Impact of Tumor Size and Tracer Uptake Heterogeneity in ^sup 18^F-FDG PET and CT Non-Small Cell Lung Cancer Tumor Delineation

The objectives of this study were to investigate the relationship between CT- and ^sup 18^F-FDG PET-based tumor volumes in nonsmall cell lung cancer (NSCLC) and the impact of tumor size and uptake heterogeneity on various approaches to delineating uptake on PET images. Methods: Twenty-five NSCLC can...

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Published inThe Journal of nuclear medicine (1978) Vol. 52; no. 11; p. 1690
Main Authors Hatt, Mathieu, Cheze-le Rest, Catherine, van Baardwijk, Angela, Lambin, Philippe, Pradier, Olivier, Visvikis, Dimitris
Format Journal Article
LanguageEnglish
Published New York Society of Nuclear Medicine 01.11.2011
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Summary:The objectives of this study were to investigate the relationship between CT- and ^sup 18^F-FDG PET-based tumor volumes in nonsmall cell lung cancer (NSCLC) and the impact of tumor size and uptake heterogeneity on various approaches to delineating uptake on PET images. Methods: Twenty-five NSCLC cancer patients with ^sup 18^F-FDG PET/CT were considered. Seventeen underwent surgical resection of their tumor, and the maximum diameter was measured. Two observers manually delineated the tumors on the CT images and the tumor uptake on the corresponding PET images, using a fixed threshold at 50% of the maximum (T^sub 50^), an adaptive threshold methodology, and the fuzzy locally adaptive Bayesian (FLAB) algorithm. Maximum diameters of the delineated volumes were compared with the histopathology reference when available. The volumes of the tumors were compared, and correlations between the anatomic volume and PET uptake heterogeneity and the differences between delineations were investigated. Results: All maximum diameters measured on PET and CT images significantly correlated with the histopathology reference (r > 0.89, P < 0.0001). Significant differences were observed among the approaches: CT delineation resulted in large overestimation (+32% ± 37%), whereas all delineations on PET images resulted in underestimation (from -15% ± 17% for T^sub 50^ to -4% ± 8% for FLAB) except manual delineation (+8% ± 17%). Overall, CT volumes were significantly larger than PET volumes (55 ± 74 cm^sup 3^ for CT vs. from 18 ± 25 to 47 ± 76 cm^sup 3^ for PET). A significant correlation was found between anatomic tumor size and heterogeneity (larger lesions were more heterogeneous). Finally, the more heterogeneous the tumor uptake, the larger was the underestimation of PET volumes by threshold-based techniques. Conclusion: Volumes based on CT images were larger than those based on PET images. Tumor size and tracer uptake heterogeneity have an impact on threshold-based methods, which should not be used for the delineation of cases of large heterogeneous NSCLC, as these methods tend to largely underestimate the spatial extent of the functional tumor in such cases. For an accurate delineation of PET volumes in NSCLC, advanced image segmentation algorithms able to deal with tracer uptake heterogeneity should be preferred. [PUBLICATION ABSTRACT]
ISSN:0161-5505
1535-5667