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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:ESMO open 2023-08, Vol.8 (4), p.101594-101594, Article 101594
Hauptverfasser: Tamura, K., Yoshida, T., Masuda, K., Matsumoto, Y., Shinno, Y., Okuma, Y., Goto, Y., Horinouchi, H., Yamamoto, N., Ohe, Y.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 101594
container_issue 4
container_start_page 101594
container_title ESMO open
container_volume 8
creator Tamura, K.
Yoshida, T.
Masuda, K.
Matsumoto, Y.
Shinno, Y.
Okuma, Y.
Goto, Y.
Horinouchi, H.
Yamamoto, N.
Ohe, Y.
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
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10485398</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S2059702923008281</els_id><sourcerecordid>2844090101</sourcerecordid><originalsourceid>FETCH-LOGICAL-c464t-48c1218a7792f3e56f96e888c93c1f80919a1d832a9c0821e286b2ebda6bd4d33</originalsourceid><addsrcrecordid>eNp9Ul1v1SAYboyLW-b-gTFczosegdIWbjTmZJuLS5aYeU0ofXsORwoV6Mz-nr9Maucyb0xIgPd9nvfzKYo3BG8IJs37wwbi6P20oZhWi6kW7EVxQnEtyhZT8fLZ-7g4i_GAMSYty8bmVXFctTVpq4adFL-2fpxUMNE75AekrXFGK4v8nLQfIS5GH80IIWVPh5Tr0WBCTOUOHASVTCZeXF1-LdNDyEAH6LtxKgIybm86k3yI6Pzuy3V8ly0oP8rZpQAqQb_yxjn9-Tjvyjgqa0sN1iI7ux3SymkI6KdJe2RhSrkiZ9wOcoEjJBXzgfi6OBqUjXD2eJ8W3y4v7rafy5vbq-vtp5tSs4alknFNKOGqbQUdKqibQTTAOdei0mTgWBChSM8rqoTGnBKgvOkodL1qup71VXVafFzjTnM3Qq8h96GsnIIZVXiQXhn5r8eZvdz5e0kw43UleI5w_hgh-B8zxCRHE5dulQM_R0k5Y1jgvM4MZStU56nGAMNTHoLlIgF5kKsE5CIBuUog094-r_GJ9HfhGfBhBUCe1L2BIKM2kKfcmwA6yd6b_2f4DdESyTk</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2844090101</pqid></control><display><type>article</type><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><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><creator>Tamura, K. ; Yoshida, T. ; Masuda, K. ; Matsumoto, Y. ; Shinno, Y. ; Okuma, Y. ; Goto, Y. ; Horinouchi, H. ; Yamamoto, N. ; Ohe, Y.</creator><creatorcontrib>Tamura, K. ; Yoshida, T. ; Masuda, K. ; Matsumoto, Y. ; Shinno, Y. ; Okuma, Y. ; Goto, Y. ; Horinouchi, H. ; Yamamoto, N. ; Ohe, Y.</creatorcontrib><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><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>
fulltext fulltext
identifier ISSN: 2059-7029
ispartof ESMO open, 2023-08, Vol.8 (4), p.101594-101594, Article 101594
issn 2059-7029
2059-7029
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10485398
source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-05T11%3A37%3A07IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Comparison%20of%20clinical%20outcomes%20of%20osimertinib%20and%20first-generation%20EGFR-tyrosine%20kinase%20inhibitors%20(TKIs)%20in%20TKI-untreated%20EGFR-mutated%20non-small-cell%20lung%20cancer%20with%20leptomeningeal%20metastases&rft.jtitle=ESMO%20open&rft.au=Tamura,%20K.&rft.date=2023-08-01&rft.volume=8&rft.issue=4&rft.spage=101594&rft.epage=101594&rft.pages=101594-101594&rft.artnum=101594&rft.issn=2059-7029&rft.eissn=2059-7029&rft_id=info:doi/10.1016/j.esmoop.2023.101594&rft_dat=%3Cproquest_pubme%3E2844090101%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2844090101&rft_id=info:pmid/37517364&rft_els_id=S2059702923008281&rfr_iscdi=true