Natural Killer Cells as a Potential Biomarker for Predicting Immunotherapy Efficacy in Patients with Non-Small Cell Lung Cancer

Background Immunotherapy with immune checkpoint inhibitors for non-small cell lung cancer (NSCLC) has emerged as an important treatment option. Although immunotherapy may significantly improve survival and quality of life, response rates are as low as 20% in NSCLC patients. Objective The identificat...

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Veröffentlicht in:Targeted oncology 2020-04, Vol.15 (2), p.241-247
Hauptverfasser: Cho, Yong-Hee, Choi, Myeong Geun, Kim, Dong Ha, Choi, Yun Jung, Kim, Seon Ye, Sung, Ki Jung, Lee, Jae Cheol, Kim, Sang-Yeob, Rho, Jin Kyung, Choi, Chang-Min
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container_end_page 247
container_issue 2
container_start_page 241
container_title Targeted oncology
container_volume 15
creator Cho, Yong-Hee
Choi, Myeong Geun
Kim, Dong Ha
Choi, Yun Jung
Kim, Seon Ye
Sung, Ki Jung
Lee, Jae Cheol
Kim, Sang-Yeob
Rho, Jin Kyung
Choi, Chang-Min
description Background Immunotherapy with immune checkpoint inhibitors for non-small cell lung cancer (NSCLC) has emerged as an important treatment option. Although immunotherapy may significantly improve survival and quality of life, response rates are as low as 20% in NSCLC patients. Objective The identification of reliable biomarkers predicting response to immunotherapy is required urgently to determine patient selection guidelines. Patients and Methods Peripheral blood mononuclear cells (PBMCs) from nine NSCLC patients were collected pre- and post-treatment with immunotherapy. The immune cell composition of PBMCs was analyzed using CyTOF with an optimized 32-marker panel. The natural killer (NK) cell activity was assessed with the measurement of interferon (INF)-γ using an NK Vue™ kit. Results We found that the percentages of NK cell populations in the immune cells of PBMCs were prominently elevated in the immunotherapy responder group when compared with non-responders. While no meaningful differences were observed in other populations of immune cells, consistent with these results, the overall activity of NK cells in responders was highly elevated compared with that of non-responders. From the analysis of NK subsets, although differences in the population of early NK cells were not observed, the functionally differentiated late NK cells were prominently high in responders. Conclusions The overall activity or number of NK cells may be a useful biomarker to predict immunotherapy response in patients with NSCLC.
doi_str_mv 10.1007/s11523-020-00712-2
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Although immunotherapy may significantly improve survival and quality of life, response rates are as low as 20% in NSCLC patients. Objective The identification of reliable biomarkers predicting response to immunotherapy is required urgently to determine patient selection guidelines. Patients and Methods Peripheral blood mononuclear cells (PBMCs) from nine NSCLC patients were collected pre- and post-treatment with immunotherapy. The immune cell composition of PBMCs was analyzed using CyTOF with an optimized 32-marker panel. The natural killer (NK) cell activity was assessed with the measurement of interferon (INF)-γ using an NK Vue™ kit. Results We found that the percentages of NK cell populations in the immune cells of PBMCs were prominently elevated in the immunotherapy responder group when compared with non-responders. While no meaningful differences were observed in other populations of immune cells, consistent with these results, the overall activity of NK cells in responders was highly elevated compared with that of non-responders. From the analysis of NK subsets, although differences in the population of early NK cells were not observed, the functionally differentiated late NK cells were prominently high in responders. Conclusions The overall activity or number of NK cells may be a useful biomarker to predict immunotherapy response in patients with NSCLC.</description><identifier>ISSN: 1776-2596</identifier><identifier>EISSN: 1776-260X</identifier><identifier>DOI: 10.1007/s11523-020-00712-2</identifier><identifier>PMID: 32285316</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Biomarkers ; Biomarkers - metabolism ; Biomedicine ; Carcinoma, Non-Small-Cell Lung - therapy ; Female ; Humans ; Immunotherapy ; Immunotherapy - methods ; Killer Cells, Natural - metabolism ; Lung cancer ; Lung Neoplasms - therapy ; Male ; Medicine ; Medicine &amp; Public Health ; Middle Aged ; Oncology ; Prospective Studies ; Short Communication ; Young Adult</subject><ispartof>Targeted oncology, 2020-04, Vol.15 (2), p.241-247</ispartof><rights>Springer Nature Switzerland AG 2020</rights><rights>Springer Nature Switzerland AG 2020.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-ea18e52a91caf40f879abf5efb7d42ef8fdd7933309d239afc4807f21fbaf5f93</citedby><cites>FETCH-LOGICAL-c375t-ea18e52a91caf40f879abf5efb7d42ef8fdd7933309d239afc4807f21fbaf5f93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11523-020-00712-2$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11523-020-00712-2$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32285316$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cho, Yong-Hee</creatorcontrib><creatorcontrib>Choi, Myeong Geun</creatorcontrib><creatorcontrib>Kim, Dong Ha</creatorcontrib><creatorcontrib>Choi, Yun Jung</creatorcontrib><creatorcontrib>Kim, Seon Ye</creatorcontrib><creatorcontrib>Sung, Ki Jung</creatorcontrib><creatorcontrib>Lee, Jae Cheol</creatorcontrib><creatorcontrib>Kim, Sang-Yeob</creatorcontrib><creatorcontrib>Rho, Jin Kyung</creatorcontrib><creatorcontrib>Choi, Chang-Min</creatorcontrib><title>Natural Killer Cells as a Potential Biomarker for Predicting Immunotherapy Efficacy in Patients with Non-Small Cell Lung Cancer</title><title>Targeted oncology</title><addtitle>Targ Oncol</addtitle><addtitle>Target Oncol</addtitle><description>Background