<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-09-20T15:59:39Z</responseDate><request verb="GetRecord" identifier="oai:dspace.mit.edu:1721.1/76942" metadataPrefix="dim">https://dspace.mit.edu/server/oai/request</request><GetRecord><record><header><identifier>oai:dspace.mit.edu:1721.1/76942</identifier><datestamp>2022-01-13T07:54:37Z</datestamp><setSpec>com_1721.1_7582</setSpec><setSpec>com_1721.1_7581</setSpec><setSpec>col_1721.1_131024</setSpec></header><metadata><dim:dim xmlns:dim="http://www.dspace.org/xmlns/dspace/dim" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.dspace.org/xmlns/dspace/dim http://www.dspace.org/schema/dim.xsd">
   <dim:field mdschema="dc" element="contributor" qualifier="advisor" lang="en_US">Richard Lanza and George T.Y. Chen.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author" lang="en_US">Wiśniowska, Agata Elżbieta</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="other" lang="en_US">Massachusetts Institute of Technology. Dept. of Nuclear Science and Engineering.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="department">Massachusetts Institute of Technology. Department of Nuclear Science and Engineering</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="accessioned">2013-02-14T15:20:04Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2013-02-14T15:20:04Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="issued" lang="en_US">2011</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri">http://hdl.handle.net/1721.1/76942</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="oclc" lang="en_US">824560127</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Thesis (S.B.)--Massachusetts Institute of Technology, Dept. of Nuclear Science and Engineering, 2011.</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">"June 2011." Cataloged from PDF version of thesis.</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Includes bibliographical references (p. 33-34).</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">The purpose of this study is to assess the difference between 4D liver dose calculations versus standard 3D treatment planning and to investigate the dosimetric gain of gating on radiation dose to normal tissue. 4DCT scans are collected for 25 patients with hepatic tumors treated by proton radiotherapy. The 4D treatment planning process explicitly takes into account respiratory motion of abdominal organs. A 4DCT scan consists of 10 3D anatomical states, each at an instant of time in the respiratory cycle. 4D treatment planning includes 1) propagating the target contours, drawn by a physician on one phase, to all breathing phases using deformable registration, 2) calculating the compensating bolus for proton therapy, and then 3) calculating 4D dose distributions. Dose volume histograms are used to compute the effective uniform dose (EUD) delivered to normal liver. We found that 4DCT planning always results in a larger EUD to normal liver when compared with dose from a 3DCT plan. The mean EUD difference between 4D and 3D planning is 3.8Gy ([sigma]= 1.9Gy, p&lt;0.000 1). Gated 4D treatment planning results in a lower EUD to normal liver compared to ungated planning, with a mean difference of 2.9 Gy ([sigma]=1.9Gy, p&lt;0.0001). The EUD difference is only weakly correlated with the magnitude of the superior-inferior (S-I) tumor motion ([tau]=0.59 for 4D/3D, [tau]=0.48 for ungated/gated). The [Delta]EUD correlation with clinical target volume (CTV) (as fraction of liver volume) is much weaker ([tau]-0.31 for 4D/3D, [tau]=0.26 for ungated/gated). There was no evidence that the tumor position within the liver influenced the [Delta]EUD. This study suggests that physicians should consider 4D treatment planning if the risk of normal tissue complications is high. Normal tissues may also be significantly spared by gated treatment as a motion management strategy.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="statementofresponsibility" lang="en_US">by Agata Elżbieta Wiśniowska.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="degree" lang="en_US">S.B.</dim:field>
   <dim:field mdschema="dc" element="format" qualifier="extent" lang="en_US">39 p.</dim:field>
   <dim:field mdschema="dc" element="language" qualifier="iso" lang="en_US">eng</dim:field>
   <dim:field mdschema="dc" element="publisher" lang="en_US">Massachusetts Institute of Technology</dim:field>
   <dim:field mdschema="dc" element="rights" lang="en_US">M.I.T. theses are protected by 
copyright. They may be viewed from this source for any purpose, but 
reproduction or distribution in any format is prohibited without written 
permission. See provided URL for inquiries about permission.</dim:field>
   <dim:field mdschema="dc" element="rights" qualifier="uri" lang="en_US">http://dspace.mit.edu/handle/1721.1/7582</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">Nuclear Science and Engineering.</dim:field>
   <dim:field mdschema="dc" element="title" lang="en_US">Analysis of 3D and 4D proton treatment planning for hepatic tumors</dim:field>
   <dim:field mdschema="dc" element="title" qualifier="alternative" lang="en_US">Analysis of three-dimensional and four-dimensional proton treatment planning for hepatic tumors</dim:field>
   <dim:field mdschema="dc" element="type" lang="en_US">Thesis</dim:field>
   <dim:field mdschema="dc" element="format" qualifier="mimetype">application/pdf</dim:field>
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	&lt;Language>eng&lt;/Language>
   	&lt;Title>Analysis of 3D and 4D proton treatment planning for hepatic tumors&lt;/Title>
   	&lt;Subtitle>Analysis of three-dimensional and four-dimensional proton treatment planning for hepatic tumors&lt;/Subtitle>
   	&lt;PublishedIn>
    	&lt;Publication>
      	&lt;/Publication>
   	&lt;/PublishedIn>
   	&lt;PublicationDate>2011&lt;/PublicationDate>
   	&lt;Authors>
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        	&lt;DisplayName>Wiśniowska, Agata Elżbieta&lt;/DisplayName>
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            &lt;DisplayName>Massachusetts Institute of Technology&lt;/DisplayName>
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    &lt;License>http://dspace.mit.edu/handle/1721.1/7582&lt;/License>
    &lt;Keyword>Nuclear Science and Engineering.&lt;/Keyword>
   	&lt;Abstract>The purpose of this study is to assess the difference between 4D liver dose calculations versus standard 3D treatment planning and to investigate the dosimetric gain of gating on radiation dose to normal tissue. 4DCT scans are collected for 25 patients with hepatic tumors treated by proton radiotherapy. The 4D treatment planning process explicitly takes into account respiratory motion of abdominal organs. A 4DCT scan consists of 10 3D anatomical states, each at an instant of time in the respiratory cycle. 4D treatment planning includes 1) propagating the target contours, drawn by a physician on one phase, to all breathing phases using deformable registration, 2) calculating the compensating bolus for proton therapy, and then 3) calculating 4D dose distributions. Dose volume histograms are used to compute the effective uniform dose (EUD) delivered to normal liver. We found that 4DCT planning always results in a larger EUD to normal liver when compared with dose from a 3DCT plan. The mean EUD difference between 4D and 3D planning is 3.8Gy ([sigma]= 1.9Gy, p&amp;lt;0.000 1). Gated 4D treatment planning results in a lower EUD to normal liver compared to ungated planning, with a mean difference of 2.9 Gy ([sigma]=1.9Gy, p&amp;lt;0.0001). The EUD difference is only weakly correlated with the magnitude of the superior-inferior (S-I) tumor motion ([tau]=0.59 for 4D/3D, [tau]=0.48 for ungated/gated). The [Delta]EUD correlation with clinical target volume (CTV) (as fraction of liver volume) is much weaker ([tau]-0.31 for 4D/3D, [tau]=0.26 for ungated/gated). There was no evidence that the tumor position within the liver influenced the [Delta]EUD. This study suggests that physicians should consider 4D treatment planning if the risk of normal tissue complications is high. Normal tissues may also be significantly spared by gated treatment as a motion management strategy.&lt;/Abstract>
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