Lenalidomide for the treatment of B-cell malignancies

被引:147
作者
Chanan-Khan, Asher A.
Cheson, Bruce D.
机构
[1] Roswell Pk Canc Inst, Buffalo, NY 14263 USA
[2] Georgetown Univ Hosp, Washington, DC 20007 USA
关键词
D O I
10.1200/JCO.2007.14.5367
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Lenalidomide is a novel anticancer agent that has made a major impact in the treatment of patients with B-cell malignancies. A more potent analog of thalidomide, lenalidomide was developed to enhance immunomodulatory properties with improved safety profile. Its antitumor activity seems mediated through modulation of both the cytokine and cellular tumor cell microenvironment. Preclinical as well as clinical observations demonstrate that lenalidomide downregulates production of various critical prosurvival cytokines in the tumor microenvironment while concurrently promoting activation of T- and natural killer (NK) cell-mediated antitumor response. Early clinical investigations noted its efficacy in relapsed and/or refractory multiple myeloma patients. Subsequently, larger randomized studies confirmed the clinical benefit of lenalidomide when added to dexamethasone compared with dexamethasone alone in previously treated myeloma patients resulting in its recent approval by the US Food and Drug Administration. Consequently, the role of lenalidomide in other B-cell malignancies has been investigated, with impressive results in chronic lymphocytic leukemia and non-Hodgkin's lymphoma. This review summarizes the data from various clinical investigations and highlights the impact of lenalidomide in the management of patients with B-cell malignancies.
引用
收藏
页码:1544 / 1552
页数:9
相关论文
共 83 条
[1]   Lenalidomide and thalidomide: Mechanisms of action - Similarities and differences [J].
Anderson, KC .
SEMINARS IN HEMATOLOGY, 2005, 42 (04) :S3-S8
[2]  
[Anonymous], BLOOD
[3]   Timeline - The evolution of thalidomide and its IMiD derivatives as anticancer agents [J].
Bartlett, JB ;
Dredge, K ;
Dalgleish, AG .
NATURE REVIEWS CANCER, 2004, 4 (04) :314-322
[4]   Lenalidomide and pegylated liposomal doxorubicin-based chemotherapy for relapsed or refractory multiple myeloma: safety and efficacy [J].
Baz, R. ;
Walker, E. ;
Karam, M. A. ;
Choueiri, T. K. ;
Jawde, R. A. ;
Bruening, K. ;
Reed, J. ;
Faiman, B. ;
Ellis, Y. ;
Brand, C. ;
Srkalovic, G. ;
Andresen, S. ;
Knight, R. ;
Zeldis, J. ;
Hussein, M. A. .
ANNALS OF ONCOLOGY, 2006, 17 (12) :1766-1771
[5]   MALIGNANT CHRONIC LYMPHOCYTIC-LEUKEMIA B-CELLS ELABORATE SOLUBLE FACTORS THAT DOWN-REGULATE T-CELL AND NK FUNCTION [J].
BURTON, JD ;
WEITZ, CH ;
KAY, NE .
AMERICAN JOURNAL OF HEMATOLOGY, 1989, 30 (02) :61-67
[6]   Randomized phase 2 study of fludarabine with concurrent versus sequential treatment with rituximab in symptomatic, untreated patients with B-cell chronic lymphocytic leukemia: results from Cancer and Leukemia Group B 9712 (CALGB 9712) [J].
Byrd, JC ;
Peterson, BL ;
Morrison, VA ;
Park, K ;
Jacobson, R ;
Hoke, E ;
Vardiman, JW ;
Rai, K ;
Schiffer, CA ;
Larson, RA .
BLOOD, 2003, 101 (01) :6-14
[7]   Addition of rituximab to fludarabine may prolong progression-free survival and overall survival in patients with previously untreated chronic lymphocytic leukemia: an updated retrospective comparative analysis of CALGB 9712 and CALGB 9011 [J].
Byrd, JC ;
Rai, K ;
Peterson, BL ;
Appelbaum, FR ;
Morrison, VA ;
Kolitz, JE ;
Shepherd, L ;
Hines, JD ;
Schiffer, CA ;
Larson, RA .
BLOOD, 2005, 105 (01) :49-53
[8]   Acquired CD40-ligand deficiency in chronic lymphocytic leukemia [J].
Cantwell, M ;
Hua, T ;
Pappas, J ;
Kipps, TJ .
NATURE MEDICINE, 1997, 3 (09) :984-989
[9]   Results of a phase 1 clinical trial of thalidomide in combination with fludarabine as initial therapy for patients with treatment-requiring chronic lymphocytic leukemia (CLL) [J].
Chanan-Khan, A ;
Miller, KC ;
Takeshita, K ;
Koryzna, A ;
Donohue, K ;
Bernstein, ZP ;
Mohr, A ;
Klippenstein, D ;
Wallace, P ;
Zeldis, JB ;
Berger, C ;
Czuczman, MS .
BLOOD, 2005, 106 (10) :3348-3352
[10]  
Chanan-Khan AA, 2005, BLOOD, V106