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直肠癌根治术前XELOX化学治疗方案对患者体液免疫及瘤组织血管内皮生长因子表达的影响

Influence of XELOX Chemotherapeutic Scheme on Humoral Immunity and VEGF Expression in Tumor Tissue before Radical Operation of Rectal Cancer
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摘要 目的探讨直肠癌根治术前应用卡培他滨联合奥沙利铂(XELOX)的新辅助化学治疗(简称化疗)方案的临床疗效,以及对瘤组织血管内皮生长因子(VEGF)及体液免疫的影响。方法选择医院收治的Ⅱ期、Ⅲ期直肠癌患者80例,按随机数字表法均分为治疗组和对照组,各40例。治疗组患者术前接受XELOX化疗方案,对照组患者术前接受5-氟尿嘧啶(5-Fu)联合亚叶酸钙(de Gramont)化疗方案。采用速度散射比浊法,于化疗第1个周期前(化疗前)、第3或4个周期前(化疗中)、第9个周期(化疗后)检测患者血清免疫球蛋白(Ig G,Ig A,Ig M)的含量,采用血细胞计数仪分析全血中淋巴细胞总数、B淋巴细胞的含量,采用免疫组化法检测化疗前后患者肿瘤组织中VEGF表达情况。结果治疗组近期疗效总有效率显著高于对照组(P<0.05);两组患者化疗后血清Ig M水平、淋巴细胞总数均较化疗前显著下降(P<0.05)。两组患者化疗后肿瘤组织中VEGF表达较化疗前显著下降(P<0.05)。结论直肠癌术前采用XELOX辅助化疗方案的疗效优于de Gramont化疗方案,可抑制肿瘤组织的VEGF表达,但同时也会损伤肿瘤患者体液的免疫功能。 Objective To observe the clinical efficacy of neoadjuvant chemotherapy scheme of capecitabine plus oxaliplatin( XELOX)and its influence on vascular endothelial growth factor( VEGF) in tumor tissue and humoral immunity before the radicaloperation of rectal cancer. Methods 80 cases of stage Ⅱ,Ⅲ rectal cancer in our hospital were selected and randomly divided into the treatment group and the control group according to the random number table method,40 cases in each group. The treatment group received the XELOX scheme before operation,while the control group received the 5- fluorouracil combined with calcium folinate before operation. The contents of serum Ig G,Ig A and Ig M were detected before 1 cycle( before chemotherapy),3 or 4 cycles( intra- chemotherapy),9 cycles( after chemotherapy) by using the speed scattering turbidimetry assay. The total number of lymphocytes and B lymphocytes in whole blood were detected by using the whole blood cytometry instrument. The VEGF expression in tumor tissue was detected by using the immunohistochemical method. Results The total effective rate of short term curative effect in the treatment group was significantly higher than that in the control group( P 0. 05); the serum Ig M level and total lymphocyte count after treatment in the two groups were significantly decreased than pre- chemotherapy( P 0. 05). The expression of VEGF in tumor tissue after treatment in the two groups were significantly decreased than pre- chemotherapy( P 0. 05). Conclusion Adopting the XELOX neoadjuvant chemotherapy scheme has better effect before operation in rectal cancer than the de Gramont chemotherapeutic scheme,which can inhibit the VEGF expression in tumor tissue,but at the same time damages the humoral immunity function.
出处 《中国药业》 CAS 2015年第6期33-35,共3页 China Pharmaceuticals
关键词 卡培他滨 奥沙利铂 直肠肿瘤 血管内皮生长因子 体液免疫 capecitabine oxaliplatin rectal tumor vascular endothelial growth factor humoral immunity
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参考文献9

