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局部晚期和晚期滤泡性淋巴瘤在基因表达谱上存在差异。

Localized- and advanced-stage follicular lymphomas differ in their gene expression profiles.

机构信息

Department of Clinical Pathology, Robert-Bosch-Krankenhaus, Stuttgart, Germany.

Dr Margarete Fischer-Bosch Institute of Clinical Pharmacology, Stuttgart, Germany.

出版信息

Blood. 2020 Jan 16;135(3):181-190. doi: 10.1182/blood.2019000560.

Abstract

The genetic background of follicular lymphomas (FLs) diagnosed in advanced clinical stages III/IV, and which are frequently characterized by t(14;18), has been substantially unraveled. Molecular features, as exemplified in the clinicogenetic risk model m7FLIPI, are important tools in risk stratification. In contrast, little information is available concerning localized-stage FL (clinical stages I/II), which accounts for ∼20% of newly diagnosed FL in which the detection rate of t(14;18) is only ∼50%. To investigate the genetic background of localized-stage FL, patient cohorts with advanced-stage FL or localized-stage FL, uniformly treated within phase 3 trials of the German Low-Grade Lymphoma Study Group, were comparatively analyzed. Targeted gene expression (GE) profiling of 184 genes using nCounter technology was performed in 110 localized-stage and 556 advanced-stage FL patients. By penalized Cox regression, a prognostic GE signature could not be identified in patients with advanced-stage FL, consistent with results from global tests and univariate regression. In contrast, it was possible to define robust GE signatures discriminating localized-stage and advanced-stage FL (area under the curve, 0.98) by penalized logistic regression. Of note, 3% of samples harboring an "advanced-stage signature" in the localized-stage cohort exhibited inferior failure-free survival (hazard ratio [HR], 7.1; P = .0003). Likewise, in the advanced-stage cohort, 7% of samples with a "localized-stage signature" had prolonged failure-free survival (HR, 2.3; P = .017) and overall survival (HR, 3.4; P = .072). These data support the concept of a biological difference between localized-stage and advanced-stage FL that might contribute to the superior outcome of localized FL.

摘要

滤泡性淋巴瘤(FL)在临床晚期 III/IV 期的遗传背景已得到充分阐明,这些肿瘤通常具有 t(14;18)。分子特征,如临床遗传风险模型 m7FLIPI 所举例说明的那样,是分层风险的重要工具。相比之下,关于局限性阶段的 FL(临床 I/II 期)的信息很少,约 20%的新诊断的 FL 为局限性阶段,其中 t(14;18)的检出率仅约为 50%。为了研究局限性阶段 FL 的遗传背景,对德国低级别淋巴瘤研究组的 3 期试验中统一治疗的晚期 FL 或局限性阶段 FL 的患者队列进行了比较分析。采用 nCounter 技术对 184 个基因进行了靶向基因表达(GE)谱分析,共分析了 110 例局限性阶段和 556 例晚期 FL 患者。通过惩罚性 Cox 回归,在晚期 FL 患者中未识别出具有预后意义的 GE 特征,与全局检验和单变量回归结果一致。相反,通过惩罚逻辑回归,可以定义出可靠的 GE 特征来区分局限性阶段和晚期 FL(曲线下面积,0.98)。值得注意的是,在局限性阶段队列中,3%的样本具有“晚期阶段特征”,其无失败生存(危险比[HR],7.1;P =.0003)较差。同样,在晚期队列中,7%具有“局限性阶段特征”的样本具有延长的无失败生存(HR,2.3;P =.017)和总生存(HR,3.4;P =.072)。这些数据支持局限性阶段和晚期 FL 之间存在生物学差异的概念,这可能有助于解释局限性 FL 的良好预后。

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