TY - JOUR
T1 - Enhanced Application of 18F-FDG PET/CT in Bladder Cancer by Adding Early Dynamic Acquisition to a Standard Delayed PET Protocol
AU - Yoon, Hai Jeon
AU - Yoo, Jang
AU - Kim, Yemi
AU - Lee, Dong Hyeon
AU - Kim, Bom Sahn
N1 - Publisher Copyright:
© Wolters Kluwer Health, Inc. All rights reserved.
PY - 2017/10/1
Y1 - 2017/10/1
N2 - Purpose We investigated the value of early dynamic (ED) PET for the detection and characterization of bladder cancer. Methods Fifty-Two bladder cancer patients were prospectively enrolled. The study protocol was composed of ED, whole-body (WB, 60 minutes after injection), and additional delayed (AD, 120 minutes after injection) PET acquisition. Early dynamic PET was acquired for 10 minutes and reconstructed as 5 frames at 2-minute intervals. A focal radiotracer accumulation confined to the bladder wall was considered as PET positive and referred for further quantitative measurement. SUVmax on ED (1fSUVmax, 2fSUVmax, 3fSUVmax, 4fSUVmax, and 5fSUVmax for 5 frames), WB (WBSUVmax), and AD PET (ADSUVmax) were measured. PET results were correlated with bladder cancer pathology variables. Results The sensitivities of ED, WB, and AD PET for bladder cancer were 84.6%, 57.7%, and 61.2%, respectively. The sensitivity of ED PET was significantly higher than that of WB (P = 0.002) and AD PET (P = 0.008). On ED PET, 2fSUVmax was significantly correlated with muscle invasiveness, histological grade, and pathological tumor size (P = 0.018, P = 0.030, and P = 0.030). On WB and AD PET, only pathological tumor size showed significant positive correlation with WBSUVmax and ADSUVmax (P = 0.043 and P = 0.007). Conclusions Early dynamic PET can help to detect and characterize bladder cancer.
AB - Purpose We investigated the value of early dynamic (ED) PET for the detection and characterization of bladder cancer. Methods Fifty-Two bladder cancer patients were prospectively enrolled. The study protocol was composed of ED, whole-body (WB, 60 minutes after injection), and additional delayed (AD, 120 minutes after injection) PET acquisition. Early dynamic PET was acquired for 10 minutes and reconstructed as 5 frames at 2-minute intervals. A focal radiotracer accumulation confined to the bladder wall was considered as PET positive and referred for further quantitative measurement. SUVmax on ED (1fSUVmax, 2fSUVmax, 3fSUVmax, 4fSUVmax, and 5fSUVmax for 5 frames), WB (WBSUVmax), and AD PET (ADSUVmax) were measured. PET results were correlated with bladder cancer pathology variables. Results The sensitivities of ED, WB, and AD PET for bladder cancer were 84.6%, 57.7%, and 61.2%, respectively. The sensitivity of ED PET was significantly higher than that of WB (P = 0.002) and AD PET (P = 0.008). On ED PET, 2fSUVmax was significantly correlated with muscle invasiveness, histological grade, and pathological tumor size (P = 0.018, P = 0.030, and P = 0.030). On WB and AD PET, only pathological tumor size showed significant positive correlation with WBSUVmax and ADSUVmax (P = 0.043 and P = 0.007). Conclusions Early dynamic PET can help to detect and characterize bladder cancer.
KW - F-FDG
KW - bladder cancer
KW - early dynamic PET/CT
KW - tumor blood flow
KW - urine activity
UR - http://www.scopus.com/inward/record.url?scp=85032342262&partnerID=8YFLogxK
U2 - 10.1097/RLU.0000000000001780
DO - 10.1097/RLU.0000000000001780
M3 - Article
C2 - 28759520
AN - SCOPUS:85032342262
SN - 0363-9762
VL - 42
SP - 749
EP - 755
JO - Clinical Nuclear Medicine
JF - Clinical Nuclear Medicine
IS - 10
ER -