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Dukes B,C期结肠癌术后两种方案化疗的临床对照研究 被引量:2

Clinical research of Dukes B,C period colon cancer treated with the two schemes of chemotherapy
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摘要 目的探讨F0LFOX与FOLFOX4两种化疗方案治疗Dukes B,C期结肠癌术后的临床效果。方法回顾性分析我院收治的应用FOL-FOX与FOLFOX4方案化疗的Dukes B,C期结肠癌术后患者的临床资料。观察两种化疗方案的复发率、5年生存率及毒副反应发生情况。结果两组患者复发率及5年生存率无显著性差异,但FOLFOX4患者复发时间明显延后;两组患者毒副反应发生率比较无显著差异,但F0LFOX4组Ⅲ度以上毒副反应发生率明显低于F0LFOX组。结论 F0LFOX4化疗方案复发率较低,5年生存率较高,且毒副反应相对较轻,更易被患者接受,值得临床广泛应用于中期结肠癌的术后化疗。 OBJECTIVE To discuss the clinical effect of Dukes B,C period after colon cancer treated with F0LFOX and FOLFOX4.METHODS The clinical data of Dukes B,C period colon cancer patients were analyzed retrospectively who were treated with F0LFOX and FOLFOX4.Watched the relapse rate,5 years survival rate and toxic reaction conditions of the two chemotherapy patients.RESULTS The recurrence rate and 5-year survival rate of the two groups had no significant difference,but FOLFOX4 patients relapse time were delayed obviously;Two groups of patients,incidence of adverse reaction had no remarkable difference,but F0LFOX4 group Ⅲ degrees above adverse reaction rate was significantly lower than the F0LFOX group.CONCLUSION F0LFOX4 chemotherapy for the recurrence rate was low,5 years survival rate was high,and it had the relatively light toxicity,patients were more likely to be accepted,and was worth using widely.
作者 曹宪伟
出处 《海峡药学》 2012年第4期74-76,共3页 Strait Pharmaceutical Journal
关键词 结肠癌 F0LFOX FOLFOX4 Colon cance F0LFOX FOLFOX4
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  • 1赵保平,韩全乡,姜祖光,邵玉山.FOLFOX6方案治疗晚期胃癌45例临床观察[J].山东医药,2008,48(14):138-139. 被引量:8
  • 2Sasaoka M,Fuwa N,Asano A,et al.Patterns of failure in carcinoma ofthe uterine cervix treated with definitive radiotherapy alone(J).Am JClin Oncol,2001,24(6):586-590.
  • 3De Gramont A,Boni C,Navarro M,et al.Oxaliplatin/5-Fu/LV in theadjuvant treatment of stageⅡandⅢcolon cancer,Efficancy resultwith a median follow-up of 4 years(J).4lth ASCO Annal MeetingProceeding,2005,2465:3501.
  • 4SchusterL.针对结直肠癌肝转移的最新化疗方案.肿瘤时讯,2005,:13-13.

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  • 1Goldberg RM,Meropol NJ,Taberuero J.Accomplishments in 2008 in the treatment of advanced metastatic colorectal cancer[J].Gastrointest Cancer Res,2009,3(5 Suppl 2):s2.
  • 2Sileri P,Dugo S,Bennavoli D,et al.Metachronous splenic metastasis from colonic carcinoma five years after surgery:a ease report and literature review[J].South Med J,2009,102(7):733-735.
  • 3Rivera E.Management of metastatic breast cancer:monotherapy options for patients resistant to anthracyclines and taxanes[J].Am J Clin Oncol,2010,33(2):176-185.
  • 4Crane CH,Eng C,Feig BW,et al.Phase 11 trial of neoadjuvant bevacizumab,capecitabine and radiotherapy for locallyadvanced rectal cancer[J].Int J Radiat Oncol Biol Phys,2010,76(3):824-830.
  • 5Sileri P,Dugo S,Bennavoli D,et al.Metachronous splenic metastasis from colonic carcinoma five years after surgery:a ease report and literature review[J].South Med J,2009,102(7):733-735.
  • 6Scott GK, Goga A,Bhaumik D, et al. Coordinatesuppression of ERBB2 and ERBB3 by enforced expressionof micro-RNA miR425b[ J]. J Biol Chen,2007 ,282(2):1479 - I486.
  • 7Slaby 0,Svoboda M,Fabian P,et al. Altered expression ofmiR-21 , miR-31,miR-143 and miR-145 is related toclinicopathologic features of colorectal cancer [ J ].Oncology,2007,72(5-6) :397 -402.
  • 8Faltejskova P, Besse A, Sevcikova S,et al. Clinicalcorrelations of miR-21 expression in colorectal cancerpatients and effects of its inhibition on DLD1 colon cancercells [ J ]. Int J Colorectal Dis, 2012, 27 ( 11 ) : 1401 -1408.
  • 9Xu L,Huang Y, Chen D, et al. Downregulation of miR-21 increases cisplatin sensitivity of non-small-cell lungcancer[ J]. Cancer Genet ,2014,207(5) :214 - 220.
  • 10Meng F,Henson R,Lang M,et al. I nvolvement of humanmicro-RNA in growth and response to chemotherapy inhuman cholangio carcinoma cell lines [ J ]. Gastroenterolo-gy,2006,130(7) :2113 -2129.

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