Sjö Lene Dissing, Poulsen Christian Bjørn, Hansen Mads, Møller Michael Boe, Ralfkiaer Elisabeth
Department of Pathology, Copenhagen University Hospital, Copenhagen, Denmark.
Eur J Haematol. 2007 Dec;79(6):501-7. doi: 10.1111/j.1600-0609.2007.00976.x. Epub 2007 Nov 7.
Diffuse large B-cell lymphoma (DLBCL) is a frequent lymphoma subtype with a heterogeneous behavior and a variable response to conventional chemotherapy. This clinical diversity is believed to reflect differences in the molecular pathways leading to lymphomagenesis. In this study, we have analyzed pretreatment, diagnostic samples from 108 DLBCL by immunohistology for expression of four markers linked to germinal center B-cells (CD10, Bcl-6), postgerminal center B-cells (MUM1) and apoptosis (Bcl-2). The results indicate that both CD10 and Bcl-6 are favorable prognostic indicators, in contrast to Bcl-2, which is an adverse parameter. Furthermore, using two algorithms for distinction between low- and high-risk patients proposed by Hans et al. (Blood, 2004; 103:275) and Muris et al. (Journal of Pathology, 2006; 208:714), it is shown that both are useful for predicting outcome in DLBCL. However, in this report, the algorithm of Hans et al. was superior to that of Muris et al. These findings confirm and extend other studies and indicate that different prognostic subgroups of DLBCL can be distinguished by simple immunohistological investigations for a limited number of markers. Whether these groups are also relevant for individual treatment decisions will be important to investigate in prospective studies.
弥漫性大B细胞淋巴瘤(DLBCL)是一种常见的淋巴瘤亚型,其行为具有异质性,对传统化疗的反应也各不相同。这种临床多样性被认为反映了导致淋巴瘤发生的分子途径的差异。在本研究中,我们通过免疫组织化学分析了108例DLBCL患者的预处理诊断样本,以检测与生发中心B细胞(CD10、Bcl-6)、生发中心后B细胞(MUM1)和细胞凋亡(Bcl-2)相关的四种标志物的表达。结果表明,与作为不良参数的Bcl-2相反,CD10和Bcl-6都是良好的预后指标。此外,使用Hans等人(《血液》,2004年;103:275)和Muris等人(《病理学杂志》,2006年;208:714)提出的两种区分低风险和高风险患者的算法,结果显示这两种算法都有助于预测DLBCL的预后。然而,在本报告中,Hans等人的算法优于Muris等人的算法。这些发现证实并扩展了其他研究,表明通过对有限数量标志物进行简单的免疫组织学研究,可以区分DLBCL的不同预后亚组。这些亚组是否也与个体治疗决策相关,将是前瞻性研究中需要重点探讨的问题。