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Immune-related RNA signature predicts outcome of PD-1 inhibitor-combined GEMCIS therapy in advanced intrahepatic cholangiocarcinoma

BackgroundImmune checkpoint inhibitor (ICI)-combined chemotherapy in advanced intrahepatic cholangiocarcinoma has been proved to have more efficacy in a series of clinical trials. However, whether the tumor microenvironment (TME) plays a vital role in immune-combined therapy has not been rigorously...

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Published in:Frontiers in immunology 2022-09, Vol.13, p.943066-943066
Main Authors: Zeng, Tian-mei, Pan, Yu-fei, Yuan, Zhen-gang, Chen, Dong-sheng, Song, Yun-jie, Gao, Yong
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Pan, Yu-fei
Yuan, Zhen-gang
Chen, Dong-sheng
Song, Yun-jie
Gao, Yong
description BackgroundImmune checkpoint inhibitor (ICI)-combined chemotherapy in advanced intrahepatic cholangiocarcinoma has been proved to have more efficacy in a series of clinical trials. However, whether the tumor microenvironment (TME) plays a vital role in immune-combined therapy has not been rigorously evaluated. MethodsFirstly, we assayed the immunogenic properties of GEM-based chemotherapy. Then, 12 ICC patients treated with PD-1 inhibitor (sintilimab) combined with gemcitabine and cisplatin (GemCis) from a phase 2 clinical trial (ChiCTR2000036652) were included and their immune-related gene expression profiles were analyzed using RNA from baseline tumor samples. Immune-related signature correlating with clinical outcome was identified according to the 12 ICC patients, and its predictive value was validated in an ICC cohort with 26 patients. Multiplexed immunofluorescence (mIF) and flow cytometry (FCM) analysis were performed to evaluate the immune-related molecules with therapeutic outcomes. ResultsGEM-based chemotherapy induced immunogenic cell death of cholangiocarcinoma cells, together with increased CD274 expression. In an ICC cohort, we found that upregulation of immune-checkpoint molecules and immune response-related pathways were significantly related to better clinical outcome. On the contrary, baseline immune-cell proportions in tumor tissues did not show any correlation with clinical benefit between responders and non-responders. Immune-related signature (including six genes) correlating with clinical outcome was identified according to the 12 ICC patients, and its predictive value was validated in a small ICC cohort with 26 patients. ConclusionImmune-related RNA signature predicts the outcome of PD-1 inhibitor-combined GEMCIS therapy in advanced intrahepatic cholangiocarcinoma, which could be tested as a biomarker for immune-chemotherapy in the future.
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However, whether the tumor microenvironment (TME) plays a vital role in immune-combined therapy has not been rigorously evaluated. MethodsFirstly, we assayed the immunogenic properties of GEM-based chemotherapy. Then, 12 ICC patients treated with PD-1 inhibitor (sintilimab) combined with gemcitabine and cisplatin (GemCis) from a phase 2 clinical trial (ChiCTR2000036652) were included and their immune-related gene expression profiles were analyzed using RNA from baseline tumor samples. Immune-related signature correlating with clinical outcome was identified according to the 12 ICC patients, and its predictive value was validated in an ICC cohort with 26 patients. Multiplexed immunofluorescence (mIF) and flow cytometry (FCM) analysis were performed to evaluate the immune-related molecules with therapeutic outcomes. ResultsGEM-based chemotherapy induced immunogenic cell death of cholangiocarcinoma cells, together with increased CD274 expression. In an ICC cohort, we found that upregulation of immune-checkpoint molecules and immune response-related pathways were significantly related to better clinical outcome. On the contrary, baseline immune-cell proportions in tumor tissues did not show any correlation with clinical benefit between responders and non-responders. Immune-related signature (including six genes) correlating with clinical outcome was identified according to the 12 ICC patients, and its predictive value was validated in a small ICC cohort with 26 patients. ConclusionImmune-related RNA signature predicts the outcome of PD-1 inhibitor-combined GEMCIS therapy in advanced intrahepatic cholangiocarcinoma, which could be tested as a biomarker for immune-chemotherapy in the future.