Imatinib improves but may not fully reverse the poor prognosis of patients with CML with derivative chromosome 9 deletions

被引:91
作者
Huntly, BJP
Guilhot, F
Reid, AG
Vassiliou, G
Hennig, E
Franke, C
Byrne, J
Brizard, A
Niederwieser, D
Freeman-Edward, J
Cuthbert, G
Bown, N
Clark, RE
Nacheva, EP
Green, AR
Deininger, MWN [7 ]
机构
[1] Univ Cambridge, Dept Hematol, Cambridge CB2 1TN, England
[2] Ctr Hosp Reg & Univ Poitiers, Dept Hematol, Poitiers, France
[3] City Hosp Nottingham, Dept Hematol, Nottingham, England
[4] Univ Hosp, Dept Hematol, Leipzig, Germany
[5] Royal Liverpool Univ Hosp, Dept Hematol, Liverpool, Merseyside, England
[6] Newcastle Univ, Cytogenet Unit, Inst Human Genet, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
[7] Oregon Hlth & Sci Univ, BMT Leukemia, Portland, OR 97201 USA
关键词
D O I
10.1182/blood-2002-09-2763
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Deletions of the derivative chromosome 9 occur in a subset of patients with Philadelphia chromosome-positive chronic myeloid leukemia (CML) and are associated with a poor prognosis on standard drug therapy. However, it is currently unknown if the presence of deletions influences the response to imatinib, an Abi-specific tyrosine kinase inhibitor, that has recently shown excellent hematologic and cytogenetic responses in patients with CML. We, therefore, compared hematologic and cytogenetic responses with imatinib in 397 patients with CML, and survival and progression in 354 of these patients, according to deletion status and disease phase. We found no difference in survival between patients with and without deletions, contrasting with previous reports in cohorts with a lower proportion of patients treated with imatinib. However, the time to disease progression on imatinib treatment was significantly shorter for patients with deletions, both in chronic phase (P = .02) and advanced phases (P = .02). Moreover, both in chronic phase and more advanced phases of CML, hematologic and cytogenetic responses were uniformly lower in patients with deletions, with significant differences seen for hematologic response (P = .04), for major cytogenetic response (P = .008) in chronic phase, and for hematologic response in advanced phases (P = .007) of CML. This finding suggests that differences in survival may become apparent with longer follow-up. (C) 2003 by The American Society of Hematology.
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页码:2205 / 2212
页数:8
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