Facts and uncertainties in monitoring treatment response in chronic myeloid leukaemia

被引:6
作者
Clark, Richard E. [1 ]
机构
[1] Royal Liverpool Univ Hosp, Dept Haematol, Liverpool L7 8XP, Merseyside, England
关键词
Chronic myeloid leukaemia; Imatinib; Drug monitoring; Tyrosine kinase inhibitor; Mutation; CHRONIC MYELOGENOUS LEUKEMIA; KINASE DOMAIN MUTATIONS; COMPLETE CYTOGENETIC RESPONSE; GIMEMA WORKING PARTY; BCR-ABL MUTATIONS; STANDARD-DOSE IMATINIB; LATE CHRONIC PHASE; CML PATIENTS; MOLECULAR RESPONSES; SUBOPTIMAL RESPONSE;
D O I
10.1016/j.leukres.2009.04.001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
For patients with chronic myeloid leukaemia (CML), current guidelines advocate frequent monitoring using haematological, cytogenetic, and molecular methods, and these have been used to set targets for disease responses at various time points. Recent clinical data, however, have provided new information on responses to treatment with tyrosine kinase inhibitors, which may have implications for how patients should be monitored. Topics of debate include whether time to complete cytogenetic response (CCyR) is clinically important, what benefit is derived from achieving a major molecular response in patients who have achieved CCyR, and what prognostic implications are associated with developing different types of BCR-ABL mutation. Here, current questions relating to CML monitoring are addressed and practical interpretations are suggested. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1151 / 1155
页数:5
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