Comparison between dynamic whole-body FDG-PET and early-delayed imaging for the assessment of motion in focal uptake in colorectal area

• Published in: Annals of nuclear medicine 2021-12, Vol.35 (12), p.1305-1311
• Main Authors: Kotani, Tomoya, Nishimura, Motoki, Tamaki, Nagara, Matsushima, Shigenori, Akiyama, Shimpei, Kanayama, Taisei, Bamba, Chisa, Tanada, Yasutomo, Nii, Takeshi, Yamada, Kei
• Format: Article
• Language: English
• Subjects: Adenoma; Adult; Aged; Aged, 80 and over; Biological Transport; Colorectal cancer; Colorectal carcinoma; Colorectal Neoplasms - diagnostic imaging; Colorectal Neoplasms - metabolism; Computed tomography; Emission analysis; Female; Fluorodeoxyglucose F18; Humans; Imaging; Lesions; Male; Medical imaging; Medicine; Medicine & Public Health; Middle Aged; Motion; Movement; Nuclear Medicine; Original Article; Physiology; Positron emission; Positron emission tomography; Positron Emission Tomography Computed Tomography; Positron-Emission Tomography - methods; Radiology; Time Factors; Tomography; Whole Body Imaging - methods
• ISSN: 0914-7187; 1864-6433; 1864-6433
• DOI: 10.1007/s12149-021-01671-y

Objectives Serial changes of focal uptake in whole-body dynamic positron emission tomography (PET) imaging were assessed and compared with those in early-delayed imaging to differentiate pathological uptake from physiological uptake in the colorectal area, based on the change in uptake shape. Methods In 60 patients with at least 1 pathologically diagnosed colorectal cancer or adenoma, a serial 3 min dynamic whole-body PET/computed tomography imaging was performed four times around 60 min after the administration of 18 F-fluorodeoxyglucose (FDG) to create a conventional (early) image by summation. Delayed imaging was performed separately at 110 min after FDG administration. High focal uptake lesions in the colorectal area were visually assessed as “changed” or “unchanged” on serial dynamic imaging and early-delayed imaging, based on the alteration in uptake shape over time. These criteria on the images were used to differentiate pathological uptake from physiological uptake. Results In this study, 334 lesions with high focal FDG uptake were observed. Among 73 histologically proven pathological FDG uptakes, no change was observed in 69 on serial dynamic imaging and 72 on early-delayed imaging (sensitivity of 95 vs. 99%, respectively; ns). In contrast, out of 261 physiological FDG uptakes, a change in uptake shape was seen in 159 on dynamic PET imaging and 66 on early-delayed imaging (specificity of 61 vs. 25%, respectively; p