Chronic lymphocytic leukaemia

被引:118
作者
Scarfo, Lydia [1 ,2 ]
Ferreri, Andres J. M. [1 ]
Ghia, Paolo [1 ,2 ]
机构
[1] IRCCS San Raffaele Hosp, Div Expt Oncol, Dept Oncohaematol, Milan, Italy
[2] Univ Vita Salute San Raffaele, Milan, Italy
关键词
Chronic lymphocytic leukaemia; Leukaemias; Lymphoproliferative disorders; PREVIOUSLY UNTREATED PATIENTS; STEM-CELL TRANSPLANTATION; MINIMAL RESIDUAL DISEASE; IDENTIFIES RECURRENT MUTATIONS; HIGH-DOSE METHYLPREDNISOLONE; GENOME-WIDE ASSOCIATION; HIGH-RISK; NOTCH1; MUTATIONS; INITIAL THERAPY; TP53; MUTATION;
D O I
10.1016/j.critrevonc.2016.06.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Chronic lymphocytic leukaemia (CLL) is the most common leukaemia among the adults in the Western World. CLL (and the corresponding nodal entity small lymphocytic lymphoma, SLL) is classified as a lymphoproliferative disorder characterised by the relentless accumulation of mature B-lymphocytes showing a peculiar immunophenotype in the peripheral blood, bone marrow, lymph nodes and spleen. CLL clinical course is very heterogeneous: the majority of patients follow an indolent clinical course with no or delayed treatment need and with a prolonged survival, while others experience aggressive disease requiring early treatment followed by frequent relapses. In the last decade, the improved understanding of CLL pathogenesis shed light on premalignant conditions (i.e., monoclonal B-cell lymphocytosis, MBL), defined new prognostic and predictive markers, improving patient stratification, but also broadened the therapeutic armamentarium with novel agents, targeting fundamental signaling pathways. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:169 / 182
页数:14
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