Development of a multivariate model to predict the likelihood of carcinoma in patients with indeterminate peripheral lung nodules after a nondiagnostic bronchoscopic evaluation
Summary Studies have shown that fluorescence in situ hybridization (FISH) testing increases lung cancer detection on cytology specimens in peripheral nodules. The goal of this study was to determine whether a predictive model using clinical features and routine cytology with FISH results could predi...
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Veröffentlicht in: | Human pathology 2014, Vol.45 (1), p.41-47 |
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creator | Voss, Jesse S., CT, MB (ASCP) Iqbal, Seher, MD Jenkins, Sarah M., MS Henry, Michael R., MD Clayton, Amy C., MD Jett, James R., MD Kipp, Benjamin R., PhD Halling, Kevin C., MD, PhD Maldonado, Fabien, MD |
description | Summary Studies have shown that fluorescence in situ hybridization (FISH) testing increases lung cancer detection on cytology specimens in peripheral nodules. The goal of this study was to determine whether a predictive model using clinical features and routine cytology with FISH results could predict lung malignancy after a nondiagnostic bronchoscopic evaluation. Patients with an indeterminate peripheral lung nodule that had a nondiagnostic bronchoscopic evaluation were included in this study (N = 220). FISH was performed on residual bronchial brushing cytology specimens diagnosed as negative (n = 195), atypical (n = 16), or suspicious (n = 9). FISH results included hypertetrasomy (n = 30) and negative (n = 190). Primary study end points included lung cancer status along with time to diagnosis of lung cancer or date of last clinical follow-up. Hazard ratios (HRs) were calculated using Cox proportional hazards regression model analyses, and P values < .05 were considered statistically significant. The mean age of the 220 patients was 66.7 years (range, 35-91), and most (58%) were men. Most patients (79%) were current or former smokers with a mean pack year history of 43.2 years (median, 40; range, 1-200). After multivariate analysis, hypertetrasomy FISH (HR = 2.96, P < .001), pack years (HR = 1.03 per pack year up to 50, P = .001), age (HR = 1.04 per year, P = .02), atypical or suspicious cytology (HR = 2.02, P = .04), and nodule spiculation (HR = 2.36, P = .003) were independent predictors of malignancy over time and were used to create a prediction model (C-statistic = 0.78). These results suggest that this multivariate model including test results and clinical features may be useful following a nondiagnostic bronchoscopic examination. |
doi_str_mv | 10.1016/j.humpath.2013.07.038 |
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The goal of this study was to determine whether a predictive model using clinical features and routine cytology with FISH results could predict lung malignancy after a nondiagnostic bronchoscopic evaluation. Patients with an indeterminate peripheral lung nodule that had a nondiagnostic bronchoscopic evaluation were included in this study (N = 220). FISH was performed on residual bronchial brushing cytology specimens diagnosed as negative (n = 195), atypical (n = 16), or suspicious (n = 9). FISH results included hypertetrasomy (n = 30) and negative (n = 190). Primary study end points included lung cancer status along with time to diagnosis of lung cancer or date of last clinical follow-up. Hazard ratios (HRs) were calculated using Cox proportional hazards regression model analyses, and P values < .05 were considered statistically significant. The mean age of the 220 patients was 66.7 years (range, 35-91), and most (58%) were men. Most patients (79%) were current or former smokers with a mean pack year history of 43.2 years (median, 40; range, 1-200). After multivariate analysis, hypertetrasomy FISH (HR = 2.96, P < .001), pack years (HR = 1.03 per pack year up to 50, P = .001), age (HR = 1.04 per year, P = .02), atypical or suspicious cytology (HR = 2.02, P = .04), and nodule spiculation (HR = 2.36, P = .003) were independent predictors of malignancy over time and were used to create a prediction model (C-statistic = 0.78). These results suggest that this multivariate model including test results and clinical features may be useful following a nondiagnostic bronchoscopic examination.