<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hormuth DA</submitter><funding>NCI NIH HHS</funding><funding>NINDS NIH HHS</funding><pagination>1270-1279</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5934308</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>100(5)</volume><pubmed_abstract>&lt;h4>Purpose&lt;/h4>To develop and investigate a set of biophysical models based on a mechanically coupled reaction-diffusion model of the spatiotemporal evolution of tumor growth after radiation therapy.&lt;h4>Methods and materials&lt;/h4>Post-radiation therapy response is modeled using a cell death model (M&lt;sub>d&lt;/sub>), a reduced proliferation rate model (M&lt;sub>p&lt;/sub>), and cell death and reduced proliferation model (M&lt;sub>dp&lt;/sub>). To evaluate each model, rats (n = 12) with C6 gliomas were imaged with diffusion-weighted magnetic resonance imaging (MRI) and contrast-enhanced MRI at 7 time points over 2 weeks. Rats received either 20 or 40 Gy between the third and fourth imaging time point. Diffusion-weighted MRI was used to estimate tumor cell number within enhancing regions in contrast-enhanced MRI data. Each model was fit to the spatiotemporal evolution of tumor cell number from time point 1 to time point 5 to estimate model parameters. The estimated model parameters were then used to predict tumor growth at the final 2 imaging time points. The model prediction was evaluated by calculating the error in tumor volume estimates, average surface distance, and voxel-based cell number.&lt;h4>Results&lt;/h4>For both the rats treated with either 20 or 40 Gy, significantly lower error in tumor volume, average surface distance, and voxel-based cell number was observed for the M&lt;sub>dp&lt;/sub> and M&lt;sub>p&lt;/sub> models compared with the M&lt;sub>d&lt;/sub> model. The M&lt;sub>dp&lt;/sub> model fit, however, had significantly lower sum squared error compared with the M&lt;sub>p&lt;/sub> and M&lt;sub>d&lt;/sub> models.&lt;h4>Conclusions&lt;/h4>The results of this study indicate that for both doses, the M&lt;sub>p&lt;/sub> and M&lt;sub>dp&lt;/sub> models result in accurate predictions of tumor growth, whereas the M&lt;sub>d&lt;/sub> model poorly describes response to radiation therapy.</pubmed_abstract><journal>International journal of radiation oncology, biology, physics</journal><pubmed_title>Biophysical Modeling of In Vivo Glioma Response After Whole-Brain Radiation Therapy in a Murine Model of Brain Cancer.</pubmed_title><pmcid>PMC5934308</pmcid><funding_grant_id>U01 CA142565</funding_grant_id><funding_grant_id>R01 CA186193</funding_grant_id><funding_grant_id>R25 CA092043</funding_grant_id><funding_grant_id>K25 CA204599</funding_grant_id><funding_grant_id>R01 CA138599</funding_grant_id><funding_grant_id>P30 CA068485</funding_grant_id><funding_grant_id>R21 CA169387</funding_grant_id><funding_grant_id>U01 CA174706</funding_grant_id><funding_grant_id>R01 NS049251</funding_grant_id><pubmed_authors>Miga MI</pubmed_authors><pubmed_authors>Quaranta V</pubmed_authors><pubmed_authors>Barnes SL</pubmed_authors><pubmed_authors>Weis JA</pubmed_authors><pubmed_authors>Hormuth DA</pubmed_authors><pubmed_authors>Yankeelov TE</pubmed_authors></additional><is_claimable>false</is_claimable><name>Biophysical Modeling of In Vivo Glioma Response After Whole-Brain Radiation Therapy in a Murine Model of Brain Cancer.</name><description>&lt;h4>Purpose&lt;/h4>To develop and investigate a set of biophysical models based on a mechanically coupled reaction-diffusion model of the spatiotemporal evolution of tumor growth after radiation therapy.&lt;h4>Methods and materials&lt;/h4>Post-radiation therapy response is modeled using a cell death model (M&lt;sub>d&lt;/sub>), a reduced proliferation rate model (M&lt;sub>p&lt;/sub>), and cell death and reduced proliferation model (M&lt;sub>dp&lt;/sub>). To evaluate each model, rats (n = 12) with C6 gliomas were imaged with diffusion-weighted magnetic resonance imaging (MRI) and contrast-enhanced MRI at 7 time points over 2 weeks. Rats received either 20 or 40 Gy between the third and fourth imaging time point. Diffusion-weighted MRI was used to estimate tumor cell number within enhancing regions in contrast-enhanced MRI data. Each model was fit to the spatiotemporal evolution of tumor cell number from time point 1 to time point 5 to estimate model parameters. The estimated model parameters were then used to predict tumor growth at the final 2 imaging time points. The model prediction was evaluated by calculating the error in tumor volume estimates, average surface distance, and voxel-based cell number.&lt;h4>Results&lt;/h4>For both the rats treated with either 20 or 40 Gy, significantly lower error in tumor volume, average surface distance, and voxel-based cell number was observed for the M&lt;sub>dp&lt;/sub> and M&lt;sub>p&lt;/sub> models compared with the M&lt;sub>d&lt;/sub> model. The M&lt;sub>dp&lt;/sub> model fit, however, had significantly lower sum squared error compared with the M&lt;sub>p&lt;/sub> and M&lt;sub>d&lt;/sub> models.&lt;h4>Conclusions&lt;/h4>The results of this study indicate that for both doses, the M&lt;sub>p&lt;/sub> and M&lt;sub>dp&lt;/sub> models result in accurate predictions of tumor growth, whereas the M&lt;sub>d&lt;/sub> model poorly describes response to radiation therapy.</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Apr</publication><modification>2024-11-09T09:46:52.686Z</modification><creation>2019-08-04T07:30:55Z</creation></dates><accession>S-EPMC5934308</accession><cross_references><pubmed>29398129</pubmed><doi>10.1016/j.ijrobp.2017.12.004</doi></cross_references></HashMap>