Smoking History as a Predictor of Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors in Patients with Non-Small Cell Lung Cancer Harboring EGFR Mutations
Background: Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKIs) therapy has been recognized as the standard treatment for patients with non-small cell lung cancer (NSCLC) harboring EGFR mutations. However, resistance to EGFR-TKIs has been observed in certain subpopulations of th...
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Veröffentlicht in: | Oncology 2018-01, Vol.95 (2), p.109-115 |
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creator | Nishinarita, Noriko Igawa, Satoshi Kasajima, Masashi Kusuhara, Seiichiro Harada, Shinya Okuma, Yuriko Sugita, Keisuke Ozawa, Takahiro Fukui, Tomoya Mitsufuji, Hisashi Yokoba, Masanori Katagiri, Masato Kubota, Masaru Sasaki, Jiichiro Naoki, Katsuhiko |
description | Background: Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKIs) therapy has been recognized as the standard treatment for patients with non-small cell lung cancer (NSCLC) harboring EGFR mutations. However, resistance to EGFR-TKIs has been observed in certain subpopulations of these patients. We aimed to evaluate the impact of smoking history on the efficacy of EGFR-TKIs. Methods: The records of patients (n = 248) with NSCLC harboring activating EGFR mutations who were treated with gefitinib or erlotinib at our institution between March 2010 and June 2016 were retrospectively reviewed, and the treatment outcomes were evaluated. Results: The overall response rate and median progression-free survival (PFS) were 59.7% and 10.7 months, respectively. The overall response rate was significantly higher in the ex- and nonsmokers than in the current smokers (64.6 vs. 51.1%, p = 0.038). PFS also differed significantly between the current smokers and the ex- and nonsmokers (12.4 vs. 7.4 months, p = 0.016). Multivariate analysis identified smoking history as an independent predictor of PFS and overall survival. Conclusion: The clinical data obtained in this study provide a valuable rationale for considering smoking history as a predictor of the efficacy of EGFR-TKI in NSCLC patients harboring activating EGFR mutations. |
doi_str_mv | 10.1159/000488594 |
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However, resistance to EGFR-TKIs has been observed in certain subpopulations of these patients. We aimed to evaluate the impact of smoking history on the efficacy of EGFR-TKIs. Methods: The records of patients (n = 248) with NSCLC harboring activating EGFR mutations who were treated with gefitinib or erlotinib at our institution between March 2010 and June 2016 were retrospectively reviewed, and the treatment outcomes were evaluated. Results: The overall response rate and median progression-free survival (PFS) were 59.7% and 10.7 months, respectively. The overall response rate was significantly higher in the ex- and nonsmokers than in the current smokers (64.6 vs. 51.1%, p = 0.038). PFS also differed significantly between the current smokers and the ex- and nonsmokers (12.4 vs. 7.4 months, p = 0.016). Multivariate analysis identified smoking history as an independent predictor of PFS and overall survival. Conclusion: The clinical data obtained in this study provide a valuable rationale for considering smoking history as a predictor of the efficacy of EGFR-TKI in NSCLC patients harboring activating EGFR mutations.</description><identifier>ISSN: 0030-2414</identifier><identifier>EISSN: 1423-0232</identifier><identifier>DOI: 10.1159/000488594</identifier><identifier>PMID: 29698957</identifier><language>eng</language><publisher>Basel, Switzerland: S. Karger AG</publisher><subject>Afatinib ; Care and treatment ; Clinical Study ; Development and progression ; Epidermal growth factors ; Erlotinib ; Gefitinib ; Genetic aspects ; Lung cancer ; Non-small cell lung cancer ; Phenols (Class of compounds) ; Small cell lung cancer ; Smokers ; Tyrosine</subject><ispartof>Oncology, 2018-01, Vol.95 (2), p.109-115</ispartof><rights>2018 S. Karger AG, Basel</rights><rights>2018 S. Karger AG, Basel.