Re-evaluation of the prognostic value of visceral pleura invasion in Stage IB non-small cell lung cancer using the prospective multicenter ACOSOG Z0030 trial data set

Abstract Purpose This study seeks to clarify the modern prognostic significance of visceral pleura invasion (VPI) in Stage IB (T2aN0M0) non-small cell lung cancer (NSCLC) within the context of the 7th edition TNM classification using the data set from a recent prospective multicenter trial. Patients...

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Veröffentlicht in:Lung cancer (Amsterdam, Netherlands) Netherlands), 2012-12, Vol.78 (3), p.259-262
Hauptverfasser: Fibla, Juan J, Cassivi, Stephen D, Brunelli, Alessandro, Decker, Paul A, Allen, Mark S, Darling, Gail E, Landreneau, Rodney J, Putnam, Joe B
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container_end_page 262
container_issue 3
container_start_page 259
container_title Lung cancer (Amsterdam, Netherlands)
container_volume 78
creator Fibla, Juan J
Cassivi, Stephen D
Brunelli, Alessandro
Decker, Paul A
Allen, Mark S
Darling, Gail E
Landreneau, Rodney J
Putnam, Joe B
description Abstract Purpose This study seeks to clarify the modern prognostic significance of visceral pleura invasion (VPI) in Stage IB (T2aN0M0) non-small cell lung cancer (NSCLC) within the context of the 7th edition TNM classification using the data set from a recent prospective multicenter trial. Patients and methods 1111 early-stage NSCLC patients participating in the ACOSOG Z0030 trial (1990–2004) underwent curative pulmonary resection. After excluding T2b tumours (>5 cm and ≤7 cm) and non-size-based T2 factors other than VPI, 289 patients were categorized as Stage IB NSCLC – T2aN0M0 – according to the AJCC 7th edition classification. The patients were divided into three groups according to size and VPI: tumours ≤ 3 cm with VPI (Group I, “VPI-alone”, n = 83), tumours > 3 cm and ≤5 cm without VPI (Group II, “Size-alone”, n = 156), and tumours > 3 cm and ≤5 cm with VPI (Group III, “VPI + Size”, n = 50). Multivariate Cox regression analysis was used to assess the association of VPI and size with survival, adjusting for age, gender, histology and type of resection. Results VPI in Stage IB was identified in 133 patients (46.0%). Survival analysis in these patients identified an optimal cutpoint for survival based on size of 3.1 cm. Group III (VPI + Size) had a 5-year survival rate of 55.0% significantly shorter when compared to Group I (VPI-alone = 68.3%, p = 0.009), and Group II (Size-alone = 67.2%, p = 0.021). No difference was found between Groups I and II. Multivariable analysis showed that VPI associated with size was an independent negative prognostic factor of long-term survival, along with older age and limited resection. Conclusions Stage IB patients with VPI and tumours >3 cm and ≤5 cm have significantly worse prognosis than those with ‘T2a’ tumours on the basis of VPI or tumour size alone. This finding would suggest upstaging these patients from the current IB status to Stage IIA.
