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Association of tumor growth rates with molecular biomarker status: a longitudinal study of high-grade glioma

机译:肿瘤生长速度与分子生物标记物状态的关联:高度神经胶质瘤的纵向研究

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摘要

To determine the association of molecular biomarkers with tumor growth in patients with high-grade gliomas (HGGs), the tumor growth rates and molecular biomarker status in 109 patients with HGGs were evaluated. Mean tumor diameter was assessed on at least two pre-surgical T -weighted and contrast-enhancement T weighted magnetic resonance images (MRIs). Tumor growth rates were calculated based on tumor volume and diameter using various methods. The association of biomarkers with increased or decreased tumor growth was calculated using linear mixed-effects models. HGGs exhibited rapid growth rates, with an equivalent volume doubling time of 63.4 days and an equivalent velocity of diameter expansion of 51.6 mm/year. The WHO grade was an independent clinical factor of eVDEs. promoter mutation C250T and promoter methylation was significantly associated with tumor growth in univariable analysis but not in multivariable analysis. Molecular groups of , and 1p/19q and and were independently associated with tumor growth. In addition, tumor enhanced area had a faster growth rate than a tumor entity in incomplete enhanced HGGs ( = 0.006). Our findings provide crucial information for the prediction of preoperative tumor growth in HGGs, and aided in the decision making for aggressive resection and adjuvant treatment strategies.
机译:为了确定高级别神经胶质瘤(HGG)患者的分子生物标记物与肿瘤生长的相关性,评估了109名HGGs患者的肿瘤生长速率和分子生物标记物状态。在至少两个术前T加权和对比增强T加权磁共振图像(MRIs)上评估平均肿瘤直径。使用各种方法基于肿瘤的体积和直径计算肿瘤的生长速率。使用线性混合效应模型计算生物标志物与肿瘤生长增加或减少的关联。 HGGs表现出快速的生长速度,等效体积倍增时间为63.4天,等效直径膨胀速度为51.6 mm /年。 WHO等级是eVDE的独立临床因素。在单变量分析中,启动子突变C250T和启动子甲基化与肿瘤的生长显着相关,而在多变量分析中却没有。 ,和1p / 19q和和的分子组与肿瘤生长独立相关。此外,在不完全增强的HGG中,肿瘤增强区域的生长速度要快于肿瘤实体(= 0.006)。我们的发现为预测HGGs术前肿瘤生长提供了重要信息,并有助于做出积极切除和辅助治疗策略的决策。

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