FDG PET for evaluating the change of glucose metabolism in prostate cancer after androgen ablation

被引:86
作者
Oyama, N [1 ]
Akino, H [1 ]
Suzuki, Y [1 ]
Kanamaru, H [1 ]
Ishida, H [1 ]
Tanase, K [1 ]
Sadato, N [1 ]
Yonekura, Y [1 ]
Okada, K [1 ]
机构
[1] Fukui Med Univ, Dept Urol, Fukui, Japan
关键词
FDG PET; prostate cancer; endocrine therapy;
D O I
10.1097/00006231-200109000-00004
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
In the clinical study of prostate cancer, the effect of androgen ablation on glucose metabolism in cancer tissue has not been elucidated. The purpose of this study was to investigate the change in glucose utilization due to endocrine therapy for prostate adenocarcinoma. Ten patients with histologically proven prostate cancer were prospectively investigated with F-18-fluorodeoxyglucose and positron emission tomography (FDG PET) prior to and after the initiation of endocrine therapy. FDG uptake was calculated to measure glucose utilization in cancer tissue. The change in FDG accumulation was compared with changes in serum prostate specific antigen (PSA) level and prostate size. FDG accumulation in the prostate decreased in all patients 1-5 months after the initiation of hormone therapy. The serum PSA level and prostate size measured on computerized tomography (CT) also decreased in these periods. A decrease in FDG accumulation was also demonstrated in metastatic sites. In this study, there appeared to be a decrease in FDG uptake in prostate cancer after endocrine therapy not only in primary prostate cancer lesions but also at metastatic sites, suggesting that the glucose utilization by tumours was suppressed by androgen ablation. ((C) 2001 Lippincott Williams & Wilkins).
引用
收藏
页码:963 / 969
页数:7
相关论文
共 19 条
[1]  
Agus DB, 1998, CANCER RES, V58, P3009
[2]  
CHERYL TL, 1995, SEMIN SURG ONCOL, V11, P23
[3]  
DEGRADO TR, 1994, J NUCL MED, V35, P1398
[4]  
Denmeade SR, 1996, PROSTATE, V28, P251
[5]   Metabolic imaging of untreated prostate cancer by positron emission tomography with (18)fluorine-labeled deoxyglucose [J].
Effert, PJ ;
Bares, R ;
Handt, S ;
Wolff, JM ;
Bull, U ;
Jakse, G .
JOURNAL OF UROLOGY, 1996, 155 (03) :994-998
[6]   How much can we rely on the level of prostate-specific antigen as an end point for evaluation of clinical trials? A word of caution! [J].
Eisenberger, MA ;
Nelson, WG .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1996, 88 (12) :779-781
[7]  
GLEASON DF, 1997, PROSTATE, P170
[8]  
Haberkorn U, 1997, J NUCL MED, V38, P1215
[9]  
HAMACHER K, 1986, J NUCL MED, V27, P235
[10]  
HOE CK, 1996, J NUCL MED, V37, pP267