术前DCE MRI结构动力学特征预测直肠癌新辅助放化疗后病理肿瘤分期

Siddhartha Nanda, J. Antunes, K. Bera, Justin T. Brady, K. Friedman, J. Willis, R. Paspulati, S. Viswanath
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引用次数: 1

摘要

动态对比增强(DCE) MRI越来越多地用于体内直肠癌的分期和评估,以便对局部晚期肿瘤进行计划和靶向干预。目前直肠癌面临的主要临床挑战是通过早期识别哪些患者将受益于单独的新辅助放化疗(nCRT),哪些患者将受益于积极的手术(辅助放疗)来进行个性化干预;通过基线成像。在这项研究中,我们使用基线DCE MRI扫描评估直肠肿瘤的结构动力学特征,以预测nCRT对病理肿瘤分期的影响。我们的纹理动力学方法利用纹理特征(来自多个DCE摄取阶段)和多项式曲线拟合的组合来唯一地量化nCRT反应者和非反应者在造影剂摄取和扩散过程中病变纹理的时空模式。我们采用了48例直肠癌患者的队列,他们在ncrt前可获得3t DCE MRI,包括前增强期、早期增强期和延迟增强期。所有DCE MRI相位通过刚性共配准处理运动和空间对齐伪影,并且所有3个对比相位的肿瘤ROI相对于非增强肌肉进行归一化。分别从3个对比阶段提取191个纹理特征,然后绘制每个特征相对于时间的曲线,得到特征增强曲线。对每个特征增强曲线进行多项式拟合,得到一个系数向量,该系数向量被认为是该特征的纹理动力学表示。通过交叉验证的QDA分类器,对所有191个特征的纹理动力学表征和原始特征增强进行评估,以预测病理回归肿瘤分期(ypT0-2)和非回归肿瘤分期(ypT3-4)。梯度XY增强的织构动力学得到的最佳总体AUC=0:762±0:053,显著高于任何特征增强表示(最佳AUC=0:696±0:050)。纹理动态表示在54.5%的特征比较中优于相应的原始特征增强表示,只有13%的比较表现明显更差。因此,通过使用DCE MRI的纹理动力学特征,可以增强对直肠癌干预措施的非侵入性指导,这可以更好地表征应答者和无应答者在基线成像上的时空差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Texture kinetic features from pre-treatment DCE MRI for predicting pathologic tumor stage regression after neoadjuvant chemoradiation in rectal cancers
Dynamic contrast-enhanced (DCE) MRI is increasingly used to stage and evaluate rectal cancer extent in vivo in order to plan and target interventions for locally advanced tumors. The major clinical challenge faced with rectal cancers today is to personalize interventions through early identification of patients will benefit from neoadjuvant chemoradiation (nCRT) alone and who will benefit from aggressive surgery (with adjuvant radiation) instead; via baseline imaging. In this study, we evaluated texture kinetic features of rectal tumors using baseline DCE MRI scans, in order to predict pathologic tumor stage regression in response to nCRT. Our texture kinetics approach utilized a combination of texture features (from multiple DCE uptake phases) and polynomial curve fitting to uniquely quantify spatiotemporal patterns of lesion texture during contrast uptake and diffusion that were different between responders and non-responders to nCRT. We utilized a cohort of 48 rectal cancer patients for whom pre-nCRT 3 T DCE MRI was available, including pre-, early-, and delayed-enhancement phases. All DCE MRI phases were processed for motion and spatial alignment artifacts via rigid co-registration, and the tumor ROI on all 3 contrast phases was normalized with respect to non-enhancing muscle. 191 texture features were extracted from each of 3 contrast phases separately, following which each feature was plotted with respect to time to yield a feature enhancement curve. Polynomial fitting was applied to each feature enhancement curve to result in a vector of coefficients which was considered the texture kinetic representation of that feature. All 191 features were evaluated in terms of their texture kinetic representation as well as the raw feature enhancement, for predicting pathologically regressed tumor stages (ypT0-2) from non-regressed tumors (ypT3-4) via a cross-validated QDA classifier. Texture kinetics of gradient XY enhancement yielded the best overall AUC=0:762±0:053, which was significantly higher than any feature enhancement representation (best AUC=0:696±0:050). Texture kinetic representations also outperformed their corresponding raw feature enhancement representations in 54.5% of the features compared, and performed significantly worse in only 13% of the comparisons. Non-invasive guidance of interventions in rectal cancers could therefore be enhanced through the use of texture kinetic features from DCE MRI, which may better characterize spatiotemporal differences between responders and non-responders on baseline imaging.
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