Kedves András, Tóth Zoltán, Emri Miklós, Fábián Krisztián, Sipos Dávid, Freihat Omar, Tollár József, Cselik Zsolt, Lakosi Ferenc, Bajzik Gábor, Repa Imre, Kovács Árpád
Doctoral School of Health Sciences, University of Pécs, Pécs, Hungary.
Department of Medical Imaging, Faculty of Health Sciences, University of Pécs, Pécs, Hungary.
Front Oncol. 2020 Sep 2;10:1484. doi: 10.3389/fonc.2020.01484. eCollection 2020.
This study aims to evaluate the predictive value of the pretreatment, metabolic, and diffusion parameters of a primary tumor assessed with PET/MR on patient clinical outcomes. Retrospective evaluation was performed using PET/MR image data sets acquired using the single tracer injection dual imaging of 68 histologically proven head and neck cancer patients 4 weeks before receiving definitive chemoradiotherapy (CRT). PET/MR was performed before the CRT and 12 weeks after the CRT for response evaluation. Image data (PET and MRI diffusion-weighted imaging [DWI]) was used to specify the maximum standard uptake value, the peak lean body mass corrected, SUV, the metabolic tumor volume, the total lesion glycolysis (SUV, SUL, MTV, and TLG), and the mean apparent diffusion coefficient (ADC) of the primary tumor. Based on the results of the therapeutic response evaluation, two patient subgroups were created: one with a viable tumor and another without. Metabolic and diffusion data, from the pretreatment PET/MR and the therapeutic response, were correlated using Spearman's correlation coefficient and Wilcoxon's test. After completing the CRT, a viable residual tumor was detected in 36/68 (53%) cases, and 32/68 (47%) patients showed complete remission. However, no significant correlation was found between the pretreatment parameter, ADC ( = 0.88), and the therapeutic success. The PET parameters, SUV and SUL, MTV, and TLG ( = 0.032, = 0.01, < 0.0001, = 0.0004) were statistically significantly different between the two patient subgroups. This study found that MRI-based (ADC) data from FDG PET/MR pretreatment could not be used to predict therapeutic response although the PET parameters SUV, SUL, MTV, and TLG proved to be more useful; thus, their inclusion in risk stratification may also be of additional value.
本研究旨在评估通过PET/MR评估的原发性肿瘤的预处理、代谢和扩散参数对患者临床结局的预测价值。使用68例经组织学证实的头颈癌患者在接受确定性放化疗(CRT)前4周进行单示踪剂注射双成像采集的PET/MR图像数据集进行回顾性评估。在CRT前和CRT后12周进行PET/MR检查以评估反应。图像数据(PET和MRI扩散加权成像[DWI])用于确定原发性肿瘤的最大标准摄取值、校正后的瘦体重峰值SUV、代谢肿瘤体积、总病变糖酵解(SUV、SUL、MTV和TLG)以及平均表观扩散系数(ADC)。根据治疗反应评估结果,创建了两个患者亚组:一个有存活肿瘤,另一个没有。使用Spearman相关系数和Wilcoxon检验对预处理PET/MR和治疗反应的代谢和扩散数据进行相关性分析。完成CRT后,在36/68(53%)例患者中检测到存活的残留肿瘤,32/68(47%)例患者显示完全缓解。然而,预处理参数ADC( = 0.88)与治疗成功之间未发现显著相关性。两个患者亚组之间的PET参数SUV、SUL、MTV和TLG( = 0.032, = 0.01, < 0.0001, = 0.0004)在统计学上有显著差异。本研究发现,尽管PET参数SUV、SUL、MTV和TLG被证明更有用,但来自FDG PET/MR预处理的基于MRI的(ADC)数据不能用于预测治疗反应;因此,将它们纳入风险分层可能也具有额外价值。