期刊文献+

髓内型骨肉瘤患者预后的多因素COX模型分析 被引量:3

Prognostic factors for intramedullary osteosarcoma: a multivariate analysis using COX proportion hazard model in 80 cases
下载PDF
导出
摘要 目的:研究病理多因素对骨肉瘤预后的影响。方法:通过计算机COX多因素分析模型,利用累积生存率,对80例有随访的长骨髓内型骨肉瘤进行预后研究。结果:80例骨肉瘤患者2年、5年生存率分别为33.8%和18.3%。在选取的14个因素中,对预后影响最大的因素依次为:骨样组织分型(RR=2.35)、p53(RR=2.27)、血管内皮生长因子(VEGF)表达(RR=2.07)、WHO分型(RR=1.87)、增殖细胞核抗原(PC-NA)(RR=1.74)、微血管密度(MVD)(RR=1.01)。治疗方法和转移抑制基因nm23-H1蛋白表达对预后影响不大。结论:该结果对综合评估骨肉瘤预后有重要意义。 Objective: To investigate the prognostic significance of pathological parameters in osteosarcoma. Methods: Fourteen individual variables were statistically evaluated using the cumulative survival rate by the computerized COX multivariate analysis model in 80 patients with intramedullary osteosarcoma of long bone. Results: The 2 and 5 year cumulative survival rates were 33.8% and 18.3% respectively. The most important prognostic variables for predicting overall survival included the neoplastic osteoid classification, p53 protein, expression of vascular endothelial growth factor, the type according to WHO classification in 1993, proliferating nuclear antigen and intratumoral microvessel density. The methods of treatment and the expression of nm23 H1 protein did not strongly influence the prognosis of the disease. Conclusion: The results are important for comprehensive evaluation of the prognosis of osteosarcoma.
出处 《第三军医大学学报》 CAS CSCD 北大核心 1999年第4期259-261,共3页 Journal of Third Military Medical University
关键词 预后 骨肉瘤 髓内型 COX模型 bone tumor/pathology multivariate analysis prognosis
  • 相关文献

参考文献3

二级参考文献4

  • 1吴祖尧,中华骨科杂志,1988年,3卷,231页
  • 2刘昌茂,实用病理学杂志,1987年,1期,1页
  • 3刘子君,中华肿瘤杂志,1983年,5卷,340页
  • 4王东,中华病理学杂志,1990年,19卷,268页

共引文献35

同被引文献26

  • 1Kim N K, Ahn J Y, Song J, et al. Expression of the DNA repair enzyme, N-methylpurine-DNA glycosylase (MPG) in astrocytic tumors[J]. Anticancer Res, 2003, 23(2B) : 1417- 1423.
  • 2Kim N K, An H J, Kim H J, et al. Altered expression of the DNA repair protein, N-methylpurine-DNA glycosylase (MPG) in human gonads[J]. Anticancer Res , 2002, 22(2A) : 793 -798.
  • 3Coquerelle T, Dosch J, Kaina B. Overexpression of N-methylpufine-DNA glycosylase in Chinese hamster ovary cells renders them more sensitive to the production of chromosomal aberrations by methylating agents-a case of imbalanced DNA repair [J]. Mutat Res, 1995, 336(1):9-17.
  • 4Rinne M, Caldwell D, Kelley M R. Transient adenoviral N-methylpurine DNA glycosylase overexpression imparts chemotherapeutic sensitivity to human breast cancer cells[ J]. Mol Cancer Ther, 2004,3(8):955 - 967.
  • 5Nagasubramanian R, Dolan M E. Temozolomide: realizing the promise and potential [J]. Curr Opin Oncol, 2003, 15(6) : 412 -418.
  • 6Fishel M L, Seo Y R, Smith M L, et al. Imbalancing the DNA base excision repair pathway in the mitochondria; targeting and overexpressing N-methylpurine DNA glycosylase in mitochondria leads to enhanced cell killing[J]. Cancer Res, 2003, 63(3): 608-615.
  • 7Kreklau E L, Limp Foster M, Liu N, et al. A novel fluorometric oligonucleotide assay to measure O6-methylguanine DNA methyltransferase,methylpurine DNA glycosylase, 8-oxoguanine DNA glycosylase and abasic endonuclease activities: DNA repair status in human breast carcinoma cells overexpressing methylpurine DNA glycosylase[J]. Nucleic Acids Res, 2001, 29(12) : 2558 -2566.
  • 8Limp Foster M, Kelley M R. DNA repair and gene therapy: implications for translational uses[ J]. Environ Mol Mutagen, 2000, 35 (2) :71 -81.
  • 9Fishel ML,Seo YR,Smith ML,et al.Imbalancing the DNA base excision repair pathway in the mitochondria:targeting and overexpression N-methylpurine DNA glycosylase in mitochondria leads to enhanced cell killing.Cancer Res,2003,63:608-615.
  • 10Limp-Foster M,Kelley MR.DNA repair and gene therapy:implications for translational uses.Environ Mol Mutagen,2000,35:71-81.

引证文献3

二级引证文献1

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