期刊文献+

MTT法在非小细胞肺癌优化治疗方案中的应用 被引量:5

Application of optimizing therapeutic regimen for non-small cell lung cancer with MTT assay
下载PDF
导出
摘要 目的:通过非小细胞肺癌体外原代细胞的培养,对其常用的化疗药物进行敏感性检测,探讨不同化疗药物之间的敏感性差异,筛选出最佳的化疗药物或联合化疗方案。方法:应用MTT显色分析法测定40例非小细胞肺癌实体瘤标本对9种化疗药物及其组成的联合化疗方案的敏感性或耐药性,并比较结果。结果:非小细胞肺癌化疗敏感性个体差异较大。联合化疗药物的敏感性明显优于单药,P=0.038。各药物平均抑制率由高到低的顺序依次为DDP+HCPT>DDP+VP16>HCPT>DDP+NVB>DDP+ADM+IFO>ADM>CTX+ADM+VCR>DDP>NVB>VP16>CBP>IFO>VP16+CBP>VCR>CTX。无论是单药组间比较,还是联合药物组间比较,其敏感性的差异均有显著差异,均P<0.01。结论:体外肿瘤细胞药敏试验对临床肿瘤化疗用药有很强的指导性,并能发现耐药病例。对非小细胞肺癌患者进行化疗时,应尽量选择联合用药方案。 To investigate the different sensitivities of commonly used chemotherapeutic drugs on nonsmall cell lung cancer(NSCLC) by the method of primary culture of NSCLC cells, and to screen the best chemotherapeutic drugs or combined drugs. Methods: The drug sensitivity or resistance of 40 NSCLC samples to 9 chemotherapeutic drugs and combined chemotherapy were detected by MTT colorimetric assay, and compared the results. Results:The individual chemosensitivity was comparatively different. The chemosensitivity of combined drugs was apparently superior to single drugs, P = 0. 038. The sequence for the average inhibition ratio of drugs was DDP + HCPT 〉 DDP + VP16 〉 HCPT 〉 DDP + NVB 〉 DDP + ADM + IFO 〉 ADM 〉 CTX + ADM + VCR 〉 DDP 〉 NVB 〉 VP16 〉 CBP 〉 IFO 〉 VP16 + CBP 〉 VCR 〉 CTX. There were significant differences in sensitivity among the single drug groups and among the combined drug groups, all P 〈 0.01. Conclusion: The tumour chemosensitivity test in vitro gave some prediction and guidances for the clinical chemotherapy, and it could discover the drug resisting cases. The combined chemotherapy should be selected for NSCLC patients.
出处 《现代肿瘤医学》 CAS 2007年第11期1566-1568,共3页 Journal of Modern Oncology
基金 广西科学研究与技术开发计划项目(桂科攻0235024-13)
关键词 非小细胞肺癌 药敏实验 MTT显色分析法 化疗 non - small cell lung cancer chemosensitivity test MTT colorimetric assay chemotherapy
  • 相关文献

参考文献10

  • 1De Vita VT Jr, Hellmau S, Rosenberg SA. Cancer:principles and practice of oncology( Sixth edition) [M]. Philadelphia:JB Lippincott,2001.21-22.
  • 2Levi F. From circadian to cancer chronotherapeutics[J]. Chronobiology International,2002,19( 1 ) : 1-19.
  • 3张天泽.肿瘤化疗药敏试验研究现况[J].中国肿瘤临床,1990,17(5):260-263. 被引量:9
  • 4Bellamy WT. Prediction of response to drag therapy of cancer:a review of in vitro assays[J]. Drags, 1992,44:690.
  • 5Oka M, Fukuda M. Phase I study of irinotecan and cisplatin with concurrent split -course radiotherapy in unresectable arid locally advanced non - small cell lung cancer[J]. Eur J Cancer,2001,37 (11) :1359-1365.
  • 6Sargent JM. The use of the MTT assay to study drug resistance in fresh tumour samples[J]. Recent Resuhs Cancer Res,2003,161 : 13-25.
  • 7Kaspers GJL,Veerman AJP,Pieters R,et al. Drag combination testing in acute lymphoblastic leukemia using the MTT assay [J]. Leuk Res, 1995,19 : 175-183.
  • 8谢晓东,李小民,蒋芹,鲍华.MTT法原代癌细胞培养药物敏感性试验及其影响因素的研究[J].河南肿瘤学杂志,2001,14(6):399-401. 被引量:7
  • 9辛华雯,王润帮,杜光祖.MTT法在恶性肿瘤体外药物敏感试验中的临床应用[J].实用癌症杂志,1994,9(2):73-75. 被引量:25
  • 10Fruehauf JP, Alberts DS. In vitro drug resistance versus chemosen- sitivity:Two sides of different coins [J]. J Clin Oncol, 2005,23 (15) :3641-3643.

二级参考文献7

共引文献36

同被引文献49

引证文献5

二级引证文献20

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