Treatment of chronic myeloid leukemia in 2007

被引:0
作者
Labussiere, Helene
Hayette, Sandrine
Tigaud, Isabelle
Michallet, Mauricette
Nicolini, Franck-Emmanuel
机构
[1] Hop Edouard Herriot, Hematol Clin, F-69437 Lyon, France
[2] Ctr Hosp Lyon Sud, Lab Cytogenet & Biol Mol, F-69495 Pierre Benite, France
关键词
chronic myeloid leukemia; imatinib mesylate; BCR-ABL; resistance;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The treatment of chronic myeloid leukemia (CML) has considerably evolved since imatinib mesylate has been introduced as a new therapeutic weapon for this disease. The 5-year updated results of the IRIS study confirmed that imatinib mesylate is the best first line therapy for chronic phase CML with an overall survival of 90 %. Responses improve with time and complete cytogenetic and major molecular levels reach 87 and 70 % respectively at 5 years. However, despite these remarkable improvements, new Problems arise as sub-optimal responses, imatinib-resistances with recently identified BCR-ABL protein point mutations, responsible for a variety of therapeutic consequences : imatinib dose increase, alternative treatments with second generation tyrosine kinase inhibitors (TKIs : dastinib, nilotinib) or allogeneic stem cell transplantation. The treatment of accelerated and blastic phases relies on imatinib +/- conventional chemotherapy, ideally followed by allogeneic stein cell transplantation, as newly developed TKIs are currently evaluated within this frame. Finally, BCR-ABL(T3151) mutations remain a new therapeutic critical challenge as none of the three TKIs (imatinib, nilotinib, dasatinib) can efficiently control such diseases. triangle.
引用
收藏
页码:863 / 869
页数:7
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