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弥漫性大 B 细胞淋巴瘤的预测和预后分子因素。

Predictive and Prognostic Molecular Factors in Diffuse Large B-Cell Lymphomas.

机构信息

Division of Haematopathology, European Institute of Oncology, IEO IRCCS, Via Ripamonti 435, 20141 Milan, Italy.

Tumor Immunology Unit, University of Palermo, 90133 Palermo, Italy.

出版信息

Cells. 2021 Mar 18;10(3):675. doi: 10.3390/cells10030675.

Abstract

Diffuse large B-cell lymphoma (DLBCL) is the commonest form of lymphoid malignancy, with a prevalence of about 40% worldwide. Its classification encompasses a common form, also termed as "not otherwise specified" (NOS), and a series of variants, which are rare and at least in part related to viral agents. Over the last two decades, DLBCL-NOS, which accounts for more than 80% of the neoplasms included in the DLBCL chapter, has been the object of an increasing number of molecular studies which have led to the identification of prognostic/predictive factors that are increasingly entering daily practice. In this review, the main achievements obtained by gene expression profiling (with respect to both neoplastic cells and the microenvironment) and next-generation sequencing will be discussed and compared. Only the amalgamation of molecular attributes will lead to the achievement of the long-term goal of using tailored therapies and possibly chemotherapy-free protocols capable of curing most (if not all) patients with minimal or no toxic effects.

摘要

弥漫性大 B 细胞淋巴瘤(DLBCL)是最常见的淋巴恶性肿瘤,全球发病率约为 40%。其分类包括一种常见形式,也称为“非特指”(NOS),以及一系列罕见的变体,这些变体至少部分与病毒有关。在过去的二十年中,占 DLBCL 章节中包含的肿瘤 80%以上的 DLBCL-NOS 已经成为越来越多分子研究的对象,这些研究导致了预后/预测因素的确定,这些因素越来越多地进入日常实践。在这篇综述中,将讨论和比较基因表达谱(针对肿瘤细胞和微环境)和下一代测序所取得的主要成果。只有将分子特征融合在一起,才能实现使用量身定制的治疗方法和可能无化疗方案治愈大多数(如果不是全部)患者的长期目标,同时尽量减少或不产生毒性作用。

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