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新辅助化疗对中期宫颈癌的疗效观察 被引量:2

Observation of the effect of neoadjuvant chemotherapy for patients with advanced cervical cancer
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摘要 目的:观察新辅助化疗对中期宫颈癌的疗效。方法106例中期宫颈癌患者按照数字表法随机分为观察组和对照组,各53例。观察组在手术前采用紫杉醇与顺铂( TP)方案新辅助化疗,对照组直接行手术治疗。观察化疗总有效率和化疗前后肿瘤直径变化,并测定观察组血清血管内皮生长因子( VEGF)和基质金属蛋白酶9(MMP-9)的变化,同时比较两组手术情况。结果化疗结束后观察组总有效率为60.4%;化疗前后观察组肿瘤平均直径分别为(5.24±1.35) cm、(2.64±0.67) cm,差异有统计学意义( t=3.947,P<0.05)。在手术时间、术中出血量及淋巴结转移方面,观察组均明显优于对照组( t=3.725、5.392,χ2=4.28, P<0.05或P<0.01)。观察组患者化疗后血清VEGF和MMP-9均比化疗前有明显降低( t=3.130、4.724,均P<0.05)。结论新辅助化疗可以明显降低中期宫颈癌患者血清VEGF和MMP-9的表达。 Objective To observe the effect of neoadjuvant chemotherapy for patients with advanced cervical cancer.Methods According to the digital table ,106 patients with advanced cervical cancer were randomly divided into the two groups ,53 cases in each group .The observation group was given TP Scheme neoadjuvant chemotherapy before surgery ,the control group underwent surgery directly .The total effective rate of chemotherapy and the changes of diameter of tumor before and after chemotherapy were observed .The serum levels of vascular endothelial growth fac-tor(VEGF) and matrix metalloproteinase-9(MMP-9) of the observation group were detected ,and the operation condi-tions were compared between the two groups .Results After chemotherapy ,the total effective rate of the observation group was 60.4%.Before and after chemotherapy ,the average tumor diameter of the observation group was (5.24 ± 1.35)cm,(2.64 ±0.67)cm,respectively,the difference was significant (t=3.947,P〈0.05).The operative time, blood loss and lymph node metastasis in the observation group were significantly less than those in the control group (t=3.725,5.392,χ2 =4.28,P〈0.05 or P〈0.01).After chemotherapy,the serum levels of VEGF and MMP-9 were significantly lower than that before chemotherapy (t=3.130,4.724,all P〈0.05).Conclusion Neoadjuvant chemotherapy in the treatment of advanced cervical cancer can significantly reduce serum VEGF and MMP-9 expression.
出处 《中国基层医药》 CAS 2014年第19期2929-2931,共3页 Chinese Journal of Primary Medicine and Pharmacy
关键词 宫颈肿瘤 抗肿瘤联合化疗方案 血管内皮生长因子 基质金属蛋白酶9 Uterine cervical neoplasms Antineoplastic combined chemotherapy protocols Vascular endothe-lial growth factors Matrix metalloproteinase 9
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  • 1杨红文,陈忠东,周波,秦永喜,赵强.局部晚期宫颈癌新辅助化疗前后细胞周期和增殖变化对化疗敏感性预测价值的探讨[J].中国医师进修杂志,2012,35(3):3-6. 被引量:4
  • 2Vagno G, Conmio G, Pignata S, et al. Cisplatin and vinorelbine as neoadjuvant chemotherapy in locally advanced cervical cancer: a phase study [ J ]. Int J Gynecol Cancer,2009,13 ( 3 ) : 308-312.
  • 3Okines AF, Norman AR, MaCloud P, et al. Meta-analysis of the REAL-2 and ML17032 trials:evaluating eapecitabine based com- bination chemotherapy and infused 5-fluorouracil based combina- tion chemotherapy for the treatment of advanced oesophagogastric cancer [ J ]. Ann 0neol,2009,20 ( 9 ) : 1529-1534.
  • 4阮晓红,钟开运,杨爱莲,罗中明,练晓勤.宫颈癌新辅助化疗疗效评估[J].中国实用妇科与产科杂志,2009,25(9):688-690. 被引量:8
  • 5Park DC,Suh MJ,Yeo SG. Neoadjuvant paclitaxel and cisplantin in uterine cervical cancer: long-term results [ J ]. Int J Gynecol Cancer,2009,19 ( 5 ) :943-947.
  • 6Gold MA, Tian C, Whitney CW, et al. Surgical versus radiographic determination of paraaoric lymph node metastases before chemoradi- ation for locally advanced cervical carcinoma:a gynecologic oncology group study[J]. Cancer,2008,112(9) :1954-1963.
  • 7Ferrandina G,Distefano M,Ludovisi M,et al. Lymph node involve- ment in locally advanced cervical cancer patients administered pre- operative chemoradiation versns chemotherapy[ J ]. Ann Surg Oncol, 2007,14(3) :1129-1135.
  • 8Loizzi V, Cormio G, Vicino M, et al. Neoadjuvant chemotherapy : an alternative option of treatment for locally advanced cervical cancer [ J ]. Gynecol Obstet Invest,2008,65 ( 2 ) :96-103.
  • 9Gerald JF,Thaddeus HG,Jeffrey WS,et al. Pharmacokinetic/pharre- codynamie modeling and simulmion of neutropenia during phase Ⅰ development of liposomeentrapped paclitaxel [ J ]. Clin Cancer Res, 2008,14 (18) :5856-5863.
  • 10Ho QT, Kuo CJ. Vascular endothelial growth factor: biology and therapeutic applications [ J ]. Int J Biochem Cell Biol, 2007,39 (7-8) : 1349-1357.

