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首页> 外文期刊>Therapeutic advances in hematology. >Prognostic molecular biomarkers in diffuse large B-cell lymphoma in the rituximab era and their therapeutic implications
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Prognostic molecular biomarkers in diffuse large B-cell lymphoma in the rituximab era and their therapeutic implications

机译:预后分子生物标志物中延长的大型B细胞淋巴瘤及其治疗意义

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Diffuse large B-cell lymphoma (DLBCL) represents a group of tumors characterized by substantial heterogeneity in terms of their pathological and biological features, a causal factor of their varied clinical outcome. This variation has persisted despite the implementation of rituximab in treatment regimens over the last 20 years. In this context, prognostic biomarkers are of great importance in order to identify high-risk patients that might benefit from treatment intensification or the introduction of novel therapeutic agents. Herein, we review current knowledge on specific immunohistochemical or genetic biomarkers that might be useful in clinical practice. Gene-expression profiling is a tool of special consideration in this effort, as it has enriched our understanding of DLBCL biology and has allowed for the classification of DLBCL by cell-of-origin as well as by more elaborate molecular signatures based on distinct gene-expression profiles. These subgroups might outperform individual biomarkers in terms of prognostication; however, their use in clinical practice is still limited. Moreover, the underappreciated role of the tumor microenvironment in DLBCL prognosis is discussed in terms of prognostic gene-expression signatures, as well as in terms of individual biomarkers of prognostic significance. Finally, the efficacy of novel therapeutic agents for the treatment of DLBCL patients are discussed and an evidence-based therapeutic approach by specific genetic subgroup is suggested.
机译:弥漫性大B细胞淋巴瘤(DLBCL)代表了一组肿瘤,其特征在于其病理和生物学特征方面,其变化的临床结果的因果因素。尽管在过去20年中,这种变异仍然存在于治疗方案中的rituximab。在这种情况下,预后生物标志物具有重要意义,以识别可能从治疗强化或引入新的治疗剂中受益的高风险患者。在此,我们审查了目前对特定免疫组织化学或遗传生物标志物的了解,这可能在临床实践中有用。基因表达分析是这种努力的特殊考虑的工具,因为它丰富了我们对DLBCL生物学的理解,并且已经通过源细胞分类DLBCL,以及基于不同基因的更精细的分子签名 - 表达式配置文件。这些亚组可能在预后表现出各个生物标志物;然而,他们在临床实践中的使用仍然有限。此外,在预后基因表达签名方面讨论了肿瘤微环境在DLBCL预后中的未被符合的作用,以及以预后意义的单独生物标志物而言。最后,讨论了用于治疗DLBCL患者的新型治疗剂的疗效,并提出了具体遗传亚组的基于证据的治疗方法。

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