Comparison of clinical outcomes of osimertinib and first-generation EGFR-tyrosine kinase inhibitors (TKIs) in TKI-untreated EGFR-mutated non-small-cell lung cancer with leptomeningeal metastases
Leptomeningeal metastases (LM) are devastating complications of epidermal growth factor receptor (EGFR)-mutated non-small-cell lung cancer (NSCLC). Although osimertinib, a third-generation EGFR-tyrosine kinase inhibitor (TKI), has better penetration into the central nervous system than first-generat...
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description | Leptomeningeal metastases (LM) are devastating complications of epidermal growth factor receptor (EGFR)-mutated non-small-cell lung cancer (NSCLC). Although osimertinib, a third-generation EGFR-tyrosine kinase inhibitor (TKI), has better penetration into the central nervous system than first-generation EGFR-TKIs, data on the distinct activity of EGFR-TKIs in untreated advanced EGFR-mutated NSCLC with LM are lacking.
We retrospectively reviewed patients treated with EGFR-TKIs for TKI-untreated common EGFR-mutated NSCLC with LM between July 2002 and July 2021 at the National Cancer Center Hospital. The patients were divided into two groups: patients treated with osimertinib (Osi group) and those treated with gefitinib or erlotinib [first-generation (1G)-TKI group].
Of the 967 patients, 71 were eligible, including 29 in the Osi group and 42 in the 1G-TKI group. The median progression-free survival (PFS) and overall survival (OS) in the Osi group were better than those in the 1G-TKI group (PFS: 16.9 months versus 8.6 months, P = 0.007, and OS: 26.6 months versus 20.0 months, P = 0.158). The LM-overall response rate (ORR) and LM-PFS were significantly better in the Osi group than in the 1G-TKI group (LM-ORR: 62.5% versus 25.7%, P = 0.007; LM-PFS: 23.4 months versus 12.1 months, P = 0.021). In the subgroup analysis of EGFR mutation status, LM-PFS for patients with exon 19 deletion was significantly longer in the Osi group than in the 1G-TKI group (32.7 months versus 13.4 months, P = 0.013), whereas those with L858R mutation in exon 21 did not differ between the two groups. In the multivariate analysis, osimertinib and exon 19 deletion were significant factors for better LM-PFS and OS.
Osimertinib can be more effective for untreated common EGFR-mutated NSCLC patients with LM, especially those with exon 19 deletion, compared to first-generation TKIs.
•The standard of care for LM remains unknown.•We evaluated 71 patients with LM treated with gefitinib/erlotinib or osimertinib.•Osimertinib showed better efficacy for LM.•Osimertinib was more effective for EGFR-mutated NSCLC patients with LM. |
doi_str_mv | 10.1016/j.esmoop.2023.101594 |
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We retrospectively reviewed patients treated with EGFR-TKIs for TKI-untreated common EGFR-mutated NSCLC with LM between July 2002 and July 2021 at the National Cancer Center Hospital. The patients were divided into two groups: patients treated with osimertinib (Osi group) and those treated with gefitinib or erlotinib [first-generation (1G)-TKI group].
Of the 967 patients, 71 were eligible, including 29 in the Osi group and 42 in the 1G-TKI group. The median progression-free survival (PFS) and overall survival (OS) in the Osi group were better than those in the 1G-TKI group (PFS: 16.9 months versus 8.6 months, P = 0.007, and OS: 26.6 months versus 20.0 months, P = 0.158). The LM-overall response rate (ORR) and LM-PFS were significantly better in the Osi group than in the 1G-TKI group (LM-ORR: 62.5% versus 25.7%, P = 0.007; LM-PFS: 23.4 months versus 12.1 months, P = 0.021). In the subgroup analysis of EGFR mutation status, LM-PFS for patients with exon 19 deletion was significantly longer in the Osi group than in the 1G-TKI group (32.7 months versus 13.4 months, P = 0.013), whereas those with L858R mutation in exon 21 did not differ between the two groups. In the multivariate analysis, osimertinib and exon 19 deletion were significant factors for better LM-PFS and OS.
Osimertinib can be more effective for untreated common EGFR-mutated NSCLC patients with LM, especially those with exon 19 deletion, compared to first-generation TKIs.
