Kridel Robert, Mottok Anja, Farinha Pedro, Ben-Neriah Susana, Ennishi Daisuke, Zheng Yvonne, Chavez Elizabeth A, Shulha Hennady P, Tan King, Chan Fong Chun, Boyle Merrill, Meissner Barbara, Telenius Adele, Sehn Laurie H, Marra Marco A, Shah Sohrab P, Steidl Christian, Connors Joseph M, Scott David W, Gascoyne Randy D
Centre for Lymphoid Cancer, BC Cancer Agency, Vancouver, BC, Canada; Department of Pathology and Laboratory Medicine, and.
Centre for Lymphoid Cancer, BC Cancer Agency, Vancouver, BC, Canada;
Blood. 2015 Oct 29;126(18):2118-27. doi: 10.1182/blood-2015-06-649905. Epub 2015 Aug 25.
Follicular lymphoma (FL) is an indolent disease but transforms in 2% to 3% of patients per year into aggressive, large cell lymphoma, a critical event in the course of the disease associated with increased lymphoma-related mortality. Early transformation cannot be accurately predicted at the time of FL diagnosis and the biology of transformed FL (TFL) is poorly understood. Here, we assembled a cohort of 126 diagnostic FL specimens including 40 patients experiencing transformation (<5 years) and 86 patients not experiencing transformation for at least 5 years. In addition, we assembled an overlapping cohort of 155 TFL patients, including 114 cases for which paired samples were available, and assessed temporal changes of routinely available biomarkers, outcome after transformation, as well as molecular subtypes of TFL. We report that the expression of IRF4 is an independent predictor of early transformation (Hazard ratio, 13.3; P < .001). We also show that composite histology at the time of transformation predicts favorable prognosis. Moreover, applying the Lymph2Cx digital gene expression assay for diffuse large B-cell lymphoma (DLBCL) cell-of-origin determination to 110 patients with DLBCL-like TFL, we demonstrate that TFL is of the germinal-center B-cell-like subtype in the majority of cases (80%) but that a significant proportion of cases is of the activated B-cell-like (ABC) subtype (16%). These latter cases are commonly negative for BCL2 translocation and arise preferentially from BCL2 translocation-negative and/or IRF4-expressing FLs. Our study demonstrates the existence of molecular heterogeneity in TFL as well as its relationship to the antecedent FL.
滤泡性淋巴瘤(FL)是一种惰性疾病,但每年有2%至3%的患者会转化为侵袭性大细胞淋巴瘤,这是疾病进程中的关键事件,与淋巴瘤相关死亡率增加有关。在FL诊断时无法准确预测早期转化,且转化型FL(TFL)的生物学特性了解甚少。在此,我们收集了126例诊断性FL标本组成的队列,其中包括40例发生转化(<5年)的患者和86例至少5年未发生转化的患者。此外,我们收集了155例TFL患者组成的重叠队列,其中包括114例有配对样本的病例,并评估了常规可用生物标志物的时间变化、转化后的结局以及TFL的分子亚型。我们报告IRF4的表达是早期转化的独立预测因子(风险比,13.3;P <.001)。我们还表明,转化时的复合组织学可预测良好预后。此外,将用于弥漫性大B细胞淋巴瘤(DLBCL)细胞起源确定的Lymph2Cx数字基因表达分析应用于110例DLBCL样TFL患者,我们证明大多数病例(80%)的TFL为生发中心B细胞样亚型,但相当一部分病例为活化B细胞样(ABC)亚型(16%)。后一类病例通常BCL2易位为阴性,且优先来源于BCL2易位阴性和/或IRF4表达的FL。我们的研究证明了TFL中存在分子异质性及其与先前FL的关系。