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Leptomeningeal metastases from NSCLC
BackgroundLeptomeningeal metastases (LM) from non‐small cell lung cancer (NSCLC) are associated with poor prognosis and optimal treatment for this subgroup of NSCLC patients is controversial. The purpose of this study is to evaluate treatment options and prognostic factors of NSCLC patients with LM....
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Published in: | Thoracic cancer 2015-07, Vol.6 (4), p.407-412 |
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creator | Xu, Qinghua Chen, Xiu Qian, Danwen Wang, Yongsheng Meng, Shuyan Liu, Hui Zhou, Caicun |
description | BackgroundLeptomeningeal metastases (LM) from non‐small cell lung cancer (NSCLC) are associated with poor prognosis and optimal treatment for this subgroup of NSCLC patients is controversial. The purpose of this study is to evaluate treatment options and prognostic factors of NSCLC patients with LM.MethodsWe retrospectively analyzed data of 108 patients who had been diagnosed with LM from NSCLC between May 2006 and August 2013.ResultsThe median survival time (MST) of the 108 patients was 5.3 months, and the one‐year survival rate was 23.7%. Forty‐nine patients received whole brain radiotherapy (WBRT) and the MST of patients who received WBRT and those who did not were 6.4 and 4.3 months, respectively. Forty‐two patients were treated with epidermal growth factor receptor‐tyrosine kinase inhibitors (EGFR‐TKIs) after being diagnosed with LM. These patients had prolonged survival (11.1 vs. 4.4 months). Patients who received concomitant WBRT and EGFR‐TKIs had the longest MST (12.3 months). Eastern Cooperative Oncology Group performance status, whether patients received WBRT, and/or EGFR‐TKIs were independent prognostic factors for patients with LM from NSCLC.ConclusionWBRT, EGFR‐TKIs or combined therapy, could lead to better clinical outcomes for NSCLC patients with LM. EGFR‐TKIs plus WBRT has the potential to be the standard strategy for LM in NSCLC patients. |
doi_str_mv | 10.1111/1759-7714.12188 |
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The purpose of this study is to evaluate treatment options and prognostic factors of NSCLC patients with LM.MethodsWe retrospectively analyzed data of 108 patients who had been diagnosed with LM from NSCLC between May 2006 and August 2013.ResultsThe median survival time (MST) of the 108 patients was 5.3 months, and the one‐year survival rate was 23.7%. Forty‐nine patients received whole brain radiotherapy (WBRT) and the MST of patients who received WBRT and those who did not were 6.4 and 4.3 months, respectively. Forty‐two patients were treated with epidermal growth factor receptor‐tyrosine kinase inhibitors (EGFR‐TKIs) after being diagnosed with LM. These patients had prolonged survival (11.1 vs. 4.4 months). Patients who received concomitant WBRT and EGFR‐TKIs had the longest MST (12.3 months). Eastern Cooperative Oncology Group performance status, whether patients received WBRT, and/or EGFR‐TKIs were independent prognostic factors for patients with LM from NSCLC.ConclusionWBRT, EGFR‐TKIs or combined therapy, could lead to better clinical outcomes for NSCLC patients with LM. EGFR‐TKIs plus WBRT has the potential to be the standard strategy for LM in NSCLC patients.</description><identifier>ISSN: 1759-7706</identifier><identifier>EISSN: 1759-7714</identifier><identifier>DOI: 10.1111/1759-7714.12188</identifier><language>eng</language><publisher>Tianjin: John Wiley & Sons, Inc</publisher><subject>Age ; Cancer therapies ; Chemotherapy ; Epidermal growth factor ; Gender ; Histology ; Lung cancer ; Medical prognosis ; Metastasis ; Mutation ; NMR ; Nuclear magnetic resonance ; Oncology ; Patients ; Radiation therapy</subject><ispartof>Thoracic cancer, 2015-07, Vol.6 (4), p.407-412</ispartof><rights>2015. This work is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2289751503/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2289751503?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,25753,27924,27925,37012,44590,75126</link.rule.ids></links><search><creatorcontrib>Xu, Qinghua</creatorcontrib><creatorcontrib>Chen, Xiu</creatorcontrib><creatorcontrib>Qian, Danwen</creatorcontrib><creatorcontrib>Wang, Yongsheng</creatorcontrib><creatorcontrib>Meng, Shuyan</creatorcontrib><creatorcontrib>Liu, Hui</creatorcontrib><creatorcontrib>Zhou, Caicun</creatorcontrib><title>Leptomeningeal metastases from NSCLC</title><title>Thoracic cancer</title><description>BackgroundLeptomeningeal metastases (LM) from non‐small cell lung cancer (NSCLC) are associated with poor prognosis and optimal treatment for this subgroup of NSCLC patients is controversial. The purpose of this study is to evaluate treatment options and prognostic factors of NSCLC patients with LM.MethodsWe retrospectively analyzed data of 108 patients who had been diagnosed with LM from NSCLC between May 2006 and August 2013.ResultsThe median survival time (MST) of the 108 patients was 5.3 months, and the one‐year survival rate was 23.7%. Forty‐nine patients received whole brain radiotherapy (WBRT) and the MST of patients who received WBRT and those who did not were 6.4 and 4.3 months, respectively. Forty‐two patients were treated with epidermal growth factor receptor‐tyrosine kinase inhibitors (EGFR‐TKIs) after being diagnosed with LM. These patients had prolonged survival (11.1 vs. 4.4 months). Patients who received concomitant WBRT and EGFR‐TKIs had the longest MST (12.3 months). Eastern Cooperative Oncology Group performance status, whether patients received WBRT, and/or EGFR‐TKIs were independent prognostic factors for patients with LM from NSCLC.ConclusionWBRT, EGFR‐TKIs or combined therapy, could lead to better clinical outcomes for NSCLC patients with LM. EGFR‐TKIs plus WBRT has the potential to be the standard strategy for LM in NSCLC patients.