Dacomitinib overcomes acquired resistance to osimertinib in advanced NSCLC patients with EGFR L718Q mutation: A two-case report
Acquired resistance still inevitably occurs in patients treated with third-generation TKI osimertinib. Although the EGFR L718Q mutation has been reported as a scarce mechanism of osimertinib resistance, advanced therapeutic strategies are still in development. In this report, we included 2 cases of...
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Veröffentlicht in: | Medicine (Baltimore) 2024-07, Vol.103 (28), p.e38789 |
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creator | Li, Jielin Jin, Meizi Diao, Yuzhu Li, Xiaoling |
description | Acquired resistance still inevitably occurs in patients treated with third-generation TKI osimertinib. Although the EGFR L718Q mutation has been reported as a scarce mechanism of osimertinib resistance, advanced therapeutic strategies are still in development. In this report, we included 2 cases of patients who acquired EGFR L858R/L718Q mutation after osimertinib and were overcome by dacomitinib.
Case 1: A 77-year-old woman was diagnosed with stage IV lung adenocarcinoma. Case 2: A 64-year-old woman was diagnosed with stage IV lung adenocarcinoma.
Case 1: The patient was diagnosed with adenocarcinoma with EGFR L858R mutation. Since then, treatment with gefitinib was administrated, leading to a progression-free survival of 18 months. The treatment was switched to osimertinib based on the detection of EGFR T790M mutation, resulting in a progression-free survival of 24 months. Subsequently, EGFR L718Q mutation was detected. Case 2: The patient was diagnosed with adenocarcinoma with EGFR L858R mutation. Icotinib was used as the first-line treatment for 7 months. Osimertinib was applied as the second-line treatment for 13 months based on the EGFR T790M mutation. Subsequently, EGFR L718Q mutation was detected.
Case 1: Dacomitinib was administered. Case 2: Dacomitinib was administered.
Case 1:The progression-free survival was 8 months. Case 2: The progression-free survival was 3 months.
Dacomitinib is a potential treatment option for NSCLC patients with EGFR L718Q mutation after resistance to Osimertinib. Further research is needed to validate the efficacy of Dacomitinib in this context. |
doi_str_mv | 10.1097/MD.0000000000038789 |
format | Article |
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Case 1: A 77-year-old woman was diagnosed with stage IV lung adenocarcinoma. Case 2: A 64-year-old woman was diagnosed with stage IV lung adenocarcinoma.
Case 1: The patient was diagnosed with adenocarcinoma with EGFR L858R mutation. Since then, treatment with gefitinib was administrated, leading to a progression-free survival of 18 months. The treatment was switched to osimertinib based on the detection of EGFR T790M mutation, resulting in a progression-free survival of 24 months. Subsequently, EGFR L718Q mutation was detected. Case 2: The patient was diagnosed with adenocarcinoma with EGFR L858R mutation. Icotinib was used as the first-line treatment for 7 months. Osimertinib was applied as the second-line treatment for 13 months based on the EGFR T790M mutation. Subsequently, EGFR L718Q mutation was detected.
Case 1: Dacomitinib was administered. Case 2: Dacomitinib was administered.
Case 1:The progression-free survival was 8 months. Case 2: The progression-free survival was 3 months.
Dacomitinib is a potential treatment option for NSCLC patients with EGFR L718Q mutation after resistance to Osimertinib. Further research is needed to validate the efficacy of Dacomitinib in this context.</description><identifier>ISSN: 0025-7974</identifier><identifier>ISSN: 1536-5964</identifier><identifier>EISSN: 1536-5964</identifier><identifier>DOI: 10.1097/MD.0000000000038789</identifier><identifier>PMID: 38996163</identifier><language>eng</language><publisher>United States</publisher><subject>Acrylamides - therapeutic use ; Adenocarcinoma of Lung - drug therapy ; Adenocarcinoma of Lung - genetics ; Aged ; Aniline Compounds - therapeutic use ; Antineoplastic Agents - therapeutic use ; Carcinoma, Non-Small-Cell Lung - drug therapy ; Carcinoma, Non-Small-Cell Lung - genetics ; Drug Resistance, Neoplasm - genetics ; ErbB Receptors - genetics ; Female ; Humans ; Indoles ; Lung Neoplasms - drug therapy ; Lung Neoplasms - genetics ; Middle Aged ; Mutation ; Protein Kinase Inhibitors - therapeutic use ; Pyrimidines ; Quinazolinones - therapeutic use</subject><ispartof>Medicine (Baltimore), 2024-07, Vol.103 (28), p.e38789</ispartof><rights>Copyright © 2024 the Author(s). Published by Wolters Kluwer Health, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c230t-82128719f06b36b51e27544556d2769f7eb2970d461f9e3e13a1278d3f4ae82e3</cites><orcidid>0000-0002-2368-4797 ; 0009-0007-0443-4438</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,864,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38996163$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Jielin</creatorcontrib><creatorcontrib>Jin, Meizi</creatorcontrib><creatorcontrib>Diao, Yuzhu</creatorcontrib><creatorcontrib>Li, Xiaoling</creatorcontrib><title>Dacomitinib overcomes acquired resistance to osimertinib in advanced NSCLC patients with EGFR L718Q mutation: A two-case report</title><title>Medicine (Baltimore)</title><addtitle>Medicine (Baltimore)</addtitle><description>Acquired resistance still inevitably occurs in patients treated with third-generation TKI osimertinib. Although the EGFR L718Q mutation has been reported as a scarce mechanism of osimertinib resistance, advanced therapeutic strategies are still in development. In this report, we included 2 cases of patients who acquired EGFR L858R/L718Q mutation after osimertinib and were overcome by dacomitinib.
