Department of Dermatology and.
Department of Molecular Medicine, Aarhus University, Aarhus, Denmark.
Blood. 2018 Feb 15;131(7):759-770. doi: 10.1182/blood-2017-06-788950. Epub 2017 Dec 5.
Mycosis fungoides (MF) is the most frequent form of cutaneous T-cell lymphoma. The disease often takes an indolent course, but in approximately one-third of the patients, the disease progresses to an aggressive malignancy with a poor prognosis. At the time of diagnosis, it is impossible to predict which patients develop severe disease and are in need of aggressive treatment. Accordingly, we investigated the prognostic potential of microRNAs (miRNAs) at the time of diagnosis in MF. Using a quantitative reverse transcription polymerase chain reaction platform, we analyzed miRNA expression in diagnostic skin biopsies from 154 Danish patients with early-stage MF. The patients were subdivided into a discovery cohort (n = 82) and an independent validation cohort (n = 72). The miRNA classifier was built using a LASSO (least absolute shrinkage and selection operator) Cox regression to predict progression-free survival (PFS). We developed a 3-miRNA classifier, based on miR-106b-5p, miR-148a-3p, and miR-338-3p, which successfully separated patients into high-risk and low-risk groups of disease progression. PFS was significantly different between these groups in both the discovery cohort and the validation cohort. The classifier was stronger than existing clinical prognostic factors and remained a strong independent prognostic tool after stratification and adjustment for these factors. Importantly, patients in the high-risk group had a significantly reduced overall survival. The 3-miRNA classifier is an effective tool to predict disease progression of early-stage MF at the time of diagnosis. The classifier adds significant prognostic value to existing clinical prognostic factors and may facilitate more individualized treatment of these patients.
蕈样肉芽肿(MF)是最常见的皮肤 T 细胞淋巴瘤形式。这种疾病通常呈惰性病程,但约有三分之一的患者疾病进展为侵袭性恶性肿瘤,预后不良。在诊断时,无法预测哪些患者会发展为严重疾病并需要积极治疗。因此,我们研究了 MF 患者在诊断时微小 RNA(miRNA)的预后潜力。我们使用定量逆转录聚合酶链反应平台分析了 154 例丹麦早期 MF 患者的诊断性皮肤活检中的 miRNA 表达。将患者分为发现队列(n = 82)和独立验证队列(n = 72)。使用 LASSO(最小绝对收缩和选择算子)Cox 回归构建 miRNA 分类器以预测无进展生存期(PFS)。我们开发了一个基于 miR-106b-5p、miR-148a-3p 和 miR-338-3p 的 3-miRNA 分类器,成功地将患者分为疾病进展的高风险和低风险组。在发现队列和验证队列中,这些组之间的 PFS 均有显著差异。该分类器强于现有的临床预后因素,并且在分层和调整这些因素后仍然是一种强大的独立预后工具。重要的是,高风险组患者的总生存期明显缩短。该 3-miRNA 分类器是一种在诊断时预测早期 MF 疾病进展的有效工具。该分类器为现有的临床预后因素增加了显著的预后价值,并可能为这些患者的个体化治疗提供便利。