TY - JOUR
T1 - 18F-FDG PET/CT is a prognostic biomarker in patients affected by bone metastases from breast cancer in comparison with 18F-NaF PET/CT
AU - Piccardo, A
AU - Puntoni, M
AU - Morbelli, S
AU - Massollo, M
AU - Bongioanni, F
AU - Paparo, F
AU - Altrinetti, V
AU - Gonella, R
AU - Gennari, Alessandra
AU - Iacozzi, M
AU - Sambuceti, G
AU - DeCensi, A.
N1 - Publisher Copyright:
© Schattauer 2015.
PY - 2015
Y1 - 2015
N2 - Aim: To compare18F-FDG PET/CT and18F-NaF PET/CT with respect to disease prognostication and outcome in patients affected by bone metastases from breast cancer (BC). Patients, methods: We retrospectively investigated 32 women with BC and documented bone metastases. Semi-quantitative parameters were applied to18F-FDG PET/CT and18F-Na PET/CT in order to evaluate disease extent and tumour metabolism. We used time-to-event analyses (Kaplan Meier and COX proportional hazard methods) to estimate progression-free (PFS) and overall survival (OS) in order to assess the independent prognostic value of18F-FDG PET/CT and18F-Na PET/CT. Results: The sensitivity of18F-NaF PET/CT (100%) was higher (p < 0.05) than that of18F-FDG PET/CT (72% and 72%). None of the18F-FDG PET/CT-negative patients showed disease progression at the end of follow-up. After adjustment for age, Ki-67 levels, presence of visceral metastases, hormone therapy, duration of bone disease and response to first-line therapy, only18F-FDG SUV mean [HR 15.7, 95% confidence interval (CI) 1.15-214.5] and18F-FDG whole-body bone metabolic burden (WB-B-MB) (HR 16.9; 95%CI 1.87-152.2) were independently and significantly associated with OS. None of the18F-NaF PET/CT parameters were associated with OS. None of the conventional clinical prognostic parameters remained significantly associated with OS after the inclusion of PET/ CT parameters in the model. Conclusion:18F-FDG PET/CT is independently associated with OS in BC patients with bone metastases and its prognostic impact seems to be higher than conventional clinical and biological rognostic factors. Although18F-NaF PET/CT has a higher diagnostic sensitivity than18F-FDG PET/ CT, it is not independently associated with OS.
AB - Aim: To compare18F-FDG PET/CT and18F-NaF PET/CT with respect to disease prognostication and outcome in patients affected by bone metastases from breast cancer (BC). Patients, methods: We retrospectively investigated 32 women with BC and documented bone metastases. Semi-quantitative parameters were applied to18F-FDG PET/CT and18F-Na PET/CT in order to evaluate disease extent and tumour metabolism. We used time-to-event analyses (Kaplan Meier and COX proportional hazard methods) to estimate progression-free (PFS) and overall survival (OS) in order to assess the independent prognostic value of18F-FDG PET/CT and18F-Na PET/CT. Results: The sensitivity of18F-NaF PET/CT (100%) was higher (p < 0.05) than that of18F-FDG PET/CT (72% and 72%). None of the18F-FDG PET/CT-negative patients showed disease progression at the end of follow-up. After adjustment for age, Ki-67 levels, presence of visceral metastases, hormone therapy, duration of bone disease and response to first-line therapy, only18F-FDG SUV mean [HR 15.7, 95% confidence interval (CI) 1.15-214.5] and18F-FDG whole-body bone metabolic burden (WB-B-MB) (HR 16.9; 95%CI 1.87-152.2) were independently and significantly associated with OS. None of the18F-NaF PET/CT parameters were associated with OS. None of the conventional clinical prognostic parameters remained significantly associated with OS after the inclusion of PET/ CT parameters in the model. Conclusion:18F-FDG PET/CT is independently associated with OS in BC patients with bone metastases and its prognostic impact seems to be higher than conventional clinical and biological rognostic factors. Although18F-NaF PET/CT has a higher diagnostic sensitivity than18F-FDG PET/ CT, it is not independently associated with OS.
UR - https://iris.uniupo.it/handle/11579/93254
M3 - Article
SN - 0029-5566
VL - 54
SP - 163
EP - 172
JO - Nuklearmedizin - NuclearMedicine
JF - Nuklearmedizin - NuclearMedicine
IS - 4
ER -