</description><identifier>ISSN: 1664-3224</identifier><identifier>EISSN: 1664-3224</identifier><identifier>DOI: 10.3389/fimmu.2022.943066</identifier><language>eng</language><publisher>Frontiers Media S.A</publisher><subject>immune-related signature ; immunochemotherapy ; Immunology ; intrahepatic cholangiocarcinoma ; prognosis ; tumor microenvironment</subject><ispartof>Frontiers in immunology, 2022-09, Vol.13, p.943066-943066</ispartof><rights>Copyright © 2022 Zeng, Pan, Yuan, Chen, Song and Gao 2022 Zeng, Pan, Yuan, Chen, Song and Gao</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c442t-54eee86738fe12c3f13964b235758f9356a82b6e46cac67906c9f105d69a55f43</citedby><cites>FETCH-LOGICAL-c442t-54eee86738fe12c3f13964b235758f9356a82b6e46cac67906c9f105d69a55f43</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/PMC9501891/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9501891/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids></links><search><creatorcontrib>Zeng, Tian-mei</creatorcontrib><creatorcontrib>Pan, Yu-fei</creatorcontrib><creatorcontrib>Yuan, Zhen-gang</creatorcontrib><creatorcontrib>Chen, Dong-sheng</creatorcontrib><creatorcontrib>Song, Yun-jie</creatorcontrib><creatorcontrib>Gao, Yong</creatorcontrib><title>Immune-related RNA signature predicts outcome of PD-1 inhibitor-combined GEMCIS therapy in advanced intrahepatic cholangiocarcinoma</title><title>Frontiers in immunology</title><description>BackgroundImmune checkpoint inhibitor (ICI)-combined chemotherapy in advanced intrahepatic cholangiocarcinoma has been proved to have more efficacy in a series of clinical trials. However, whether the tumor microenvironment (TME) plays a vital role in immune-combined therapy has not been rigorously evaluated. MethodsFirstly, we assayed the immunogenic properties of GEM-based chemotherapy. Then, 12 ICC patients treated with PD-1 inhibitor (sintilimab) combined with gemcitabine and cisplatin (GemCis) from a phase 2 clinical trial (ChiCTR2000036652) were included and their immune-related gene expression profiles were analyzed using RNA from baseline tumor samples. Immune-related signature correlating with clinical outcome was identified according to the 12 ICC patients, and its predictive value was validated in an ICC cohort with 26 patients. Multiplexed immunofluorescence (mIF) and flow cytometry (FCM) analysis were performed to evaluate the immune-related molecules with therapeutic outcomes. ResultsGEM-based chemotherapy induced immunogenic cell death of cholangiocarcinoma cells, together with increased CD274 expression. In an ICC cohort, we found that upregulation of immune-checkpoint molecules and immune response-related pathways were significantly related to better clinical outcome. On the contrary, baseline immune-cell proportions in tumor tissues did not show any correlation with clinical benefit between responders and non-responders. Immune-related signature (including six genes) correlating with clinical outcome was identified according to the 12 ICC patients, and its predictive value was validated in a small ICC cohort with 26 patients. ConclusionImmune-related RNA signature predicts the outcome of PD-1 inhibitor-combined GEMCIS therapy in advanced intrahepatic cholangiocarcinoma, which could be tested as a biomarker for immune-chemotherapy in the future.</description><subject>immune-related signature</subject><subject>immunochemotherapy</subject><subject>Immunology</subject><subject>intrahepatic cholangiocarcinoma</subject><subject>prognosis</subject><subject>tumor microenvironment</subject><issn>1664-3224</issn><issn>1664-3224</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpVkktr3DAQx01poWGbD9Cbjr14q7elSyFs03QhTUsfZyHL47WCbbmSHMg5X7zabCiJDqNhHr8ZiX9VvSd4y5jSH3s_TeuWYkq3mjMs5avqjEjJa0Ypf_3Mf1udp3SLy-GaMSbOqod9aZ2hjjDaDB36eXOBkj_MNq8R0BKh8y4nFNbswgQo9OjH55ogPw--9TnEuoRbP5fOq8tvu_0vlAeIdrkvFch2d3Z2JeXnHO0Ai83eITeE0c4HH5yNzs9hsu-qN70dE5w_3Zvqz5fL37uv9fX3q_3u4rp2nNNcCw4ASjZM9UCoYz1hWvKWMtEI1WsmpFW0lcCls042Gkune4JFJ7UVoudsU-1P3C7YW7NEP9l4b4L15jEQ4sHYWFYcwYCgWMiOtsKVEarTmnW4a0AR0nLqoLA-nVjL2k7QOTg-cXwBfZmZ_WAO4c5ogYnSpAA-PAFi-LtCymbyycFY_gbCmgxtiJJM4WI2FTmVuhhSitD_H0OwOQrAPArAHAVgTgJg_wDFbKbu</recordid><startdate>20220909</startdate><enddate>20220909</enddate><creator>Zeng, Tian-mei</creator><creator>Pan, Yu-fei</creator><creator>Yuan, Zhen-gang</creator><creator>Chen, Dong-sheng</creator><creator>Song, Yun-jie</creator><creator>Gao, Yong</creator><general>Frontiers