18F-FDG PET/CT对肺癌间质性肺病患者化疗相关急性加重的预测价值

K. Akaike, K. Saruwatari, S. Oda, S. Hamada, Y. Tomita, S. Saeki, H. Ichiyasu, K. Fujii, S. Shiraishi, T. Sakagami
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摘要

背景:肺癌(LC)间质性肺炎(ILD)患者急性加重(AE)可能是化疗相关的致死性不良反应之一。本研究的目的是确定化疗前18F-FDG PET/CT结果是否可以预测LC合并ILD患者化疗相关AE-ILD的发病。方法:2006年4月至2018年3月,33例LC和ILD患者在熊本大学医院进行了18F-FDG PET/CT检查并接受了化疗。测量间质病变的SUVmax以量化背景ILD活性。采用logistic回归和ROC曲线分析建立了化疗相关AE的预测模型。结果:33例患者中,有7例发生了ILD的AE (AE组),26例未发生AE(非AE组),AE组对侧间质病变SUVmax显著高于非AE组(中位SUVmax 2.22 vs. 1.80, P = 0.041)。单变量logistic回归分析显示,对侧间质病变SUVmax可能与化疗相关的ILD AE相关(优势比8.683;95%置信区间[CI], 0.88-85.83;P = 0.064)。SUVmax预测ILD化疗相关AE的AUC为0.780 (95% CI: 0.579 ~ 0.982, P = 0.025)。SUVmax的最佳临界值为2.005。该分界点的敏感性和特异性分别为0.857和0.769。结论:18F-FDG PET/CT对侧间质病变SUVmax可用于预测LC合并ILD患者化疗相关AE。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Predictive value of 18F-FDG PET/CT for chemotherapy-related acute exacerbation of interstitial lung disease in lung cancer patients with interstitial lung disease
Background: Acute exacerbation (AE) of interstitial pneumonia disease (ILD) in lung cancer (LC) patients with ILD could be one of the lethal adverse effect related to chemotherapy. The purpose of this study was to determine if the result of 18F-FDG PET/CT before chemotherapy could predict onset of chemotherapy-related AE-ILD in LC patients with ILD. Methods: Between April 2006 and March 2018, 33 patients with LC and ILD performed 18F-FDG PET/CT and treated with chemotherapy in Kumamoto University Hospital. The SUVmax of interstitial lesion was measured to quantify the background ILD activity. A prediction model chemotherapy-related AE of ILD was developed using a logistic regression and ROC curve analysis. Results: Among 33 patients, 7 experienced AE of ILD (AE group) and 26 did not (non-AE group), the SUVmax of contralateral interstitial lesion in AE group was significantly higher than that in non-AE group (median SUVmax 2.22 vs. 1.80, P = 0.041). An univariable logistic regression analysis showed that the SUVmax of contralateral interstitial lesion had potential to be associated with chemotherapy-related AE of ILD (odds ratio, 8.683; 95% confidence interval [CI], 0.88–85.83; P = 0.064). The AUC of the SUVmax for predicting chemotherapy-related AE of ILD was 0.780 (95% CI: 0.579-0.982, P = 0.025). The optimal cut-off value for SUVmax was 2.005. Sensitivity and specificity value for this cut-off point were 0.857 and 0.769, respectively. Conclusions: The SUVmax of contralateral interstitial lesion in 18F-FDG PET/CT might be useful to predict chemotherapy-related AE of ILD in LC with ILD.
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