Mantle cell lymphoma

被引:23
作者
Bertoni, F [1 ]
Zucca, E [1 ]
Cavalli, F [1 ]
机构
[1] Oncol Inst So Switzerland, CH-6500 Bellinzona, Switzerland
关键词
lymphoma; ATM; bone marrow transplant; prognosis factors;
D O I
10.1097/01.moh.0000138682.13354.da
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose of review Mantle cell lymphoma is the B-cell lymphoma with the worst prognosis. Until now, no standard treatment has resulted in cure. Improvements in understanding of the disease are needed to advance therapeutic efforts. Recent findings Pathology and immunohistochemistry can identify the subset of patients with the worse prognosis. New data suggest that at least a subset of mantle cell lymphoma cases have undergone some form of antigene selection, and particular types of lg gene rearrangement seem to give a better prognosis. The cell cycle, the ATM, gene and the nuclear factor kappaB pathways are the main targets of the genetic abnormalities occurring in mantle cell lymphoma: new genomic and expression data have been recently published. Unfortunately, this progress has not yet brought any major improvements in therapeutic approaches, which still remain highly unsatisfactory. Autologous and allogenic bone marrow transplantations appear to be the only current treatments that might improve the outcome of patients with PMCL. New additional treatment modalities are currently under investigation. Summary This review summarizes all the most recent data published on the biology and treatment of mantle cell lymphoma.
引用
收藏
页码:411 / 418
页数:8
相关论文
共 108 条
[11]   Inhibition of the proteasome induces cell cycle arrest and apoptosis in mantle cell lymphoma cells [J].
Bogner, C ;
Ringshausen, I ;
Schneller, F ;
Fend, F ;
Quintanilla-Martinez, L ;
Häcker, G ;
Goetze, K ;
Oostendorp, R ;
Peschel, C ;
Decker, T .
BRITISH JOURNAL OF HAEMATOLOGY, 2003, 122 (02) :260-268
[12]   Clearing minimal residual disease with rituximab consolidation therapy [J].
Brugger, W .
SEMINARS IN ONCOLOGY, 2004, 31 (01) :33-37
[13]  
CABANILLAS F, 2002, AM SOC CLIN ONCOLOGY, P416
[14]   ATM gene inactivation in mantle cell lymphoma mainly occurs by truncating mutations and missense mutations involving the phosphatidylinositol-3 kinase domain and is associated with increasing numbers of chromosomal imbalances [J].
Camacho, E ;
Hernández, L ;
Hernández, S ;
Tort, F ;
Bellosillo, B ;
Beà, S ;
Bosch, F ;
Montserrat, E ;
Cardesa, A ;
Fernández, PL ;
Campo, E .
BLOOD, 2002, 99 (01) :238-244
[15]   Molecular heterogeneity in MCL defined by the use of specific VH genes and the frequency of somatic mutations [J].
Camacho, FI ;
Algara, P ;
Rodríguez, A ;
Ruíz-Ballesteros, E ;
Mollejo, M ;
Martínez, N ;
Martínez-Climent, JA ;
González, M ;
Mateo, M ;
Caleo, A ;
Sánchez-Beato, M ;
Menárguez, J ;
García-Conde, J ;
Solé, F ;
Campo, E ;
Piris, MA .
BLOOD, 2003, 101 (10) :4042-4046
[16]   Genetic and molecular genetic studies in the diagnosis of B-cell lymphomas I: Mantle cell lymphoma, follicular lymphoma, and Burkitt's lymphoma [J].
Campo, E .
HUMAN PATHOLOGY, 2003, 34 (04) :330-335
[17]  
Chan WC, 1997, BLOOD, V89, P3909
[18]   Consistent immunostaining for cyclin D1 can be achieved on a routine basis using a newly available rabbit monoclonal antibody [J].
Cheuk, W ;
Wong, KOY ;
Wong, CSC ;
Chan, JKC .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2004, 28 (06) :801-807
[19]   Increased proteasome degradation of cyclin-dependent kinase inhibitor p27 is associated with a decreased overall survival in mantle cell lymphoma [J].
Chiarle, R ;
Budel, LM ;
Skolnik, J ;
Frizzera, G ;
Chilosi, M ;
Corato, A ;
Pizzolo, G ;
Magidson, J ;
Montagnoli, A ;
Pagano, M ;
Maes, B ;
De Wolf-Peeters, C ;
Inghirami, G .
BLOOD, 2000, 95 (02) :619-626
[20]  
COIFFIER B, 2003, ECCO ED BOOK, P23