Comparison of efficacy of gefitinib and osimertinib for untreated EGFR mutation-positive non-small-cell lung cancer in patients with poor performance status
There is a dearth of studies on the efficacy and safety of the tyrosine kinase inhibitors osimertinib (OSI) and gefitinib (GEF) in treating epidermal growth factor receptor (EGFR) mutation-positive non-small cell lung cancer (NSCLC), even in patients with poor performance status (PS). We retrospecti...
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creator | Nakashima, Kazuhisa Kodama, Hiroaki Murakami, Haruyasu Takahashi, Toshiaki Kawakado, Keita Yanagawa, Takashi Kitani, Kashu Hottta, Takamasa Abe, Masaaki Hamai, Kosuke Tanimoto, Takuya Ishikawa, Nobuhisa Tamura, Tomoki Kuyama, Shoichi Isobe, Takeshi Tsubata, Yukari |
description | There is a dearth of studies on the efficacy and safety of the tyrosine kinase inhibitors osimertinib (OSI) and gefitinib (GEF) in treating epidermal growth factor receptor (EGFR) mutation-positive non-small cell lung cancer (NSCLC), even in patients with poor performance status (PS).
We retrospectively reviewed and compared data of 113 patients with EGFR mutation-positive NSCLC with Eastern Cooperative Oncology Group PS 2–4 who were administered OSI 80 mg/day or GEF 250 mg/day from May 2016 to March 2022.
The GEF group (39 patients; median age: 74 years) included 20 patients with a PS of 2, 17 with a PS of 3, and 2 with a PS of 4. The OSI group (74 patients; median age: 76 years) included 48 patients with a PS of 2, 24 with a PS of 3, and 2 with a PS of 4. The overall response rates were 69% and 66% in the GEF and OSI groups, respectively. The disease control and PS improvement rates were 89% and 51% in both groups, respectively. The median progression-free survival in the GEF and OSI groups was 6.9 and 9.2 months, respectively (p = 0.15). The OSI group experienced better overall survival than the GEF group (median: 20.9 vs. 13.0 months, p = 0.0031). The incidence of pneumonitis was 10% and 11% in the GEF and OSI groups, respectively. One treatment-related death owing to pneumonitis occurred in the GEF group.
OSI may be a useful treatment for untreated EGFR mutation-positive NSCLC with poor PS. |
doi_str_mv | 10.1016/j.resinv.2024.09.010 |
format | Article |
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We retrospectively reviewed and compared data of 113 patients with EGFR mutation-positive NSCLC with Eastern Cooperative Oncology Group PS 2–4 who were administered OSI 80 mg/day or GEF 250 mg/day from May 2016 to March 2022.
The GEF group (39 patients; median age: 74 years) included 20 patients with a PS of 2, 17 with a PS of 3, and 2 with a PS of 4. The OSI group (74 patients; median age: 76 years) included 48 patients with a PS of 2, 24 with a PS of 3, and 2 with a PS of 4. The overall response rates were 69% and 66% in the GEF and OSI groups, respectively. The disease control and PS improvement rates were 89% and 51% in both groups, respectively. The median progression-free survival in the GEF and OSI groups was 6.9 and 9.2 months, respectively (p = 0.15). The OSI group experienced better overall survival than the GEF group (median: 20.9 vs. 13.0 months, p = 0.0031). The incidence of pneumonitis was 10% and 11% in the GEF and OSI groups, respectively. One treatment-related death owing to pneumonitis occurred in the GEF group.