•The standard of care for LM remains unknown.•We evaluated 71 patients with LM treated with gefitinib/erlotinib or osimertinib.•Osimertinib showed better efficacy for LM.•Osimertinib was more effective for EGFR-mutated NSCLC patients with LM.</description><identifier>ISSN: 2059-7029</identifier><identifier>EISSN: 2059-7029</identifier><identifier>DOI: 10.1016/j.esmoop.2023.101594</identifier><identifier>PMID: 37517364</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Carcinoma, Non-Small-Cell Lung - drug therapy ; Carcinoma, Non-Small-Cell Lung - genetics ; Carcinoma, Non-Small-Cell Lung - pathology ; ErbB Receptors - genetics ; erlotinib ; gefitinib ; Humans ; leptomeningeal metastases ; Lung Neoplasms - drug therapy ; Lung Neoplasms - genetics ; Lung Neoplasms - pathology ; non-small-cell lung cancer ; Original Research ; osimertinib ; Protein Kinase Inhibitors - therapeutic use ; Retrospective Studies ; Tyrosine Kinase Inhibitors</subject><ispartof>ESMO open, 2023-08, Vol.8 (4), p.101594-101594, Article 101594</ispartof><rights>2023 The Authors</rights><rights>Copyright © 2023 The Authors. Published by Elsevier Ltd.. All rights reserved.</rights><rights>2023 The Authors 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c464t-48c1218a7792f3e56f96e888c93c1f80919a1d832a9c0821e286b2ebda6bd4d33</citedby><cites>FETCH-LOGICAL-c464t-48c1218a7792f3e56f96e888c93c1f80919a1d832a9c0821e286b2ebda6bd4d33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10485398/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10485398/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37517364$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tamura, K.</creatorcontrib><creatorcontrib>Yoshida, T.</creatorcontrib><creatorcontrib>Masuda, K.</creatorcontrib><creatorcontrib>Matsumoto, Y.</creatorcontrib><creatorcontrib>Shinno, Y.</creatorcontrib><creatorcontrib>Okuma, Y.</creatorcontrib><creatorcontrib>Goto, Y.</creatorcontrib><creatorcontrib>Horinouchi, H.</creatorcontrib><creatorcontrib>Yamamoto, N.</creatorcontrib><creatorcontrib>Ohe, Y.</creatorcontrib><title>Comparison of clinical outcomes of osimertinib and first-generation EGFR-tyrosine kinase inhibitors (TKIs) in TKI-untreated EGFR-mutated non-small-cell lung cancer with leptomeningeal metastases</title><title>ESMO open</title><addtitle>ESMO Open</addtitle><description>Leptomeningeal metastases (LM) are devastating complications of epidermal growth factor receptor (EGFR)-mutated non-small-cell lung cancer (NSCLC). Although osimertinib, a third-generation EGFR-tyrosine kinase inhibitor (TKI), has better penetration into the central nervous system than first-generation EGFR-TKIs, data on the distinct activity of EGFR-TKIs in untreated advanced EGFR-mutated NSCLC with LM are lacking.
We retrospectively reviewed patients treated with EGFR-TKIs for TKI-untreated common EGFR-mutated NSCLC with LM between July 2002 and July 2021 at the National Cancer Center Hospital. The patients were divided into two groups: patients treated with osimertinib (Osi group) and those treated with gefitinib or erlotinib [first-generation (1G)-TKI group].
Of the 967 patients, 71 were eligible, including 29 in the Osi group and 42 in the 1G-TKI group. The median progression-free survival (PFS) and overall survival (OS) in the Osi group were better than those in the 1G-TKI group (PFS: 16.9 months versus 8.6 months, P = 0.007, and OS: 26.6 months versus 20.0 months, P = 0.158). The LM-overall response rate (ORR) and LM-PFS were significantly better in the Osi group than in the 1G-TKI group (LM-ORR: 62.5% versus 25.7%, P = 0.007; LM-PFS: 23.4 months versus 12.1 months, P = 0.021). In the subgroup analysis of EGFR mutation status, LM-PFS for patients with exon 19 deletion was significantly longer in the Osi group than in the 1G-TKI group (32.7 months versus 13.4 months, P = 0.013), whereas those with L858R mutation in exon 21 did not differ between the two groups. In the multivariate analysis, osimertinib and exon 19 deletion were significant factors for better LM-PFS and OS.
Osimertinib can be more effective for untreated common EGFR-mutated NSCLC patients with LM, especially those with exon 19 deletion, compared to first-generation TKIs.
