BCL6公司
淋巴瘤
医学
染色体易位
免疫组织化学
癌症研究
耐火材料(行星科学)
肿瘤科
病理
免疫学
B细胞
抗体
基因
生物
生发中心
遗传学
天体生物学
作者
Clémentine Sarkozy,Alexandra Traverse‐Glehen,Bertrand Coiffier
出处
期刊:Lancet Oncology
[Elsevier]
日期:2015-11-01
卷期号:16 (15): e555-e567
被引量:133
标识
DOI:10.1016/s1470-2045(15)00005-4
摘要
Double-hit lymphoma (DHL) is a subgroup of aggressive lymphomas with both MYC and BCL2 gene rearrangements, characterised by a rapidly progressing clinical course that is refractory to aggressive treatment and short survival. Over time, the definition was modified and now includes diffuse large B-cell lymphoma (DLBCL) with MYC translocation combined with an additional translocation involving BCL2 or BCL6. Some cases that have a similar clinical course with concomitant overexpression of MYC or BCL2 proteins were recently characterised as immunohistochemical double-hit lymphomas (ie, double-protein-expression lymphomas [DPLs]). The clinical course of these DPLs is worse than so-called standard DLBCL but suggested by some studies to be slightly better than DHL, although there is overlap between the two categories. Present treatment does not allow cure or long-term survival in patients with genetic or immunohistochemical double-hit lymphomas, but several new drugs are being developed.
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