Low levels of PSMA expression limit the utility of 18F-DCFPyL PET/CT for imaging urothelial carcinoma

被引:28
|
作者
Campbell, Scott P. [1 ,2 ]
Baras, Alexander S. [3 ]
Ball, Mark W. [1 ,2 ]
Kates, Max [1 ,2 ]
Hahn, Noah M. [4 ]
Bivalacqua, Trinity J. [1 ,2 ,4 ]
Johnson, Michael H. [1 ,2 ]
Pomper, Martin G. [1 ,2 ,4 ,5 ]
Allaf, Mohamad E. [1 ,2 ,4 ]
Rowe, Steven P. [1 ,2 ,5 ]
Gorin, Michael A. [1 ,2 ,3 ,4 ,5 ,6 ]
机构
[1] Johns Hopkins Univ, Sch Med, James Buchanan Brady Urol Inst, Baltimore, MD 21218 USA
[2] Johns Hopkins Univ, Sch Med, Dept Urol, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Sch Med, Dept Pathol, Baltimore, MD 21205 USA
[4] Johns Hopkins Univ, Sch Med, Dept Oncol, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD 21205 USA
[5] Johns Hopkins Univ, Russell H Morgan Dept Radiol & Radiol Sci, Sch Med, Baltimore, MD 21218 USA
[6] 600 North Wolfe St,Pk 213, Baltimore, MD 21287 USA
基金
美国国家卫生研究院;
关键词
Prostate-specific membrane antigen; PSMA; F-18-DCFPyL PET/CT; Urothelial carcinoma; Bladder cancer; Transitional cell carcinoma; RENAL-CELL CARCINOMA; TUMOR-ASSOCIATED NEOVASCULATURE; POSITRON-EMISSION-TOMOGRAPHY; MEMBRANE ANTIGEN; PROSTATE-CANCER; BLADDER-CANCER; COMPUTED-TOMOGRAPHY; SOLID TUMORS; METAANALYSIS; EXPERIENCE;
D O I
10.1007/s12149-017-1216-x
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
To explore the clinical utility of PSMA-targeted F-18-DCFPyL PET/CT in patients with metastatic urothelial carcinoma. Three patients with metastatic urothelial carcinoma were imaged with F-18-DCFPyL PET/CT. All lesions with perceptible radiotracer uptake above background were considered positive. Maximum standardized uptake values were recorded for each detected lesion and findings on F-18-DCFPyL PET/CT were compared to those on conventional imaging studies. To further explore PSMA as a molecular target of urothelial carcinoma, RNA-sequencing data from The Cancer Genome Atlas were used to compare the relative expression of PSMA among cases of bladder cancer, prostate cancer, and clear cell renal cell carcinoma. Additionally, immunohistochemical staining for PSMA was performed on a biopsy specimen from one of the imaged patients. F-18-DCFPyL PET/CT allowed for the detection of sites of urothelial carcinoma, albeit with low levels of radiotracer uptake. Analysis of RNA-sequencing data revealed that bladder cancer had significantly lower levels of PSMA expression than both prostate cancer and clear cell renal cell carcinoma. Consistent with this observation, immunohistochemical staining of tissue from one of the imaged patients demonstrated a low level of neovascularization and nearly absent PSMA expression. The relatively scant expression of PSMA by urothelial carcinoma likely limits the utility of PSMA-targeted PET imaging of this malignancy. Future research efforts should focus on the development of other molecularly targeted imaging agents for urothelial carcinoma.
引用
收藏
页码:69 / 74
页数:6
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