Perioperative immunotherapy for patients with EGFR mutant non-small cell lung cancer: Unexpected potential benefits
Given that immunotherapy has resulted in a significant overall survival (OS) benefit in advanced-stage disease, it is of notable interest to determine the effectiveness of these agents in early-stage non-small cell lung cancer (NSCLC). The potential exists for the immunotherapeutic approach in early...
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description | Given that immunotherapy has resulted in a significant overall survival (OS) benefit in advanced-stage disease, it is of notable interest to determine the effectiveness of these agents in early-stage non-small cell lung cancer (NSCLC). The potential exists for the immunotherapeutic approach in early-stage NSCLC to mirror the paradigm seen in advanced NSCLC, wherein survival enhancements have notably benefited the majority of patients. However, their performance in early-stage epidermal growth factor receptor (EGFR) mutant NSCLC is controversial. In the limited studies that included patients with EGFR mutation status, we found unexpected, good survival benefits of perioperative immune checkpoint inhibitors (ICIs) in resectable EGFR-positive NSCLC, which is controversial with those in advanced EGFR-mutant NSCLC. It is possible because of the shift toward immunosuppression that the immune environment undergoes during tumor progression. In the early disease stages, the anti-tumor immune response can be activated with fewer hindrances. In the context of EGFR mutant tumors, intratumor genetic heterogeneity can generate treatment-sensitive and -resistant subclones. The subclonality of the resistant subclone is pivotal in therapy response, with tyrosine kinase inhibitors (TKIs) selectively controlling EGFR-mutant cell proliferation and “competitive release” potentially explaining lower pathological responses in adjuvant TKIs trials. This review delves into emerging data on perioperative treatment modalities for early-stage EGFR mutant NSCLC, exploring unique mechanisms and predictive biomarkers to guide perioperative management strategies.
•Unveils unexpected ICIs benefits in early EGFR+ NSCLC.•Explored adjuvant EGFR-TKIs in resected EGFR-mutant NSCLC.•Exploring biomarkers for perioperative strategies in EGFR-mutant groups.•Revealed “competitive release” in EGFR mutant tumors. |
doi_str_mv | 10.1016/j.bbcan.2024.189194 |
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•Unveils unexpected ICIs benefits in early EGFR+ NSCLC.•Explored adjuvant EGFR-TKIs in resected EGFR-mutant NSCLC.•Exploring biomarkers for perioperative strategies in EGFR-mutant groups.•Revealed “competitive release” in EGFR mutant tumors.</description><identifier>ISSN: 0304-419X</identifier><identifier>ISSN: 1879-2561</identifier><identifier>EISSN: 1879-2561</identifier><identifier>DOI: 10.1016/j.bbcan.2024.189194</identifier><identifier>PMID: 39413856</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Adjuvant ; Carcinoma, Non-Small-Cell Lung - drug therapy ; Carcinoma, Non-Small-Cell Lung - genetics ; Carcinoma, Non-Small-Cell Lung - immunology ; Carcinoma, Non-Small-Cell Lung - pathology ; EGFR ; ErbB Receptors - genetics ; Humans ; Immune Checkpoint Inhibitors - pharmacology ; Immune Checkpoint Inhibitors - therapeutic use ; Immune-checkpoint inhibitors ; Immunotherapy ; Immunotherapy - methods ; Lung cancer ; Lung Neoplasms - drug therapy ; Lung Neoplasms - genetics ; Lung Neoplasms - immunology ; Lung Neoplasms - pathology ; Mutation ; Neoadjuvant</subject><ispartof>Biochimica et biophysica acta. Reviews on cancer, 2024-11, Vol.1879 (6), p.189194, Article 189194</ispartof><rights>2024</rights><rights>Copyright © 2024. Published by Elsevier B.V.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c239t-efbbfe08a359da270d96d65eaca41450b1cf6673c930a13a6bb86093ac3aa8243</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0304419X24001252$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39413856$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Teng, Feifei</creatorcontrib><creatorcontrib>Ju, Xiao</creatorcontrib><creatorcontrib>Gao, Zhenhua</creatorcontrib><creatorcontrib>Xu, Junhao</creatorcontrib><creatorcontrib>Li, Yikun</creatorcontrib><creatorcontrib>Wang, Yungang</creatorcontrib><creatorcontrib>Zou, Bingwen</creatorcontrib><creatorcontrib>Yu, Jinming</creatorcontrib><title>Perioperative immunotherapy for patients with EGFR mutant non-small cell lung cancer: Unexpected potential benefits</title><title>Biochimica et biophysica acta. Reviews on cancer</title><addtitle>Biochim Biophys Acta Rev Cancer</addtitle><description>Given that immunotherapy has resulted in a significant overall survival (OS) benefit in advanced-stage disease, it is of notable interest to determine the effectiveness of these agents in early-stage non-small cell lung cancer (NSCLC). The potential exists for the immunotherapeutic approach in early-stage NSCLC to mirror the paradigm seen in advanced NSCLC, wherein survival enhancements have notably benefited the majority of patients. However, their performance in early-stage epidermal growth factor receptor (EGFR) mutant NSCLC is controversial. In the limited studies that included patients with EGFR mutation status, we found unexpected, good survival benefits of perioperative immune checkpoint inhibitors (ICIs) in resectable EGFR-positive NSCLC, which is controversial with those in advanced EGFR-mutant NSCLC. It is possible because of the shift toward immunosuppression that the immune environment undergoes during tumor progression. In the early disease stages, the anti-tumor immune response can be activated with fewer hindrances. In the context of EGFR mutant tumors, intratumor genetic heterogeneity can generate treatment-sensitive and -resistant subclones. The subclonality of the resistant subclone is pivotal in therapy response, with tyrosine kinase inhibitors (TKIs) selectively controlling EGFR-mutant cell proliferation and “competitive release” potentially explaining lower pathological responses in adjuvant TKIs trials. This review delves into emerging data on perioperative treatment modalities for early-stage EGFR mutant NSCLC, exploring unique mechanisms and predictive biomarkers to guide perioperative management strategies.
