Novel Agents for Follicular Lymphoma

被引:7
作者
Leonard, John P. [1 ,2 ,3 ]
Martin, Peter [1 ,2 ,3 ]
机构
[1] Weill Cornell Med Coll, Ctr Lymphoma & Myeloma, New York, NY 10065 USA
[2] Weill Cornell Med Coll, Div Hematol & Med Oncol, New York, NY 10065 USA
[3] New York Presbyterian Hosp, New York, NY 10065 USA
关键词
HUMANIZED ANTI-CD22 ANTIBODY; NON-HODGKINS-LYMPHOMA; PROTEASOME INHIBITOR BORTEZOMIB; MONOCLONAL-ANTIBODY; PHASE-I/II; HUMAN CD20; EPRATUZUMAB; THERAPY; LENALIDOMIDE; COMBINATION;
D O I
10.1182/asheducation-2010.1.259
中图分类号
G40 [教育学];
学科分类号
040101 ; 120403 ;
摘要
Unlabeled and radiolabeled anti-CD20 monoclonal antibodies have had a significant impact in the care of patients with follicular lymphoma (FL) over the past decade. More recently, bendamustine has demonstrated activity in refractory FL, and has been explored as initial therapy and in novel combinations. Whereas outcomes for this patient population have significantly improved, there remains substantial unmet need for patients who require more effective and better-tolerated therapies. Novel anti-CD20 antibodies and other immunotherapies against different B-cell antigens are under active investigation. The proteosome inhibitor bortezomib and the immunomodulatory agent lenalidomide have demonstrated single-agent activity and are currently in randomized trials. Other novel compounds have demonstrated activity in broad-based clinical studies in B-cell malignancies. However, considerable challenges remain in efficiently demonstrating which patient subsets can benefit from these novel compounds and which combinations may have the greatest clinical benefit in further improving outcomes for patients with FL.
引用
收藏
页码:259 / 264
页数:6
相关论文
共 58 条
[1]   BCL6 gene translocation in follicular lymphoma:: a harbinger of eventual transformation to diffuse aggressive lymphoma [J].
Akasaka, T ;
Lossos, IS ;
Levy, R .
BLOOD, 2003, 102 (04) :1443-1448
[2]  
ALSINA M, 2007, BLOOD, V110
[3]   Lenalidomide and thalidomide: Mechanisms of action - Similarities and differences [J].
Anderson, KC .
SEMINARS IN HEMATOLOGY, 2005, 42 (04) :S3-S8
[4]  
Andritsos L, 2009, J CLIN ONCOL, V27
[5]  
[Anonymous], BLOOD
[6]   Tumor regression in cancer patients by very low doses of a T cell-engaging antibody [J].
Bargou, Ralf ;
Leo, Eugen ;
Zugmaier, Gerhard ;
Klinger, Matthias ;
Goebeler, Mariele ;
Knop, Stefan ;
Noppeney, Richard ;
Viardot, Andreas ;
Hess, Georg ;
Schuler, Martin ;
Einsele, Hermann ;
Brandl, Christian ;
Wolf, Andreas ;
Kirchinger, Petra ;
Klappers, Petra ;
Schmidt, Margit ;
Riethmueller, Gert ;
Reinhardt, Carsten ;
Baeuerle, Patrick A. ;
Kufer, Peter .
SCIENCE, 2008, 321 (5891) :974-977
[7]  
Baum PR, 2009, J CLIN ONCOL, V27
[8]   Anti-CD20 monoclonal antibody with enhanced affinity for CD16 activates NK cells at lower concentrations and more effectively than rituximab [J].
Bowles, Julie A. ;
Wang, Siao-Yi ;
Link, Brian K. ;
Allan, Barrett ;
Beuerlein, Gregory ;
Campbell, Mary-Ann ;
Marquis, David ;
Ondek, Brian ;
Wooldridge, James E. ;
Smith, Brian J. ;
Breitmeyer, James B. ;
Weiner, George J. .
BLOOD, 2006, 108 (08) :2648-2654
[9]   Epratuzumab, a CD22-targeting recombinant humanized antibody with a different mode of action from rituximab [J].
Carnahan, Josette ;
Stein, Rhona ;
Qu, Zhengxing ;
Hess, Kristen ;
Cesano, Alessandra ;
Hansen, Hans J. ;
Goldenberg, David M. .
MOLECULAR IMMUNOLOGY, 2007, 44 (06) :1331-1341
[10]   A purine scaffold Hsp90 inhibitor destabilizes BCL-6 and has specific antitumor activity in BCL-6-dependent B cell lymphomas [J].
Cerchietti, Leandro C. ;
Lopes, Eloisi C. ;
Yang, Shao Ning ;
Hatzi, Katerina ;
Bunting, Karen L. ;
Tsikitas, Lucas A. ;
Mallik, Alka ;
Robles, Ana I. ;
Walling, Jennifer ;
Varticovski, Lyuba ;
Shaknovich, Rita ;
Bhalla, Kapil N. ;
Chiosis, Gabriela ;
Melnick, Ari .
NATURE MEDICINE, 2009, 15 (12) :1369-U3