期刊文献+

Construction and clinical significance of a predictive system for prognosis of hepatocellular carcinoma 被引量:8

Construction and clinical significance of a predictive system for prognosis of hepatocellular carcinoma
下载PDF
导出
摘要 AIM: The aims of this study were to explore individualized treatment method for hepatocellular carcinoma (HCC)patients whose maximum tumor size was less than 5 cm to improve prognosis and survival quality. METHODS: Thirty cases of primary HCC patients undergoing tumor resection were retrospectively analyzed (resection group). All the tumors were proved as primary HCC with pathologic examination. The patients were divided into two groups according to follow-up results: group A, with tumor recurrence within 1 year after resection; group B, without tumor recurrence within 1 year. Immunohist ochemical stainings were performed using 11 kinds of monoclonal antibodies (AFP, c-erbB2, c-met, c-myc, HBsAg, HCV, Ki-67, MMP-2, nm23-H1, P53, and VEGF), and expressing intensities were quantitatively analyzed. Regression equation using factors affecting prognosis of HCC was constructed with binary logistic method. HCC patients undergoing percutaneous microwave coagulation therapy (PMCT) were also retrospectively analyzed (PMCT group). Immunohistochemical stainings of tumor biopsy samples were performed with molecules related to HCC prognosis, staining intensities were quantitatively analyzed, coincidence rate of prediction was calculated. RESULTS: In resection group, the expressing intensities of c-myc, Ki-67, MMP-2 and VEGF in cancer tissue in group A were significantly higher than those in group B (t = 2.97, P= 0.01; t= 2.42,P= 0.03<0.05; t= 2.57,P= 0.02<0.05;t = 3.43, P = 0.004<0.01, respectively); the expressingintensities of 11 kinds of detected molecules in para-cancer tissue in groups A and B were not significantly different (P>0.05). The regression equation predicting prognosis of HCC is as follows: P(1) = 1/[1+e-(3.663-0.412mycc-2.187Ki-67c-0.387vegfc)].It demonstrates that prognosis of HCC in resection group was related with c-myc, Ki-67 and VEGF expressing intensity in cancer tissue. In PMCT group, the expressing intensities of c-myc, Ki-67 and VEGF in cancer tissue in group A were significantly higher than those in group B (t= 4.57, P= 0.000<0.01; t= 2.08, P= 0.04<0.05;t = 2.38, ,P = 0.02<0.05, respectively); the expressing intensities of c-myc, Ki-67 and VEGF in para-cancer tissue in groups A and B were not significantly different (P>0.05). The coincidence rate of patients undergoing PMCT in group A was 88.00% (22/25), in group B 68.75% (11/16), the total coincidence rate was 80.49% (33/41). CONCLUSION: The regression equation is accurate and feasible and could be used for predicting prognosis of HCC, it helps to select treatment method (resection or PMCT) for HCC patients to realize individualized treatment to improve prognosis. AIM: The aims of this study were to explore individualized treatment method for hepatocellular carcinoma (HCC) patients whose maximum tumor size was less than 5 cm to improve prognosis and survival quality. METHODS: Thirty cases of primary HCC patients undergoing tumor resection were retrospectively analyzed (resection group). All the tumors were proved as primary HCC with pathologic examination. The patients were divided into two groups according to follow-up results: group A, with tumor recurrence within 1 year after resection; group B, without tumor recurrence within 1 year. Immunohist-ochemical stainings were performed using 11 kinds of monoclonal antibodies (AFP, c-erbB2, c-met, c-myc, HBsAg, HCV, Ki-67, MMP-2, nm23-H1, P53, and VEGF), and expressing intensities were quantitatively analyzed. Regression equation using factors affecting prognosis of HCC was constructed with binary logistic method. HCC patients undergoing percutaneous microwave coagulation therapy (PMCT) were also retrospectively analyzed (PMCT group). Immunohistochemical stainings of tumor biopsy samples were performed with molecules related to HCC prognosis, staining intensities were quantitatively analyzed, coincidence rate of prediction was calculated. RESULTS: In resection group, the expressing intensities of c-myc, Ki-67, MMP-2 and VEGF in cancer tissue in group A were significantly higher than those in group B (t = 2.97, P= 0.01; t = 2.42, P= 0.03<0.05; t = 2.57, P= 0.02<0.05; t = 3.43, P = 0.004<0.01, respectively); the expressing intensities of 11 kinds of detected molecules in para-cancer tissue in groups A and B were not significantly different (P>0.05). The regression equation predicting prognosis of HCC is as follows: P(1) = 1/[1+e-(3.663-0.412mycc-2.187kl-67c-0.397vegfc)]. It demonstrates that prognosis of HCC in resection group was related with c-myc, Ki-67 and VEGF expressing intensity in cancer tissue. In PMCT group, the expressing intensities of c-myc, Ki-67 and VEGF in cancer tissue in group A were significantly higher than those in group B (t = 4.57, P= 0.000<0.01; t = 2.08, P= 0.04<0.05; t = 2.38, P= 0.02<0.05, respectively); the expressing intensities of c-myc, Ki-67 and VEGF in para-cancer tissue in groups A and B were not significantly different (P>0.05). The coincidence rate of patients undergoing PMCT in group A was 88.00% (22/25), in group B 68.75% (11/16), the total coincidence rate was 80.49% (33/41). CONCLUSION: The regression equation is accurate and feasible and could be used for predicting prognosis of HCC, it helps to select treatment method (resection or PMCT) for HCC patients to realize individualized treatment to improve prognosis.
机构地区 DepartmentofUltrasound
出处 《World Journal of Gastroenterology》 SCIE CAS CSCD 2005年第20期3027-3033,共7页 世界胃肠病学杂志(英文版)
基金 Supported by the Medical and Health Science Foundation of PLA During the 10th five-year plan period, No. 01Z038
关键词 疾病预后 预测体系 肝细胞癌 肿瘤切除手术 Hepatocellular carcinoma Prognosis Prediction
  • 相关文献

