TY - JOUR
T1 - Is response assessment of breast cancer bone metastases better with measurement of
18
F-fluoride metabolic flux than with measurement of
18
F-fluoride PET/CT SUV?
AU - Azad, Gurdip K.
AU - Siddique, Musib
AU - Taylor, Benjamin
AU - Green, Adrian
AU - O’Doherty, Jim
AU - Gariani, Joanna
AU - Blake, Glen M.
AU - Mansi, Janine
AU - Goh, Vicky
AU - Cook, Gary J.R.
PY - 2019/3/1
Y1 - 2019/3/1
N2 -
Our purpose was to establish whether noninvasive measurement of changes in
18
F-fluoride metabolic flux to bone mineral (K
i
) by PET/ CT can provide incremental value in response assessment of bone metastases in breast cancer compared with SUV
max
and SUV
mean
. Methods: Twelve breast cancer patients starting endocrine treatment for de novo or progressive bone metastases were included. Static
18
F-fluoride PET/CT scans were acquired 60 min after injection, before and 8 wk after commencing treatment. Venous blood samples were taken at 55 and 85 min after injection to measure plasma
18
F-fluoride activity concentrations, and K
i
in individual bone metastases was calculated using a previously validated method. Percentage changes in K
i
, SUV
max
, and SUV
mean
were calculated from the same index lesions (#5 lesions) from each patient. Clinical response up to 24 wk, assessed in consensus by 2 experienced oncologists masked to PET imaging findings, was used as a reference standard. Results: Of the 4 patients with clinically progressive disease (PD), mean K
i
significantly increased (.25%) in all, SUV
max
in 3, and SUV
mean
in 2. Of the 8 non-PD patients, K
i
decreased or remained stable in 7, SUV
max
in 5, and SUV
mean
in 6. A significant mean percentage increase from baseline for K
i
, compared with SUV
max
and SUV
mean
, occurred in the 4 patients with PD (89.7% vs. 41.8% and 43.5%, respectively; P, 0.001). Conclusion: After 8 wk of endocrine treatment for bone-predominant metastatic breast cancer, K
i
more reliably differentiated PD from non-PD than did SUV
max
and SUV
mean
, probably because measurement of SUV underestimates fluoride clearance by not considering changes in input function.
AB -
Our purpose was to establish whether noninvasive measurement of changes in
18
F-fluoride metabolic flux to bone mineral (K
i
) by PET/ CT can provide incremental value in response assessment of bone metastases in breast cancer compared with SUV
max
and SUV
mean
. Methods: Twelve breast cancer patients starting endocrine treatment for de novo or progressive bone metastases were included. Static
18
F-fluoride PET/CT scans were acquired 60 min after injection, before and 8 wk after commencing treatment. Venous blood samples were taken at 55 and 85 min after injection to measure plasma
18
F-fluoride activity concentrations, and K
i
in individual bone metastases was calculated using a previously validated method. Percentage changes in K
i
, SUV
max
, and SUV
mean
were calculated from the same index lesions (#5 lesions) from each patient. Clinical response up to 24 wk, assessed in consensus by 2 experienced oncologists masked to PET imaging findings, was used as a reference standard. Results: Of the 4 patients with clinically progressive disease (PD), mean K
i
significantly increased (.25%) in all, SUV
max
in 3, and SUV
mean
in 2. Of the 8 non-PD patients, K
i
decreased or remained stable in 7, SUV
max
in 5, and SUV
mean
in 6. A significant mean percentage increase from baseline for K
i
, compared with SUV
max
and SUV
mean
, occurred in the 4 patients with PD (89.7% vs. 41.8% and 43.5%, respectively; P, 0.001). Conclusion: After 8 wk of endocrine treatment for bone-predominant metastatic breast cancer, K
i
more reliably differentiated PD from non-PD than did SUV
max
and SUV
mean
, probably because measurement of SUV underestimates fluoride clearance by not considering changes in input function.
KW - F-fluoride PET/CT
KW - Bone metastases
KW - Breast cancer
KW - Heterogeneity
UR - http://www.scopus.com/inward/record.url?scp=85063323722&partnerID=8YFLogxK
U2 - 10.2967/jnumed.118.208710
DO - 10.2967/jnumed.118.208710
M3 - Article
C2 - 30042160
AN - SCOPUS:85063323722
SN - 0161-5505
VL - 60
SP - 322
EP - 327
JO - Journal of Nuclear Medicine
JF - Journal of Nuclear Medicine
IS - 3
ER -