•The standard of care for LM remains unknown.•We evaluated 71 patients with LM treated with gefitinib/erlotinib or osimertinib.•Osimertinib showed better efficacy for LM.•Osimertinib was more effective for EGFR-mutated NSCLC patients with LM.</description><subject>Carcinoma, Non-Small-Cell Lung - drug therapy</subject><subject>Carcinoma, Non-Small-Cell Lung - genetics</subject><subject>Carcinoma, Non-Small-Cell Lung - pathology</subject><subject>ErbB Receptors - genetics</subject><subject>erlotinib</subject><subject>gefitinib</subject><subject>Humans</subject><subject>leptomeningeal metastases</subject><subject>Lung Neoplasms - drug therapy</subject><subject>Lung Neoplasms - genetics</subject><subject>Lung Neoplasms - pathology</subject><subject>non-small-cell lung cancer</subject><subject>Original Research</subject><subject>osimertinib</subject><subject>Protein Kinase Inhibitors - therapeutic use</subject><subject>Retrospective Studies</subject><subject>Tyrosine Kinase Inhibitors</subject><issn>2059-7029</issn><issn>2059-7029</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9Ul1v1SAYboyLW-b-gTFczosegdIWbjTmZJuLS5aYeU0ofXsORwoV6Mz-nr9Maucyb0xIgPd9nvfzKYo3BG8IJs37wwbi6P20oZhWi6kW7EVxQnEtyhZT8fLZ-7g4i_GAMSYty8bmVXFctTVpq4adFL-2fpxUMNE75AekrXFGK4v8nLQfIS5GH80IIWVPh5Tr0WBCTOUOHASVTCZeXF1-LdNDyEAH6LtxKgIybm86k3yI6Pzuy3V8ly0oP8rZpQAqQb_yxjn9-Tjvyjgqa0sN1iI7ux3SymkI6KdJe2RhSrkiZ9wOcoEjJBXzgfi6OBqUjXD2eJ8W3y4v7rafy5vbq-vtp5tSs4alknFNKOGqbQUdKqibQTTAOdei0mTgWBChSM8rqoTGnBKgvOkodL1qup71VXVafFzjTnM3Qq8h96GsnIIZVXiQXhn5r8eZvdz5e0kw43UleI5w_hgh-B8zxCRHE5dulQM_R0k5Y1jgvM4MZStU56nGAMNTHoLlIgF5kKsE5CIBuUog094-r_GJ9HfhGfBhBUCe1L2BIKM2kKfcmwA6yd6b_2f4DdESyTk</recordid><startdate>20230801</startdate><enddate>20230801</enddate><creator>Tamura, K.</creator><creator>Yoshida, T.</creator><creator>Masuda, K.</creator><creator>Matsumoto, Y.</creator><creator>Shinno, Y.</creator><creator>Okuma, Y.</creator><creator>Goto, Y.</creator><creator>Horinouchi, H.</creator><creator>Yamamoto, N.</creator><creator>Ohe, Y.</creator><general>Elsevier Ltd</general><general>Elsevier</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><scope>5PM</scope></search><sort><creationdate>20230801</creationdate><title>Comparison of clinical outcomes of osimertinib and first-generation EGFR-tyrosine kinase inhibitors (TKIs) in TKI-untreated EGFR-mutated non-small-cell lung cancer with leptomeningeal metastases</title><author>Tamura, K. ; Yoshida, T. ; Masuda, K. ; Matsumoto, Y. ; Shinno, Y. ; Okuma, Y. ; Goto, Y. ; Horinouchi, H. ; Yamamoto, N. ; Ohe, Y.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c464t-48c1218a7792f3e56f96e888c93c1f80919a1d832a9c0821e286b2ebda6bd4d33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Carcinoma, Non-Small-Cell Lung - drug therapy</topic><topic>Carcinoma, Non-Small-Cell Lung - genetics</topic><topic>Carcinoma, Non-Small-Cell Lung - pathology</topic><topic>ErbB Receptors - genetics</topic><topic>erlotinib</topic><topic>gefitinib</topic><topic>Humans</topic><topic>leptomeningeal metastases</topic><topic>Lung Neoplasms - drug therapy</topic><topic>Lung Neoplasms - genetics</topic><topic>Lung Neoplasms - pathology</topic><topic>non-small-cell lung cancer</topic><topic>Original Research</topic><topic>osimertinib</topic><topic>Protein Kinase Inhibitors - therapeutic use</topic><topic>Retrospective Studies</topic><topic>Tyrosine Kinase Inhibitors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tamura, K.</creatorcontrib><creatorcontrib>Yoshida, T.</creatorcontrib><creatorcontrib>Masuda, K.</creatorcontrib><creatorcontrib>Matsumoto, Y.</creatorcontrib><creatorcontrib>Shinno, Y.</creatorcontrib><creatorcontrib>Okuma, Y.</creatorcontrib><creatorcontrib>Goto, Y.</creatorcontrib><creatorcontrib>Horinouchi, H.</creatorcontrib><creatorcontrib>Yamamoto, N.</creatorcontrib><creatorcontrib>Ohe, Y.