Quantitative Analysis of Response to Treatment with Erlotinib in Advanced Non–Small Cell Lung Cancer Using 18F-FDG and 3′-Deoxy-3′-18F-Fluorothymidine PET

Standardized uptake value
DOI: 10.2967/jnumed.111.094458 Publication Date: 2011-11-08T03:55:11Z
ABSTRACT
The purpose of this study was to evaluate the relevance for prediction clinical benefit first-line treatment with erlotinib using different quantitative parameters PET both <sup>18</sup>F-FDG and 3′-deoxy-3′-<sup>18</sup>F-fluorothymidine (<sup>18</sup>F-FLT) in patients advanced non–small cell lung cancer. <b>Methods:</b> Data were used from a prospective trial involving untreated stage IV <sup>18</sup>F-FLT performed before 1 (early) 6 (late) weeks after treatment. Several standardized uptake values (SUVs) definitions volumes interest varying isocontours (maximum SUV [SUV<sub>max</sub>], 2-dimensional peak [SUV<sub>2Dpeak</sub>], 3-dimensional [3D] [SUV<sub>3Dpeak</sub>], 3D isocontour at 50% maximum pixel value [SUV<sub>50</sub>], adapted background [SUV<sub>A50</sub>], 41% [SUV<sub>A41</sub>], 70% [SUV<sub>70</sub>], [SUV<sub>A70</sub>], relative threshold level [SUV<sub>RTL</sub>]) metabolically active volume measurements obtained hottest single tumor lesion sum up 5 lesions per scan 30 patients. Metabolic response defined as minimum reduction 30% each SUVs 45% volume. Progression-free survival (PFS) compared between without metabolic measured parameters, Kaplan–Meier statistics log-rank test. <b>Results:</b> Patients on early well had significantly longer PFS, regardless method calculate SUV. However, highest significance SUV<sub>max</sub>, SUV<sub>50</sub>, SUV<sub>A50</sub>, SUV<sub>A41.</sub> by SUV<sub>max</sub> SUV<sub>3Dpeak</sub> late PFS. Furthermore, analyses showed strong association PFS seen volume, either or <sup>18</sup>F-FDG. <b>Conclusion:</b> Early can predict calculation. SUV<sub>A41</sub> might be best robust use prediction. Metabolically measurement may have an additional predictive monitoring cancer treated erlotinib.
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