{"title":"估计人类胶质母细胞瘤异种移植对贝伐单抗治疗的DCE-MRI反应","authors":"J. Carl, K. Nielsen, Soeren Ravn","doi":"10.15761/JTBR.1000117","DOIUrl":null,"url":null,"abstract":"Background and purpose: It has been suggested that consecutive DCE-MRI in the early phase of treatment with bevacizumab could provide a better estimate of treatment response. Materials and methods: The xenograft study was performed using adult (8-12 weeks of age) male type NMRINUM Mice (Taconic, Denmark). A human glioblastoma xenograft was inoculated subcutaneously in the posterior flank of the mouse. DCE MRI and compartment analysis was performed extended Toft´s model. Pathology immunohistochemistry of Glial fibrillary acidic protein (GFAP) of excised tumors slides were analyzed using an ImageJ threshold watershed technique to determine tissue fraction of glial tumor cells. Results: A total of 15 intervention tumors and two C16MG control tumors were subjected to DCE MRI. A significant correlation between Ktrans and GFAP was observed. Furthermore a significant reduction in Ktrans following Bevacizumab was observed. Conclusion: To conclude this study successfully established a technique, which allowed small animals with Xenograft heterotopic implanted GBM tumors to be scanned with a DCE-MRI technique using a clinical 3T MR scanner setting. Furthermore the Ktrans parameters derived was demonstrated to be a potential imaging biomarker of GBM GFAP activity and treatment response to Bevacizumab.","PeriodicalId":75256,"journal":{"name":"Trends in biomedical research","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Estimating human glioblastoma xenograft DCE-MRI response to Bevacizumab treatment\",\"authors\":\"J. Carl, K. Nielsen, Soeren Ravn\",\"doi\":\"10.15761/JTBR.1000117\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Background and purpose: It has been suggested that consecutive DCE-MRI in the early phase of treatment with bevacizumab could provide a better estimate of treatment response. Materials and methods: The xenograft study was performed using adult (8-12 weeks of age) male type NMRINUM Mice (Taconic, Denmark). A human glioblastoma xenograft was inoculated subcutaneously in the posterior flank of the mouse. DCE MRI and compartment analysis was performed extended Toft´s model. Pathology immunohistochemistry of Glial fibrillary acidic protein (GFAP) of excised tumors slides were analyzed using an ImageJ threshold watershed technique to determine tissue fraction of glial tumor cells. Results: A total of 15 intervention tumors and two C16MG control tumors were subjected to DCE MRI. A significant correlation between Ktrans and GFAP was observed. Furthermore a significant reduction in Ktrans following Bevacizumab was observed. Conclusion: To conclude this study successfully established a technique, which allowed small animals with Xenograft heterotopic implanted GBM tumors to be scanned with a DCE-MRI technique using a clinical 3T MR scanner setting. Furthermore the Ktrans parameters derived was demonstrated to be a potential imaging biomarker of GBM GFAP activity and treatment response to Bevacizumab.\",\"PeriodicalId\":75256,\"journal\":{\"name\":\"Trends in biomedical research\",\"volume\":\"1 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Trends in biomedical research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.15761/JTBR.1000117\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Trends in biomedical research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15761/JTBR.1000117","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Estimating human glioblastoma xenograft DCE-MRI response to Bevacizumab treatment
Background and purpose: It has been suggested that consecutive DCE-MRI in the early phase of treatment with bevacizumab could provide a better estimate of treatment response. Materials and methods: The xenograft study was performed using adult (8-12 weeks of age) male type NMRINUM Mice (Taconic, Denmark). A human glioblastoma xenograft was inoculated subcutaneously in the posterior flank of the mouse. DCE MRI and compartment analysis was performed extended Toft´s model. Pathology immunohistochemistry of Glial fibrillary acidic protein (GFAP) of excised tumors slides were analyzed using an ImageJ threshold watershed technique to determine tissue fraction of glial tumor cells. Results: A total of 15 intervention tumors and two C16MG control tumors were subjected to DCE MRI. A significant correlation between Ktrans and GFAP was observed. Furthermore a significant reduction in Ktrans following Bevacizumab was observed. Conclusion: To conclude this study successfully established a technique, which allowed small animals with Xenograft heterotopic implanted GBM tumors to be scanned with a DCE-MRI technique using a clinical 3T MR scanner setting. Furthermore the Ktrans parameters derived was demonstrated to be a potential imaging biomarker of GBM GFAP activity and treatment response to Bevacizumab.