Is now the time for molecular driven therapy for diffuse large B-cell lymphoma?

被引:16
作者
Di Rocco, Alice [1 ]
De Angelis, Federico [1 ]
Ansuinelli, Michela [1 ]
Foa, Robin [1 ]
Martelli, Maurizio [1 ]
机构
[1] Sapienza Univ Rome, Dept Cellular Biotechnol & Hematol, Via Benevento 6, I-00161 Rome, Italy
关键词
Diffuse large B cell lymphoma (DLBCL); cell of origin (COO); germinal centre-B cell like (GCB); activated B cell (ABC); rituximab; CHOP regimen; immunohistochemistry (IHC); gene expression profiling (GEP); RITUXIMAB PLUS CYCLOPHOSPHAMIDE; DOUBLE-HIT LYMPHOMA; NF-KAPPA-B; R-CHOP; PROGNOSTIC-SIGNIFICANCE; GENE-EXPRESSION; PROTEIN EXPRESSION; ELDERLY-PATIENTS; BCL6; REARRANGEMENTS; MUTATIONS PREDICT;
D O I
10.1080/17474086.2017.1356714
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Recent genetic and molecular discoveries regarding alterations in diffuse large B-cell lymphoma (DLBCL) deeply changed the approach to this lymphoproliferative disorder. Novel additional predictors of outcomes and new therapeutic strategies are being introduced to improve outcomes.Areas covered: This review aims to analyse the recent molecular discoveries in DLBCL, the rationale of novel molecular driven treatments and their impact on DLBCL prognosis, especially in ABC-DLBCL and High Grade B Cell Lymphoma. Pre-clinical and clinical evidences are reviewed to critically evaluate the novel DLBCL management strategies.Expert commentary: New insights in DLBCL molecular characteristics should guide the therapeutic approach; the results of the current studies which are investigating safety and efficacy of novel X-RCHOP' will probably lead, in future, to a cell of origin (COO) based upfront therapy. Moreover, it is necessary to identify early patients with DLBCL who carried MYC, BCL2 and/or BCL6 rearrangements double hit lymphomas (DHL) because they should not receive standard R-CHOP but high intensity treatment as reported in many retrospective studies. New prospective trials are needed to investigate the more appropriate treatment of DHL.
引用
收藏
页码:761 / 774
页数:14
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