期刊文献+

同期放化疗对食管癌患者血清血管内皮生长因子表达水平的影响——附43例临床资料分析 被引量:2

Effect of Concurrent Chemoradiotherapy on Serum Vascular Endothelial Growth Factor in Esophageal Squamous Cell Carcinoma Patients——A Report of 43 Cases
下载PDF
导出
摘要 背景与目的:食管癌患者的预后,除与临床分期有关外,还与血清血管内皮生长因子(serumvascularendothelialgrowthfactor,S-VEGF)的表达水平有关。本研究采用酶联反应吸附试验,探讨食管癌患者同期放化疗对血清中VEGF表达水平的影响及其与预后的关系。方法:收集自2002年12月~2004年1月期间就诊于中山大学肿瘤医院进行同期放化疗,符合入组条件的食管鳞癌患者;血清标本分别在治疗前和治疗结束后1个月抽取,同时选取性别、年龄比例相当的健康人血清作为对照组。采用酶联免疫吸附试验测定S-VEGF表达水平。放射治疗采用常规分割方案进行,放疗剂量60~64Gy,分别在放疗过程中的第1~2天和第29~30天给予顺铂+氟尿嘧啶方案化疗。比较食管癌患者组和正常人组之间S-VEGF表达水平有无差异。以无肿瘤进展生存率为指标,观察治疗前和治疗后,食管癌患者S-VEGF表达水平的变化情况及其与无进展生存率的关系。结果:食管癌患者治疗前、治疗后1个月的S-VEGF表达水平均高于和健康对照组,分别为(516.27±67.89)ng/L、(347.19±35.42)ng/L和(294.20±23.40)ng/L(P<0.01、P=0.002)。同期放化疗显著降低S-VEGF的表达(P<0.01)。完全缓解(CR)患者和部分缓解(PR)+进展(PD)的患者治疗前S-VEGF表达水平分别为(345.82±76.29)ng/L和(669.37±99.04)ng/L(P=0.020)。根据治疗前后S-VEGF表达的动态变化进行分组,即S-VEGF治疗前、治疗后水平>516.27ng/L、>347.19ng/L组(A组),>516.27ng/L、<347.19ng/L组(B组),<516.27ng/L、>347.19ng/L组(C组),<516.27ng/L、<347.19ng/L组(D组),则A、B、C、D四组的1年无肿瘤进展率分别为0%、17%、57%、72%(P=0.005)。结论:食管癌患者S-VEGF的表达水平明显高于健康人;同期放化疗能够降低食管癌患者S-VEGF的表达;治疗前和治疗后S-VEGF的变化情况有可能成为一个判断患者预后参考指标。 BACKGROUND & OBJECTIVE. The prognosis of esophageal cancer is not only affected by TNM stage but also by the level of serum vascular endothelial growth factor (S-VEGF). This study was to investigate the effect of concurrent chemoradiotherapy on S-VEGF in esophageal squamous cell carcinoma (ESCC), and to explore the correlation of S-VEGF to the prognosis of ESCC. METHODS. Serum samples were obtained from ESCC patients, treated with concurrent chemoradiotherapy in Cancer Center of Sun Yat-sen University from Dec. 2002 to May 2004, before treatment and 1 month after treatment. The serum samples from sex- and age-matched healthy donors were used as controls. Two courses of chemotherapy, comprised of cisplatin and 5-fluorouracil, were given during radiotherapy at 4-week intervals. S-VEGF level was measured by ELISA. The changes of S- VEGF level before and after treatment were observed, and its correlation to progress-freely survival rate of ESCC patients was analyzed. RESULTS. S- VEGF level was significantly higher in ESCC patients before and 1 month after treatment than in healthy controls [(516.27±67.89) ng/L and (347.19± 35.42) ng/L vs. (294.20±23.40) ng/L, P〈0.01, P=0.002]; concurrent chemoradiotherapy significantly reduced S-VEGF level (P〈0.01). S-VEGF level before treatment was significantly lower in the patients achieved complete remission than in those achieved partial remission or had progressive disease [(345.82±76.29) ng/L vs. (669.37±99.04) ng/L, P = 0.020]. The 1-year progress-freely survival rate was 0 in the patients with S- VEGF level of 〉 516.27 ng/L before treatment and 〉347.19 ng/L after treatment, 17% in the patients with S-VEGF level of 〉 516.27 ng/L and 〈 347.19 ng/L, respectively, 57% in the patients with S-VEGF level of 〈 516.27 ng/L and 〉347.19 ng/L, respectively, and 72% in the patients with S-VEGF level of 〈 516.27 ng/L and 〈347.19 ng/L, respectively (P= 0.005). CONCLUSIONS: S-VEGF level is higher in ESCC patients than in healthy control. Concurrent chemoradiotherapy could reduce S-VEGF level in ESCC. The changes of S-VEGF level before and after treatment may provide prognostic information for ESCC patients.
出处 《癌症》 SCIE CAS CSCD 北大核心 2006年第11期1428-1432,共5页 Chinese Journal of Cancer
关键词 食管肿瘤 放射治疗 化学治疗 VEGF 预后 Esophageal neoplasm Radiotherapy Chemotherapy Serum vascular endothelial growth factor (S-VEGF) Prognosis
  • 相关文献

