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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Human pathology 2014, Vol.45 (1), p.41-47
Hauptverfasser: 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
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 47
container_issue 1
container_start_page 41
container_title Human pathology
container_volume 45
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
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1467062799</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>1_s2_0_S0046817713003304</els_id><sourcerecordid>3147544791</sourcerecordid><originalsourceid>FETCH-LOGICAL-c448t-c3d32ce492a4a797d5b2bb9b11b63e0e083ec04dfaa29e80e41f84d82cd76ce43</originalsourceid><addsrcrecordid>eNqFks1u1TAQhSMEoreFRwBZYsMmwX_524CqQgGpEgtgbTn2pPGtYwfbuahvxSPi6F5A6oaVZes7Z8ZzpiheEFwRTJo3-2pa50WmqaKYsAq3FWbdo2JHakbLjvX0cbHDmDdlR9r2rDiPcY8xITWvnxZnlJNMELYrfr2HA1i_zOAS8iOSaF5tMgcZjEyAZq_BouTREkAblVCaAFlzB9ZM3utNoWRQxvlZIuNQbshkp4h-mjTlBw0Jwmzc5rVAMMsEQVpkV3eLnNerhYjkmJlc2Hmnjbx1Piaj0BC8U5OPyi_5Bgdp1-zt3bPiyShthOen86L4fv3h29Wn8ubLx89Xlzel4rxLpWKaUQW8p5LLtm91PdBh6AdChoYBBtwxUJjrUUraQ4eBk7HjuqNKt03WsYvi9dF3Cf7HCjGJ2UQF1koHfo2C8KbFDW37PqOvHqB7vwaXu9uonEeXx52p-kip4GMMMIolmFmGe0Gw2CIVe3GKVGyRCtyKHGnWvTy5r8MM-q_qT4YZeHcEII_jYCCIqHIIKgcWQCWhvflvibcPHJQ1zihp7-Ae4r_fiEgFFl-3vdrWijCMGcOc_QZxPM8u</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1465328413</pqid></control><display><type>article</type><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><source>MEDLINE</source><source>Elsevier ScienceDirect Journals Complete</source><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</creator><creatorcontrib>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</creatorcontrib><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 &lt; .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 &lt; .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 &lt; .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 &lt; .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 &amp; 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 &lt; .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 &lt; .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>
fulltext fulltext
identifier ISSN: 0046-8177
ispartof Human pathology, 2014, Vol.45 (1), p.41-47
issn 0046-8177
1532-8392
language eng
recordid cdi_proquest_miscellaneous_1467062799
source MEDLINE; Elsevier ScienceDirect Journals Complete
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T11%3A44%3A04IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Development%20of%20a%20multivariate%20model%20to%20predict%20the%20likelihood%20of%20carcinoma%20in%20patients%20with%20indeterminate%20peripheral%20lung%20nodules%20after%20a%20nondiagnostic%20bronchoscopic%20evaluation&rft.jtitle=Human%20pathology&rft.au=Voss,%20Jesse%20S.,%20CT,%20MB%20(ASCP)&rft.date=2014&rft.volume=45&rft.issue=1&rft.spage=41&rft.epage=47&rft.pages=41-47&rft.issn=0046-8177&rft.eissn=1532-8392&rft_id=info:doi/10.1016/j.humpath.2013.07.038&rft_dat=%3Cproquest_cross%3E3147544791%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1465328413&rft_id=info:pmid/24139213&rft_els_id=1_s2_0_S0046817713003304&rfr_iscdi=true