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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Veröffentlicht in:Clinical cancer research 2005-08, Vol.11 (15), p.5440-5443
Hauptverfasser: ZLOBEC, Inti, STEELE, Russell, NIGAM, Nilima, COMPTON, Carolyn C
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container_title Clinical cancer research
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creator ZLOBEC, Inti
STEELE, Russell
NIGAM, Nilima
COMPTON, Carolyn C
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
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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. 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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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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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