参考文献14

  • 1Al-Sarraf M,Martz K,Herskovic A,et al.Progress reporter of combined chemoradiotherapy versus radiotherapy alone in patients with esophageal cancer:an intergroup study[J].J Clin Oncol,1997,15 (1):277-284.
  • 2Herskovic A,Martz K,Al-Sarraf M,et al.Combined chemotherapy and radiation therapy compared with radiotherapy alone in patients with cancer of the esophagus[J].N Engl J Med,1992,326(24):1593-1598.
  • 3Urchel J D,Vasan H.A meta-analysis of randomized controlled trials that compared neoadjuvant chemoradiation and surgery alone for resectable esophageal cancer[J].Am J Surg,2003,185(6):538-543.
  • 4Maeda K,Chung Y S,Ogawa Y,et al.Prognostic value of vascular endothelial growth factor expression in gastric carcinoma[J].Cancer,1996,77 (5):858-836.
  • 5Inoue K,Ozeki Y,Suganuma T,et al.Vascular endothelial growth factor expression in primary esophageal squamous cell carcinoma.Association with angiogenesis and tumor progression[J].Cancer,1997,79(2):206-213.
  • 6Sato F,Shimada Y,Watanabe G,et al.Expression of vascular endothelial growth factor,matrix metalloproteinase-9 and E-cadherin in the process of lymph node metastasic in oesophageal cancer[J].Br J Cancer,1999,80 (9):1366-1372.
  • 7洪明晃.随访率应逐年计算[J].中国肿瘤,1997,6(6):27-27.
  • 8Poon R T,Fan S T,Wong J,et al.Clinical implications of circulation angiogenic factor in cancer patients[J].J Clin Oncol,2001,19(4):1207-1225.
  • 9Wallner G,Ciechanski A,Dabrowski A,et al.Vascular endothelial growth factor and basic growth factor in patients with squamous cell oesophageal cancer[J].Folia Histochem Cytobiol,2001,39(Suppl 2):122-123.
  • 10Shimada H,Takeda A,Nabeya Y,et al.Clincal significance of serum vascular endothelial growth factor in esophageal squamous cell carcinoma[J].Cancer,2001,92 (3):663-669.

共引文献1

同被引文献20

  • 1王其春,李国平.血管内皮生长因子在肝细胞癌及慢性肝病检测中的应用[J].医学检验与临床,2008,20(3):36-38. 被引量:4
  • 2康静波,聂青,张丽萍,李建国,齐文杰.立体定向放射(体部伽玛刀)治疗原发性肝癌的疗效分析[J].海军总医院学报,2005,18(1):16-19. 被引量:24
  • 3孙燕,石远凯.临床肿瘤内科手册[M].5版.北京:人民卫生出版社,2009.
  • 4Jain RK. Normalization of tumor vasculature: an emerging concept in antiangiogenic therapy [ J ]. Science,2005,307 ( 5706 ) : 58 -62.
  • 5Ma J, Waxman DJ. Combination of antiangiogenesis with chemotherapy for more effective cancer treatment [ J ]. Mol Cancer Ther, 2008, 7(12) :3670-3684.
  • 6Ma J, Chen CS, Blute T, et al. Antiangiogencsis enhances intratumoral drug retention [ J ]. Cancer Res,2011,71 (7) :2675-2685.
  • 7Jain RK, Duda DG, Clark JW, et al. Lessons from phase Ⅲ clinical trails on anti-VEGF therapy for cancer[ J]. Nat Clin Pract Oncol, 2006,3 ( 1 ) :24-40.
  • 8Peng F, Xu Z, Wang J, et al. Recombinant human endostatin normalize tumor vasculature and enhances responses in xenograf- ted human nasopharyngeal carcinoma models [ J ]. PLoS One, 2012,7(4) :e34-e46.
  • 9Jiang XD, Qiao Y, Dai P, et al. Enhancement of recombinant human endostatin on the radiosensitivity of human pulmonary adenocarcino- ma A549 cells and its mechanism[ J]. J Biomed Biotechnol,2012, 30(7) :19-31.
  • 10Chang L, Guo F, Lu Y, et al. The inhibitory effects of Endostar com- bined with chemotherapy on human esophageal squamous cell carcino- ma xenograft in mice[ J]. Mol Biol Rep,2013,40( 1 ) :669-673.

引证文献2

二级引证文献8

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