Case 1: A 77-year-old woman was diagnosed with stage IV lung adenocarcinoma. Case 2: A 64-year-old woman was diagnosed with stage IV lung adenocarcinoma.
Case 1: The patient was diagnosed with adenocarcinoma with EGFR L858R mutation. Since then, treatment with gefitinib was administrated, leading to a progression-free survival of 18 months. The treatment was switched to osimertinib based on the detection of EGFR T790M mutation, resulting in a progression-free survival of 24 months. Subsequently, EGFR L718Q mutation was detected. Case 2: The patient was diagnosed with adenocarcinoma with EGFR L858R mutation. Icotinib was used as the first-line treatment for 7 months. Osimertinib was applied as the second-line treatment for 13 months based on the EGFR T790M mutation. Subsequently, EGFR L718Q mutation was detected.
Case 1: Dacomitinib was administered. Case 2: Dacomitinib was administered.
Case 1:The progression-free survival was 8 months. Case 2: The progression-free survival was 3 months.
Dacomitinib is a potential treatment option for NSCLC patients with EGFR L718Q mutation after resistance to Osimertinib. Further research is needed to validate the efficacy of Dacomitinib in this context.</description><subject>Acrylamides - therapeutic use</subject><subject>Adenocarcinoma of Lung - drug therapy</subject><subject>Adenocarcinoma of Lung - genetics</subject><subject>Aged</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>Drug Resistance, Neoplasm - genetics</subject><subject>ErbB Receptors - genetics</subject><subject>Female</subject><subject>Humans</subject><subject>Indoles</subject><subject>Lung Neoplasms - drug therapy</subject><subject>Lung Neoplasms - genetics</subject><subject>Middle Aged</subject><subject>Mutation</subject><subject>Protein Kinase Inhibitors - therapeutic use</subject><subject>Pyrimidines</subject><subject>Quinazolinones - therapeutic use</subject><issn>0025-7974</issn><issn>1536-5964</issn><issn>1536-5964</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkElLxEAQhRtRdBz9BYL00UvGXtKbN5lxg1FxO4dOUsGWSXrs7ox48q8bGRewLkXxvvcKHkIHlEwoMer4ejYhf8O10mYDjajgMhNG5ptoRAgTmTIq30G7Mb4QQrli-Tba4doYSSUfoY-ZrXzrkutcif0KwnBBxLZ67V2AGgeILibbVYCTxz66FsIadh229epLqfHNw3Q-xUubHHQp4jeXnvHZxfk9niuq73Dbp0Hy3Qk-xenNZ5WNMCQvfUh7aKuxiwj733uMns7PHqeX2fz24mp6Os8qxknKNKNMK2oaIksuS0GBKZHnQsiaKWkaBSUzitS5pI0BDpRbypSueZNb0Az4GB2tc5fBv_YQU9G6WMFiYTvwfSw4UUYLoYQZUL5Gq-BjDNAUy-BaG94LSoqv5ovrWfG_-cF1-P2gL1uofz0_VfNPVOx9uQ</recordid><startdate>20240712</startdate><enddate>20240712</enddate><creator>Li, Jielin</creator><creator>Jin, Meizi</creator><creator>Diao, Yuzhu</creator><creator>Li, Xiaoling</creator><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/0000-0002-2368-4797</orcidid><orcidid>https://orcid.org/0009-0007-0443-4438</orcidid></search><sort><creationdate>20240712</creationdate><title>Dacomitinib overcomes acquired resistance to osimertinib in advanced NSCLC patients with EGFR L718Q mutation: A two-case report</title><author>Li, Jielin ; Jin, Meizi ; Diao, Yuzhu ; Li, Xiaoling</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c230t-82128719f06b36b51e27544556d2769f7eb2970d461f9e3e13a1278d3f4ae82e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Acrylamides - therapeutic use</topic><topic>Adenocarcinoma of Lung - drug therapy</topic><topic>Adenocarcinoma of Lung - genetics</topic><topic>Aged</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>Drug Resistance, Neoplasm - genetics</topic><topic>ErbB Receptors - genetics</topic><topic>Female</topic><topic>Humans</topic><topic>Indoles</topic><topic>Lung Neoplasms - drug therapy</topic><topic>Lung