二级参考文献36

  • 1邵四海,王荣江,石麒麟,赵红星,郑银元,李辉,陈晓农.动脉化疗栓塞对膀胱癌组织中增殖细胞核抗原表达的影响[J].中国全科医学,2009,12(9):732-733. 被引量:2
  • 2杨琳,谢榕,林玉珍.宫颈癌术前新辅助化疗的临床应用[J].中国肿瘤,2009,18(12):1021-1022. 被引量:2
  • 3Mukherjee P, EI-Abbadi MM, kasperzyk JL, et al. Dietary restriction reduces angiogenesis and growth in an orthotopic mouse brain tumor model[ J]. Br J Cancer,2002,86(10) : 1615-1621.
  • 4Weidner N, Folkman J, Pozza F, et al. Tumor angiogenesis: a new signifieant and independent prognostic indicator in earlystage breast carcinoma[ J ]. J Natl Cancer Inst, 1992,84 ( 24 ) : 1875-1887.
  • 5Reddy VG, Khanna N, Singh N. Vitamin C augments chemotherapeutic response of cervical carcinoma Hela cells by stabilizing p53 [ J ]. Biochem Biophys Res Commun, 2001,282 ( 2 ) : 409-415.
  • 6Sultana H, Kigawa J, Kanamori Y, et al. Chemosensitivity and p53-Bax pathway-mediated apoptosis in patients with uterine cervical cancer[J]. Ann Oncol, 2003,14(2) :214-219.
  • 7Folkman J. Angiogenesis and apoptosis[ J]. Semin Cancer Biol, 2003,13(2) :159-167.
  • 8Gadducci A, Viacava P, Cosio S, et al. Intratumoral microvessel density, response to chemotherapy and clinical outcome of patients with advanced ovarian carcinoma [ J]. Anticancer Res, 2003,23(1B) :549-556.
  • 9Tannock IF, Lee CM, Tunggal JK, et al. Limited penetration of anticancer drugs through tumor tissue : a potential cause of resistance of solid tumors to chemotherapy [ J ]. Clin Cancer Res, 2002, 8(3) :878-884.
  • 10de Campo JM, Prat A, Gil-Moreno A, et al. Update on novel therapeutic agents for cervical cancer[ J ]. Gynecol Oneol, 2008, 110(3 Suppl 2) :S72-S76.

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