Diffuse large B cell lymphoma: molecular targeted therapy

被引:20
|
作者
Roschewski, Mark [1 ]
Dunleavy, Kieron [1 ]
Wilson, Wyndham H. [1 ]
机构
[1] NCI, Lymphoma Therapeut Sect, Metab Branch, NIH, Bethesda, MD 20892 USA
关键词
Diffuse large B cell lymphoma; DLBCL; NF-kappa B; STAT3; BCR signaling; PROTEASOME INHIBITOR BORTEZOMIB; RITUXIMAB PLUS CYCLOPHOSPHAMIDE; TYROSINE KINASE INHIBITOR; CHOP-LIKE CHEMOTHERAPY; DOSE-ADJUSTED EPOCH; NF-KAPPA-B; GERMINAL-CENTER; PHASE-II; YOUNG-PATIENTS; NEDD8-ACTIVATING ENZYME;
D O I
10.1007/s12185-012-1198-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Diffuse large B cell lymphoma (DLBCL) is a biologically heterogeneous disease and the most common subtype of B cell non-Hodgkin's lymphoma in the USA. Even though it is a curable lymphoma in advanced stages, up to 40 % of patients eventually relapse or fail to achieve remission. Improved understanding of the biologic complexity of DLBCL reveals a diverse range of oncogenic driver mutations and signaling pathways that are essential for growth and survival of malignant cells. Since many of these signaling pathways can be targeted by small-molecule inhibitors, the therapy for DLBCL is currently undergoing a paradigm shift away from conventional chemotherapy and toward targeted agents that capitalize on an improved biologic understanding of the subsets with the highest risk of treatment failure. Participation in well-conducted and rationally designed clinical trials will be essential to realize the potential of these targeted agents and realize the goal of improving overall outcomes in the most common B cell lymphoma in the world.
引用
收藏
页码:552 / 561
页数:10
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