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首页> 外文期刊>Blood: The Journal of the American Society of Hematology >Immunoblastic morphology but not the immunohistochemical GCBonGCB classifier predicts outcome in diffuse large B-cell lymphoma in the RICOVER-60 trial of the DSHNHL.
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Immunoblastic morphology but not the immunohistochemical GCBonGCB classifier predicts outcome in diffuse large B-cell lymphoma in the RICOVER-60 trial of the DSHNHL.

机译:在RICOVER-60的DSHNHL试验中,免疫母细胞形态而非免疫组织化学GCB / nonGCB分类器预测了弥漫性大B细胞淋巴瘤的预后。

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摘要

The survival of diffuse large B-cell lymphoma patients varies considerably, reflecting the molecular diversity of tumors. In view of the controversy whether cytologic features, immunohistochemical markers or gene expression signatures may capture this molecular diversity, we investigated which features provide prognostic information in a prospective trial in the R-CHOP treatment era. Within the cohort of DLBCLs patients treated in the RICOVER-60 trial of the German High-Grade Lymphoma Study Group (DSHNHL), we tested the prognostic impact of IB morphology in 949 patients. The expression of immunohistochemical markers CD5, CD10, BCL2, BCL6, human leukocyte antigen (HLA)-DR, interferon regulatory factor-4/multiple myeloma-1 (IRF4/MUM1), and Ki-67 was assessed in 506 patients. Expression of the immunohistochemical markers tested was of modest, if any, prognostic relevance. Moreover, the Hans algorithm using the expression patterns of CD10, BCL6, and interferon regulatory factor-4/multiple myeloma-1 failed to show prognostic significance in the entire cohort as well as in patient subgroups. IB morphology, however, emerged as a robust, significantly adverse prognostic factor in multivariate analysis, and its diagnosis showed a good reproducibility among expert hematopathologists. We conclude, therefore, that IB morphology in DLBCL is likely to capture some of the adverse molecular alterations that are currently not detectable in a routine diagnostic setting, and that its recognition has significant prognostic power.
机译:弥漫性大B细胞淋巴瘤患者的生存率差异很大,反映出肿瘤的分子多样性。鉴于是否存在细胞学特征,免疫组织化学标记物或基因表达特征可以捕获这种分子多样性的争论,我们在R-C​​HOP治疗时代的一项前瞻性试验中调查了哪些特征可提供预后信息。在德国高级别淋巴瘤研究组(DSHNHL)的RICOVER-60试验中治疗的DLBCLs患者队列中,我们测试了IB形态对949位患者的预后影响。在506例患者中评估了免疫组化标记CD5,CD10,BCL2,BCL6,人白细胞抗原(HLA)-DR,干扰素调节因子-4 /多发性骨髓瘤1(IRF4 / MUM1)和Ki-67的表达。所测试的免疫组织化学标记物的表达与预后有关,如果有的话。此外,使用CD10,BCL6和干扰素调节因子4 /多发性骨髓瘤1的表达模式的Hans算法未能在整个队列以及患者亚组中显示出预后意义。然而,IB形态在多变量分析中作为一种强有力的,显着不利的预后因素出现,其诊断在专业的血液病理学家中显示出良好的可重复性。因此,我们得出的结论是,DLBCL中的IB形态可能捕获了一些目前在常规诊断环境中无法检测到的不利分子改变,并且其识别具有重大的预后能力。

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