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The presence of large focal lesions is a strong independent prognostic factor in multiple myeloma

机译:大局灶性病变的存在是多发性骨髓瘤的强烈独立预后因子

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摘要

Spatial intratumor heterogeneity is frequently seen in multiple myeloma (MM) and poses a significant challenge for risk classifiers, which rely on tumor samples from the iliac crest. Because biopsy-based assessment of multiple skeletal sites is difficult, alternative strategies for risk stratification are required. Recently, the size of focal lesions (FLs) was shown to be a surrogate marker for spatial heterogeneity, suggesting that data from medical imaging could be used to improve risk stratification approaches. Here, we investigated the prognostic value of FL size in 404 transplant-eligible, newly diagnosed MM patients. Using diffusion-weighted magnetic resonance imaging with background suppression, we identified the presence of multiple large FLs as a strong prognostic factor. Patients with at least 3 large FLs with a product of the perpendicular diameters 5 cm(2) were associated with poor progression-free survival (PFS) and overall survival (OS; median, 2.3 and 3.6 years, respectively). This pattern, seen in 13.8% of patients, was independent of the Revised International Staging System (RISS), gene expression profiling (GEP)-based risk score, gain(1q), or extramedullary disease (hazard ratio, 2.7 and 2.2 for PFS and OS in multivariate analysis, respectively). The number of FLs lost its negative impact on outcome after adjusting for FL size. In conclusion, the presence of at least 3 large FL is a feature of high risk, which can be used to refine the diagnosis of this type of disease behavior and as an entry criterion for risk-stratified trials.
机译:在多发性骨髓瘤(mm)中经常看到空间毒液异质性,并对风险分类器构成重大挑战,依赖于髂嵴肿瘤样本。因为基于活检的评估是难以困难的,所以需要进行风险分层的替代策略。最近,焦点病变(FL)的大小被证明是用于空间异质性的替代标记,表明来自医学成像的数据可用于改善风险分层方法。在这里,我们研究了404例移植符合条件的新诊断的MM患者的FL大小的预后值。使用与背景抑制的扩散加权磁共振成像,我们将多种大杂种的存在确定为强预后因素。具有至少3个大的垂直直径&gt的含量的患者。5cm(2)与无进展的存活率(PFS)和总存活(OS;中位数,2.3和3.6岁有关。在13.8%的患者中看到的这种模式与修订后的国际分期系统(RIS),基因表达分析(GEP)的风险评分,增益(1Q)或仿毒性疾病(PFS危害比例为2.7和2.2)无关和多变量分析中的操作系统)。在调整FL尺寸后,FL的数量对结果产生了负面影响。总之,至少3种大的存在是高风险的特征,可用于优化这种类型的疾病行为的诊断和风险分层试验的进入标准。

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    Univ Arkansas Med Sci Myeloma Inst 4301 W Markham 816 Little Rock AR 72205 USA;

    Univ Arkansas Med Sci Dept Radiol Little Rock AR 72205 USA;

    Univ Arkansas Med Sci Myeloma Inst 4301 W Markham 816 Little Rock AR 72205 USA;

    Univ Arkansas Med Sci Myeloma Inst 4301 W Markham 816 Little Rock AR 72205 USA;

    Univ Arkansas Med Sci Dept Radiol Little Rock AR 72205 USA;

    Univ Arkansas Med Sci Dept Radiol Little Rock AR 72205 USA;

    Univ Arkansas Med Sci Dept Radiol Little Rock AR 72205 USA;

    Univ Arkansas Med Sci Dept Radiol Little Rock AR 72205 USA;

    Univ Arkansas Med Sci Myeloma Inst 4301 W Markham 816 Little Rock AR 72205 USA;

    Univ Arkansas Med Sci Myeloma Inst 4301 W Markham 816 Little Rock AR 72205 USA;

    Univ Arkansas Med Sci Myeloma Inst 4301 W Markham 816 Little Rock AR 72205 USA;

    Univ Arkansas Med Sci Myeloma Inst 4301 W Markham 816 Little Rock AR 72205 USA;

    Roswell Pk Comprehens Canc Ctr Buffalo NY USA;

    Univ Arkansas Med Sci Myeloma Inst 4301 W Markham 816 Little Rock AR 72205 USA;

    Univ Arkansas Med Sci Myeloma Inst 4301 W Markham 816 Little Rock AR 72205 USA;

    Univ Arkansas Med Sci Myeloma Inst 4301 W Markham 816 Little Rock AR 72205 USA;

    Univ Arkansas Med Sci Myeloma Inst 4301 W Markham 816 Little Rock AR 72205 USA;

    Univ Arkansas Med Sci Myeloma Inst 4301 W Markham 816 Little Rock AR 72205 USA;

    Univ Arkansas Med Sci Myeloma Inst 4301 W Markham 816 Little Rock AR 72205 USA;

    Univ Arkansas Med Sci Myeloma Inst 4301 W Markham 816 Little Rock AR 72205 USA;

    Univ Arkansas Med Sci Myeloma Inst 4301 W Markham 816 Little Rock AR 72205 USA;

    Univ Arkansas Med Sci Myeloma Inst 4301 W Markham 816 Little Rock AR 72205 USA;

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  • 正文语种 eng
  • 中图分类 血液及淋巴系疾病;
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