</description><identifier>ISSN: 0046-8177</identifier><identifier>EISSN: 1532-8392</identifier><identifier>DOI: 10.1016/j.humpath.2013.07.038</identifier><identifier>PMID: 24139213</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adult ; Age ; Aged ; Aged, 80 and over ; Bronchoscopy ; Cellular biology ; Confidence intervals ; Cytodiagnosis ; Cytology ; Disease Progression ; Female ; Humans ; In Situ Hybridization, Fluorescence ; Lung cancer ; Lung Diseases - diagnosis ; Lung Neoplasms - diagnosis ; Male ; Middle Aged ; Multivariate Analysis ; Pathology ; Pulmonary nodule</subject><ispartof>Human pathology, 2014, Vol.45 (1), p.41-47</ispartof><rights>Elsevier Inc.</rights><rights>2014 Elsevier Inc.</rights><rights>2013.</rights><rights>Copyright Elsevier Limited Jan 2014</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c448t-c3d32ce492a4a797d5b2bb9b11b63e0e083ec04dfaa29e80e41f84d82cd76ce43</citedby><cites>FETCH-LOGICAL-c448t-c3d32ce492a4a797d5b2bb9b11b63e0e083ec04dfaa29e80e41f84d82cd76ce43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.humpath.2013.07.038$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,4024,27923,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24139213$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Voss, Jesse S., CT, MB (ASCP)</creatorcontrib><creatorcontrib>Iqbal, Seher, MD</creatorcontrib><creatorcontrib>Jenkins, Sarah M., MS</creatorcontrib><creatorcontrib>Henry, Michael R., MD</creatorcontrib><creatorcontrib>Clayton, Amy C., MD</creatorcontrib><creatorcontrib>Jett, James R., MD</creatorcontrib><creatorcontrib>Kipp, Benjamin R., PhD</creatorcontrib><creatorcontrib>Halling, Kevin C., MD, PhD</creatorcontrib><creatorcontrib>Maldonado, Fabien, MD</creatorcontrib><title>Development of a multivariate model to predict the likelihood of carcinoma in patients with indeterminate peripheral lung nodules after a nondiagnostic bronchoscopic evaluation</title><title>Human pathology</title><addtitle>Hum Pathol</addtitle><description>Summary Studies have shown that fluorescence in situ hybridization (FISH) testing increases lung cancer detection on cytology specimens in peripheral nodules. The goal of this study was to determine whether a predictive model using clinical features and routine cytology with FISH results could predict lung malignancy after a nondiagnostic bronchoscopic evaluation. Patients with an indeterminate peripheral lung nodule that had a nondiagnostic bronchoscopic evaluation were included in this study (N = 220). FISH was performed on residual bronchial brushing cytology specimens diagnosed as negative (n = 195), atypical (n = 16), or suspicious (n = 9). FISH results included hypertetrasomy (n = 30) and negative (n = 190). Primary study end points included lung cancer status along with time to diagnosis of lung cancer or date of last clinical follow-up. Hazard ratios (HRs) were calculated using Cox proportional hazards regression model analyses, and P values < .05 were considered statistically significant. The mean age of the 220 patients was 66.7 years (range, 35-91), and most (58%) were men. Most patients (79%) were current or former smokers with a mean pack year history of 43.2 years (median, 40; range, 1-200). After multivariate analysis, hypertetrasomy FISH (HR = 2.96, P < .001), pack years (HR = 1.03 per pack year up to 50, P = .001), age (HR = 1.04 per year, P = .02), atypical or suspicious cytology (HR = 2.02, P = .04), and nodule spiculation (HR = 2.36, P = .003) were independent predictors of malignancy over time and were used to create a prediction model (C-statistic = 0.78). These results suggest that this multivariate model including test results and clinical features may be useful following a nondiagnostic bronchoscopic examination.