Update on Therapy of Chronic Lymphocytic Leukemia

被引:85
作者
Gribben, John G. [1 ]
O'Brien, Susan
机构
[1] Queen Mary Univ London, Barts Canc Inst, Barts & London Sch Med, London EC1M 6BQ, England
关键词
FLUDARABINE PLUS CYCLOPHOSPHAMIDE; PREVIOUSLY UNTREATED PATIENTS; PROGRESSION-FREE SURVIVAL; PHASE-III TRIAL; GENE MUTATION STATUS; TERM-FOLLOW-UP; 1ST-LINE THERAPY; CD38; EXPRESSION; GENOMIC ABERRATIONS; PROGNOSTIC-FACTORS;
D O I
10.1200/JCO.2010.32.3865
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
There have been tremendous advances in the treatment of chronic lymphocytic leukemia (CLL) over the past decade, with the goal of therapy no longer being just to palliate symptoms but now to achieve complete remission, eradicate minimal residual disease, and improve survival. During this period, there have also been major advances in identification of molecular factors associated with increased risk of progression. The clinical utility of these factors is being explored to determine whether we can identify groups of patients who should be treated earlier in their disease course and whether we can tailor therapy for groups of patients with specific molecular markers of disease. First-line chemoimmunotherapy approaches now offer prolonged survival, and there is a need to identify patients who are suitable candidates for allogeneic stem-cell transplantation that uses reduced-intensity conditioning regimens. The vast majority of CLL patients are either too old or do not have sufficiently high-risk disease to warrant these approaches, and effective therapies that can be tolerated by the more frail elderly patients with this disease are urgently needed. Numerous novel agents are being developed, and their role in the first-line treatment of frail patients or those who relapse after previous treatment is being explored in clinical trials. J Clin Oncol 29:544-550. (C) 2011 by American Society of Clinical Oncology
引用
收藏
页码:544 / 550
页数:7
相关论文
共 68 条
[1]
[Anonymous], 1999, J Natl Cancer Inst, V91, P861
[2]
[Anonymous], 2010, SURV EP END RES SEER
[3]
Clinical implications of ZAP-70 expression in chronic lymphocytic leukemia [J].
Bosch, Francesc ;
Muntanola, Ana ;
Gine, Eva ;
Carrio, Ana ;
Villamor, Neus ;
Moreno, Carolina ;
Crespo, Marta ;
Montserrat, Emili .
CYTOMETRY PART B-CLINICAL CYTOMETRY, 2006, 70B (04) :214-217
[4]
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
[5]
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
[6]
Select high-risk genetic features predict earlier progression following chemoimmunotherapy with fludarabine and rituximab in chronic lymphocytic leukemia: Justification for risk-adapted therapy [J].
Byrd, JC ;
Gribben, JG ;
Peterson, BL ;
Grever, MR ;
Lozanski, G ;
Lucas, DM ;
Lampson, B ;
Larson, RA ;
Caligiuri, MA ;
Heerema, NA .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (03) :437-443
[7]
Rituximab using a thrice weekly dosing schedule in B-Cell chronic lymphocytic leukemia and small lymphocytic lymphoma demonstrates clinical activity and acceptable toxicity [J].
Byrd, JC ;
Murphy, T ;
Howard, RS ;
Lucas, MS ;
Goodrich, A ;
Park, K ;
Pearson, M ;
Waselenko, JK ;
Ling, G ;
Grever, MR ;
Grillo-Lopez, AJ ;
Rosenberg, J ;
Kunkel, L ;
Flinn, IW .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (08) :2153-2164
[8]
Frequent deletions and down-regulation of micro-RNA genes miR15 and miR16 at 13q14 in chronic lymphocytic leukemia [J].
Calin, GA ;
Dumitru, CD ;
Shimizu, M ;
Bichi, R ;
Zupo, S ;
Noch, E ;
Aldler, H ;
Rattan, S ;
Keating, M ;
Rai, K ;
Rassenti, L ;
Kipps, T ;
Negrini, M ;
Bullrich, F ;
Croce, CM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (24) :15524-15529
[9]
A MicroRNA signature associated with prognosis and progression in chronic lymphocytic leukemia [J].
Calin, GA ;
Ferracin, M ;
Cimmino, A ;
Di Leva, G ;
Shimizu, M ;
Wojcik, SE ;
Iorio, MV ;
Visone, R ;
Sever, NI ;
Fabbri, M ;
Iuliano, R ;
Palumbo, T ;
Pichiorri, F ;
Roldo, C ;
Garzon, R ;
Sevignani, C ;
Rassenti, L ;
Alder, H ;
Volinia, S ;
Liu, CG ;
Kipps, TJ ;
Negrini, M ;
Croce, CM .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 353 (17) :1793-1801
[10]
MicroRNA profiling reveals distinct signatures in B cell chronic lymphocytic leukemias [J].
Calin, GA ;
Liu, CG ;
Sevignani, C ;
Ferracin, M ;
Felli, N ;
Dumitru, CD ;
Shimizu, M ;
Cimmino, A ;
Zupo, S ;
Dono, M ;
Dell'Aquila, ML ;
Alder, H ;
Rassenti, L ;
Kipps, TJ ;
Bullrich, F ;
Negrini, M ;
Croce, CM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (32) :11755-11760