2007 Fiscal Year Final Research Report Summary
Radiotoxicity after iodine-131 MIBG therapy using the micronucleus assay
| Project/Area Number |
17591251
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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 | University of Toyama |
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Principal Investigator |
WATANABE Naoto University of Toyama, Radiology, Associate Professor (40210926)
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| Co-Investigator(Kenkyū-buntansha) |
KINUYA Seigo Kanazawa University, School of Medicine, Professor (20281024)
OGAWA Shinichi Toyama University, Hospital Radiology, Instructor (60377265)
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| Project Period (FY) |
2005 – 2007
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| Keywords | I-131 MIBG therapy / Micronucleus assay / Lymphocyte / Radiotoxicity |
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| Research Abstract |
The purpose of the present study was to evaluate the degree of cytological radiation damage to lymphocytes after I-131 Metaiodobenzylguanidine (MIBG) therapy using the cytokinesis-blocked micronucleus assay. The chromosomal damage to lymphocytes induced by I-131 in vivo should result in augmentation of the cells with micronuclei.
Methods: We studied 18 patients with pheochromocytoma (17/18) or ganglioneuroma (1/18), who were treated initially with 7.4 GBq of I-131-MIBG. Isolated lymphocytes collected from patients 10 days after the therapy were harvested and treated according to the cytokinesis-blocked method of Fenech and Morley. Serial blood samples were obtained periodically only from two patients for two years after therapy. Micronucleus number of micronulei per 500 binucleated cells was scored by visual inspection. As controls, lymphocytes from the same patients before the therapy were also studied. In an in vitro study, lymphocytes from eight normal volunteers were exposed to doses varying from 0.5 to 2 Gy and studied with the same method.
Results: The mean number (mean±SD) of micronuclei after treatment was significantly increased (p<0.001) as compared to control subjects (46.1±7.7 vs. 9.6±2.6). Internal radiation absorbed doses estimated for 18 patients were 1.5±0.3 Gy in this external irradiation study. The frequency of micronuclei post-administration of I-131-MIBG gradually decreased to near baseline (ie pre-therapy) levels by two years.
Conclusions: The relatively low frequency of lymphocyte micronuclei induced by I-131-MIBG in vivo and recovery of increasing frequency of lymphocyte micronuclei after therapy supported the contention that short-term non-stochastic damage of this therapy with 7.4 GBq of I-131-MIBG in pheochromocytoma or ganglioneuroma patients is limited and reversible.
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