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树突状细胞联合化疗治疗晚期胃肠道肿瘤的临床研究 被引量:2

Clinical study of dendritic cell combined with chemotherapy for advanced gastrointestinal cancer
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摘要 目的探讨致敏的树突状细胞联合化疗治疗晚期胃肠道恶性肿瘤的临床疗效和毒副作用。方法40例晚期的胃癌和结直肠癌患者随机分为树突状细胞联合化疗组(观察组)和单纯化疗组(对照组),治疗组化疗前分离患者外周血单核细胞,体外培养成致敏的树突状细胞,培养期间给予患者一周期的5-FU、CF和奥沙利铂方案的化疗,化疗后回输树突状细胞,对照组给予患者同一方案的化疗,观察临床获益率、卡氏评分和毒副作用等临床指标。结果两组临床获益率无统计学差异(P>0.05),骨髓抑制毒副反应较对照组明显减轻(P<0.05),观察组行树突状细胞回输时,常见的不良反应为发热,未发现III级以上的毒副作用。结论两组临床疗效相近,树突状细胞能够减轻化疗的毒副反应,改变免疫抑制状态,提高免疫功能,改善患者的生活质量。 Objective To observe the clinical curative effect and side effect of dendritic cell combined chemotherapy in advanced gastrointestinal cancer. Methods Forty patients with advanced gastric cancer or coloreetal cancer were randomly divided into chemotherapy group (control goup) and dendritic cell combined with chemotherapy group (observing group), sensitized matured DCs were derived from peripheal blood monocytes of the patients in observing group before chemotherapy which were loaded tumor lysate and cultivated in vitro, in the course of cultivation, the patients in observing group received oxaliplatin (L- OHP) plus 5 -FU/CF, sensitized matured DCs were administered after chemotherapy, the patients in control group received the treatment of the same regimen, toxicity, clinical benefit response rate and KPS were obseved. Results No statistical difference was found in clinical benefit response rate between two groups (P 〉 0.05 ). Compared with control group, bone marrow suppression was mild in obversing goup (P 〈 0. 05). In observing group, when sensitized matured DCs were administered, fever was a common side effect, serious side effect was not obversed. Conclusions The response rate of bioehmotherapy is the same with chemotherapy;dendritic cell can decrease side effect of chemotherapy, change immunosuppression, enhance immune function and improve patients' quality of life.
出处 《医学信息(手术学分册)》 2008年第11期993-995,共3页 Medical Information Operations Sciences Fascicule
关键词 树突状细胞 IFN—γ IL-10 IL-12 化疗 胃肠道肿瘤 dendritic cell IFN - γ IL - 10 IL - 12 chemotherapy gastrointestinal cancer
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  • 1[4]Louvet C,Andre T,Tigaud JM,et al.Phase study of oxaliplatin,fluorouracil,and folinic acid in locally advanced or metastatic gastric cancer patients[J].J Clin Oncol,2002,20(23):4543~4548.
  • 2[5]Grolleau F,Gamelin L,Boisdron-Celle M,et al.A possible explanation for a neurotoxic effect of the anticancer agent oxaliplatin on neuronal voltage-gated sodium channels[J].J Neurophysiol,2001,85(5):2293~2297.
  • 3Liu Y, Chiriva-Internati M, You C, et al. Use and specificity of breast cancer antigen/milk protein BA46 for generating anti-selfcytotoxic T lymphocytes by recombinant adeno-associated virusbased gene loading of dendritic cells [ J ]. Cancer Gene Ther,2005,12(3) :304 - 312.
  • 4Midgley R, Kerr DJ, Mirza N, et al. A phase Ⅱ dendritic cell (DC) immunotherapy trial for hepatocellular carcinoma (HC) [J]. Proc Am Soc Clin Oncol,2002,21:23b.
  • 5Chang JWC,Hsieh JJ,Chen J S, et al. Immunotherapy with dendritic cells pulsed by autologous dactinomycin-treated melanoma apoptotic cells for patients with malignant melanoma [ J ]. ProcAm Soc Clin Oncol,2002,21:3b.
  • 6Chiriva-Internati M, Liu Y, Salati E, et al. Efficient generation of cytotoxic T lymphocytes against cervical cancer cells by adeno associated virus/human papillomavirus type 16 E7 antigen gene transduction into dendritic cells[J ]. Eur J Immunol, 2002,32(1) :30 - 38.
  • 7Slichenmyer WJ,Fry DW. Anticancer therapy targeting the erbB family of receptor tyrosine kinases[J]. Semin Oncol, 2001,28 (Suppl 16) :S67 - S79.
  • 8Hainsworth JD, Litchy S, Burris HA, et al. Rituximab as firstline and maintenance therapy for patients with indolent nonhodgkin's lymphoma[J]. J Clin Oncol,2002,20(20):4261 -4267.
  • 9Cohen RB. Epidermal growth factor receptor as a therapeutic target in colorectal cancer[J]. Clin Colorectal Cancer ,2003,2(4): 246 - 251.
  • 10Goodman L. Persistance-luck-Avastin[J]. J Clin Invest,2004, 113(7) :934 - 940.

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  • 1王娟,陶贞霞,刘荣英,曹艳丽,许卫星,李静,沈杰,王庆,王瑞环,赵芳,刘春燕,张睿,张敏娟,马洪玉,苏国宏.DC-CIK细胞免疫治疗恶性肿瘤的临床研究[J].免疫学杂志,2009,25(1):71-74. 被引量:16
  • 2罗荣城,尤长宣.肿瘤生物治疗新进展[J].中国新药杂志,2005,14(2):143-146. 被引量:18
  • 3王科,王晓雄,石炳毅.肾细胞癌患者肿瘤免疫状况的监测[J].北京生物医学工程,2005,24(3):217-219. 被引量:2
  • 4骆云鹏,余南生,黄文州,谢鸿寿,田秀荣,李永安,胡万发,杨路保,赵多兰,张文兵,王中民,朱永,谢保琴,廖璐荣.极高频电磁波对恶性肿瘤化疗患者外周血辅助淋巴细胞亚群Th1/Th2免疫应答平衡的影响[J].免疫学杂志,2006,22(5):562-565. 被引量:12
  • 5Gcige JD, Hutchinson J, Hohenkik LF, et al. Vaccination of pediatic solid-tumo patients with tumo lysate-pulsed dendritic cells can expand specific T cells and mediate tumor regression[J]. Cancer Res, 2001, 61 (23):8513-8519.
  • 6Ishikawa A, Motohashi S, Ishikawa E, et al. A phase I study of alpha-galactosylceamide(KN7000)-pulsed dendritic cells in patients with advanced and recurrent non-small cell lung cancer[J]. Clin Cancer Res, 2005, 11(5):1910-1917.
  • 7Rains N, Cannan J, Chen W, et al. Development of a dendritic cell (DC)-based vaccine for patients with advanced colorectal cancer [J]. Hepatogastroenterology, 2001, 48 (38): 347-351.
  • 8Bang S, Kim HS, Choo YS,et al. Differences in immune cells engaged in cell-mediated immunity after chemotherapy for far advanced pancreatic cancer[J]. Pancreas, 2006, 32(1): 29-36.
  • 9Ridgway D. The first 1000 dendritic cell vaccinees [J]. Cancer Invest, 2003, 21 (6):969-970.
  • 10Kim SH,Bianco NR,Shufesky WJ,et al.Effective treatment of inflammatory disease models with exosomes derived from dendritic cells genetically modified to express IL-4[J].J Immunol,2007,179(4):2242-2249.

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