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小剂量环磷酰胺联合参一胶囊治疗进展期非小细胞肺癌 被引量:11

The efficacy analysis of low-dose cyclophosphamide combined with ginsenoside Rg3 on advanced non-small cell lung cancer
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摘要 目的:应用小剂量环磷酰胺(CTX)联合参一胶囊治疗IIII、V期非小细胞肺癌,观察其临床疗效及毒副作用。方法:III、IV期非小细胞肺癌患者经标准化、放疗后随机分为两组,治疗组(38例):CTX 50mg每日一次、参一胶囊20mg每日两次口服,三至六个月;对照组(34例):化疗后不用任何药物治疗。结果:联合治疗组患者外周血血管内皮生长因子(VEGF)表达下降,T淋巴细胞亚群CD4+及CD4+/CD8+升高,病人生存质量及生存期提高。结论:III、IV期NSCLC患者化疗后联合应用小剂量CTX联合参一胶囊治疗是一种安全有效的治疗方法,可以提高患者的生存质量及生存期。 Objective: To investigate its toxicity and efficacy of low - dose cyclophesphamide(CTX) and ginsenoside Rg3 in treating patients with advanced non-small cell lung cancer. Methods: 72 patients with non-small cell lung cancer, who were diagnosed Stage Ⅲ or Ⅳ by pathology and had been treated with chemotherapy and radiotherapy,were randomly divided into two groups; the therapeutic group(n = 38) was given CTX 50mg qd po plus ginsenoside Rg3 20mg bid po for three to six months; the control group wasn't given any medication after chemotherapy. The clinical data of all the patients in the two groups were analysed when and after medication. Results: The results showed that in the therapeutic group, TTP( = tumor time of progression) was 7 months and meso life span was 19.5 months and annual survival rate was 63.2% ; while in the control group, TTP4 months and meso life span 13.5% and annual survival rate 52.9%. The serum VEGF( = vascular endothelial growth factor) in the therapeutic group was lower than that in the control group after medication. CD4 + , CD4 +/CD8 + after treatment in the therapeutic group were higher than those before treatment. Conclusion: This experiment is proved to be a new safe antieancer therapy,which can improve life quality of the patients and prolong their life span.
出处 《现代生物医学进展》 CAS 2006年第2期50-52,共3页 Progress in Modern Biomedicine
关键词 小剂量环磷酰胺(CTX) 人参皂甙RG3 抗血管生成 非小细胞肺癌 疗效 Low- dose cyclophosphamide(CTX) Ginsenoside Rg3 Antiangiogensis Advanced non- small cell lung cancer Efficacy
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