Division of Haematopathology, European Institute of Oncology, IEO IRCCS, Via Ripamonti 435, 20141 Milan, Italy.
Tumor Immunology Unit, University of Palermo, 90133 Palermo, Italy.
Cells. 2021 Mar 18;10(3):675. doi: 10.3390/cells10030675.
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.
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。