  • 1申丽君,章真.直肠癌新辅助放化疗的适宜人群及疗效评价[J].中华胃肠外科杂志,2014,17(3):201-205. 被引量:5
  • 2De Gramont A, Krulik M ,Cady J,et al. High - dose folinic acid and 5 fluo- rouracil bolus and continuous infusion in advanced colorectal eancer[J]. Eur J Cancer Clin Oncol, 2008,24 (9) : 1 499 - 1 503.
  • 3Feliu J, Salud A, Escudero P, et al. XEI,OX (capecitabine plus oxaliplatin) as first - line treatment for elderly patients over 70 years of age with ad- vanced colorectal cancer [ J ]. Br J Cancer, 2006,94 (7) : 969 - 975.
  • 4Gohji K, Katsuoka Y, Okamoto M, et al. Human heparanase: roles in in- vasion and metastasis of eancer[J] . Hinyokika Kiyo, 2000, 46( 10): 757 - 762.
  • 5Lebe B, Sagol O, Ulukus C, et al. The importance of cyclin DI and Ki67 expression on the biological behavior of pancreatic adenocarcinomas[J]. Pathol Res Pract, 2004,200 (5) : 389 - 396.
  • 6Hoff PM, Saud ED, Ajani JA, et al. P base ls tudyw harmacokinelics of S - 1 on an oral daily schedule for 28 days in patients with solidtumlJ]. Clin Cancer Rcs,2003,9( 1 ) : 134 - 142.
  • 7余辉,吴一龙,戎铁华,李锦添,王思愚,区伟,侯景辉,林素瑕.p53 c-erbB-2 VEGF蛋白表达对非小细胞肺癌辅助化疗的临床预测[J].中国肿瘤临床,2003,30(1):1-4. 被引量:5
  • 8赵刚,肖刚,黄美雄,龙海空.腹腔镜结直肠癌根治对机体免疫状态的影响[J].中华胃肠外科杂志,2005,8(5):407-409. 被引量:41
  • 9Mackall CL. T- cell immunodeficieney following cytotoxic antineoplastic therapy : a review [ J ]. Stem Cells, 2000,18 ( I ) : 10 - 18.

二级参考文献44

  • 1沈坤炜,王坚,沈铭昌,韩企夏,沈镇宙.C-erbB-2基因蛋白表达和肺鳞癌及腺癌生物学行为的关系[J].齐鲁肿瘤杂志,1996,3(2):94-96. 被引量:3
  • 2吴一龙 张昌卿 王思愚.肺癌组织病理学特征和p53蛋白增殖细胞核抗原的表达[J].中华肿瘤杂志,1995,17:112-113.
  • 3步宏 庞宗国.c—erbB—2基因在乳腺癌中的研究进展[J].基因快讯,2001,1:12-14.
  • 4Braga M,Vingali A,Zuliami W,et al. Metabolic and functional results after laparoscopic colorectal surgery. Dis Colon Rectum,2002,45:1070-1077.
  • 5Ordemann J,Jacobi C,Mansmann U,et al. Cellular and humoral inflammatory response after laparoscopic and conventional colorectal resections. Results of a prospective randomized trial. Surg Endosc,2001,15:600-608.
  • 6Hildebrandt U,Kessler K,Plusczyk T,et al. Comparison of surgical stress between laproscopic and open colonic resections. Surg Endosc,2003,17:242-246.
  • 7Walker CBJ,Bruce DM,Heys SD,et al. Minimal modulation of lymphocyte and nature killer cell subsets following minimal access surgery. Am J Surg,1999,177:48-54.
  • 8Sauer R, Becker H, Hohenberger W, et al. Preoperative versus postoperative chemoradiotherapy for rectal cancer [J]. N Engl J Med, 2004,351 : 1731-1740.
  • 9Bosset JF, Collette L, Calais G, et al. Chemotherapy with preoperative radiotherapy in rectal cancer [J]. N Engl J Med, 2006,355 : 1114-1123.
  • 10Swedish Rectal Cancer Trial. Improved survival with preoperative radiotherapy in resectable rectal cancer[J]. N Engl J Med, 1997,336:980-987.

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