A Predictive Model of Rectal Tumor Response to Preoperative Radiotherapy Using Classification and Regression Tree Methods
Purpose: The ability to predict rectal tumor response to preoperative radiotherapy before treatment would significantly impact patient selection. In this study, classification and regression tree (CART) methods were used to model tumor response to preoperative conformal high-dose rate brachytherapy...
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description | Purpose: The ability to predict rectal tumor response to preoperative radiotherapy before treatment would significantly impact patient
selection. In this study, classification and regression tree (CART) methods were used to model tumor response to preoperative
conformal high-dose rate brachytherapy by assessing the predictive value of vascular endothelial growth factor (VEGF), Bcl-2,
p21, p53, and APAF-1.
Experimental Design: Immunohistochemistry was used to detect VEGF, Bcl-2, p21, p53, and APAF-1 from 62 pretreatment rectal tumor biopsies. Scores
were assigned as percentages of positive tumor cell staining and were used in CART analysis to identify the proteins that
best predicted response to radiotherapy. Ten-fold cross-validation was used to prevent overfitting and multiple cross-validation
experiments were run to estimate the prediction error.
Results: Postoperative pathologic evaluation of the irradiated tumor bed revealed 43 responsive tumors [20 with complete response
(T 0 ) and 23 with partial response] and 19 nonresponsive tumors. The optimal tree resulting from CART analysis had five terminal
nodes with a misclassification rate of 18%. Of the five proteins selected for their predictive value, VEGF and Bcl-2 contributed
most to the classification of responsive and nonresponsive tumors. All 10 tumors with no VEGF were completely responsive (T 0 ) to radiotherapy; 85% of those with VEGF and negative for Bcl-2 were responsive to therapy.
Conclusions: VEGF and Bcl-2 status in pretreatment rectal tumor biopsies may be predictive of response to preoperative high-dose rate
brachytherapy. |
doi_str_mv | 10.1158/1078-0432.CCR-04-2587 |
format | Article |
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selection. In this study, classification and regression tree (CART) methods were used to model tumor response to preoperative
conformal high-dose rate brachytherapy by assessing the predictive value of vascular endothelial growth factor (VEGF), Bcl-2,
p21, p53, and APAF-1.
Experimental Design: Immunohistochemistry was used to detect VEGF, Bcl-2, p21, p53, and APAF-1 from 62 pretreatment rectal tumor biopsies. Scores
were assigned as percentages of positive tumor cell staining and were used in CART analysis to identify the proteins that
best predicted response to radiotherapy. Ten-fold cross-validation was used to prevent overfitting and multiple cross-validation
experiments were run to estimate the prediction error.
Results: Postoperative pathologic evaluation of the irradiated tumor bed revealed 43 responsive tumors [20 with complete response
(T 0 ) and 23 with partial response] and 19 nonresponsive tumors. The optimal tree resulting from CART analysis had five terminal
nodes with a misclassification rate of 18%. Of the five proteins selected for their predictive value, VEGF and Bcl-2 contributed
most to the classification of responsive and nonresponsive tumors. All 10 tumors with no VEGF were completely responsive (T 0 ) to radiotherapy; 85% of those with VEGF and negative for Bcl-2 were responsive to therapy.
