ABSTRACT
Objective: To evaluate the performance of 18F-fluorodeoxyglucose positron emission tomography (18F-FDG PET/CT) radiomic features to predict overall survival (OS) in patients with locally advanced uterine cervical carcinoma. Methods: Longitudinal and retrospective study that evaluated 50 patients with cervical epidermoid carcinoma (clinical stage IB2 to IVA according to FIGO). Segmentation of the 18F-FDG PET/CT tumors was performed using the LIFEx software, generating the radiomic features. We used the Mann-Whitney test to select radiomic features associated with the clinical outcome (death), excluding the features highly correlated with each other with Spearman correlation. Subsequently, ROC curves and a Kaplan-Meier analysis were performed. A p-value < 0.05 were considered significant. Results: The median follow-up was 23.5 months and longer than 24 months in all surviving patients. Independent predictors for OS were found-SUVpeak with an AUC of 0.74, sensitivity of 77.8%, and specificity of 72.7% (p = 0.006); and the textural feature gray-level run-length matrix GLRLM_LRLGE, with AUC of 0.74, sensitivity of 72.2%, and specificity of 81.8% (p = 0.005). When we used the derived cut-off points from these ROC curves (12.76 for SUVpeak and 0.001 for GLRLM_LRLGE) in a Kaplan-Meier analysis, we can see two different groups (one with an overall survival probability of approximately 90% and the other with 30%). These biomarkers are independent of FIGO staging. Conclusion: By radiomic 18F-FDG PET/CT data analysis, SUVpeak and GLRLM_LRLGE textural feature presented the best performance to predict OS in patients with cervical cancer undergoing chemo-radiotherapy and brachytherapy.
ABSTRACT
(18)FDG, an analogue of glucose labelled with the radionuclide (18)F, is the most widely used radiopharmaceutical in positron emission tomography/computed tomography technique. In Brazil, there are currently eight (18)FDG plants in operation and other facilities are expected to start their production in the near future. The growth in the production and clinical use of (18)FDG represents an increasing risk of worker exposures. According to national regulations and international recommendations, internal exposures should be effectively controlled in order to keep doses as low as possible. The implementation of a routine monitoring programme towards the estimation of internal doses related to the incorporation of (18)F is difficult, mainly due to its short physical half-life, the cost of a bioassay laboratory and the need of a monitoring service promptly available near the production plant. This paper describes the implementation and evaluation of a methodology for in vivo brain monitoring of (18)F to be applied in cases of suspected incorporation of (18)FDG. The technique presented a minimum detectable effective dose in the order of nanoSieverts, which allows its application for occupational monitoring purposes.