期刊文献+

达沙替尼与伊马替尼治疗慢性粒细胞白血病慢性期患者效果的Meta分析 被引量:5

Meta-analysis of efficacies of dasatinib and imatinib for patients with chronic myeloid leukemiachronic phase
原文传递
导出
摘要 目的比较达沙替尼和伊马替尼治疗慢性粒细胞白血病慢性期(CML—CP)患者的效果。方法通过计算机检索Cochrane图书馆、OVID数据库、Embase数据库、PubMed数据库、中国期刊全文数据库(CNKI)、SpringerLink数据库、万方数据库、维普数据库,并进一步对纳入文献的参考文献扩大检索。对纳入的随机对照研究采用Cochrane风险偏倚评估工具进行质量评价。采用RevMan5.1软件进行统计学分析。结果共纳入5篇文献,CML—CP患者2031例。Meta分析结果显示,达沙替尼组12个月完全细胞遗传学反应(CCyR)率高于伊马替尼组[83.6%(478/572)比70.6%(406/575),合并比值比(OR)=2.11,95%CI1.59~2.80,P〈0.05];达沙替尼组12个月主要分子生物学反应(MMR)率高于伊马替尼组[49.3%(296/600)比30.6%(185/605),OR=2.22,95%CI1.75~2.82,P〈0.05]。结论达沙替尼可以提高CML—CP患者12个月的CCyR率和MMR率。 Objective To compare the efficiencies of imatinib and dasatinib in patients with chronic myeloid leukemia-chronic phase (CML-CP). Methods The databases were retrieved, ineluding Cochrane Library, OVID, Embase, PubMed, China National Knowledge Infrastructure (CNKI), WanFang database and VIP database, besides, references of articles were further to search. The quality of randomized controlled trials (RCTs) was assessed by the Cochrane collaboration's risk tool. Meta-analysis was performed by RevMan 5.1 software. Results A total of 5 articles involved 2 031 patients with CML-CP were included. Meta-analysis showed that the rate of complete cytogenetic response (CCyR) at the 12th month in dasatinib group was higher than that in imatinib group [83.6 % (478/572) vs 70.6 % (406/575), OR = 2.11, 95 % CI 1.59-2.80, P 〈 0.05], and the rate of major molecular response (MMR) at the 12th month in dasatinib group was higher than that in imatinib group [49.3 % (296/600) vs 30.6 % (185/605), OR = 2.22, 95 % CI 1.75-2.82, P 〈 0.05]. Conclusion Dasatinib can improve CCyR and MMR rate at the 12th month in CML-CP patients.
出处 《白血病.淋巴瘤》 CAS 2016年第4期228-233,共6页 Journal of Leukemia & Lymphoma
关键词 白血病 髓样 慢性 达沙替尼 伊马替尼 META分析 Leukemia, myeloid, chronic Dasatinib Imatinib Meta-analysis
  • 相关文献

参考文献2

二级参考文献14

  • 1O'Brien SG,Guilhot F,Larson RA,et al.Imatinib compared with interferon and low-dose cytarabine for newly diagnosed chronic-phase chronic myeloid leukemia.N Engl J Med,2003,348:994-1004.
  • 2Kantarjian HM,O'Brien S,Cortes J,et al.Imatinib mesylate therapy improves survival in patients with newly diagnosed Philadelphia chromosome-positive chronic myelogenous leukemia in the chronic phase:comparison with historic data.Cancer,2003,98:2636-2642.
  • 3Simonsson B.Beneficial effects of cytogenetic and molecular response on long-term outcome in patients with newly diagnosed chronic myeloid leukemia in chronic phase (CML-CP) treated with imatinib (IM):update from the IRIS study.Blood,2005,106:abstract # 166.
  • 4Goldman JM,Hughes T,Radich J,et al.Continuing reduction in level of residual disease after 4 years in patients with CML in chronic phase responding to first-line imatinib (IM) in the IBIS study.Blood,2005,106:abstract #163.
  • 5Kantarjian HM,Cortes JE,O'Brien S,et al.Long-term survival benefit and improved complete cytogenetic and molecular response rates with imatinib mesylate in Philadelphia chromosome-positive chronic-phase chronic myeloid leukemia after failure of interferon-alpha.Blood,2004,104:1979-1988.
  • 6Talpaz M,Silver RT,Druker BJ,et al.Imatinib induces durable hematologic and cytogenetic responses in patients with accelerated phase chronic myeloid leukemia:results of a phase 2 study.Blood,2002,99:1928-1937.
  • 7Kantarjian HM,Cortes J,O'Brien S,et al.Imatinib mesylate (STI571) therapy for Philadelphia chromosome-positive chronic myelogenous leukemia in blast phase.Blood,2002,99:3547-3553.
  • 8Dagher R,Cohen M,Williams G,et al.Approval summary:imatinib mesylate in the treatment of metastatic and/or unresectable malignant gastrointestinal stromal tumors.Clin Cancer Res,2002,8:3034-3038.
  • 9Bartolovic K,Balabanov S,Hartmann U,et al.Inhibitory effect of imatinib on normal progenitor cells in vitro.Blood,2004,103:523-529.
  • 10Sneed TB,Kantarjian HM,Talpaz M,et al.The significance of myelosuppression during therapy with imatinib mesylate in patients with chronic myelogenous leukemia in chronic phase.Cancer,2004,100:116-121.

共引文献60

同被引文献33

引证文献5

二级引证文献16

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部