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Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) are effective for leptomeningeal metastasis from non-small cell lung cancer patients with sensitive EGFR mutation or other predictive factors of good response for EGFR TKI
Abstract The purpose of this study was to demonstrate the beneficial effect of epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) in the treatment of leptomeningeal metastasis (LM) for a select group of non-small cell lung cancer (NSCLC) patients who had a sensitive EGFR mutat...
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Published in: | Lung cancer (Amsterdam, Netherlands) Netherlands), 2009-07, Vol.65 (1), p.80-84 |
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creator | Yi, Hyeon Gyu Kim, Hye Jin Kim, Yu Jung Han, Sae-Won Oh, Do-Youn Lee, Se-Hoon Kim, Dong-Wan Im, Seock-Ah Kim, Tae-You Kim, Chul Soo Heo, Dae Seog Bang, Yung-Jue |
description | Abstract The purpose of this study was to demonstrate the beneficial effect of epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) in the treatment of leptomeningeal metastasis (LM) for a select group of non-small cell lung cancer (NSCLC) patients who had a sensitive EGFR mutation or good predictive clinical factors for EGFR TKI treatment. Eleven patients with NSCLC and LM were treated with a standard dose of erlotinib ( n = 9), or higher than standard dose of gefitinib followed by erlotinib ( n = 2). They were treated with various therapies including whole brain radiotherapy or intrathecal chemotherapy for CNS lesion previously and concurrently with EGFR TKI. Nine of 11 patients showed overt improvement in ECOG performance status. Six patients were alive >6 months, and 2 additional patients were alive 2.5+ and 4.4+ months with clinical improvement. Two patients showed responses to higher than standard dose of gefitinib. The median overall survival was not reached. In conclusion, EGFR TKIs are effective in the treatment of LM from NSCLC when patients were selected properly. |
doi_str_mv | 10.1016/j.lungcan.2008.10.016 |
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Eleven patients with NSCLC and LM were treated with a standard dose of erlotinib ( n = 9), or higher than standard dose of gefitinib followed by erlotinib ( n = 2). They were treated with various therapies including whole brain radiotherapy or intrathecal chemotherapy for CNS lesion previously and concurrently with EGFR TKI. Nine of 11 patients showed overt improvement in ECOG performance status. Six patients were alive >6 months, and 2 additional patients were alive 2.5+ and 4.4+ months with clinical improvement. Two patients showed responses to higher than standard dose of gefitinib. The median overall survival was not reached. In conclusion, EGFR TKIs are effective in the treatment of LM from NSCLC when patients were selected properly.</description><identifier>ISSN: 0169-5002</identifier><identifier>EISSN: 1872-8332</identifier><identifier>DOI: 10.1016/j.lungcan.2008.10.016</identifier><identifier>PMID: 19059670</identifier><identifier>CODEN: LUCAE5</identifier><language>eng</language><publisher>Oxford: Elsevier Ireland Ltd</publisher><subject>Adult ; Aged ; Antineoplastic Combined Chemotherapy Protocols - administration & dosage ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Biological and medical sciences ; Carcinoma, Non-Small-Cell Lung - drug therapy ; Carcinoma, Non-Small-Cell Lung - enzymology ; Carcinoma, Non-Small-Cell Lung - pathology ; Epidermal growth factor receptor ; Erlotinib Hydrochloride ; Female ; Hematology, Oncology and Palliative Medicine ; Humans ; Leptomeningeal metastasis ; Lung Neoplasms - drug therapy ; Lung Neoplasms - enzymology ; Lung Neoplasms - genetics ; Lung Neoplasms - pathology ; Male ; Medical sciences ; Meningeal Neoplasms - drug therapy ; Meningeal Neoplasms - enzymology ; Meningeal Neoplasms - genetics ; Meningeal Neoplasms - secondary ; Middle Aged ; Non-small cell lung cancer ; Pneumology ; Protein Kinase Inhibitors - administration & dosage ; Protein Kinase Inhibitors - therapeutic use ; Pulmonary/Respiratory ; Quinazolines - administration & dosage ; Quinazolines - therapeutic use ; Receptor, Epidermal Growth Factor - antagonists & inhibitors ; Receptor, Epidermal Growth Factor - genetics ; Retrospective Studies ; Survival ; Treatment Outcome ; Tumors ; Tumors of the respiratory system and mediastinum ; Tyrosine kinase inhibitor</subject><ispartof>Lung cancer (Amsterdam, Netherlands), 2009-07, Vol.65 (1), p.80-84</ispartof><rights>Elsevier Ireland Ltd</rights><rights>2008 Elsevier Ireland Ltd</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c448t-2827a84a5e6af7d0d07f117357b2e16c371e42808f8d78260c1e216f0564337b3</citedby><cites>FETCH-LOGICAL-c448t-2827a84a5e6af7d0d07f117357b2e16c371e42808f8d78260c1e216f0564337b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21674451$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19059670$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yi, Hyeon Gyu</creatorcontrib><creatorcontrib>Kim, Hye Jin</creatorcontrib><creatorcontrib>Kim, Yu Jung</creatorcontrib><creatorcontrib>Han, Sae-Won</creatorcontrib><creatorcontrib>Oh, Do-Youn</creatorcontrib><creatorcontrib>Lee, Se-Hoon</creatorcontrib><creatorcontrib>Kim, Dong-Wan</creatorcontrib><creatorcontrib>Im, Seock-Ah</creatorcontrib><creatorcontrib>Kim, Tae-You</creatorcontrib><creatorcontrib>Kim, Chul Soo</creatorcontrib><creatorcontrib>Heo, Dae Seog</creatorcontrib><creatorcontrib>Bang, Yung-Jue</creatorcontrib><title>Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) are effective for leptomeningeal metastasis from non-small cell lung cancer patients with sensitive EGFR mutation or other predictive factors of good response for EGFR TKI</title><title>Lung cancer (Amsterdam, Netherlands)</title><addtitle>Lung Cancer</addtitle><description>Abstract The purpose of this study was to demonstrate the beneficial effect of epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) in the treatment of leptomeningeal metastasis (LM) for a select group of non-small cell lung cancer (NSCLC) patients who had a sensitive EGFR mutation or good predictive clinical factors for EGFR TKI treatment. Eleven patients with NSCLC and LM were treated with a standard dose of erlotinib ( n = 9), or higher than standard dose of gefitinib followed by erlotinib ( n = 2). They were treated with various therapies including whole brain radiotherapy or intrathecal chemotherapy for CNS lesion previously and concurrently with EGFR TKI. Nine of 11 patients showed overt improvement in ECOG performance status. Six patients were alive >6 months, and 2 additional patients were alive 2.5+ and 4.4+ months with clinical improvement. Two patients showed responses to higher than standard dose of gefitinib. The median overall survival was not reached. In conclusion, EGFR TKIs are effective in the treatment of LM from NSCLC when patients were selected properly.</description><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic Combined Chemotherapy Protocols - administration & dosage</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Carcinoma, Non-Small-Cell Lung - drug therapy</subject><subject>Carcinoma, Non-Small-Cell Lung - enzymology</subject><subject>Carcinoma, Non-Small-Cell Lung - pathology</subject><subject>Epidermal growth factor receptor</subject><subject>Erlotinib Hydrochloride</subject><subject>Female</subject><subject>Hematology, Oncology and Palliative Medicine</subject><subject>Humans</subject><subject>Leptomeningeal metastasis</subject><subject>Lung Neoplasms - drug therapy</subject><subject>Lung Neoplasms - enzymology</subject><subject>Lung Neoplasms - genetics</subject><subject>Lung Neoplasms - pathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Meningeal Neoplasms - drug therapy</subject><subject>Meningeal Neoplasms - enzymology</subject><subject>Meningeal Neoplasms - genetics</subject><subject>Meningeal Neoplasms - secondary</subject><subject>Middle Aged</subject><subject>Non-small cell lung cancer</subject><subject>Pneumology</subject><subject>Protein Kinase Inhibitors - administration & dosage</subject><subject>Protein Kinase Inhibitors - therapeutic use</subject><subject>Pulmonary/Respiratory</subject><subject>Quinazolines - administration & dosage</subject><subject>Quinazolines - therapeutic use</subject><subject>Receptor, Epidermal Growth Factor - antagonists & inhibitors</subject><subject>Receptor, Epidermal Growth Factor - genetics</subject><subject>Retrospective Studies</subject><subject>Survival</subject><subject>Treatment Outcome</subject><subject>Tumors</subject><subject>Tumors of the respiratory system and mediastinum</subject><subject>Tyrosine kinase inhibitor</subject><issn>0169-5002</issn><issn>1872-8332</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNqFUk1vEzEQXSEQLYWfAPIF1B4S7P2ycwGhKi0VlZCgnC3HO06c7trBs9sqP5w7s8kKJC5IK681fjPvzbzJsteCzwUX9fvtvB3C2powzzlXFJtT9El2KpTMZ6oo8qfZKUUWs4rz_CR7gbjlXEjBF8-zE7Hg1aKW_DT7tdz5BlJnWrZO8bHfMGdsHxNLYGE3Xs6X11ffLli_TxF9AHbvg0FgPmz8yhMA2fndlxu8YCYBA-fA9v4BmKPUdqzQQfBhDUTQQW-QPo_MpdixEMMMibllFugY-2HUkIXEdqb3EHpkj54kIQT0h6qjFtYNPT3HwIgi9psRnqDxE-9BPrLo2DrGhvrAXQx4FHRIJ7Uvs2fOtAivpv9Z9uNqeXf5eXb79frm8tPtzJal6me5yqVRpamgNk42vOHSCSGLSq5yELUtpIAyV1w51UiV19wKyEXteFWXRSFXxVn27lh3l-LPAbDXncexWRMgDqhrWYiyUIqA1RFoacqYwOld8p1Jey24Hv3WWz35rUe_xzBFKe_NRDCsOmj-Zk0GE-DtBDBoTesSzdfjHxyplWVZCcJ9POKAxvHgIWm05ICludIm9LqJ_r9SPvxTwbY-eCK9hz3gNg4p0Ky10Jhrrr-PyznuJlecV1WVF78BpArksg</recordid><startdate>20090701</startdate><enddate>20090701</enddate><creator>Yi, Hyeon Gyu</creator><creator>Kim, Hye Jin</creator><creator>Kim, Yu Jung</creator><creator>Han, Sae-Won</creator><creator>Oh, Do-Youn</creator><creator>Lee, Se-Hoon</creator><creator>Kim, Dong-Wan</creator><creator>Im, Seock-Ah</creator><creator>Kim, Tae-You</creator><creator>Kim, Chul Soo</creator><creator>Heo, Dae Seog</creator><creator>Bang, Yung-Jue</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></search><sort><creationdate>20090701</creationdate><title>Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) are effective for leptomeningeal metastasis from non-small cell lung cancer patients with sensitive EGFR mutation or other predictive factors of good response for EGFR TKI</title><author>Yi, Hyeon Gyu ; Kim, Hye Jin ; Kim, Yu Jung ; Han, Sae-Won ; Oh, Do-Youn ; Lee, Se-Hoon ; Kim, Dong-Wan ; Im, Seock-Ah ; Kim, Tae-You ; Kim, Chul Soo ; Heo, Dae Seog ; Bang, Yung-Jue</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c448t-2827a84a5e6af7d0d07f117357b2e16c371e42808f8d78260c1e216f0564337b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Antineoplastic Combined Chemotherapy Protocols - administration & dosage</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Carcinoma, Non-Small-Cell Lung - drug therapy</topic><topic>Carcinoma, Non-Small-Cell Lung - enzymology</topic><topic>Carcinoma, Non-Small-Cell Lung - pathology</topic><topic>Epidermal growth factor receptor</topic><topic>Erlotinib Hydrochloride</topic><topic>Female</topic><topic>Hematology, Oncology and Palliative Medicine</topic><topic>Humans</topic><topic>Leptomeningeal metastasis</topic><topic>Lung Neoplasms - drug therapy</topic><topic>Lung Neoplasms - enzymology</topic><topic>Lung Neoplasms - genetics</topic><topic>Lung Neoplasms - pathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Meningeal Neoplasms - drug therapy</topic><topic>Meningeal Neoplasms - enzymology</topic><topic>Meningeal Neoplasms - genetics</topic><topic>Meningeal Neoplasms - secondary</topic><topic>Middle Aged</topic><topic>Non-small cell lung cancer</topic><topic>Pneumology</topic><topic>Protein Kinase Inhibitors - administration & dosage</topic><topic>Protein Kinase Inhibitors - therapeutic use</topic><topic>Pulmonary/Respiratory</topic><topic>Quinazolines - administration & dosage</topic><topic>Quinazolines - therapeutic use</topic><topic>Receptor, Epidermal Growth Factor - antagonists & inhibitors</topic><topic>Receptor, Epidermal Growth Factor - genetics</topic><topic>Retrospective Studies</topic><topic>Survival</topic><topic>Treatment Outcome</topic><topic>Tumors</topic><topic>Tumors of the respiratory system and mediastinum</topic><topic>Tyrosine kinase inhibitor</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yi, Hyeon Gyu</creatorcontrib><creatorcontrib>Kim, Hye Jin</creatorcontrib><creatorcontrib>Kim, Yu