</rights><rights>COPYRIGHT 2018 S. Karger AG</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c365t-8be46f70940df442a3e30ec72b1abf464380a2596d5d69fac7d562abfbabb3983</citedby><cites>FETCH-LOGICAL-c365t-8be46f70940df442a3e30ec72b1abf464380a2596d5d69fac7d562abfbabb3983</cites><orcidid>0000-0002-5294-7832</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,2423,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29698957$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nishinarita, Noriko</creatorcontrib><creatorcontrib>Igawa, Satoshi</creatorcontrib><creatorcontrib>Kasajima, Masashi</creatorcontrib><creatorcontrib>Kusuhara, Seiichiro</creatorcontrib><creatorcontrib>Harada, Shinya</creatorcontrib><creatorcontrib>Okuma, Yuriko</creatorcontrib><creatorcontrib>Sugita, Keisuke</creatorcontrib><creatorcontrib>Ozawa, Takahiro</creatorcontrib><creatorcontrib>Fukui, Tomoya</creatorcontrib><creatorcontrib>Mitsufuji, Hisashi</creatorcontrib><creatorcontrib>Yokoba, Masanori</creatorcontrib><creatorcontrib>Katagiri, Masato</creatorcontrib><creatorcontrib>Kubota, Masaru</creatorcontrib><creatorcontrib>Sasaki, Jiichiro</creatorcontrib><creatorcontrib>Naoki, Katsuhiko</creatorcontrib><title>Smoking History as a Predictor of Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors in Patients with Non-Small Cell Lung Cancer Harboring EGFR Mutations</title><title>Oncology</title><addtitle>Oncology</addtitle><description>Background: Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKIs) therapy has been recognized as the standard treatment for patients with non-small cell lung cancer (NSCLC) harboring EGFR mutations. However, resistance to EGFR-TKIs has been observed in certain subpopulations of these patients. We aimed to evaluate the impact of smoking history on the efficacy of EGFR-TKIs. Methods: The records of patients (n = 248) with NSCLC harboring activating EGFR mutations who were treated with gefitinib or erlotinib at our institution between March 2010 and June 2016 were retrospectively reviewed, and the treatment outcomes were evaluated. Results: The overall response rate and median progression-free survival (PFS) were 59.7% and 10.7 months, respectively. The overall response rate was significantly higher in the ex- and nonsmokers than in the current smokers (64.6 vs. 51.1%, p = 0.038). PFS also differed significantly between the current smokers and the ex- and nonsmokers (12.4 vs. 7.4 months, p = 0.016). Multivariate analysis identified smoking history as an independent predictor of PFS and overall survival. Conclusion: The clinical data obtained in this study provide a valuable rationale for considering smoking history as a predictor of the efficacy of EGFR-TKI in NSCLC patients harboring activating EGFR mutations.</description><subject>Afatinib</subject><subject>Care and treatment</subject><subject>Clinical Study</subject><subject>Development and progression</subject><subject>Epidermal growth factors</subject><subject>Erlotinib</subject><subject>Gefitinib</subject><subject>Genetic aspects</subject><subject>Lung cancer</subject><subject>Non-small cell lung cancer</subject><subject>Phenols (Class of compounds)</subject><subject>Small cell lung cancer</subject><subject>Smokers</subject><subject>Tyrosine</subject><issn>0030-2414</issn><issn>1423-0232</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNptkUtv1DAUhS0EokNhwR4hS0gIFgE_k3hZRfOoGGjVlnXkJDczpokd7ETV_B1-KZ6mzIqN7avznXuvfBB6S8kXSqX6SggReS6VeIYWVDCeEMbZc7QghJOECSrO0KsQfkUskyJ9ic6YSlWuZLZAf257d2_sDm9MGJ0_YB2wxtceGlPHGrsWLwfTgO91h9fePYx7vNKP0g3UMBwfdwfvgrGAvxmrA-BLuzeViUrAxuJrPRqwY8APJnp_OJvcxl4dLiAe2ymOLrStweON9pXzx12W69UN_j6N0elseI1etLoL8ObpPkc_V8u7YpNsr9aXxcU2qXkqxySvQKRtRpQgTSsE0xw4gTpjFdVVK1LBc6KZVGkjm1S1us4ambIoVbqquMr5Ofo09x28-z1BGMvehDpuqS24KZSMcMaVEpmM6McZ3ekOyj3obtwH102P-5YXUimaS5ode36ewTp-UfDQloM3vfaHkpLymF15yi6y75_mT1UPzYn8F1YE3s3AvfY78Cfg5P_wX_mq2M5EOTQt_wsXHqou</recordid><startdate>20180101</startdate><enddate>20180101</enddate><creator>Nishinarita, Noriko</creator><creator>Igawa, Satoshi</creator><creator>Kasajima, Masashi</creator><creator>Kusuhara, Seiichiro</creator><creator>Harada, Shinya</creator><creator>Okuma, Yuriko</creator><creator>Sugita, Keisuke</creator><creator>Ozawa, Takahiro</creator><creator>Fukui, Tomoya</creator><creator>Mitsufuji, Hisashi</creator><creator>Yokoba, Masanori</creator><creator>Katagiri, Masato</creator><creator>Kubota, Masaru</creator><creator>Sasaki, Jiichiro</creator><creator>Naoki, Katsuhiko</creator><general>S. Karger AG</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-5294-7832</orcidid></search><sort><creationdate>20180101</creationdate><title>Smoking History as a Predictor of Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors in Patients with Non-Small Cell Lung Cancer Harboring EGFR Mutations</title><author>Nishinarita, Noriko ; Igawa, Satoshi ; Kasajima, Masashi ; Kusuhara, Seiichiro ; Harada, Shinya ; Okuma, Yuriko ; Sugita, Keisuke ; Ozawa, Takahiro ; Fukui, Tomoya ; Mitsufuji, Hisashi ; Yokoba, Masanori ; Katagiri, Masato ; Kubota, Masaru ; Sasaki, Jiichiro ; Naoki, Katsuhiko</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c365t-8be46f70940df442a3e30ec72b1abf464380a2596d5d69fac7d562abfbabb3983</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Afatinib</topic><topic>Care and treatment</topic><topic>Clinical Study</topic><topic>Development and progression</topic><topic>Epidermal growth factors</topic><topic>Erlotinib</topic><topic>Gefitinib</topic><topic>Genetic aspects</topic><topic>Lung cancer</topic><topic>Non-small cell lung cancer</topic><topic>Phenols (Class of compounds)</topic><topic>Small cell lung cancer</topic><topic>Smokers</topic><topic>Tyrosine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nishinarita, Noriko</creatorcontrib><creatorcontrib>Igawa, Satoshi</creatorcontrib><creatorcontrib>Kasajima, Masashi</creatorcontrib><creatorcontrib>Kusuhara, Seiichiro</creatorcontrib><creatorcontrib>Harada, Shinya</creatorcontrib><creatorcontrib>Okuma, Yuriko</creatorcontrib><creatorcontrib>Sugita, Keisuke</creatorcontrib><creatorcontrib>Ozawa, Takahiro</creatorcontrib><creatorcontrib>Fukui, Tomoya</creatorcontrib><creatorcontrib>Mitsufuji, Hisashi</creatorcontrib><creatorcontrib>Yokoba, Masanori</creatorcontrib><creatorcontrib>Katagiri, Masato</creatorcontrib><creatorcontrib>Kubota, Masaru</creatorcontrib><creatorcontrib>Sasaki, Jiichiro</creatorcontrib><creatorcontrib>Naoki, Katsuhiko</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nishinarita, Noriko</au><au>Igawa, Satoshi</au><au>Kasajima, Masashi</au><au>Kusuhara, Seiichiro</au><au>Harada, Shinya</au><au>Okuma, Yuriko</au><au>Sugita, Keisuke</au><au>Ozawa, Takahiro</au><au>Fukui, Tomoya</au><au>Mitsufuji, Hisashi</au><au>Yokoba, Masanori</au><au>Katagiri, Masato</au><au>Kubota, Masaru</au><au>Sasaki, Jiichiro</au><au>Naoki, Katsuhiko</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Smoking History as a Predictor of Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors in Patients with Non-Small Cell Lung Cancer Harboring EGFR Mutations</atitle><jtitle>Oncology</jtitle><addtitle>Oncology</addtitle><date>2018-01-01</date><risdate>2018</risdate><volume>95</volume><issue>2</issue><spage>109</spage><epage>115</epage><pages>109-115</pages><issn>0030-2414</issn><eissn>1423-0232</eissn><abstract>Background: Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKIs) therapy has been recognized as the standard treatment for patients with non-small cell lung cancer (NSCLC) harboring EGFR mutations. However, resistance to EGFR-TKIs has been observed in certain subpopulations of these patients. We aimed to evaluate the impact of smoking history on the efficacy of EGFR-TKIs. Methods: The records of patients (n = 248) with NSCLC harboring activating EGFR mutations who were treated with gefitinib or erlotinib at our institution between March 2010 and June 2016 were retrospectively reviewed, and the treatment outcomes were evaluated. Results: The overall response rate and median progression-free survival (PFS) were 59.7% and 10.7 months, respectively. The overall response rate was significantly higher in the ex- and nonsmokers than in the current smokers (64.6 vs. 51.1%, p = 0.038). PFS also differed significantly between the current smokers and the ex- and nonsmokers (12.4 vs. 7.4 months, p = 0.016). Multivariate analysis identified smoking history as an independent predictor of PFS and overall survival. Conclusion: The clinical data obtained in this study provide a valuable rationale for considering smoking history as a predictor of the efficacy of EGFR-TKI in NSCLC patients harboring activating EGFR mutations.</abstract><cop>Basel, Switzerland</cop><pub>S. Karger AG</pub><pmid>29698957</pmid><doi>10.1159/000488594</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-5294-7832</orcidid></addata></record> |
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subjects | Afatinib Care and treatment Clinical Study Development and progression Epidermal growth factors Erlotinib Gefitinib Genetic aspects Lung cancer Non-small cell lung cancer Phenols (Class of compounds) Small cell lung cancer Smokers Tyrosine |
title | Smoking History as a Predictor of Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors in Patients with Non-Small Cell Lung Cancer Harboring EGFR Mutations |
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