参考文献3

二级参考文献31

  • 1朱力,周树夏,杨连甲,孙庆妹.实验性骨折愈合中β转化生长因子的免疫组织化学定位[J].华西口腔医学杂志,1995,13(3):167-169. 被引量:2
  • 2李亚非,李青,陈万录,Lars Grimelius,胡蕴玉.人骨折骨痂中转化生长因子β_1的免疫组化研究[J].中华骨科杂志,1997,17(3):191-193. 被引量:9
  • 3Bonewald LF, Mundy GR. Role of transforming growth factor beta in bone remolding[J ]. Clin Orthop, 1990, (250) :261 - 268.
  • 4Lind M. TGF - β stimulation of bone healing[J]. Acta Orthop Scand Oct, 283: 2 - 37.
  • 5Erbe EM, Marx JG, Clineff TD, et al. Potential of an ultroporous beta- tricalcium phosphate synthetic cancellous bone void filler and bone marrow aspirate composite graft[J]. Eur spine J, 2001,10 suppl 2:s141 - 6.
  • 6R Z Wang, F z Cui, H B Liu, et al. Synthesis of nanophase hydroxapatite/collagen composite[J ]. Mater Sci Lett, 1995, 14:490 -6.
  • 7Stratmann A;Risau W;Plate KH.Cell type-specific expression of angiopoietin-1 and angiopoietin-2 suggests a role in glioblastoma angiogenesis,1998.
  • 8Millauer B;Longhi MP;Plate KH.Dominant-negative inhibition of Flk-1 suppresses the growth of many tumor types in vivo,1996.
  • 9Suzuki K;Hayashi N;Miyamoto Y.Expression of vascular permeability factor/vascular endothelial growth factor in human hepatocellular carcinoma,1996.
  • 10Lauren J;Gunji Y;Alitalo K.Is angiopoietin-2 necessary for the initiation of tumor angiogenesis?,1998.

共引文献70

同被引文献46

引证文献8

二级引证文献34

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