Conclusions: VEGF and Bcl-2 status in pretreatment rectal tumor biopsies may be predictive of response to preoperative high-dose rate
brachytherapy.</description><identifier>ISSN: 1078-0432</identifier><identifier>EISSN: 1557-3265</identifier><identifier>DOI: 10.1158/1078-0432.CCR-04-2587</identifier><identifier>PMID: 16061859</identifier><language>eng</language><publisher>Philadelphia, PA: American Association for Cancer Research</publisher><subject>Antineoplastic agents ; Apoptotic Protease-Activating Factor 1 ; Bcl-2 ; Biological and medical sciences ; Biomarkers, Tumor ; Biopsy ; brachytherapy ; Brachytherapy - methods ; Cyclin-Dependent Kinase Inhibitor p21 - biosynthesis ; Gastroenterology. Liver. Pancreas. Abdomen ; Humans ; Immunohistochemistry ; Intracellular Signaling Peptides and Proteins - metabolism ; Medical sciences ; Neoplasms - pathology ; Oxygen - metabolism ; Pharmacology. Drug treatments ; predicting response ; Proteins - metabolism ; Proto-Oncogene Proteins c-bcl-2 - biosynthesis ; Radiotherapy, Adjuvant - methods ; Radiotherapy, Conformal - methods ; Rectal cancer ; Rectal Neoplasms - classification ; Rectal Neoplasms - diagnosis ; Rectal Neoplasms - radiotherapy ; Regression Analysis ; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus ; Time Factors ; Tumor Suppressor Protein p53 - biosynthesis ; Tumors ; Vascular Endothelial Growth Factor A - biosynthesis ; Vascular Endothelial Growth Factor A - metabolism ; VEGF</subject><ispartof>Clinical cancer research, 2005-08, Vol.11 (15), p.5440-5443</ispartof><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c437t-d7b9996a18ffeabe4ae04fb5fbe52496a88de393c212a10cd435db4fd1a9255c3</citedby><cites>FETCH-LOGICAL-c437t-d7b9996a18ffeabe4ae04fb5fbe52496a88de393c212a10cd435db4fd1a9255c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,3356,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16988745$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16061859$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>ZLOBEC, Inti</creatorcontrib><creatorcontrib>STEELE, Russell</creatorcontrib><creatorcontrib>NIGAM, Nilima</creatorcontrib><creatorcontrib>COMPTON, Carolyn C</creatorcontrib><title>A Predictive Model of Rectal Tumor Response to Preoperative Radiotherapy Using Classification and Regression Tree Methods</title><title>Clinical cancer research</title><addtitle>Clin Cancer Res</addtitle><description>Purpose: The ability to predict rectal tumor response to preoperative radiotherapy before treatment would significantly impact patient
selection. In this study, classification and regression tree (CART) methods were used to model tumor response to preoperative
conformal high-dose rate brachytherapy by assessing the predictive value of vascular endothelial growth factor (VEGF), Bcl-2,
p21, p53, and APAF-1.
Experimental Design: Immunohistochemistry was used to detect VEGF, Bcl-2, p21, p53, and APAF-1 from 62 pretreatment rectal tumor biopsies. Scores
were assigned as percentages of positive tumor cell staining and were used in CART analysis to identify the proteins that
best predicted response to radiotherapy. Ten-fold cross-validation was used to prevent overfitting and multiple cross-validation
experiments were run to estimate the prediction error.
Results: Postoperative pathologic evaluation of the irradiated tumor bed revealed 43 responsive tumors [20 with complete response
(T 0 ) and 23 with partial response] and 19 nonresponsive tumors. The optimal tree resulting from CART analysis had five terminal
nodes with a misclassification rate of 18%. Of the five proteins selected for their predictive value, VEGF and Bcl-2 contributed
most to the classification of responsive and nonresponsive tumors. All 10 tumors with no VEGF were completely responsive (T 0 ) to radiotherapy; 85% of those with VEGF and negative for Bcl-2 were responsive to therapy.
