Imaging of metastatic clear cell renal cell carcinoma with PSMA-targeted 18F-DCFPyL PET/CT

• Published in: Annals of nuclear medicine Vol. 29; no. 10; pp. 877 - 882
• Main Authors: Rowe, Steven P., Gorin, Michael A., Hammers, Hans J., Som Javadi, M., Hawasli, Hazem, Szabo, Zsolt, Cho, Steve Y., Pomper, Martin G., Allaf, Mohamad E.
• Format: Journal Article
• Language: English
• Published: Tokyo Springer Japan 01.12.2015
• Subjects: Aged; Antigens, Surface - metabolism; Carcinoma, Renal Cell - diagnosis; Carcinoma, Renal Cell - diagnostic imaging; Carcinoma, Renal Cell - pathology; Glutamate Carboxypeptidase II - metabolism; Humans; Imaging; Kidney Neoplasms - diagnosis; Kidney Neoplasms - diagnostic imaging; Kidney Neoplasms - pathology; Lysine - analogs & derivatives; Male; Medicine; Medicine & Public Health; Middle Aged; Multimodal Imaging; Neoplasm Metastasis; Nuclear Medicine; Original Article; Positron-Emission Tomography; Radiology; Tomography, X-Ray Computed; Urea - analogs & derivatives; Prostate-specific membrane antigen (PSMA); Renal cell carcinoma (RCC); Positron emission tomography (PET); DCFPyL
• ISSN: 0914-7187; 1864-6433
• DOI: 10.1007/s12149-015-1017-z

Objective Molecular imaging with positron emission tomography (PET) provides a powerful means of identifying and characterizing cancerous processes, as well as providing a quantitative framework within which response to therapy can be ascertained. Unfortunately, the most commonly used PET radiotracer, 18 F-fluorodeoxyglucose (FDG), has not demonstrated a definitive role in determining response to therapy in metastatic renal cell carcinoma (RCC). As a result, new radiotracers able to reliably image RCC could be of tremendous value for this purpose. Methods Five patients with known metastatic RCC were imaged with the low-molecular weight radiotracer 18 F-DCFPyL, an inhibitor of the prostate-specific membrane antigen at 60 min post injection. 18 F-DCFPyL PET/CT and conventional images (either contrast-enhanced computed tomography or magnetic resonance imaging) were centrally reviewed for suspected sites of disease. Results In all five patients imaged, sites of putative metastatic disease were readily identifiable by abnormal 18 F-DCFPyL uptake, with overall more lesions detected than on conventional imaging. These PET-detected sites included lymph nodes, pancreatic parenchymal lesions, lung parenchymal lesions, a brain parenchymal lesion, and other soft tissue sites. 18 F-DCFPyL uptake ranged from subtle to intense with maximum standardized uptake values (SUV max ) for the identified lesions of 1.6–19.3. Based upon this small patient series, limited pathology and imaging follow-up of these patients suggests a higher sensitivity for 18 F-DCFPyL compared to conventional imaging in the detection of metastatic RCC (94.7 versus 78.9 %). Conclusions PSMA expression in the tumor neovasculature of RCC has been previously established and is believed to provide the basis for the imaging findings presented here. PSMA-based PET/CT with radiotracers such as 18 F-DCFPyL may allow more accurate staging of patients with RCC and conceivably the ability to predict and follow therapy in patients treated with agents targeting the neovasculature.