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作 者:刘福[1] 何梅[1] 李胜前[1] 周玥[1] 赵曜[1] 杨明[1]
机构地区:[1]川北医学院附属医院药剂科,四川南充637000
出 处:《中华肿瘤防治杂志》2015年第11期891-896,共6页Chinese Journal of Cancer Prevention and Treatment
基 金:"十二五"国家科技支撑计划(2013BAI06B04)
摘 要:目的评价高剂量强度环磷酰胺治疗非霍奇金淋巴瘤的疗效。方法计算机检索PubMed、Medline、Embase、Cochrane图书馆、CBM、VIP和CNKI数据库,检索时间至2013-12。纳入以CHOP(环磷酰胺、多柔比星、长春新碱、泼尼松)化疗方案为对照组,且试验组加用环磷酰胺〔剂量强度〉250mg/(m2·周)〕的相关研究,评价纳入研究的方法学质量,并提取资料,用Stata 11.0软件对数据进行Meta分析。结果共纳入9篇随机对照试验,3 509例患者。Meta分析显示,高剂量强度环磷酰胺的方案较标准CHOP的5年总生存率(SHR=0.83,95%CI为0.73~0.94)、5年无事件生存率(SHR=0.80,95%CI为0.72~0.89)、完全缓解率(SOR=0.70,95%CI为0.63~0.77),差异均有统计学意义(P值均〈0.05),此获益在中高危或预后差的非霍奇金淋巴瘤患者中更加显著。结论高剂量强度环磷酰胺联合CHOP方案较CHOP方案可改善非霍奇金淋巴瘤患者的5年总生存率、5年无事件生存率及完全缓解率,该方案适用于中高危或预后差的非霍奇金淋巴瘤患者,但尚需更多大样本高质量随机对照试验进一步确认。OBJECTIVE To evaluate the efficacy of dose-intensified cyclophosphamide in the treatment of Non Hodgkin's lymphoma.METHODS Data were searched in PubMed,Medline,Embase,Cochrane Library,CBM,VIP,CNKI databases(up to December).Eligible trials had CHOP(cyclophosphamide,doxorubicin,vincristine,prednisone)as control arm and any regimen administering cyclophosphamide at a higher dose intensity〔250mg/(m2·week)〕as the investigational arm.Methodology of eligible was assessed and relevant data were extracted.Meta-analysis was conducted with Stata 11.0software.RESULTS Nine trials involved with 3 509 participants were eligible.Patients receiving high dose intensity-based cyclophosphamide had a significantly better 5year-overall survival(SHR=0.83,95%CI:0.73-0.94),5year-event-free survival(SHR=0.80,95%CI:0.72-0.89)and complete response rate(SOR=0.70,95%CI:0.63-0.77).CONCLUSION Dose-intensified cyclophosphamide regimen has significant benefit on 5-year-overall survival,5year-event-free survival and complete response,this benefit is more prominent in intermediate+high-risk nonHodgkin's lymphoma,but more large sample and high quality randomized controll trials are needed.
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