Conclusions: VEGF and Bcl-2 status in pretreatment rectal tumor biopsies may be predictive of response to preoperative high-dose rate
brachytherapy.</description><subject>Antineoplastic agents</subject><subject>Apoptotic Protease-Activating Factor 1</subject><subject>Bcl-2</subject><subject>Biological and medical sciences</subject><subject>Biomarkers, Tumor</subject><subject>Biopsy</subject><subject>brachytherapy</subject><subject>Brachytherapy - methods</subject><subject>Cyclin-Dependent Kinase Inhibitor p21 - biosynthesis</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Intracellular Signaling Peptides and Proteins - metabolism</subject><subject>Medical sciences</subject><subject>Neoplasms - pathology</subject><subject>Oxygen - metabolism</subject><subject>Pharmacology. Drug treatments</subject><subject>predicting response</subject><subject>Proteins - metabolism</subject><subject>Proto-Oncogene Proteins c-bcl-2 - biosynthesis</subject><subject>Radiotherapy, Adjuvant - methods</subject><subject>Radiotherapy, Conformal - methods</subject><subject>Rectal cancer</subject><subject>Rectal Neoplasms - classification</subject><subject>Rectal Neoplasms - diagnosis</subject><subject>Rectal Neoplasms - radiotherapy</subject><subject>Regression Analysis</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><subject>Time Factors</subject><subject>Tumor Suppressor Protein p53 - biosynthesis</subject><subject>Tumors</subject><subject>Vascular Endothelial Growth Factor A - biosynthesis</subject><subject>Vascular Endothelial Growth Factor A - metabolism</subject><subject>VEGF</subject><issn>1078-0432</issn><issn>1557-3265</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkE1v1DAQhiNERUvhJ4B8AYlDih3biXOsIr6kVqDV9mw59nhjlI2DnQXtv--EXURPfsd-ZsZ6iuINozeMSfWR0UaVVPDqpus2GMpKquZZccWkbEpe1fI55n_MZfEy55-UMsGoeFFcsprWTMn2qjjekh8JXLBL-A3kPjoYSfRkA3YxI9ke9jFhkec4ZSBLXOE4QzJ_8Y1xIS4DlvORPOQw7Ug3mpyDDxaJOBEzOWzfJcBLLLcJcAksQ3T5VXHhzZjh9fm8Lh4-f9p2X8u771--dbd3pRW8WUrX9G3b1oYp78H0IAxQ4Xvpe5CVwAelHPCW24pVhlHrBJeuF94x01ZSWn5dvD_NnVP8dYC86H3IFsbRTBAPWddK8LoWAkF5Am2KOSfwek5hb9JRM6pX53r1qVefGp1j0Ktz7Ht7XnDo9-D-d50lI_DuDJhszeiTmWzIT7hWqUZI5D6cuCHshj8hgbZIQkJ7YJId8BOaSS2FoPwRVWSajw</recordid><startdate>20050801</startdate><enddate>20050801</enddate><creator>ZLOBEC, Inti</creator><creator>STEELE, Russell</creator><creator>NIGAM, Nilima</creator><creator>COMPTON, Carolyn C</creator><general>American Association for Cancer Research</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20050801</creationdate><title>A Predictive Model of Rectal Tumor Response to Preoperative Radiotherapy Using Classification and Regression Tree Methods</title><author>ZLOBEC, Inti ; STEELE, Russell ; NIGAM, Nilima ; COMPTON, Carolyn C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c437t-d7b9996a18ffeabe4ae04fb5fbe52496a88de393c212a10cd435db4fd1a9255c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Antineoplastic agents</topic><topic>Apoptotic Protease-Activating Factor 1</topic><topic>Bcl-2</topic><topic>Biological and medical sciences</topic><topic>Biomarkers, Tumor</topic><topic>Biopsy</topic><topic>brachytherapy</topic><topic>Brachytherapy - methods</topic><topic>Cyclin-Dependent Kinase Inhibitor p21 - biosynthesis</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Intracellular Signaling Peptides and Proteins - metabolism</topic><topic>Medical sciences</topic><topic>Neoplasms - pathology</topic><topic>Oxygen - metabolism</topic><topic>Pharmacology. Drug treatments</topic><topic>predicting response</topic><topic>Proteins - metabolism</topic><topic>Proto-Oncogene Proteins c-bcl-2 - biosynthesis</topic><topic>Radiotherapy, Adjuvant - methods</topic><topic>Radiotherapy, Conformal - methods</topic><topic>Rectal cancer</topic><topic>Rectal Neoplasms - classification</topic><topic>Rectal Neoplasms - diagnosis</topic><topic>Rectal Neoplasms - radiotherapy</topic><topic>Regression Analysis</topic><topic>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</topic><topic>Time Factors</topic><topic>Tumor Suppressor Protein p53 - biosynthesis</topic><topic>Tumors</topic><topic>Vascular Endothelial Growth Factor A - biosynthesis</topic><topic>Vascular Endothelial