doi_str_mv 10.1016/j.lungcan.2012.09.010
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Patients and methods 1111 early-stage NSCLC patients participating in the ACOSOG Z0030 trial (1990–2004) underwent curative pulmonary resection. After excluding T2b tumours (&gt;5 cm and ≤7 cm) and non-size-based T2 factors other than VPI, 289 patients were categorized as Stage IB NSCLC – T2aN0M0 – according to the AJCC 7th edition classification. The patients were divided into three groups according to size and VPI: tumours ≤ 3 cm with VPI (Group I, “VPI-alone”, n = 83), tumours &gt; 3 cm and ≤5 cm without VPI (Group II, “Size-alone”, n = 156), and tumours &gt; 3 cm and ≤5 cm with VPI (Group III, “VPI + Size”, n = 50). Multivariate Cox regression analysis was used to assess the association of VPI and size with survival, adjusting for age, gender, histology and type of resection. Results VPI in Stage IB was identified in 133 patients (46.0%). Survival analysis in these patients identified an optimal cutpoint for survival based on size of 3.1 cm. Group III (VPI + Size) had a 5-year survival rate of 55.0% significantly shorter when compared to Group I (VPI-alone = 68.3%, p = 0.009), and Group II (Size-alone = 67.2%, p = 0.021). No difference was found between Groups I and II. Multivariable analysis showed that VPI associated with size was an independent negative prognostic factor of long-term survival, along with older age and limited resection. Conclusions Stage IB patients with VPI and tumours &gt;3 cm and ≤5 cm have significantly worse prognosis than those with ‘T2a’ tumours on the basis of VPI or tumour size alone. This finding would suggest upstaging these patients from the current IB status to Stage IIA.</description><identifier>ISSN: 0169-5002</identifier><identifier>EISSN: 1872-8332</identifier><identifier>DOI: 10.1016/j.lungcan.2012.09.010</identifier><identifier>PMID: 23040416</identifier><identifier>CODEN: LUCAE5</identifier><language>eng</language><publisher>Oxford: Elsevier Ireland Ltd</publisher><subject>7th edition TNM classification ; Adenocarcinoma - mortality ; Adenocarcinoma - pathology ; Adenocarcinoma - surgery ; Adult ; Aged ; Aged, 80 and over ; Biological and medical sciences ; Carcinoma, Non-Small-Cell Lung - mortality ; Carcinoma, Non-Small-Cell Lung - pathology ; Carcinoma, Non-Small-Cell Lung - surgery ; Female ; Hematology, Oncology and Palliative Medicine ; Humans ; Kaplan-Meier Estimate ; Lung Neoplasms - mortality ; Lung Neoplasms - pathology ; Lung Neoplasms - surgery ; Lymph Node Excision ; Male ; Medical sciences ; Middle Aged ; Multicenter Studies as Topic ; Multivariate Analysis ; Neoplasm Invasiveness ; Neoplasm Staging ; Non-small cell lung cancer ; Pleura - pathology ; Pneumology ; Prognosis ; Prognostic factor ; Proportional Hazards Models ; Prospective Studies ; Pulmonary/Respiratory ; Randomized Controlled Trials as Topic ; Tumors ; Tumors of the respiratory system and mediastinum ; Visceral pleura</subject><ispartof>Lung cancer (Amsterdam, Netherlands), 2012-12, Vol.78 (3), p.259-262</ispartof><rights>Elsevier Ireland Ltd</rights><rights>2012 Elsevier Ireland Ltd</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2012 Elsevier Ireland Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c552t-9084e3ef8b6edde32ff2432cd547fc775e34c65bc3f1c4d7796c65d1d679d253</citedby><cites>FETCH-LOGICAL-c552t-9084e3ef8b6edde32ff2432cd547fc775e34c65bc3f1c4d7796c65d1d679d253</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.lungcan.2012.09.010$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,780,784,885,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=26606847$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23040416$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fibla, Juan J</creatorcontrib><creatorcontrib>Cassivi, Stephen