Second-generation tyrosine kinase inhibitors improve the survival of patients with chronic myeloid leukemia in whom imatinib therapy has failed

被引:14
作者
Ibrahim, Amr R. [1 ]
Clark, Richard E. [2 ]
Holyoake, Tessa L. [3 ]
Byrne, Jenny [4 ]
Shepherd, Pat [5 ]
Apperley, Jane F. [1 ]
Milojkovic, Dragana [1 ]
Szydlo, Richard [1 ]
Goldman, John [1 ]
Marin, David [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Hammersmith Hosp, Dept Haematol, London W12 0NN, England
[2] Royal Liverpool Univ Hosp, Dept Haematol, Liverpool, Merseyside, England
[3] Univ Glasgow, Inst Canc Sci, Glasgow, Lanark, Scotland
[4] Nottingham Univ Hosp Trust, Nottingham, England
[5] Western Gen Hosp, Dept Haematol, Edinburgh EH4 2XU, Midlothian, Scotland
来源
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL | 2011年 / 96卷 / 12期
关键词
imatinib failure; chronic myeloid leukemia; second-generation tyrosine kinase inhibitors; overall survival; CHRONIC-PHASE; RANDOMIZED-TRIALS; DASATINIB; RESPONSES; FAILURE;
D O I
10.3324/haematol.2011.049759
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background It has not been clearly established whether second-generation tyrosine kinase inhibitors actually improve the survival of patients with chronic myeloid leukemia in chronic phase who are given nilotinib or dasatinib therapy after treatment failure with imatinib. Design and Methods To address this issue we compared the survival of 104 patients in whom first-line therapy with imatinib failed and who were then treated with second-generation tyrosine kinase inhibitors with the outcome of 246 patients in whom interferon-a therapy failed and who did not receive tyrosine kinase inhibitor therapy. Results atients treated with second-generation tyrosine kinase inhibitors had longer overall survival than the interferon controls (adjusted relative risk = 0.28, P = 0.0001). However this survival advantage was limited to the 64.4% of patients in whom imatinib failed but who achieved complete cytogenetic response with the subsequent tyrosine kinase inhibitor (adjusted relative risk = 0.05, P = 0.003), whereas the 35.6% of patients who failed to achieve complete cytogenetic response on the second or third inhibitor had similar overall survival to that of the controls (adjusted relative risk = 0.76, P = 0.65). Conclusions Patients in whom imatinib treatment fails who receive sequential therapy with second-generation tyrosine kinase inhibitors have an enormous advantage in survival over controls (palliative therapy); this advantage is, however, limited to the majority of the patients who achieve a complete cytogenetic response.
引用
收藏
页码:1779 / 1782
页数:4
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