OSI may be a useful treatment for untreated EGFR mutation-positive NSCLC with poor PS.</description><identifier>ISSN: 2212-5345</identifier><identifier>ISSN: 2212-5353</identifier><identifier>EISSN: 2212-5353</identifier><identifier>DOI: 10.1016/j.resinv.2024.09.010</identifier><identifier>PMID: 39366122</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Acrylamides - therapeutic use ; Aged ; Aged, 80 and over ; Aniline Compounds - therapeutic use ; Antineoplastic Agents - therapeutic use ; Carcinoma, Non-Small-Cell Lung - drug therapy ; Carcinoma, Non-Small-Cell Lung - genetics ; EGFR mutation ; ErbB Receptors - genetics ; Female ; Gefitinib ; Gefitinib - administration & dosage ; Gefitinib - therapeutic use ; Humans ; Indoles ; Lung Neoplasms - drug therapy ; Lung Neoplasms - genetics ; Lung Neoplasms - mortality ; Male ; Middle Aged ; Mutation ; Non-small-cell lung cancer ; Osimertinib ; Poor performance status ; Protein Kinase Inhibitors - administration & dosage ; Protein Kinase Inhibitors - therapeutic use ; Pyrimidines ; Retrospective Studies ; Treatment Outcome</subject><ispartof>Respiratory investigation, 2024-11, Vol.62 (6), p.1137-1141</ispartof><rights>2024 [The Author]</rights><rights>Copyright © 2024 [The Author]. Published by Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c287t-e9dbc31c20353b6f014dfa9528aa0a881d41816d394c99cf7daec0c340a9543f3</cites><orcidid>0000-0002-2480-9029 ; 0000-0002-4260-2849 ; 0000-0002-3498-9772 ; 0000-0002-0208-2180</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39366122$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nakashima, Kazuhisa</creatorcontrib><creatorcontrib>Kodama, Hiroaki</creatorcontrib><creatorcontrib>Murakami, Haruyasu</creatorcontrib><creatorcontrib>Takahashi, Toshiaki</creatorcontrib><creatorcontrib>Kawakado, Keita</creatorcontrib><creatorcontrib>Yanagawa, Takashi</creatorcontrib><creatorcontrib>Kitani, Kashu</creatorcontrib><creatorcontrib>Hottta, Takamasa</creatorcontrib><creatorcontrib>Abe, Masaaki</creatorcontrib><creatorcontrib>Hamai, Kosuke</creatorcontrib><creatorcontrib>Tanimoto, Takuya</creatorcontrib><creatorcontrib>Ishikawa, Nobuhisa</creatorcontrib><creatorcontrib>Tamura, Tomoki</creatorcontrib><creatorcontrib>Kuyama, Shoichi</creatorcontrib><creatorcontrib>Isobe, Takeshi</creatorcontrib><creatorcontrib>Tsubata, Yukari</creatorcontrib><title>Comparison of efficacy of gefitinib and osimertinib for untreated EGFR mutation-positive non-small-cell lung cancer in patients with poor performance status</title><title>Respiratory investigation</title><addtitle>Respir Investig</addtitle><description>There is a dearth of studies on the efficacy and safety of the tyrosine kinase inhibitors osimertinib (OSI) and gefitinib (GEF) in treating epidermal growth factor receptor (EGFR) mutation-positive non-small cell lung cancer (NSCLC), even in patients with poor performance status (PS).
We retrospectively reviewed and compared data of 113 patients with EGFR mutation-positive NSCLC with Eastern Cooperative Oncology Group PS 2–4 who were administered OSI 80 mg/day or GEF 250 mg/day from May 2016 to March 2022.
The GEF group (39 patients; median age: 74 years) included 20 patients with a PS of 2, 17 with a PS of 3, and 2 with a PS of 4. The OSI group (74 patients; median age: 76 years) included 48 patients with a PS of 2, 24 with a PS of 3, and 2 with a PS of 4. The overall response rates were 69% and 66% in the GEF and OSI groups, respectively. The disease control and PS improvement rates were 89% and 51% in both groups, respectively. The median progression-free survival in the GEF and OSI groups was 6.9 and 9.2 months, respectively (p = 0.15). The OSI group experienced better overall survival than the GEF group (median: 20.9 vs. 13.0 months, p = 0.0031). The incidence of pneumonitis was 10% and 11% in the GEF and OSI groups, respectively. One treatment-related death owing to pneumonitis occurred in the GEF group.
