于甬华,陈延条,于金明,梁超前,孙新东,田世禹,韩俊庆,李建彬.马蔺子素在食管癌放疗中增敏作用的临床研究[J].中华放射医学与防护杂志,1999,19(5):313-315
马蔺子素在食管癌放疗中增敏作用的临床研究
A clinical study of radiosensitizing effect of irrisquinone combined with radiotherapy in esophageal cancer
投稿时间:1998-02-11  修订日期:1998-08-11
DOI:
中文关键词:  马蔺子素  食管癌  放疗  放射增敏剂
英文关键词:Irrisquinones  Esophageal carcinoma  Radiotherapy  Radiosensitizer
基金项目:山东省科委自然科学基金
作者单位
于甬华 250117 济南, 山东省肿瘤防治研究院放一科南京东南大学生物医学系影像科学与技术实验室 
陈延条 250117 济南, 山东省肿瘤防治研究院放一科南京东南大学生物医学系影像科学与技术实验室 
于金明 250117 济南, 山东省肿瘤防治研究院放一科南京东南大学生物医学系影像科学与技术实验室 
梁超前 250117 济南, 山东省肿瘤防治研究院放一科南京东南大学生物医学系影像科学与技术实验室 
孙新东 250117 济南, 山东省肿瘤防治研究院放一科南京东南大学生物医学系影像科学与技术实验室 
田世禹 250117 济南, 山东省肿瘤防治研究院放一科南京东南大学生物医学系影像科学与技术实验室 
韩俊庆 250117 济南, 山东省肿瘤防治研究院放一科南京东南大学生物医学系影像科学与技术实验室 
李建彬 250117 济南, 山东省肿瘤防治研究院放一科南京东南大学生物医学系影像科学与技术实验室 
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中文摘要:
      目的 观察马蔺子素对食管癌放疗的增敏作用及毒副反应。方法 1996年1月至1997年8月,将60例胸中段髓质型食管鳞癌病人随机分为试验组和对照组。试验组:在放疗的同时口服马蔺子素胶囊2次/日,110mg/次,直到放疗结束。放疗用60Co或6MV或15MVX射线为放射源,5次/周,DT2Gy/次,前后两野对穿照射DT40Gy后,再两野成角照射DT20~30Gy,中位剂量为DT66.1Gy.对照组单纯放疗,其设野和剂量分别同试验组,中位剂量为DT68.6Gy.结果 放疗结束时,试验组完全消退率(CR)为53.33%,对照组CR为26.67%,P<0.05;放疗后3个月CR分别为73.33%和46.67%,依据40Gy及60Gy时病变消退情况计算的增敏比分别为1.68和1.27.试验组出现的临床反应主要为恶心、呕吐和腹泻,发生率为56.6%,高于对照组的30%,但病人均可耐受。结论 马蔺子素对食管癌有明显的放射增敏作用,毒副作用轻微,值得临床上进一步推广应用。
英文摘要:
      Objective To observe the radiosensitization and side effects of irrisquinones in combination with radiotherapy in treatment of esophageal cancer. Methods From January 1996 to August 1997, 60 cases of esophageal cancer were randomly divided into two groups——the trial group (irisquinone plus irradiation, 30 cases) and the control group(radiotherapy alone, 30 cases).In the trial group, irisquinone provided by Shangdong Xinhua Pharmaceutical Factory was administered at 220mg/m2/day (110mg/m2, twice daily), in combination with radiotherapy throughout the course of treatment.Irradiation was administered with 1.25 MeV 60 Coγ rays and /or 6MV or 15MV X rays, 2 Gy per day and 5 times per week.Total dose was about 60-70 Gy over 6-7 weeks, and the median doses to the trial group and the control group were 66.1 Gy and 68.6 Gy, respectively. Results At the end of treatment course, complete remission rate(CR) in the trial group was 53.33% whereas that in the control group was 26.67% ( P< 0.05), and three months later, the CR were 73.33% and 46.67%, respectively.Sensitization ratios of irrisquinones were 1.68 and 1.27 by the the partial remission at doses of 40 Gy and 60 Gy.The acute toxicity of irrisquinones were diarrhea, nausea and vomiting.The diarrhea rate was 56.6% in the trial group which was higher than that in the control group, but it was generally not severe and the patients were adapted to it soon without interruption of its administration. Conclusion Irrisquinones in combination with radiotherapy in treatment of esophageal cancer can increase the complete remission rate at the end of treatment course.
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