Lenalidomide can be highly effective in chronic lymphocytic leukaemia despite T-cell depletion and deletion of chromosome 17p

被引:6
|
作者
Arumainathan, Arvind [1 ]
Kalakonda, Nagesh [1 ,2 ]
Pettitt, Andrew R. [1 ,2 ]
机构
[1] Royal Liverpool & Broadgreen Univ Hosp NHS Trust, Directorate Clin Haematol, Liverpool, Merseyside, England
[2] Univ Liverpool, Dept Mol & Clin Canc Med, Liverpool L69 3BX, Merseyside, England
关键词
chronic lymphocytic leukaemia; lenalidomide; 17p deletion; T-cell depletion; glucocorticoid; alemtuzumab; THALIDOMIDE; ALEMTUZUMAB; ANALOGS; CYTOTOXICITY; FLUDARABINE; COMBINATION; RITUXIMAB; THERAPY;
D O I
10.1111/j.1600-0609.2011.01667.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Lenalidomide is an immunomodulatory agent with activity in a range of haematological cancers including chronic lymphocytic leukaemia (CLL). However, major questions remain concerning its effectiveness in patients with T-cell depletion or deletion of TP53 on chromosome 17p. This case report provides insight into these questions by showing that lenalidomide/dexamethasone in combination can be highly effective as induction therapy for refractory 17p- CLL, that remission quality can be improved by subsequent maintenance with lenalidomide alone and that the anti-leukaemic effects of lenalidomide and its stimulatory effects on non-malignant B cells are preserved despite prolonged T-cell depletion resulting from prior alemtuzumab/methylprednisolone.
引用
收藏
页码:372 / 375
页数:4
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