Jung</creatorcontrib><creatorcontrib>Han, Sae-Won</creatorcontrib><creatorcontrib>Oh, Do-Youn</creatorcontrib><creatorcontrib>Lee, Se-Hoon</creatorcontrib><creatorcontrib>Kim, Dong-Wan</creatorcontrib><creatorcontrib>Im, Seock-Ah</creatorcontrib><creatorcontrib>Kim, Tae-You</creatorcontrib><creatorcontrib>Kim, Chul Soo</creatorcontrib><creatorcontrib>Heo, Dae Seog</creatorcontrib><creatorcontrib>Bang, Yung-Jue</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>Lung cancer (Amsterdam, Netherlands)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yi, Hyeon Gyu</au><au>Kim, Hye Jin</au><au>Kim, Yu Jung</au><au>Han, Sae-Won</au><au>Oh, Do-Youn</au><au>Lee, Se-Hoon</au><au>Kim, Dong-Wan</au><au>Im, Seock-Ah</au><au>Kim, Tae-You</au><au>Kim, Chul Soo</au><au>Heo, Dae Seog</au><au>Bang, Yung-Jue</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) are effective for leptomeningeal metastasis from non-small cell lung cancer patients with sensitive EGFR mutation or other predictive factors of good response for EGFR TKI</atitle><jtitle>Lung cancer (Amsterdam, Netherlands)</jtitle><addtitle>Lung Cancer</addtitle><date>2009-07-01</date><risdate>2009</risdate><volume>65</volume><issue>1</issue><spage>80</spage><epage>84</epage><pages>80-84</pages><issn>0169-5002</issn><eissn>1872-8332</eissn><coden>LUCAE5</coden><abstract>Abstract The purpose of this study was to demonstrate the beneficial effect of epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) in the treatment of leptomeningeal metastasis (LM) for a select group of non-small cell lung cancer (NSCLC) patients who had a sensitive EGFR mutation or good predictive clinical factors for EGFR TKI treatment. Eleven patients with NSCLC and LM were treated with a standard dose of erlotinib ( n = 9), or higher than standard dose of gefitinib followed by erlotinib ( n = 2). They were treated with various therapies including whole brain radiotherapy or intrathecal chemotherapy for CNS lesion previously and concurrently with EGFR TKI. Nine of 11 patients showed overt improvement in ECOG performance status. Six patients were alive >6 months, and 2 additional patients were alive 2.5+ and 4.4+ months with clinical improvement. Two patients showed responses to higher than standard dose of gefitinib. The median overall survival was not reached. In conclusion, EGFR TKIs are effective in the treatment of LM from NSCLC when patients were selected properly.</abstract><cop>Oxford</cop><pub>Elsevier Ireland Ltd</pub><pmid>19059670</pmid><doi>10.1016/j.lungcan.2008.10.016</doi><tpages>5</tpages></addata></record> |
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subjects | Adult Aged Antineoplastic Combined Chemotherapy Protocols - administration & dosage Antineoplastic Combined Chemotherapy Protocols - therapeutic use Biological and medical sciences Carcinoma, Non-Small-Cell Lung - drug therapy Carcinoma, Non-Small-Cell Lung - enzymology Carcinoma, Non-Small-Cell Lung - pathology Epidermal growth factor receptor Erlotinib Hydrochloride Female Hematology, Oncology and Palliative Medicine Humans Leptomeningeal metastasis Lung Neoplasms - drug therapy Lung Neoplasms - enzymology Lung Neoplasms - genetics Lung Neoplasms - pathology Male Medical sciences Meningeal Neoplasms - drug therapy Meningeal Neoplasms - enzymology Meningeal Neoplasms - genetics Meningeal Neoplasms - secondary Middle Aged Non-small cell lung cancer Pneumology Protein Kinase Inhibitors - administration & dosage Protein Kinase Inhibitors - therapeutic use Pulmonary/Respiratory Quinazolines - administration & dosage Quinazolines - therapeutic use Receptor, Epidermal Growth Factor - antagonists & inhibitors Receptor, Epidermal Growth Factor - genetics Retrospective Studies Survival Treatment Outcome Tumors Tumors of the respiratory system and mediastinum Tyrosine kinase inhibitor |
title | Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) are effective for leptomeningeal metastasis from non-small cell lung cancer patients with sensitive EGFR mutation or other predictive factors of good response for EGFR TKI |
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