D</creatorcontrib><creatorcontrib>Brunelli, Alessandro</creatorcontrib><creatorcontrib>Decker, Paul A</creatorcontrib><creatorcontrib>Allen, Mark S</creatorcontrib><creatorcontrib>Darling, Gail E</creatorcontrib><creatorcontrib>Landreneau, Rodney J</creatorcontrib><creatorcontrib>Putnam, Joe B</creatorcontrib><title>Re-evaluation of the prognostic value of visceral pleura invasion in Stage IB non-small cell lung cancer using the prospective multicenter ACOSOG Z0030 trial data set</title><title>Lung cancer (Amsterdam, Netherlands)</title><addtitle>Lung Cancer</addtitle><description>Abstract Purpose This study seeks to clarify the modern prognostic significance of visceral pleura invasion (VPI) in Stage IB (T2aN0M0) non-small cell lung cancer (NSCLC) within the context of the 7th edition TNM classification using the data set from a recent prospective multicenter trial. Patients and methods 1111 early-stage NSCLC patients participating in the ACOSOG Z0030 trial (1990–2004) underwent curative pulmonary resection. After excluding T2b tumours (&gt;5 cm and ≤7 cm) and non-size-based T2 factors other than VPI, 289 patients were categorized as Stage IB NSCLC – T2aN0M0 – according to the AJCC 7th edition classification. The patients were divided into three groups according to size and VPI: tumours ≤ 3 cm with VPI (Group I, “VPI-alone”, n = 83), tumours &gt; 3 cm and ≤5 cm without VPI (Group II, “Size-alone”, n = 156), and tumours &gt; 3 cm and ≤5 cm with VPI (Group III, “VPI + Size”, n = 50). Multivariate Cox regression analysis was used to assess the association of VPI and size with survival, adjusting for age, gender, histology and type of resection. Results VPI in Stage IB was identified in 133 patients (46.0%). Survival analysis in these patients identified an optimal cutpoint for survival based on size of 3.1 cm. Group III (VPI + Size) had a 5-year survival rate of 55.0% significantly shorter when compared to Group I (VPI-alone = 68.3%, p = 0.009), and Group II (Size-alone = 67.2%, p = 0.021). No difference was found between Groups I and II. Multivariable analysis showed that VPI associated with size was an independent negative prognostic factor of long-term survival, along with older age and limited resection. Conclusions Stage IB patients with VPI and tumours &gt;3 cm and ≤5 cm have significantly worse prognosis than those with ‘T2a’ tumours on the basis of VPI or tumour size alone. This finding would suggest upstaging these patients from the current IB status to Stage IIA.</description><subject>7th edition TNM classification</subject><subject>Adenocarcinoma - mortality</subject><subject>Adenocarcinoma - pathology</subject><subject>Adenocarcinoma - surgery</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Biological and medical sciences</subject><subject>Carcinoma, Non-Small-Cell Lung - mortality</subject><subject>Carcinoma, Non-Small-Cell Lung - pathology</subject><subject>Carcinoma, Non-Small-Cell Lung - surgery</subject><subject>Female</subject><subject>Hematology, Oncology and Palliative Medicine</subject><subject>Humans</subject><subject>Kaplan-Meier Estimate</subject><subject>Lung Neoplasms - mortality</subject><subject>Lung Neoplasms - pathology</subject><subject>Lung Neoplasms - surgery</subject><subject>Lymph Node Excision</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Multicenter Studies as Topic</subject><subject>Multivariate Analysis</subject><subject>Neoplasm Invasiveness</subject><subject>Neoplasm Staging</subject><subject>Non-small cell lung cancer</subject><subject>Pleura - pathology</subject><subject>Pneumology</subject><subject>Prognosis</subject><subject>Prognostic factor</subject><subject>Proportional Hazards Models</subject><subject>Prospective Studies</subject><subject>Pulmonary/Respiratory</subject><subject>Randomized Controlled Trials as Topic</subject><subject>Tumors</subject><subject>Tumors