Allogeneic Stem Cell Transplantation in Mantle Cell Lymphoma: Where Are We Now and Which Way Should We Go?

被引:11
作者
Le Gouill, Steven [1 ,2 ,3 ]
Mohty, Mohamad [1 ,2 ,3 ]
Guillaume, Thierry [1 ,3 ]
Gastinne, Thomas [1 ,3 ]
Moreau, Philippe [1 ,2 ,3 ]
机构
[1] CHU Nantes, Serv Hematol Clin, F-44093 Nantes 1, France
[2] INSERM, Ctr Rech Cancerol Nantes Angers, UMR 892, Nantes, France
[3] CHU Nantes, Ctr Invest Clin Cancerol CI2C, F-44093 Nantes 1, France
关键词
HIGH-DOSE THERAPY; BONE-MARROW-TRANSPLANTATION; NON-HODGKINS-LYMPHOMA; PROTEASOME INHIBITOR BORTEZOMIB; PROGRESSION-FREE SURVIVAL; LOW-GRADE LYMPHOMA; REDUCED-INTENSITY; SEQUENTIAL CHEMOTHERAPY; MOLECULAR REMISSIONS; PROGNOSTIC-FACTORS;
D O I
10.1053/j.seminhematol.2011.03.009
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Despite the use of intensive chemotherapy regimens with or without autologous stern cell transplant (auto-SCT) support, the clinical course of mantle cell lymphoma (MCL) remains characterized by iterative relapses and is still an incurable disease. The impact of allogeneic stem cell transplantation (allo-SCT) in MCL emerged in the late 1990s when it was shown that myeloablative allo-SCT could potentially cure some relapsed/refractory MCL patients. This curative impact is sustained by a graft-versus-disease (GVD-MCL) effect. However, toxicity and mortality following myeloablative allo-SCT are too high and have limited its use for patients aged under 65 years at diagnosis. Reduced-intensity conditioning regimens (RIC-allo) entail lower toxicity and reduced transplant-related mortality (TRM), making allogeneic transplant a valid option for a larger MCL population. At present, RIC-allo should be considered a valid therapeutic option for relapsed MCL patients and innovative therapeutic strategies including RIC-allo need to be investigated. Herein, the role of GVD-MCL and place of allo-SCT in MCL is discussed, taking into account the most recent literature, and several ways to improve RIC-allo in MCL that deserve to be explored are presented. Semin Hematol 48:227-239. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:227 / 239
页数:13
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