Immunotherapy with immune checkpoint inhibitors for non-small cell lung cancer (NSCLC) has emerged as an important treatment option. Although immunotherapy may significantly improve survival and quality of life, response rates are as low as 20% in NSCLC patients. Objective The identification of reliable biomarkers predicting response to immunotherapy is required urgently to determine patient selection guidelines. Patients and Methods Peripheral blood mononuclear cells (PBMCs) from nine NSCLC patients were collected pre- and post-treatment with immunotherapy. The immune cell composition of PBMCs was analyzed using CyTOF with an optimized 32-marker panel. The natural killer (NK) cell activity was assessed with the measurement of interferon (INF)-γ using an NK Vue™ kit. Results We found that the percentages of NK cell populations in the immune cells of PBMCs were prominently elevated in the immunotherapy responder group when compared with non-responders. While no meaningful differences were observed in other populations of immune cells, consistent with these results, the overall activity of NK cells in responders was highly elevated compared with that of non-responders. From the analysis of NK subsets, although differences in the population of early NK cells were not observed, the functionally differentiated late NK cells were prominently high in responders. 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Choi, Myeong Geun ; Kim, Dong Ha ; Choi, Yun Jung ; Kim, Seon Ye ; Sung, Ki Jung ; Lee, Jae Cheol ; Kim, Sang-Yeob ; Rho, Jin Kyung ; Choi, Chang-Min</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-ea18e52a91caf40f879abf5efb7d42ef8fdd7933309d239afc4807f21fbaf5f93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Biomarkers</topic><topic>Biomarkers - metabolism</topic><topic>Biomedicine</topic><topic>Carcinoma, Non-Small-Cell Lung - therapy</topic><topic>Female</topic><topic>Humans</topic><topic>Immunotherapy</topic><topic>Immunotherapy - methods</topic><topic>Killer Cells, Natural - metabolism</topic><topic>Lung cancer</topic><topic>Lung Neoplasms - therapy</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Middle Aged</topic><topic>Oncology</topic><topic>Prospective Studies</topic><topic>Short Communication</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cho, Yong-Hee</creatorcontrib><creatorcontrib>Choi, Myeong Geun</creatorcontrib><creatorcontrib>Kim, Dong Ha</creatorcontrib><creatorcontrib>Choi, Yun Jung</creatorcontrib><creatorcontrib>Kim, Seon Ye</creatorcontrib><creatorcontrib>Sung, Ki Jung</creatorcontrib><creatorcontrib>Lee, Jae Cheol</creatorcontrib><creatorcontrib>Kim, Sang-Yeob</creatorcontrib><creatorcontrib>Rho, Jin Kyung</creatorcontrib><creatorcontrib>Choi, Chang-Min</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing &amp; 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Allied Health Database (Alumni Edition)</collection><collection>Consumer Health Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Targeted oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cho, Yong-Hee</au><au>Choi, Myeong Geun</au><au>Kim, Dong Ha</au><au>Choi, Yun Jung</au><au>Kim, Seon Ye</au><au>Sung, Ki Jung</au><au>Lee, Jae Cheol</au><au>Kim, Sang-Yeob</au><au>Rho, Jin Kyung</au><au>Choi, Chang-Min</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Natural Killer Cells as a Potential Biomarker for Predicting Immunotherapy Efficacy in Patients with Non-Small Cell Lung Cancer</atitle><jtitle>Targeted oncology</jtitle><stitle>Targ Oncol</stitle><addtitle>Target Oncol</addtitle><date>2020-04-01</date><risdate>2020</risdate><volume>15</volume><issue>2</issue><spage>241</spage><epage>247</epage><pages>241-247</pages><issn>1776-2596</issn><eissn>1776-260X</eissn><abstract>Background Immunotherapy with immune checkpoint inhibitors for non-small cell lung cancer (NSCLC) has emerged as an important treatment option. Although immunotherapy may significantly improve survival and quality of life, response rates are as low as 20% in NSCLC patients. Objective The identification of reliable biomarkers predicting response to immunotherapy is required urgently to determine patient selection guidelines. Patients and Methods Peripheral blood mononuclear cells (PBMCs) from nine NSCLC patients were collected pre- and post-treatment with immunotherapy. The immune cell composition of PBMCs was analyzed using CyTOF with an optimized 32-marker panel. The natural killer (NK) cell activity was assessed with the measurement of interferon (INF)-γ using an NK Vue™ kit. Results We found that the percentages of NK cell populations in the immune cells of PBMCs were prominently elevated in the immunotherapy responder group when compared with non-responders. While no meaningful differences were observed in other populations of immune cells, consistent with these results, the overall activity of NK cells in responders was highly elevated compared with that of non-responders. From the analysis of NK subsets, although differences in the population of early NK cells were not observed, the functionally differentiated late NK cells were prominently high in responders. Conclusions The overall activity or number of NK cells may be a useful biomarker to predict immunotherapy response in patients with NSCLC.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>32285316</pmid><doi>10.1007/s11523-020-00712-2</doi><tpages>7</tpages></addata></record>
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subjects Adult
Aged
Aged, 80 and over
Biomarkers
Biomarkers - metabolism
Biomedicine
Carcinoma, Non-Small-Cell Lung - therapy
Female
Humans
Immunotherapy
Immunotherapy - methods
Killer Cells, Natural - metabolism
Lung cancer
Lung Neoplasms - therapy
Male
Medicine
Medicine & Public Health
Middle Aged
Oncology
Prospective Studies
Short Communication
Young Adult
title Natural Killer Cells as a Potential Biomarker for Predicting Immunotherapy Efficacy in Patients with Non-Small Cell Lung Cancer
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