OSI may be a useful treatment for untreated EGFR mutation-positive NSCLC with poor PS.</description><subject>Acrylamides - therapeutic use</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Aniline Compounds - therapeutic use</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Carcinoma, Non-Small-Cell Lung - drug therapy</subject><subject>Carcinoma, Non-Small-Cell Lung - genetics</subject><subject>EGFR mutation</subject><subject>ErbB Receptors - genetics</subject><subject>Female</subject><subject>Gefitinib</subject><subject>Gefitinib - administration & dosage</subject><subject>Gefitinib - therapeutic use</subject><subject>Humans</subject><subject>Indoles</subject><subject>Lung Neoplasms - drug therapy</subject><subject>Lung Neoplasms - genetics</subject><subject>Lung Neoplasms - mortality</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Mutation</subject><subject>Non-small-cell lung cancer</subject><subject>Osimertinib</subject><subject>Poor performance status</subject><subject>Protein Kinase Inhibitors - administration & dosage</subject><subject>Protein Kinase Inhibitors - therapeutic use</subject><subject>Pyrimidines</subject><subject>Retrospective Studies</subject><subject>Treatment Outcome</subject><issn>2212-5345</issn><issn>2212-5353</issn><issn>2212-5353</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kctq3TAQhkVoSUKaNwhFy27s6GbH3hTKITcIBEqzFjrSKNXBllxJPuW8Sx42Mk6yzGxmBr75R6MfoQtKakpoe7mrIyTn9zUjTNSkrwklR-iUMcqqhjf8y0ctmhN0ntKOlGgbJmh7jE54z9uWMnaKXjZhnFR0KXgcLAZrnVb6sNTPYF123m2x8gaH5EaIa29DxLPPEVQGg69vb37jcc4qu-CrqYDZ7QH70qRRDUOlYRjwMPtnrJXXELHzeCo0-Jzwf5f_4ikUxQliER4XBKeiNqdv6KtVQ4Lzt3yGnm6u_2zuqofH2_vNr4dKs-4qV9CbreZUM1Iu37aWUGGs6hvWKUVU11EjaEdbw3uh-17bK6NAE80FKZDglp-hH6vuFMO_GVKWo0vLq5WHMCfJKeWUNU3DCypWVMeQUgQrp-hGFQ-SErlYI3dytUYu1kjSy2JNGfv-tmHejmA-ht6NKMDPFYBy595BlEmXD9JgXASdpQnu8w2viJOlCQ</recordid><startdate>202411</startdate><enddate>202411</enddate><creator>Nakashima, Kazuhisa</creator><creator>Kodama, Hiroaki</creator><creator>Murakami, Haruyasu</creator><creator>Takahashi, Toshiaki</creator><creator>Kawakado, Keita</creator><creator>Yanagawa, Takashi</creator><creator>Kitani, Kashu</creator><creator>Hottta, Takamasa</creator><creator>Abe, Masaaki</creator><creator>Hamai, Kosuke</creator><creator>Tanimoto, Takuya</creator><creator>Ishikawa, Nobuhisa</creator><creator>Tamura, Tomoki</creator><creator>Kuyama, Shoichi</creator><creator>Isobe, Takeshi</creator><creator>Tsubata, Yukari</creator><general>Elsevier B.V</general><scope>6I.</scope><scope>AAFTH</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><orcidid>https://orcid.org/0000-0002-2480-9029</orcidid><orcidid>https://orcid.org/0000-0002-4260-2849</orcidid><orcidid>https://orcid.org/0000-0002-3498-9772</orcidid><orcidid>https://orcid.org/0000-0002-0208-2180</orcidid></search><sort><creationdate>202411</creationdate><title>Comparison of efficacy of gefitinib and osimertinib for untreated EGFR mutation-positive non-small-cell lung cancer in patients with poor performance status</title><author>Nakashima, Kazuhisa ; Kodama, Hiroaki ; Murakami, Haruyasu ; Takahashi, Toshiaki ; Kawakado, Keita ; Yanagawa, Takashi ; Kitani, Kashu ; Hottta, Takamasa ; Abe, Masaaki ; Hamai, Kosuke ; Tanimoto, Takuya ; Ishikawa, Nobuhisa ; Tamura, Tomoki ; Kuyama, Shoichi ; Isobe, Takeshi ; Tsubata, Yukari</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c287t-e9dbc31c20353b6f014dfa9528aa0a881d41816d394c99cf7daec0c340a9543f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Acrylamides - therapeutic use</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Aniline Compounds - therapeutic use</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Carcinoma, Non-Small-Cell Lung - drug therapy</topic><topic>Carcinoma, Non-Small-Cell Lung - genetics</topic><topic>EGFR mutation</topic><topic>ErbB Receptors - genetics</topic><topic>Female</topic><topic>Gefitinib</topic><topic>Gefitinib - administration & dosage</topic><topic>Gefitinib - therapeutic use</topic><topic>Humans</topic><topic>Indoles</topic><topic>Lung Neoplasms - drug therapy</topic><topic>Lung Neoplasms - genetics</topic><topic>Lung Neoplasms - mortality</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Mutation</topic><topic>Non-small-cell lung cancer</topic><topic>Osimertinib</topic><topic>Poor performance status</topic><topic>Protein Kinase Inhibitors - administration & dosage</topic><topic>Protein Kinase Inhibitors - therapeutic use</topic><topic>Pyrimidines</topic><topic>Retrospective