The limitation of PET imaging for biological adaptive-IMRT assessed in animal models

被引:45
作者
Christian, Nicolas [2 ]
Lee, John A. [2 ]
Bol, Anne [2 ]
De Bast, Marc [2 ]
Jordan, B. [3 ]
Gregoire, Vincent [1 ,2 ]
机构
[1] Clin Univ St Luc, Dept Radiat Oncol, B-1200 Brussels, Belgium
[2] Catholic Univ Louvain, Ctr Mol Imaging & Expt Radiotherapy, B-1200 Brussels, Belgium
[3] Catholic Univ Louvain, Biomed Magnet Resonance Unit, B-1200 Brussels, Belgium
关键词
Mouse tumor; Animal PET; Autoradiography; Image-guided radiotherapy; FDG; Molecular imaging; POSITRON-EMISSION-TOMOGRAPHY; SQUAMOUS-CELL CARCINOMAS; PERFORMANCE EVALUATION; HEAD; VOLUME; RADIOTHERAPY; RESISTANCE; HYPOXIA; TUMORS;
D O I
10.1016/j.radonc.2008.11.014
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Purpose: Biological image-guided radiotherapy aims at specifically irradiating biologically relevant sub-volumes within the tumor, as determined for instance by PET imaging. This approach requires that PET imaging be sensitive and specific enough to image various biological pathways of interest, e.g. tumor metabolism, proliferation and hypoxia. In this framework, a validation of PET imaging used for adaptive radiotherapy was undertaken in animal models by comparing small-animal PET images (2.7 mm resolution) with autoradiography (AR) (100 mu m resolution) in various tumors under various physiological situations. Methods: A specific template for tumor-bearing mouse imaging has been designed (Christian, R&O, 2008). It allows for the registration between MRI images (Biospec, Bruker), FDG-PET images (Mosaic, Philips) and AR (FLA-5100, Fujifilm). After registration, the tumors on the PET and AR images were segmented using a threshold-based method. The thresholds were selected to obtain absolute equal volumes in the PET and AR images. Matching indexes were then calculated between the various volumes. The entire imaging process was performed for FSAII tumors (n = 5), SCCVII (n = 5) and irradiated (35 Gy) FSAII tumors (n = 5). Results: In regions with high FDG activity delineated using high value thresholds, low matching values of 39% +/- 11% (mean +/- SD) were observed between the volumes delineated on the PET images and those delineated on AR. The matching values progressively increased when considering larger volumes obtained with lower thresholds. These findings were independent of tumor type, tumor metabolism or tumor size. The relationship between the matching values and the percentage of overall tumor volume was fitted through a power regression (r = 0.93). As shown by simulations, the matching improved with higher PET resolution. The results can be extrapolated to human tumors imaged with a whole-body PET system. Conclusion: Discrepancies were found between the PET images and the underlying microscopic reality represented by AR images. These differences, attributed to the finite resolution of PET, were important when considering small and highly active regions of the tumors. Dose painting based on PET images should therefore be carefully considered and should take these limitations into account. (C) 2008 Elsevier Ireland Ltd. All rights reserved. Radiotherapy and Oncology 91 (2009) 101-106
引用
收藏
页码:101 / 106
页数:6
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