•Unveils unexpected ICIs benefits in early EGFR+ NSCLC.•Explored adjuvant EGFR-TKIs in resected EGFR-mutant NSCLC.•Exploring biomarkers for perioperative strategies in EGFR-mutant groups.•Revealed “competitive release” in EGFR mutant tumors.</description><subject>Adjuvant</subject><subject>Carcinoma, Non-Small-Cell Lung - drug therapy</subject><subject>Carcinoma, Non-Small-Cell Lung - genetics</subject><subject>Carcinoma, Non-Small-Cell Lung - immunology</subject><subject>Carcinoma, Non-Small-Cell Lung - pathology</subject><subject>EGFR</subject><subject>ErbB Receptors - genetics</subject><subject>Humans</subject><subject>Immune Checkpoint Inhibitors - pharmacology</subject><subject>Immune Checkpoint Inhibitors - therapeutic use</subject><subject>Immune-checkpoint inhibitors</subject><subject>Immunotherapy</subject><subject>Immunotherapy - methods</subject><subject>Lung cancer</subject><subject>Lung Neoplasms - drug therapy</subject><subject>Lung Neoplasms - genetics</subject><subject>Lung Neoplasms - immunology</subject><subject>Lung Neoplasms - pathology</subject><subject>Mutation</subject><subject>Neoadjuvant</subject><issn>0304-419X</issn><issn>1879-2561</issn><issn>1879-2561</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1v1DAQhi1ERZfCL0BCPnLJ4okTJ0bigKp-SZWoqlbiZtnOhHqV2MF2Cv33eNnCkcuMRvO-8_EQ8g7YFhiIj7utMVb7bc3qZgu9BNm8IBvoO1nVrYCXZMM4a6oG5Ldj8jqlHWPQci5ekWMuG-B9KzYk3WB0YcGos3tE6uZ59SE_lHp5omOIdCkN9DnRny4_0LOL81s6r1n7TH3wVZr1NFGLJUyr_07LPRbjJ3rv8deCNuNAl5CL3-mJGvQ4upzekKNRTwnfPucTcn9-dnd6WV1_vbg6_XJd2ZrLXOFozIis17yVg647NkgxiBa11Q00LTNgRyE6biVnGrgWxvSCSa4t17qvG35CPhzmLjH8WDFlNbu0v1V7DGtSHKAT0AHURcoPUhtDShFHtUQ36_ikgKk9bbVTf2irPW11oF1c758XrGbG4Z_nL94i-HwQYHnz0WFUyRaaFgcXCx01BPffBb8BJ6WTtw</recordid><startdate>202411</startdate><enddate>202411</enddate><creator>Teng, Feifei</creator><creator>Ju, Xiao</creator><creator>Gao, Zhenhua</creator><creator>Xu, Junhao</creator><creator>Li, Yikun</creator><creator>Wang, Yungang</creator><creator>Zou, Bingwen</creator><creator>Yu, Jinming</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></search><sort><creationdate>202411</creationdate><title>Perioperative immunotherapy for patients with EGFR mutant non-small cell lung cancer: Unexpected potential benefits</title><author>Teng, Feifei ; Ju, Xiao ; Gao, Zhenhua ; Xu, Junhao ; Li, Yikun ; Wang, Yungang ; Zou, Bingwen ; Yu, Jinming</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c239t-efbbfe08a359da270d96d65eaca41450b1cf6673c930a13a6bb86093ac3aa8243</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adjuvant</topic><topic>Carcinoma, Non-Small-Cell Lung - drug therapy</topic><topic>Carcinoma, Non-Small-Cell Lung - genetics</topic><topic>Carcinoma, Non-Small-Cell Lung - immunology</topic><topic>Carcinoma, Non-Small-Cell Lung - pathology</topic><topic>EGFR</topic><topic>ErbB Receptors - genetics</topic><topic>Humans</topic><topic>Immune Checkpoint Inhibitors - pharmacology</topic><topic>Immune Checkpoint Inhibitors - therapeutic use</topic><topic>Immune-checkpoint inhibitors</topic><topic>Immunotherapy</topic><topic>Immunotherapy - methods</topic><topic>Lung cancer</topic><topic>Lung Neoplasms - drug therapy</topic><topic>Lung Neoplasms - genetics</topic><topic>Lung Neoplasms - immunology</topic><topic>Lung Neoplasms - pathology</topic><topic>Mutation</topic><topic>Neoadjuvant</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Teng, Feifei</creatorcontrib><creatorcontrib>Ju, Xiao</creatorcontrib><creatorcontrib>Gao, Zhenhua</creatorcontrib><creatorcontrib>Xu, Junhao</creatorcontrib><creatorcontrib>Li, Yikun</creatorcontrib><creatorcontrib>Wang, Yungang</creatorcontrib><creatorcontrib>Zou, Bingwen</creatorcontrib><creatorcontrib>Yu, Jinming</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>Biochimica