Studies</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nakashima, Kazuhisa</creatorcontrib><creatorcontrib>Kodama, Hiroaki</creatorcontrib><creatorcontrib>Murakami, Haruyasu</creatorcontrib><creatorcontrib>Takahashi, Toshiaki</creatorcontrib><creatorcontrib>Kawakado, Keita</creatorcontrib><creatorcontrib>Yanagawa, Takashi</creatorcontrib><creatorcontrib>Kitani, Kashu</creatorcontrib><creatorcontrib>Hottta, Takamasa</creatorcontrib><creatorcontrib>Abe, Masaaki</creatorcontrib><creatorcontrib>Hamai, Kosuke</creatorcontrib><creatorcontrib>Tanimoto, Takuya</creatorcontrib><creatorcontrib>Ishikawa, Nobuhisa</creatorcontrib><creatorcontrib>Tamura, Tomoki</creatorcontrib><creatorcontrib>Kuyama, Shoichi</creatorcontrib><creatorcontrib>Isobe, Takeshi</creatorcontrib><creatorcontrib>Tsubata, Yukari</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</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>Respiratory investigation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nakashima, Kazuhisa</au><au>Kodama, Hiroaki</au><au>Murakami, Haruyasu</au><au>Takahashi, Toshiaki</au><au>Kawakado, Keita</au><au>Yanagawa, Takashi</au><au>Kitani, Kashu</au><au>Hottta, Takamasa</au><au>Abe, Masaaki</au><au>Hamai, Kosuke</au><au>Tanimoto, Takuya</au><au>Ishikawa, Nobuhisa</au><au>Tamura, Tomoki</au><au>Kuyama, Shoichi</au><au>Isobe, Takeshi</au><au>Tsubata, Yukari</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparison of efficacy of gefitinib and osimertinib for untreated EGFR mutation-positive non-small-cell lung cancer in patients with poor performance status</atitle><jtitle>Respiratory investigation</jtitle><addtitle>Respir Investig</addtitle><date>2024-11</date><risdate>2024</risdate><volume>62</volume><issue>6</issue><spage>1137</spage><epage>1141</epage><pages>1137-1141</pages><issn>2212-5345</issn><issn>2212-5353</issn><eissn>2212-5353</eissn><abstract>There is a dearth of studies on the efficacy and safety of the tyrosine kinase inhibitors osimertinib (OSI) and gefitinib (GEF) in treating epidermal growth factor receptor (EGFR) mutation-positive non-small cell lung cancer (NSCLC), even in patients with poor performance status (PS).
We retrospectively reviewed and compared data of 113 patients with EGFR mutation-positive NSCLC with Eastern Cooperative Oncology Group PS 2–4 who were administered OSI 80 mg/day or GEF 250 mg/day from May 2016 to March 2022.
The GEF group (39 patients; median age: 74 years) included 20 patients with a PS of 2, 17 with a PS of 3, and 2 with a PS of 4. The OSI group (74 patients; median age: 76 years) included 48 patients with a PS of 2, 24 with a PS of 3, and 2 with a PS of 4. The overall response rates were 69% and 66% in the GEF and OSI groups, respectively. The disease control and PS improvement rates were 89% and 51% in both groups, respectively. The median progression-free survival in the GEF and OSI groups was 6.9 and 9.2 months, respectively (p = 0.15). The OSI group experienced better overall survival than the GEF group (median: 20.9 vs. 13.0 months, p = 0.0031). The incidence of pneumonitis was 10% and 11% in the GEF and OSI groups, respectively. One treatment-related death owing to pneumonitis occurred in the GEF group.
OSI may be a useful treatment for untreated EGFR mutation-positive NSCLC with poor PS.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>39366122</pmid><doi>10.1016/j.resinv.2024.09.010</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0002-2480-9029</orcidid><orcidid>https://orcid.org/0000-0002-4260-2849</orcidid><orcidid>https://orcid.org/0000-0002-3498-9772</orcidid><orcidid>https://orcid.org/0000-0002-0208-2180</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acrylamides - therapeutic use Aged Aged, 80 and over Aniline Compounds - therapeutic use Antineoplastic Agents - therapeutic use Carcinoma, Non-Small-Cell Lung - drug therapy Carcinoma, Non-Small-Cell Lung - genetics EGFR mutation ErbB Receptors - genetics Female Gefitinib Gefitinib - administration & dosage Gefitinib - therapeutic use Humans Indoles Lung Neoplasms - drug therapy Lung Neoplasms - genetics Lung Neoplasms - mortality Male Middle Aged Mutation Non-small-cell lung cancer Osimertinib Poor performance status Protein Kinase Inhibitors - administration & dosage Protein Kinase Inhibitors - therapeutic use Pyrimidines Retrospective Studies Treatment Outcome |
title | Comparison of efficacy of gefitinib and osimertinib for untreated EGFR mutation-positive non-small-cell lung cancer in patients with poor performance status |
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