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DOX方案与DOS-1方案治疗进展期胃癌的临床对比研究 被引量:3

Retrospective study on DOX versus DOS-1 in patients with advanced gastric cancer
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摘要 目的比较多西他赛联合奥沙利铂及卡培他滨(DOX方案)与多西他赛联合奥沙利铂及替吉奥(DOS-1方案)治疗进展期胃癌的有效性和安全性。另外,进一步证实检测肿瘤标记物CAl99在胃癌诊治中的意义。方法54例进展期胃癌患者随机分为两组,A组(DOX方案)29例,具体为:多西他赛Docetaxel35mg/m2静滴第l、8天,Oxaliplatin85mg/m2静滴2h,第1天:CAPE1000mg/m2bid,po,dl—d14,21天为1周期;DOS-1组(DOS-1方案)25例,具体为:Docetaxel35mg/m2静滴第1、8天,Oxaliplatin85mg/m2静滴2h,第1天:s-140mg/m2分早晚2次餐后服用,第1~14天,2l天为1周期。2个周期评价疗效及毒性。治疗前后分别进行血常规、肝肾功能、胸腹部cT扫描及胃镜等检查,观察肿瘤病灶大小及肿瘤标志物的变化,记录临床症状变化和化疗毒副反应,随访两组的无疾病进展生存时间。结果54例均可评价疗效,根据RECIST1.0实体瘤疗效评价标准,分cR、PR、sD和PD,以CR+PR计算有效率(RR),以CR+PR+SD计算疾病控制率(DCR),DOX组和DOS-1组的有效率分别为48.3%和52.0%,疾病控制率分别为75.9%和80.0%,中位无疾病进展时间分别为9.6个月和10.4个月,上述两组比较均无统计学差异(P〉0.05)。两组毒副反应主要包括恶心呕吐、腹泻、末梢神经毒性、手足综合征、口腔黏膜炎、血液学毒性和肝肾功能异常等,以l~2级为主,均可耐受。其中DOX组手足综合症发生率高于DOS-1组(P〈0.05),DOS-1组口腔粘膜炎发生率高于DOX(P〈0.05)。结论DOX方案与DOS-1方案治疗进展期胃癌的近期疗效略好于既往的联合方案研究结果,而且它们的生存优于既往的研究结果,耐受性好。但DOS-1方案的优势值得进一步深入研究。 Objective To evaluate the efficacy and toxicity of two different oral fluoropyrimidines capecitabine or S-1 in combination with oxaliplatin and docetaxel in patients with advanced gastric. In addition, to prove significance of tumor marker CA199 on astric carcinoma. Methods Fifty-four advanced gastric patients were divided into two groups: Group DOX: 29 patients were treated with Docetaxel 35 rag/toLd 1,dS, oxaliplatin 85mg/mL d 1 and ca2Petabine 1 000mg/m2 bid dl-14, Three weeks was a cycle. Group DOS-l: 25 patients were treated with Docetaxel 35 mg/mEdl,d8, oxaliplatin 85 mg/m dl and S-1 40mg/m~ orally twice daily aiter meal dl-dl4. Three weeks was a cycle. Blood routine, function of liver and kidney chest and abdomen-CT or MRI and gastroscopy were examined before and after treatment. The changes of cancer focus size, clinical symptoms, turner marker, toxic and side effects were recorded arid compared after 2 cycles. The progress flee survival were observed. Results All patients were assessable for toxicity and response to treatment. In group DOX and group DOS-l, the remission rate were 48.3 % and 52.0%, the disease control rate were 75.9% and 80.0 %, the median progress free survival were 10.4 months and 9.6 months. There was no significance, between group A and group B (P〉0.05). Side effects were similar in the two groups, mainly in bone marrow depression, nausea and vomiting, diahrrea, dysfunction of liver and kidney, and hand-foot syndrome. All these side effects were of slage 1~2, and well tolerated. Incidence of hand-foot syndrome DOX group is higher than the DOS-1 Group (P〈0.05), oral muensitis happen than DOX DOS-1 Group (P〈0.05). Conclusions DOX programme and recent effect of DOS-1 in treatment of advanced gastric cancer was slightly better than previous joint programmes of research results, research results and they're living better than the past, and well tolerated. DOS-1 the advantages of the programme worthy of further study.
出处 《疾病监测与控制》 2015年第9期627-630,共4页 Journal of Diseases Monitor and Control
关键词 胃癌 多西他赛 奥沙利铂 卡培他滨 替吉奥 化疗 Gastric cancer Docetaxeh Oxaliplatin: Capecitabine: S-1 Chemotherapy
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