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Recurrent tumor and treatment-induced effects have different MR signatures in contrast enhancing and non-enhancing lesions of high-grade gliomas

医学 胶质瘤 接收机工作特性 病变 切断 脑瘤 核医学 灌注 曲线下面积 灌注扫描 放射科 病理 内科学 物理 癌症研究 量子力学
作者
Julia Cluceru,Sarah J. Nelson,Qiuting Wen,Joanna J. Phillips,Anny Shai,Annette M. Molinaro,Paula Alcaide‐Leon,Marram P. Olson,Devika Nair,Marisa Lafontaine,Pranathi Chunduru,Javier Villanueva-Meyer,Soonmee Cha,Susan M. Chang,Mitchel S. Berger,Janine Lupo
出处
期刊:Neuro-oncology [Oxford University Press]
卷期号:22 (10): 1516-1526 被引量:8
标识
DOI:10.1093/neuonc/noaa094
摘要

Abstract Background Differentiating treatment-induced injury from recurrent high-grade glioma is an ongoing challenge in neuro-oncology, in part due to lesion heterogeneity. This study aimed to determine whether different MR features were relevant for distinguishing recurrent tumor from the effects of treatment in contrast-enhancing lesions (CEL) and non-enhancing lesions (NEL). Methods This prospective study analyzed 291 tissue samples (222 recurrent tumor, 69 treatment-effect) with known coordinates on imaging from 139 patients who underwent preoperative 3T MRI and surgery for a suspected recurrence. 8 MR parameter values were tested from perfusion-weighted, diffusion-weighted, and MR spectroscopic imaging at each tissue sample location for association with histopathological outcome using generalized estimating equation models for CEL and NEL tissue samples. Individual cutoff values were evaluated using receiver operating characteristic curve analysis with 5-fold cross-validation. Results In tissue samples obtained from CEL, elevated relative cerebral blood volume (rCBV) was associated with the presence of recurrent tumor pathology (P < 0.03), while increases in normalized choline (nCho) and choline-to-NAA index (CNI) were associated with the presence of recurrent tumor pathology in NEL tissue samples (P < 0.008). A mean CNI cutoff value of 2.7 had the highest performance, resulting in mean sensitivity and specificity of 0.61 and 0.81 for distinguishing treatment-effect from recurrent tumor within the NEL. Conclusion Although our results support prior work that underscores the utility of rCBV in distinguishing the effects of treatment from recurrent tumor within the contrast enhancing lesion, we found that metabolic parameters may be better at differentiating recurrent tumor from treatment-related changes in the NEL of high-grade gliomas.
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