of the respiratory system and mediastinum</subject><subject>Visceral pleura</subject><issn>0169-5002</issn><issn>1872-8332</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUstuEzEUHSEQDYVPAHmDxGbCtT2PeFPURlAqVYpEumJjOZ47qYPjCfbMSP0hvpM7SiiPDbJky_Y55x7f4yx7zWHOgVfvd3M_hK01YS6AizmoOXB4ks34ohb5QkrxNJsRTuUlgDjLXqS0A-A1B_U8OxMSCih4Nct-fMEcR-MH07susK5l_T2yQ-y2oUu9s2y6w-l8dMliNJ4dPA7RMBdGkyaOC2zdmy2ymysWupCnvfGeWaRpssjIIxHZkBxtTurpgLZ3I7L94KkKhp4Ql8vVenXNvgJIYH10VKsxvWEJ-5fZs9b4hK9O63l29-nj3fJzfru6vlle3ua2LEWfK1gUKLFdbCpsGpSibUUhhW3Kom5tXZcoC1uVGytbboumrlVF24Y3Va0aUcrz7OIoexg2e2wmX_RifYhub-KD7ozTf98Ed6-33ajLGhQNEnh3Eojd9wFTr_dT27w3Abshac6lqoRQhSRoeYRaakeK2D6W4aCniPVOnyLWU8QalKaIiffmT4-PrF-ZEuDtCWCSNb6N1H-XfuOqCqpFURPuwxGH1NDRYdTJOqSsGhcpHd107r9WLv5RsN4FR0W_4QOmXTfEQGlprhNx9Hr6j9N35AKglErJn58732o</recordid><startdate>20121201</startdate><enddate>20121201</enddate><creator>Fibla, Juan J</creator><creator>Cassivi, Stephen D</creator><creator>Brunelli, Alessandro</creator><creator>Decker, Paul A</creator><creator>Allen, Mark S</creator><creator>Darling, Gail E</creator><creator>Landreneau, Rodney J</creator><creator>Putnam, Joe B</creator><general>Elsevier Ireland Ltd</general><general>Elsevier</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><scope>5PM</scope></search><sort><creationdate>20121201</creationdate><title>Re-evaluation of the prognostic value of visceral pleura invasion in Stage IB non-small cell lung cancer using the prospective multicenter ACOSOG Z0030 trial data set</title><author>Fibla, Juan J ; Cassivi, Stephen D ; Brunelli, Alessandro ; Decker, Paul A ; Allen, Mark S ; Darling, Gail E ; Landreneau, Rodney J ; Putnam, Joe B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c552t-9084e3ef8b6edde32ff2432cd547fc775e34c65bc3f1c4d7796c65d1d679d253</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>7th edition TNM classification</topic><topic>Adenocarcinoma - mortality</topic><topic>Adenocarcinoma - pathology</topic><topic>Adenocarcinoma - surgery</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Biological and medical sciences</topic><topic>Carcinoma, Non-Small-Cell Lung - mortality</topic><topic>Carcinoma, Non-Small-Cell Lung - pathology</topic><topic>Carcinoma, Non-Small-Cell Lung - surgery</topic><topic>Female</topic><topic>Hematology, Oncology and Palliative Medicine</topic><topic>Humans</topic><topic>Kaplan-Meier Estimate</topic><topic>Lung Neoplasms - mortality</topic><topic>Lung Neoplasms - pathology</topic><topic>Lung Neoplasms - surgery</topic><topic>Lymph Node Excision</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Multicenter Studies as Topic</topic><topic>Multivariate Analysis</topic><topic>Neoplasm Invasiveness</topic><topic>Neoplasm Staging</topic><topic>Non-small cell lung cancer</topic><topic>Pleura - pathology</topic><topic>Pneumology</topic><topic>Prognosis</topic><topic>Prognostic factor</topic><topic>Proportional Hazards Models</topic><topic>Prospective Studies</topic><topic>Pulmonary/Respiratory</topic><topic>Randomized Controlled Trials as Topic</topic><topic>Tumors</topic><topic>Tumors of the respiratory system and mediastinum</topic><topic>Visceral pleura</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fibla, Juan J</creatorcontrib><creatorcontrib>Cassivi, Stephen D</creatorcontrib><creatorcontrib>Brunelli, Alessandro</creatorcontrib><creatorcontrib>Decker, Paul A</creatorcontrib><creatorcontrib>Allen, Mark S</creatorcontrib><creatorcontrib>Darling, Gail E</creatorcontrib><creatorcontrib>Landreneau, Rodney J</creatorcontrib><creatorcontrib>Putnam, Joe B</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Lung cancer (Amsterdam, Netherlands)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fibla, Juan J</au><au>Cassivi, Stephen D</au><au>Brunelli, Alessandro</au><au>Decker, Paul A</au><au>Allen, Mark