Beck Enemark Marie, Monrad Ida, Madsen Charlotte, Lystlund Lauridsen Kristina, Honoré Bent, Plesner Trine Lindhardt, Hamilton-Dutoit Stephen Jacques, d'Amore Francesco, Ludvigsen Maja
Department of Hematology, Aarhus University Hospital, Aarhus, Denmark.
Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.
Onco Targets Ther. 2021 Jan 18;14:481-489. doi: 10.2147/OTT.S289337. eCollection 2021.
Follicular lymphoma (FL) is an indolent, yet generally incurable neoplasia with a median survival exceeding 10 years. However, a subset of FL patients experiences histological transformation (HT) to a more aggressive lymphoma, in the majority of cases to diffuse large B-cell lymphoma (DLBCL). This affects both the clinical course and the prognostic outcome, resulting in a markedly reduced survival after transformation. Thus, early risk stratification and prediction of patients at risk of HT would be highly valuable in the clinical setting. Here, we investigated the potential of the immune inhibitory programmed death 1 (PD-1) receptor as a biomarker predictive of HT.
Immunohistochemical staining and quantification by digital image analysis of PD-1 was performed on diagnostic tumor-tissue samples from FL patients with and without subsequent transformation (n=34 and n=46, respectively), and on paired samples from the transformed lymphoma (n=34).
At the time of initial FL diagnosis, samples from patients with subsequent HT had significantly higher tumor-tissue expression of PD-1 compared with diagnostic FL samples from patients without subsequent HT (p=0.010). At the time of transformation, PD-1 expression was significantly reduced (p<0.001). No difference was observed in intra-follicular PD-1 expression at FL diagnosis between samples from patients with or without HT; however, high intra-follicular levels of PD-1 were associated with significantly shorter transformation-free survival times (p<0.043).
Our data suggest that pre-treatment tumor-tissue PD-1 expression already predicts the risk of subsequent transformation to DLBCL, as early as the time of FL diagnosis.
滤泡性淋巴瘤(FL)是一种惰性但通常无法治愈的肿瘤,中位生存期超过10年。然而,一部分FL患者会发生组织学转化(HT),转变为侵袭性更强的淋巴瘤,在大多数情况下转变为弥漫性大B细胞淋巴瘤(DLBCL)。这会影响临床病程和预后结果,导致转化后的生存期显著缩短。因此,在临床环境中,早期风险分层以及预测有HT风险的患者将具有很高的价值。在此,我们研究了免疫抑制性程序性死亡1(PD-1)受体作为预测HT的生物标志物的潜力。
对有或无后续转化的FL患者(分别为n = 34和n = 46)的诊断性肿瘤组织样本,以及转化型淋巴瘤的配对样本(n = 34)进行PD-1的免疫组织化学染色和通过数字图像分析进行定量。
在最初诊断FL时,后续发生HT的患者的样本中PD-1的肿瘤组织表达显著高于未发生后续HT的患者的诊断性FL样本(p = 0.010)。在转化时,PD-1表达显著降低(p < 0.001)。在FL诊断时,有或无HT的患者样本之间在滤泡内PD-1表达上未观察到差异;然而,滤泡内高水平的PD-1与显著缩短的无转化生存期相关(p < 0.043)。
我们的数据表明,早在FL诊断时,治疗前肿瘤组织中的PD-1表达就已经可以预测后续转化为DLBCL的风险。