Media S.A</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20220909</creationdate><title>Immune-related RNA signature predicts outcome of PD-1 inhibitor-combined GEMCIS therapy in advanced intrahepatic cholangiocarcinoma</title><author>Zeng, Tian-mei ; Pan, Yu-fei ; Yuan, Zhen-gang ; Chen, Dong-sheng ; Song, Yun-jie ; Gao, Yong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c442t-54eee86738fe12c3f13964b235758f9356a82b6e46cac67906c9f105d69a55f43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>immune-related signature</topic><topic>immunochemotherapy</topic><topic>Immunology</topic><topic>intrahepatic cholangiocarcinoma</topic><topic>prognosis</topic><topic>tumor microenvironment</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zeng, Tian-mei</creatorcontrib><creatorcontrib>Pan, Yu-fei</creatorcontrib><creatorcontrib>Yuan, Zhen-gang</creatorcontrib><creatorcontrib>Chen, Dong-sheng</creatorcontrib><creatorcontrib>Song, Yun-jie</creatorcontrib><creatorcontrib>Gao, Yong</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>Frontiers in immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zeng, Tian-mei</au><au>Pan, Yu-fei</au><au>Yuan, Zhen-gang</au><au>Chen, Dong-sheng</au><au>Song, Yun-jie</au><au>Gao, Yong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immune-related RNA signature predicts outcome of PD-1 inhibitor-combined GEMCIS therapy in advanced intrahepatic cholangiocarcinoma</atitle><jtitle>Frontiers in immunology</jtitle><date>2022-09-09</date><risdate>2022</risdate><volume>13</volume><spage>943066</spage><epage>943066</epage><pages>943066-943066</pages><issn>1664-3224</issn><eissn>1664-3224</eissn><abstract>BackgroundImmune checkpoint inhibitor (ICI)-combined chemotherapy in advanced intrahepatic cholangiocarcinoma has been proved to have more efficacy in a series of clinical trials. However, whether the tumor microenvironment (TME) plays a vital role in immune-combined therapy has not been rigorously evaluated. MethodsFirstly, we assayed the immunogenic properties of GEM-based chemotherapy. Then, 12 ICC patients treated with PD-1 inhibitor (sintilimab) combined with gemcitabine and cisplatin (GemCis) from a phase 2 clinical trial (ChiCTR2000036652) were included and their immune-related gene expression profiles were analyzed using RNA from baseline tumor samples. Immune-related signature correlating with clinical outcome was identified according to the 12 ICC patients, and its predictive value was validated in an ICC cohort with 26 patients. Multiplexed immunofluorescence (mIF) and flow cytometry (FCM) analysis were performed to evaluate the immune-related molecules with therapeutic outcomes. ResultsGEM-based chemotherapy induced immunogenic cell death of cholangiocarcinoma cells, together with increased CD274 expression. In an ICC cohort, we found that upregulation of immune-checkpoint molecules and immune response-related pathways were significantly related to better clinical outcome. On the contrary, baseline immune-cell proportions in tumor tissues did not show any correlation with clinical benefit between responders and non-responders. Immune-related signature (including six genes) correlating with clinical outcome was identified according to the 12 ICC patients, and its predictive value was validated in a small ICC cohort with 26 patients. ConclusionImmune-related RNA signature predicts the outcome of PD-1 inhibitor-combined GEMCIS therapy in advanced intrahepatic cholangiocarcinoma, which could be tested as a biomarker for immune-chemotherapy in the future.</abstract><pub>Frontiers Media S.A</pub><doi>10.3389/fimmu.2022.943066</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
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immunochemotherapy
Immunology
intrahepatic cholangiocarcinoma
prognosis
tumor microenvironment
title Immune-related RNA signature predicts outcome of PD-1 inhibitor-combined GEMCIS therapy in advanced intrahepatic cholangiocarcinoma
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