</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>ESMO open</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tamura, K.</au><au>Yoshida, T.</au><au>Masuda, K.</au><au>Matsumoto, Y.</au><au>Shinno, Y.</au><au>Okuma, Y.</au><au>Goto, Y.</au><au>Horinouchi, H.</au><au>Yamamoto, N.</au><au>Ohe, Y.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparison of clinical outcomes of osimertinib and first-generation EGFR-tyrosine kinase inhibitors (TKIs) in TKI-untreated EGFR-mutated non-small-cell lung cancer with leptomeningeal metastases</atitle><jtitle>ESMO open</jtitle><addtitle>ESMO Open</addtitle><date>2023-08-01</date><risdate>2023</risdate><volume>8</volume><issue>4</issue><spage>101594</spage><epage>101594</epage><pages>101594-101594</pages><artnum>101594</artnum><issn>2059-7029</issn><eissn>2059-7029</eissn><abstract>Leptomeningeal metastases (LM) are devastating complications of epidermal growth factor receptor (EGFR)-mutated non-small-cell lung cancer (NSCLC). Although osimertinib, a third-generation EGFR-tyrosine kinase inhibitor (TKI), has better penetration into the central nervous system than first-generation EGFR-TKIs, data on the distinct activity of EGFR-TKIs in untreated advanced EGFR-mutated NSCLC with LM are lacking.
We retrospectively reviewed patients treated with EGFR-TKIs for TKI-untreated common EGFR-mutated NSCLC with LM between July 2002 and July 2021 at the National Cancer Center Hospital. The patients were divided into two groups: patients treated with osimertinib (Osi group) and those treated with gefitinib or erlotinib [first-generation (1G)-TKI group].
Of the 967 patients, 71 were eligible, including 29 in the Osi group and 42 in the 1G-TKI group. The median progression-free survival (PFS) and overall survival (OS) in the Osi group were better than those in the 1G-TKI group (PFS: 16.9 months versus 8.6 months, P = 0.007, and OS: 26.6 months versus 20.0 months, P = 0.158). The LM-overall response rate (ORR) and LM-PFS were significantly better in the Osi group than in the 1G-TKI group (LM-ORR: 62.5% versus 25.7%, P = 0.007; LM-PFS: 23.4 months versus 12.1 months, P = 0.021). In the subgroup analysis of EGFR mutation status, LM-PFS for patients with exon 19 deletion was significantly longer in the Osi group than in the 1G-TKI group (32.7 months versus 13.4 months, P = 0.013), whereas those with L858R mutation in exon 21 did not differ between the two groups. In the multivariate analysis, osimertinib and exon 19 deletion were significant factors for better LM-PFS and OS.
Osimertinib can be more effective for untreated common EGFR-mutated NSCLC patients with LM, especially those with exon 19 deletion, compared to first-generation TKIs.
•The standard of care for LM remains unknown.•We evaluated 71 patients with LM treated with gefitinib/erlotinib or osimertinib.•Osimertinib showed better efficacy for LM.•Osimertinib was more effective for EGFR-mutated NSCLC patients with LM.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>37517364</pmid><doi>10.1016/j.esmoop.2023.101594</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Carcinoma, Non-Small-Cell Lung - drug therapy Carcinoma, Non-Small-Cell Lung - genetics Carcinoma, Non-Small-Cell Lung - pathology ErbB Receptors - genetics erlotinib gefitinib Humans leptomeningeal metastases Lung Neoplasms - drug therapy Lung Neoplasms - genetics Lung Neoplasms - pathology non-small-cell lung cancer Original Research osimertinib Protein Kinase Inhibitors - therapeutic use Retrospective Studies Tyrosine Kinase Inhibitors |
title | Comparison of clinical outcomes of osimertinib and first-generation EGFR-tyrosine kinase inhibitors (TKIs) in TKI-untreated EGFR-mutated non-small-cell lung cancer with leptomeningeal metastases |
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