factor receptor expression as a predictive factor for response to gefitinib ('Iressa', ZD1839) in non-small-cell lung cancer [J].Br J Cancer,2004,91(2):208-212.
  • 2Kosmidis P A, Dimopoulos M A, Syrigos K, et al. Gemcitahine versus gemcitahine-carboptatin for patients with advanced non-small cell lung cancer and a performance status of 2 : a prospective randomized phase Ⅱ study of the Hellenic Cooperative Oncology Group [J]. J Thorac Oncol, 2007,2 (2):135-140.
  • 3Cappuzzo F, Hirseh F R, Rossi E, et al. Epidermal growth faetor receptor gene and protein and gefitinib sensitivity in non- small-cell lung cancer[J]. J Natl Caneer Inst, 2005,97 (9):643-655.
  • 4Huang S F, Liu H P, Li L H, et al. High frequency of epidermal growth factor receptor mutations with complex patterns in non-small cell lung cancers related to gefitinib responsiveness in Taiwan.[J]. Clin Cancer Res, 2004, 10(24): 8195- 8203.
  • 5邬露丹,徐炜峰,熊逸群.恶性肿瘤患者淋巴细胞亚群的测定及与癌胚抗原的关系[J].实验与检验医学,2008,26(1):57-58. 被引量:10

二级参考文献6

  • 1[1]Hemberg M.Lymphocyte subset as.prognostic markers for cancer patients receiving immunomodul ative therapy[J].Med oncol,1999,16(3):145.
  • 2[2]Hong C,Lee H,Oh M,Kang CY,Hong S,Park SH.CD4+ T cells in the absence of the CD8+cytotoxic T cells are critical and sufficient for NKT cell-dependent tumor rejection[J].J lmmunol,2006 Nov 15;177(1 01:6747~6777.
  • 3[4]Grossmann I,de Bock GH,Meershoek-Klein Kranenbarg WM,vande Velde CJ,Wiggem T Carcinoembryonic antigen(CEA)measurement during follow-up for rectal c.arcinonla is useful even if normal levels exist before surgery.A retrospective study of CEA values in the TME trial[J].Eur J Surg Oncol,2007 Mar,33(2):183~187.
  • 4[5]Sica A,Saccani A,Bottazzi B,et al.Autocrine production of IL-10 mediates defective IL-12 production and NF-kappa B activation in tumor-associated macrophages[J].J Immunol,2000,164(2):762~767.
  • 5[6]Koehler H,Kofler D,Hombach A,Abken H.CD28 costimulation overcomes transforming growth factor-beta-mediated repression of proliferation of redirected human CD4+ and CD8+ T cells in an antitumor cell attack[J].Cancer Res,2007 Mar 1,67(5):2265~2273.
  • 6卢香兰,李霞,王萍萍,李玲,李艳.恶性肿瘤患者T细胞亚群和SIL-2R的变化及意义[J].中国医科大学学报,2004,33(3):243-244. 被引量:18

共引文献9

同被引文献35

引证文献3

二级引证文献24

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