Neoplasms - genetics</topic><topic>Middle Aged</topic><topic>Mutation</topic><topic>Protein Kinase Inhibitors - therapeutic use</topic><topic>Pyrimidines</topic><topic>Quinazolinones - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Jielin</creatorcontrib><creatorcontrib>Jin, Meizi</creatorcontrib><creatorcontrib>Diao, Yuzhu</creatorcontrib><creatorcontrib>Li, Xiaoling</creatorcontrib><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>Medicine (Baltimore)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Jielin</au><au>Jin, Meizi</au><au>Diao, Yuzhu</au><au>Li, Xiaoling</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dacomitinib overcomes acquired resistance to osimertinib in advanced NSCLC patients with EGFR L718Q mutation: A two-case report</atitle><jtitle>Medicine (Baltimore)</jtitle><addtitle>Medicine (Baltimore)</addtitle><date>2024-07-12</date><risdate>2024</risdate><volume>103</volume><issue>28</issue><spage>e38789</spage><pages>e38789-</pages><issn>0025-7974</issn><issn>1536-5964</issn><eissn>1536-5964</eissn><abstract>Acquired resistance still inevitably occurs in patients treated with third-generation TKI osimertinib. Although the EGFR L718Q mutation has been reported as a scarce mechanism of osimertinib resistance, advanced therapeutic strategies are still in development. In this report, we included 2 cases of patients who acquired EGFR L858R/L718Q mutation after osimertinib and were overcome by dacomitinib.
Case 1: A 77-year-old woman was diagnosed with stage IV lung adenocarcinoma. Case 2: A 64-year-old woman was diagnosed with stage IV lung adenocarcinoma.
Case 1: The patient was diagnosed with adenocarcinoma with EGFR L858R mutation. Since then, treatment with gefitinib was administrated, leading to a progression-free survival of 18 months. The treatment was switched to osimertinib based on the detection of EGFR T790M mutation, resulting in a progression-free survival of 24 months. Subsequently, EGFR L718Q mutation was detected. Case 2: The patient was diagnosed with adenocarcinoma with EGFR L858R mutation. Icotinib was used as the first-line treatment for 7 months. Osimertinib was applied as the second-line treatment for 13 months based on the EGFR T790M mutation. Subsequently, EGFR L718Q mutation was detected.
Case 1: Dacomitinib was administered. Case 2: Dacomitinib was administered.
Case 1:The progression-free survival was 8 months. Case 2: The progression-free survival was 3 months.
Dacomitinib is a potential treatment option for NSCLC patients with EGFR L718Q mutation after resistance to Osimertinib. Further research is needed to validate the efficacy of Dacomitinib in this context.</abstract><cop>United States</cop><pmid>38996163</pmid><doi>10.1097/MD.0000000000038789</doi><orcidid>https://orcid.org/0000-0002-2368-4797</orcidid><orcidid>https://orcid.org/0009-0007-0443-4438</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acrylamides - therapeutic use Adenocarcinoma of Lung - drug therapy Adenocarcinoma of Lung - genetics Aged Aniline Compounds - therapeutic use Antineoplastic Agents - therapeutic use Carcinoma, Non-Small-Cell Lung - drug therapy Carcinoma, Non-Small-Cell Lung - genetics Drug Resistance, Neoplasm - genetics ErbB Receptors - genetics Female Humans Indoles Lung Neoplasms - drug therapy Lung Neoplasms - genetics Middle Aged Mutation Protein Kinase Inhibitors - therapeutic use Pyrimidines Quinazolinones - therapeutic use |
title | Dacomitinib overcomes acquired resistance to osimertinib in advanced NSCLC patients with EGFR L718Q mutation: A two-case report |
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