The study of differentiation tumor lesion from inflammatory lesion using FDG microPET
| Project/Area Number |
16591219
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Radiation science
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| Research Institution | OSAKA CITY UNIVERSITY GRADUATE SCHOOL OF MEDICINE |
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Principal Investigator |
INOUE Yuichi OSAKA CITY UNIVERSITY GRADUATE SCHOOL OF MEDICINE, 大学院・医学研究科, Professor (00101288)
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| Co-Investigator(Kenkyū-buntansha) |
WATANABE Yasuyoshi Osaka City University Graduate School of Medicine, 大学院・医学研究科, Professor (40144399)
OKAMURA Terue Osaka City University Graduate School of Medicine, 大学院・医学研究科, Assistant Professor (00221143)
NAKAYAMA Keiko Osaka City University Graduate School of Medicine, 大学院・医学研究科, Assistant (80326264)
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| Project Period (FY) |
2004 – 2005
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| Project Status |
Completed (Fiscal Year 2005)
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| Budget Amount *help |
¥1,000,000 (Direct Cost: ¥1,000,000)
Fiscal Year 2005: ¥500,000 (Direct Cost: ¥500,000)
Fiscal Year 2004: ¥500,000 (Direct Cost: ¥500,000)
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| Keywords | FDG PET / microPET / tumor / inflammation / differentiation / glucose loading / FDG-PET |
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| Research Abstract |
PURPOSE : We investigated the optimum time for the differentiation tumor from inflammation using dynamic FDG-microPET scans obtained by a MicroPET P4 scanner in animal models. MATERIALS AND METHODS : Forty-six rabbits with 92 inflammatory lesions that were induced 2, 5, 7, 14, 30 and 60 days after 0.2ml (Group 1) or 1.0ml (Group 2) of turpentine oil injection were used as inflammatory models. Five rabbits with 10 VX2 tumors were used as the tumor model. Helical CT scans were performed before the PET studies. In the PET study, after 4 hours fasting, and following transmission scans and dynamic emission data acquisitions were performed until 2 hours after intravenous FDG injection. Images were reconstructed every 10 minutes using a filtered-back projection method. PET images were analyzed visually referring to CT images. For quantitative analysis, the inflammation-to-muscle (I/M) ratio and tumor-to-muscle (T/M) ratio were calculated after regions of interest were set in tumors and muscle
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s referring to CT images and the time-I/M ratio and time-T/M ratio curves (TRCs) were prepared to show the change over time in these ratios. The histological appearance of both inflammatory lesions and tumor lesions were examined and compared with the CT and FDG-microPET images. RESULTS : In visual and quantitative analysis, All the I/M ratios and the T/M ratios increased over time except that Day 60 of Group 1 showed an almost flat curve. The TRC of the T/M ratio showed a linear increasing curve over time, while that of the I/M ratios showed a parabolic increasing over time at the most. FDG uptake in the inflammatory lesions reflected the histological findings. For differentiating tumors from inflammatory lesions with the early image acquired at 40 min for dual-time imaging, the delayed image must be acquired 30 min after the early image, while imaging at 90 min or later after intravenous FDG injection was necessary in single-time-point imaging. CONCLUSION : Our results suggest the possibility of shortening the overall testing time in clinical practice by adopting dual-time-point imaging rather than single-time-point imaging. Less
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Report
(3 results)
Research Products
(12 results)