</description><subject>Age</subject><subject>Cancer therapies</subject><subject>Chemotherapy</subject><subject>Epidermal growth factor</subject><subject>Gender</subject><subject>Histology</subject><subject>Lung cancer</subject><subject>Medical prognosis</subject><subject>Metastasis</subject><subject>Mutation</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Oncology</subject><subject>Patients</subject><subject>Radiation therapy</subject><issn>1759-7706</issn><issn>1759-7714</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNpjYBA3NNAzBAJ9Q3NTS11zc0MTPUMjQwsLJgZOuAgLnG1gxsHAW1ycZQAExhaWBkamnAwqPqkFJfm5qXmZeempiTkKuaklicVAlFqskFaUn6vgF-zs48zDwJqWmFOcyguluRmU3VxDnD10C4ryC0tTi0vis_JLi_KAUvFGRhaW5qaGpgbGxsSpAgBVQTUE</recordid><startdate>20150701</startdate><enddate>20150701</enddate><creator>Xu, Qinghua</creator><creator>Chen, Xiu</creator><creator>Qian, Danwen</creator><creator>Wang, Yongsheng</creator><creator>Meng, Shuyan</creator><creator>Liu, Hui</creator><creator>Zhou, Caicun</creator><general>John Wiley & Sons, Inc</general><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20150701</creationdate><title>Leptomeningeal metastases from NSCLC</title><author>Xu, Qinghua ; Chen, Xiu ; Qian, Danwen ; Wang, Yongsheng ; Meng, Shuyan ; Liu, Hui ; Zhou, Caicun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_journals_22897515033</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Age</topic><topic>Cancer therapies</topic><topic>Chemotherapy</topic><topic>Epidermal growth factor</topic><topic>Gender</topic><topic>Histology</topic><topic>Lung cancer</topic><topic>Medical prognosis</topic><topic>Metastasis</topic><topic>Mutation</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Oncology</topic><topic>Patients</topic><topic>Radiation therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xu, Qinghua</creatorcontrib><creatorcontrib>Chen, Xiu</creatorcontrib><creatorcontrib>Qian, Danwen</creatorcontrib><creatorcontrib>Wang, Yongsheng</creatorcontrib><creatorcontrib>Meng, Shuyan</creatorcontrib><creatorcontrib>Liu, Hui</creatorcontrib><creatorcontrib>Zhou, Caicun</creatorcontrib><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Health and Medical</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>Thoracic cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xu, Qinghua</au><au>Chen, Xiu</au><au>Qian, Danwen</au><au>Wang, Yongsheng</au><au>Meng, Shuyan</au><au>Liu, Hui</au><au>Zhou, Caicun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Leptomeningeal metastases from NSCLC</atitle><jtitle>Thoracic cancer</jtitle><date>2015-07-01</date><risdate>2015</risdate><volume>6</volume><issue>4</issue><spage>407</spage><epage>412</epage><pages>407-412</pages><issn>1759-7706</issn><eissn>1759-7714</eissn><abstract>BackgroundLeptomeningeal metastases (LM) from non‐small cell lung cancer (NSCLC) are associated with poor prognosis and optimal treatment for this subgroup of NSCLC patients is controversial. The purpose of this study is to evaluate treatment options and prognostic factors of NSCLC patients with LM.MethodsWe retrospectively analyzed data of 108 patients who had been diagnosed with LM from NSCLC between May 2006 and August 2013.ResultsThe median survival time (MST) of the 108 patients was 5.3 months, and the one‐year survival rate was 23.7%. Forty‐nine patients received whole brain radiotherapy (WBRT) and the MST of patients who received WBRT and those who did not were 6.4 and 4.3 months, respectively. Forty‐two patients were treated with epidermal growth factor receptor‐tyrosine kinase inhibitors (EGFR‐TKIs) after being diagnosed with LM. These patients had prolonged survival (11.1 vs. 4.4 months). Patients who received concomitant WBRT and EGFR‐TKIs had the longest MST (12.3 months). Eastern Cooperative Oncology Group performance status, whether patients received WBRT, and/or EGFR‐TKIs were independent prognostic factors for patients with LM from NSCLC.ConclusionWBRT, EGFR‐TKIs or combined therapy, could lead to better clinical outcomes for NSCLC patients with LM. EGFR‐TKIs plus WBRT has the potential to be the standard strategy for LM in NSCLC patients.</abstract><cop>Tianjin</cop><pub>John Wiley & Sons, Inc</pub><doi>10.1111/1759-7714.12188</doi><oa>free_for_read</oa></addata></record> |
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subjects | Age Cancer therapies Chemotherapy Epidermal growth factor Gender Histology Lung cancer Medical prognosis Metastasis Mutation NMR Nuclear magnetic resonance Oncology Patients Radiation therapy |
title | Leptomeningeal metastases from NSCLC |
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