S</au><au>Darling, Gail E</au><au>Landreneau, Rodney J</au><au>Putnam, Joe B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Re-evaluation of the prognostic value of visceral pleura invasion in Stage IB non-small cell lung cancer using the prospective multicenter ACOSOG Z0030 trial data set</atitle><jtitle>Lung cancer (Amsterdam, Netherlands)</jtitle><addtitle>Lung Cancer</addtitle><date>2012-12-01</date><risdate>2012</risdate><volume>78</volume><issue>3</issue><spage>259</spage><epage>262</epage><pages>259-262</pages><issn>0169-5002</issn><eissn>1872-8332</eissn><coden>LUCAE5</coden><abstract>Abstract Purpose This study seeks to clarify the modern prognostic significance of visceral pleura invasion (VPI) in Stage IB (T2aN0M0) non-small cell lung cancer (NSCLC) within the context of the 7th edition TNM classification using the data set from a recent prospective multicenter trial. Patients and methods 1111 early-stage NSCLC patients participating in the ACOSOG Z0030 trial (1990–2004) underwent curative pulmonary resection. After excluding T2b tumours (&gt;5 cm and ≤7 cm) and non-size-based T2 factors other than VPI, 289 patients were categorized as Stage IB NSCLC – T2aN0M0 – according to the AJCC 7th edition classification. The patients were divided into three groups according to size and VPI: tumours ≤ 3 cm with VPI (Group I, “VPI-alone”, n = 83), tumours &gt; 3 cm and ≤5 cm without VPI (Group II, “Size-alone”, n = 156), and tumours &gt; 3 cm and ≤5 cm with VPI (Group III, “VPI + Size”, n = 50). Multivariate Cox regression analysis was used to assess the association of VPI and size with survival, adjusting for age, gender, histology and type of resection. Results VPI in Stage IB was identified in 133 patients (46.0%). Survival analysis in these patients identified an optimal cutpoint for survival based on size of 3.1 cm. Group III (VPI + Size) had a 5-year survival rate of 55.0% significantly shorter when compared to Group I (VPI-alone = 68.3%, p = 0.009), and Group II (Size-alone = 67.2%, p = 0.021). No difference was found between Groups I and II. Multivariable analysis showed that VPI associated with size was an independent negative prognostic factor of long-term survival, along with older age and limited resection. Conclusions Stage IB patients with VPI and tumours &gt;3 cm and ≤5 cm have significantly worse prognosis than those with ‘T2a’ tumours on the basis of VPI or tumour size alone. This finding would suggest upstaging these patients from the current IB status to Stage IIA.</abstract><cop>Oxford</cop><pub>Elsevier Ireland Ltd</pub><pmid>23040416</pmid><doi>10.1016/j.lungcan.2012.09.010</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record>
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subjects 7th edition TNM classification
Adenocarcinoma - mortality
Adenocarcinoma - pathology
Adenocarcinoma - surgery
Adult
Aged
Aged, 80 and over
Biological and medical sciences
Carcinoma, Non-Small-Cell Lung - mortality
Carcinoma, Non-Small-Cell Lung - pathology
Carcinoma, Non-Small-Cell Lung - surgery
Female
Hematology, Oncology and Palliative Medicine
Humans
Kaplan-Meier Estimate
Lung Neoplasms - mortality
Lung Neoplasms - pathology
Lung Neoplasms - surgery
Lymph Node Excision
Male
Medical sciences
Middle Aged
Multicenter Studies as Topic
Multivariate Analysis
Neoplasm Invasiveness
Neoplasm Staging
Non-small cell lung cancer
Pleura - pathology
Pneumology
Prognosis
Prognostic factor
Proportional Hazards Models
Prospective Studies
Pulmonary/Respiratory
Randomized Controlled Trials as Topic
Tumors
Tumors of the respiratory system and mediastinum
Visceral pleura
title Re-evaluation of the prognostic value of visceral pleura invasion in Stage IB non-small cell lung cancer using the prospective multicenter ACOSOG Z0030 trial data set
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