</description><subject>Adult</subject><subject>Age</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Bronchoscopy</subject><subject>Cellular biology</subject><subject>Confidence intervals</subject><subject>Cytodiagnosis</subject><subject>Cytology</subject><subject>Disease Progression</subject><subject>Female</subject><subject>Humans</subject><subject>In Situ Hybridization, Fluorescence</subject><subject>Lung cancer</subject><subject>Lung Diseases - diagnosis</subject><subject>Lung Neoplasms - diagnosis</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Multivariate Analysis</subject><subject>Pathology</subject><subject>Pulmonary nodule</subject><issn>0046-8177</issn><issn>1532-8392</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFks1u1TAQhSMEoreFRwBZYsMmwX_524CqQgGpEgtgbTn2pPGtYwfbuahvxSPi6F5A6oaVZes7Z8ZzpiheEFwRTJo3-2pa50WmqaKYsAq3FWbdo2JHakbLjvX0cbHDmDdlR9r2rDiPcY8xITWvnxZnlJNMELYrfr2HA1i_zOAS8iOSaF5tMgcZjEyAZq_BouTREkAblVCaAFlzB9ZM3utNoWRQxvlZIuNQbshkp4h-mjTlBw0Jwmzc5rVAMMsEQVpkV3eLnNerhYjkmJlc2Hmnjbx1Piaj0BC8U5OPyi_5Bgdp1-zt3bPiyShthOen86L4fv3h29Wn8ubLx89Xlzel4rxLpWKaUQW8p5LLtm91PdBh6AdChoYBBtwxUJjrUUraQ4eBk7HjuqNKt03WsYvi9dF3Cf7HCjGJ2UQF1koHfo2C8KbFDW37PqOvHqB7vwaXu9uonEeXx52p-kip4GMMMIolmFmGe0Gw2CIVe3GKVGyRCtyKHGnWvTy5r8MM-q_qT4YZeHcEII_jYCCIqHIIKgcWQCWhvflvibcPHJQ1zihp7-Ae4r_fiEgFFl-3vdrWijCMGcOc_QZxPM8u</recordid><startdate>2014</startdate><enddate>2014</enddate><creator>Voss, Jesse S., CT, MB (ASCP)</creator><creator>Iqbal, Seher, MD</creator><creator>Jenkins, Sarah M., MS</creator><creator>Henry, Michael R., MD</creator><creator>Clayton, Amy C., MD</creator><creator>Jett, James R., MD</creator><creator>Kipp, Benjamin R., PhD</creator><creator>Halling, Kevin C., MD, PhD</creator><creator>Maldonado, Fabien, MD</creator><general>Elsevier Inc</general><general>Elsevier Limited</general><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>K9.</scope><scope>7X8</scope></search><sort><creationdate>2014</creationdate><title>Development of a multivariate model to predict the likelihood of carcinoma in patients with indeterminate peripheral lung nodules after a nondiagnostic bronchoscopic evaluation</title><author>Voss, Jesse S., CT, MB (ASCP) ; Iqbal, Seher, MD ; Jenkins, Sarah M., MS ; Henry, Michael R., MD ; Clayton, Amy C., MD ; Jett, James R., MD ; Kipp, Benjamin R., PhD ; Halling, Kevin C., MD, PhD ; Maldonado, Fabien, MD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c448t-c3d32ce492a4a797d5b2bb9b11b63e0e083ec04dfaa29e80e41f84d82cd76ce43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adult</topic><topic>Age</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Bronchoscopy</topic><topic>Cellular biology</topic><topic>Confidence intervals</topic><topic>Cytodiagnosis</topic><topic>Cytology</topic><topic>Disease Progression</topic><topic>Female</topic><topic>Humans</topic><topic>In Situ Hybridization, Fluorescence</topic><topic>Lung cancer</topic><topic>Lung Diseases - diagnosis</topic><topic>Lung Neoplasms - diagnosis</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Multivariate Analysis</topic><topic>Pathology</topic><topic>Pulmonary nodule</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Voss, Jesse S., CT, MB (ASCP)</creatorcontrib><creatorcontrib>Iqbal, Seher, MD</creatorcontrib><creatorcontrib>Jenkins, Sarah M., MS</creatorcontrib><creatorcontrib>Henry, Michael R., MD</creatorcontrib><creatorcontrib>Clayton, Amy C., MD</creatorcontrib><creatorcontrib>Jett, James R., MD</creatorcontrib><creatorcontrib>Kipp, Benjamin R., PhD</creatorcontrib><creatorcontrib>Halling, Kevin C., MD, PhD</creatorcontrib><creatorcontrib>Maldonado, Fabien, MD</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Human pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Voss, Jesse S., CT, MB (ASCP)</au><au>Iqbal, Seher, MD</au><au>Jenkins, Sarah M., MS</au><au>Henry, Michael R., MD</au><au>Clayton, Amy C., MD</au><au>Jett, James R., MD</au><au>Kipp, Benjamin R., PhD</au><au>Halling, Kevin C., MD, PhD</au><au>Maldonado, Fabien, MD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of a multivariate model to predict the likelihood of carcinoma in patients with indeterminate peripheral lung nodules after a nondiagnostic bronchoscopic evaluation</atitle><jtitle>Human pathology</jtitle><addtitle>Hum Pathol</addtitle><date>2014</date><risdate>2014</risdate><volume>45</volume><issue>1</issue><spage>41</spage><epage>47</epage><pages>41-47</pages><issn>0046-8177</issn><eissn>1532-8392</eissn><abstract>Summary Studies have shown that fluorescence in situ hybridization (FISH) testing increases lung cancer detection on cytology specimens in peripheral nodules. The goal of this study was to determine whether a predictive model using clinical features and routine cytology with FISH results could predict lung malignancy after a nondiagnostic bronchoscopic evaluation. Patients with an indeterminate peripheral lung nodule that had a nondiagnostic bronchoscopic evaluation were included in this study (N = 220). FISH was performed on residual bronchial brushing cytology specimens diagnosed as negative (n = 195), atypical (n = 16), or suspicious (n = 9). FISH results included hypertetrasomy (n = 30) and negative (n = 190). Primary study end points included lung cancer status along with time to diagnosis of lung cancer or date of last clinical follow-up. Hazard ratios (HRs) were calculated using Cox proportional hazards regression model analyses, and P values < .05 were considered statistically significant. The mean age of the 220 patients was 66.7 years (range, 35-91), and most (58%) were men. Most patients (79%) were current or former smokers with a mean pack year history of 43.2 years (median, 40; range, 1-200). After multivariate analysis, hypertetrasomy FISH (HR = 2.96, P < .001), pack years (HR = 1.03 per pack year up to 50, P = .001), age (HR = 1.04 per year, P = .02), atypical or suspicious cytology (HR = 2.02, P = .04), and nodule spiculation (HR = 2.36, P = .003) were independent predictors of malignancy over time and were used to create a prediction model (C-statistic = 0.78). These results suggest that this multivariate model including test results and clinical features may be useful following a nondiagnostic bronchoscopic examination.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>24139213</pmid><doi>10.1016/j.humpath.2013.07.038</doi><tpages>7</tpages></addata></record> |
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subjects | Adult Age Aged Aged, 80 and over Bronchoscopy Cellular biology Confidence intervals Cytodiagnosis Cytology Disease Progression Female Humans In Situ Hybridization, Fluorescence Lung cancer Lung Diseases - diagnosis Lung Neoplasms - diagnosis Male Middle Aged Multivariate Analysis Pathology Pulmonary nodule |
title | Development of a multivariate model to predict the likelihood of carcinoma in patients with indeterminate peripheral lung nodules after a nondiagnostic bronchoscopic evaluation |
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