[101], the aggressiveness of BC, based on histological features,

[101], the aggressiveness of BC, based on histological features, is directly correlated with the glucose metabolism. Triple negative tumors and non-differentiated cancer (Grade 3) demonstrated a higher uptake of FDG at PET/CT than the other histological type and features. Isasi et al. [102] performed a meta-analysis to assess FDG-PET for the evaluation of BC recurrences and metastases and reported these results: the sensitivity and specificity were approximately 92% (56–100%) and 82% (0–100%), respectively. All studies comparing the diagnostic accuracy of PET with PET/CT, consistently

Sotrastaurin in vitro showed that PET/CT have improved sensitivity compared with PET but not significant differences in specificity. In these studies, PET/CT was used for the diagnosis of local disease and metastases in different locations and the advantage of PET/CT over PET appears to be true when considered for the detection of disease over a range of locations. Several studies investigated the diagnostic accuracy of CITs compared with PET or PET/CT on a patient basis [78], [97], [103], [104], [105], [106], [107] and [108]; in 2010 Pennant and Colleagues give www.selleckchem.com/products/BKM-120.html pooled summary estimates related with the two diagnostic strategies: PET had significantly higher sensitivity [89%, 95% confidence interval (CI) 83%–93% vs 79%, 95%

CI 72%–85%, relative sensitivity 1.12, 95% CI 1.04–1.21, p = 0.005] and significantly higher specificity (93%, 95% CI 83% to 97% vs 83%, 95% CI 67%–92%, relative specificity 1.12, 95% CI 1.01–1.24, p = 0.036) [75]. For bone involvement this gain in diagnostic accuracy obtained with PET is controversial and certainly less evident. In 2011, Houssami and Costelloe [86] reported a systematic review that updates the evidence on comparative test accuracy for imaging of bone involvement in women with BC; the median sensitivity (based on seven studies) for PET was 84% (range 77.7%–95.2%), and for bone scan, it was 80% (67.0%–93.3%). The median specificity (seven studies) for PET was 92% (88.2%–99.0%) and for bone scan

82.4% (9.1%–99.0%). Overall, PET and PET/CT appear to give improved diagnostic accuracy compared with CIT and in the patient-based analysis, absolute Interleukin-2 receptor estimates of sensitivity and specificity were around 10% higher for PET compared with CIT. Despite this, the impact of these results on patient management is uncertain. Individual studies emphasize that these technologies do lead to changes in management, but it is difficult to determine to what extent these changes would have taken place with CITs and, more significantly, whether they modified final patient outcome. Furthermore there are two important limitations of PET and PET/CT: economic cost, and biological cost. In Europe, a PET and a PET/CT scan range between approximately €600 ($885) and €1000 ($1474), and reimbursement for these examinations varies significantly depending on the respective health care systems [109]. With regards to biological costs, Huang et al.

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