et biophysica acta. Reviews on cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Teng, Feifei</au><au>Ju, Xiao</au><au>Gao, Zhenhua</au><au>Xu, Junhao</au><au>Li, Yikun</au><au>Wang, Yungang</au><au>Zou, Bingwen</au><au>Yu, Jinming</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Perioperative immunotherapy for patients with EGFR mutant non-small cell lung cancer: Unexpected potential benefits</atitle><jtitle>Biochimica et biophysica acta. Reviews on cancer</jtitle><addtitle>Biochim Biophys Acta Rev Cancer</addtitle><date>2024-11</date><risdate>2024</risdate><volume>1879</volume><issue>6</issue><spage>189194</spage><pages>189194-</pages><artnum>189194</artnum><issn>0304-419X</issn><issn>1879-2561</issn><eissn>1879-2561</eissn><abstract>Given that immunotherapy has resulted in a significant overall survival (OS) benefit in advanced-stage disease, it is of notable interest to determine the effectiveness of these agents in early-stage non-small cell lung cancer (NSCLC). The potential exists for the immunotherapeutic approach in early-stage NSCLC to mirror the paradigm seen in advanced NSCLC, wherein survival enhancements have notably benefited the majority of patients. However, their performance in early-stage epidermal growth factor receptor (EGFR) mutant NSCLC is controversial. In the limited studies that included patients with EGFR mutation status, we found unexpected, good survival benefits of perioperative immune checkpoint inhibitors (ICIs) in resectable EGFR-positive NSCLC, which is controversial with those in advanced EGFR-mutant NSCLC. It is possible because of the shift toward immunosuppression that the immune environment undergoes during tumor progression. In the early disease stages, the anti-tumor immune response can be activated with fewer hindrances. In the context of EGFR mutant tumors, intratumor genetic heterogeneity can generate treatment-sensitive and -resistant subclones. The subclonality of the resistant subclone is pivotal in therapy response, with tyrosine kinase inhibitors (TKIs) selectively controlling EGFR-mutant cell proliferation and “competitive release” potentially explaining lower pathological responses in adjuvant TKIs trials. This review delves into emerging data on perioperative treatment modalities for early-stage EGFR mutant NSCLC, exploring unique mechanisms and predictive biomarkers to guide perioperative management strategies.
•Unveils unexpected ICIs benefits in early EGFR+ NSCLC.•Explored adjuvant EGFR-TKIs in resected EGFR-mutant NSCLC.•Exploring biomarkers for perioperative strategies in EGFR-mutant groups.•Revealed “competitive release” in EGFR mutant tumors.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>39413856</pmid><doi>10.1016/j.bbcan.2024.189194</doi><oa>free_for_read</oa></addata></record> |
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subjects | Adjuvant Carcinoma, Non-Small-Cell Lung - drug therapy Carcinoma, Non-Small-Cell Lung - genetics Carcinoma, Non-Small-Cell Lung - immunology Carcinoma, Non-Small-Cell Lung - pathology EGFR ErbB Receptors - genetics Humans Immune Checkpoint Inhibitors - pharmacology Immune Checkpoint Inhibitors - therapeutic use Immune-checkpoint inhibitors Immunotherapy Immunotherapy - methods Lung cancer Lung Neoplasms - drug therapy Lung Neoplasms - genetics Lung Neoplasms - immunology Lung Neoplasms - pathology Mutation Neoadjuvant |
title | Perioperative immunotherapy for patients with EGFR mutant non-small cell lung cancer: Unexpected potential benefits |
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