Growth Factor A - metabolism</topic><topic>VEGF</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>ZLOBEC, Inti</creatorcontrib><creatorcontrib>STEELE, Russell</creatorcontrib><creatorcontrib>NIGAM, Nilima</creatorcontrib><creatorcontrib>COMPTON, Carolyn C</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical cancer research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>ZLOBEC, Inti</au><au>STEELE, Russell</au><au>NIGAM, Nilima</au><au>COMPTON, Carolyn C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Predictive Model of Rectal Tumor Response to Preoperative Radiotherapy Using Classification and Regression Tree Methods</atitle><jtitle>Clinical cancer research</jtitle><addtitle>Clin Cancer Res</addtitle><date>2005-08-01</date><risdate>2005</risdate><volume>11</volume><issue>15</issue><spage>5440</spage><epage>5443</epage><pages>5440-5443</pages><issn>1078-0432</issn><eissn>1557-3265</eissn><abstract>Purpose: The ability to predict rectal tumor response to preoperative radiotherapy before treatment would significantly impact patient
selection. In this study, classification and regression tree (CART) methods were used to model tumor response to preoperative
conformal high-dose rate brachytherapy by assessing the predictive value of vascular endothelial growth factor (VEGF), Bcl-2,
p21, p53, and APAF-1.
Experimental Design: Immunohistochemistry was used to detect VEGF, Bcl-2, p21, p53, and APAF-1 from 62 pretreatment rectal tumor biopsies. Scores
were assigned as percentages of positive tumor cell staining and were used in CART analysis to identify the proteins that
best predicted response to radiotherapy. Ten-fold cross-validation was used to prevent overfitting and multiple cross-validation
experiments were run to estimate the prediction error.
Results: Postoperative pathologic evaluation of the irradiated tumor bed revealed 43 responsive tumors [20 with complete response
(T 0 ) and 23 with partial response] and 19 nonresponsive tumors. The optimal tree resulting from CART analysis had five terminal
nodes with a misclassification rate of 18%. Of the five proteins selected for their predictive value, VEGF and Bcl-2 contributed
most to the classification of responsive and nonresponsive tumors. All 10 tumors with no VEGF were completely responsive (T 0 ) to radiotherapy; 85% of those with VEGF and negative for Bcl-2 were responsive to therapy.
Conclusions: VEGF and Bcl-2 status in pretreatment rectal tumor biopsies may be predictive of response to preoperative high-dose rate
brachytherapy.</abstract><cop>Philadelphia, PA</cop><pub>American Association for Cancer Research</pub><pmid>16061859</pmid><doi>10.1158/1078-0432.CCR-04-2587</doi><tpages>4</tpages></addata></record> |
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ispartof | Clinical cancer research, 2005-08, Vol.11 (15), p.5440-5443 |
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source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; American Association for Cancer Research; Alma/SFX Local Collection |
subjects | Antineoplastic agents Apoptotic Protease-Activating Factor 1 Bcl-2 Biological and medical sciences Biomarkers, Tumor Biopsy brachytherapy Brachytherapy - methods Cyclin-Dependent Kinase Inhibitor p21 - biosynthesis Gastroenterology. Liver. Pancreas. Abdomen Humans Immunohistochemistry Intracellular Signaling Peptides and Proteins - metabolism Medical sciences Neoplasms - pathology Oxygen - metabolism Pharmacology. Drug treatments predicting response Proteins - metabolism Proto-Oncogene Proteins c-bcl-2 - biosynthesis Radiotherapy, Adjuvant - methods Radiotherapy, Conformal - methods Rectal cancer Rectal Neoplasms - classification Rectal Neoplasms - diagnosis Rectal Neoplasms - radiotherapy Regression Analysis Stomach. Duodenum. Small intestine. Colon. Rectum. Anus Time Factors Tumor Suppressor Protein p53 - biosynthesis Tumors Vascular Endothelial Growth Factor A - biosynthesis Vascular Endothelial Growth Factor A - metabolism VEGF |
title | A Predictive Model of Rectal Tumor Response to Preoperative Radiotherapy Using Classification and Regression Tree Methods |
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