Utility of FDG-PET in clinical neuroendocrine prostate cancer.
Utility of FDG-PET in clinical neuroendocrine prostate cancer.
复制标题
FDG-PET在临床神经内分泌前列腺癌中的效用。
DOI:
10.1002/pros.22831
复制
发表时间:
2014-08
期刊:
影响因子:
2.8
通讯作者:
Osborne, Joseph R.
中科院分区:
文献类型:
--
作者:
Spratt, Daniel E.;Gavane, Somali;Tarlinton, Lisa;Fareedy, Shoaib B.;Doran, Michael G.;Zelefsky, Michael J.;Osborne, Joseph R.
Fluorodeoxyglucose (FDG) positron emission tomography (PET) has well-characterized limitations in prostate adenocarcinoma (PCA). However, data assessing the utility of PET in neuroendocrine prostate cancer (NEPC) is limited to isolated case reports. Herein, we describe the first case series to assess the utility of FDG-PET in NEPC. Inclusion criteria consisted of clinically progressive metastatic PCA in the setting of a chromogranin-A levels >1.5x the upper limit of normal, and ≥1 FDG-PET scan after the diagnosis of NEPC, which yielded 23 patients. All metastatic lesions on CT, PET, and bone scan were read by two independent physicians. Five hundred ninety two unique lesions were identified across all imaging modalities, 510 were bone metastases, and 82 were soft tissue metastases. Of bone lesions, 22.2%, 92.7%, and 77.6% were detected by PET, CT, and bone scan, respectively. Of soft tissue lesions, 95.1% and 97.5% were detected by PET and CT, respectively. Stratified by the median survival from NEPC diagnosis, patients who survived <2.2 versus ≥2.2 years had more PET avid bone (8 vs. 2, P=0.06) and soft tissue lesions (7 vs. 1, P=0.01), and higher average SUVmax of bone (5.49 vs. 3.40, P=0.04) and soft tissue lesions (8.02 vs. 3.90, P=0.0002). In patients with clinical NEPC, we demonstrate that FDG-PET has clinical utility in the detection of metastatic disease. In addition to detection, PET allows for treatment response to determine tumor viability. With novel therapies on the horizon to treat NEPC, consideration to investigate the use of FDG-PET to monitor response is warranted.
登录
查看更多内容
DOI:
10.6004/jnccn.2013.0174
发表时间:
2013-12-01
影响因子:
13.4
作者:
Mohler, James L.;Kantoff, Philip W.;Ho, Maria
通讯作者:
Ho, Maria
DOI:
10.1038/modpathol.2011.56
发表时间:
2011-08
期刊:
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc
影响因子:
--
作者:
通讯作者:
--
影响因子:
254.7
作者:
Siegel, Rebecca;Ma, Jiemin;Jemal, Ahmedin
通讯作者:
Jemal, Ahmedin
影响因子:
2.8
作者:
ABRAHAMSSON, PA;FALKMER, S;GRIMELIUS, L
通讯作者:
GRIMELIUS, L
影响因子:
45.3
作者:
Anker, Christopher J.;Dechet, Christopher;Shrieve, Dennis C.
通讯作者:
Shrieve, Dennis C.