A prospective study of neoadjuvant pembrolizumab plus chemotherapy for resectable esophageal squamous cell carcinoma: The Keystone-001 trial
In this phase II study, 47 patients with locally advanced, resectable esophageal squamous cell carcinoma (ESCC) received three cycles of pembrolizumab plus chemotherapy, followed by Da Vinci robot-assisted surgery. The primary endpoints were safety and major pathological response (MPR). Key secondar...
Gespeichert in:
Veröffentlicht in: | Cancer cell 2024-10, Vol.42 (10), p.1747-1763.e7 |
---|---|
Hauptverfasser: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1763.e7 |
---|---|
container_issue | 10 |
container_start_page | 1747 |
container_title | Cancer cell |
container_volume | 42 |
creator | Shang, Xiaobin Xie, Yongjie Yu, Jinpu Zhang, Chen Zhao, Gang Liang, Fei Liu, Liang Zhang, Weihong Li, Runmei Yu, Wenwen Yue, Jie Chen, Chuangui Duan, Xiaofeng Ma, Zhao Chen, Zuoyu Xiong, Yanjuan Yang, Fan Xiao, Jianyu Zhang, Rui Liu, Pengpeng Cheng, Yanan Cao, Fuliang Guo, Feng Liu, Guoyan Meng, Bin Zhou, Dejun Sun, Yan Ren, Xiubao Yu, Jun Hao, Jihui Jiang, Hongjing |
description | In this phase II study, 47 patients with locally advanced, resectable esophageal squamous cell carcinoma (ESCC) received three cycles of pembrolizumab plus chemotherapy, followed by Da Vinci robot-assisted surgery. The primary endpoints were safety and major pathological response (MPR). Key secondary endpoints included complete pathological response (pCR) and survival. No grade ≥3 adverse events or surgical delays occurred during neoadjuvant therapy. Among 46 patients studied for efficacy, the MPR and pCR rates were 72% and 41%, respectively. After a median follow-up of 27.2 months, the 2-year overall survival (OS) and disease-free survival (DFS) rates were 91% and 89%, respectively. Expansion of TRGC2+ NKT cells in peripheral blood correlated with neoadjuvant treatment effectiveness, which was validated by in vitro organoid experiments and external cancer datasets, and its functional classification and mechanism of action were further explored. These findings show preoperative pembrolizumab plus chemotherapy is a promising therapeutic strategy for resectable ESCC.
[Display omitted]
•Neoadjuvant pembrolizumab + chemotherapy was explored in resectable stage III ESCC•Quality of life and nutritional status improved following neoadjuvant therapy•After a median follow-up of 27.2 months, the 2-year overall survival rate was 91%•TRGC2+ NKT cells in peripheral blood are a potential response biomarker
Shang et al. demonstrate the efficacy and safety of neoadjuvant pembrolizumab plus chemotherapy for patients with locally advanced, resectable esophageal squamous cell carcinoma in a phase II clinical trial. They identify TRGC2+ NKT cells as potential biomarkers of response using single-cell RNA-seq in peripheral blood. |
doi_str_mv | 10.1016/j.ccell.2024.09.008 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_3117073999</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1535610824003568</els_id><sourcerecordid>3117073999</sourcerecordid><originalsourceid>FETCH-LOGICAL-c1901-c22865d80f5e22ff1bbe90db6536fe0c0f19429a105ec4d569a50ef0f080e1f43</originalsourceid><addsrcrecordid>eNp9Uclu2zAQJYoGievkCwoUPPYiZaiFJgv0EBhdggTIJTkTFDWsaUiiTEoGnG_IR4eu0x5zmjm8N_MWQj4zyBkwfr3NjcGuywsoqhxkDiA-kAUTK5GVXPCPaa_LOuMMxAX5FOMWEout5Dm5KGUFnAm-IC83dAw-jmgmt0cap7k9UG_pgF6323mvh4mO2DfBd-557nVDx26O1Gyw99MGgx4P1PpAA8Z0QjcdUox-3Og_qDsad7Pu_RGfhFKjg3GD7_U3-rhBeoeHOPkBs6SLTsHp7pKcWd1FvHqbS_L088fj-nd2__Drdn1znxkmgWWmKASvWwG2xqKwljUNSmgbXpfcIhiwTFaF1AxqNFVbc6lrQAsWBCCzVbkkX093k_XdjHFSvYtHiTrZnqMqGVvBqpRSJmh5gpqUUgxo1Rhcr8NBMVDHGtRW_a1BHWtQIFWqIbG-vD2Ymx7b_5x_uSfA9xMAk829w6CicTgYbF1IOarWu3cfvAK-NJzB</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3117073999</pqid></control><display><type>article</type><title>A prospective study of neoadjuvant pembrolizumab plus chemotherapy for resectable esophageal squamous cell carcinoma: The Keystone-001 trial</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Shang, Xiaobin ; Xie, Yongjie ; Yu, Jinpu ; Zhang, Chen ; Zhao, Gang ; Liang, Fei ; Liu, Liang ; Zhang, Weihong ; Li, Runmei ; Yu, Wenwen ; Yue, Jie ; Chen, Chuangui ; Duan, Xiaofeng ; Ma, Zhao ; Chen, Zuoyu ; Xiong, Yanjuan ; Yang, Fan ; Xiao, Jianyu ; Zhang, Rui ; Liu, Pengpeng ; Cheng, Yanan ; Cao, Fuliang ; Guo, Feng ; Liu, Guoyan ; Meng, Bin ; Zhou, Dejun ; Sun, Yan ; Ren, Xiubao ; Yu, Jun ; Hao, Jihui ; Jiang, Hongjing</creator><creatorcontrib>Shang, Xiaobin ; Xie, Yongjie ; Yu, Jinpu ; Zhang, Chen ; Zhao, Gang ; Liang, Fei ; Liu, Liang ; Zhang, Weihong ; Li, Runmei ; Yu, Wenwen ; Yue, Jie ; Chen, Chuangui ; Duan, Xiaofeng ; Ma, Zhao ; Chen, Zuoyu ; Xiong, Yanjuan ; Yang, Fan ; Xiao, Jianyu ; Zhang, Rui ; Liu, Pengpeng ; Cheng, Yanan ; Cao, Fuliang ; Guo, Feng ; Liu, Guoyan ; Meng, Bin ; Zhou, Dejun ; Sun, Yan ; Ren, Xiubao ; Yu, Jun ; Hao, Jihui ; Jiang, Hongjing</creatorcontrib><description>In this phase II study, 47 patients with locally advanced, resectable esophageal squamous cell carcinoma (ESCC) received three cycles of pembrolizumab plus chemotherapy, followed by Da Vinci robot-assisted surgery. The primary endpoints were safety and major pathological response (MPR). Key secondary endpoints included complete pathological response (pCR) and survival. No grade ≥3 adverse events or surgical delays occurred during neoadjuvant therapy. Among 46 patients studied for efficacy, the MPR and pCR rates were 72% and 41%, respectively. After a median follow-up of 27.2 months, the 2-year overall survival (OS) and disease-free survival (DFS) rates were 91% and 89%, respectively. Expansion of TRGC2+ NKT cells in peripheral blood correlated with neoadjuvant treatment effectiveness, which was validated by in vitro organoid experiments and external cancer datasets, and its functional classification and mechanism of action were further explored. These findings show preoperative pembrolizumab plus chemotherapy is a promising therapeutic strategy for resectable ESCC.
[Display omitted]
•Neoadjuvant pembrolizumab + chemotherapy was explored in resectable stage III ESCC•Quality of life and nutritional status improved following neoadjuvant therapy•After a median follow-up of 27.2 months, the 2-year overall survival rate was 91%•TRGC2+ NKT cells in peripheral blood are a potential response biomarker
Shang et al. demonstrate the efficacy and safety of neoadjuvant pembrolizumab plus chemotherapy for patients with locally advanced, resectable esophageal squamous cell carcinoma in a phase II clinical trial. They identify TRGC2+ NKT cells as potential biomarkers of response using single-cell RNA-seq in peripheral blood.</description><identifier>ISSN: 1535-6108</identifier><identifier>ISSN: 1878-3686</identifier><identifier>EISSN: 1878-3686</identifier><identifier>DOI: 10.1016/j.ccell.2024.09.008</identifier><identifier>PMID: 39406186</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adult ; Aged ; Antibodies, Monoclonal, Humanized - administration & dosage ; Antibodies, Monoclonal, Humanized - therapeutic use ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Disease-Free Survival ; esophageal ; Esophageal Neoplasms - drug therapy ; Esophageal Neoplasms - pathology ; Esophageal Squamous Cell Carcinoma - drug therapy ; Esophageal Squamous Cell Carcinoma - mortality ; Esophageal Squamous Cell Carcinoma - pathology ; Esophageal Squamous Cell Carcinoma - surgery ; Esophageal Squamous Cell Carcinoma - therapy ; Female ; Humans ; immune checkpoint inhibitor ; locally advanced ; major pathological response ; Male ; Middle Aged ; neoadjuvant therapy ; Neoadjuvant Therapy - methods ; NKT cell subsets ; Prospective Studies ; robotic-assisted surgery ; single-cell RNA-seq ; squamous cell cancer ; TRGC2</subject><ispartof>Cancer cell, 2024-10, Vol.42 (10), p.1747-1763.e7</ispartof><rights>2024 Elsevier Inc.</rights><rights>Copyright © 2024 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c1901-c22865d80f5e22ff1bbe90db6536fe0c0f19429a105ec4d569a50ef0f080e1f43</cites><orcidid>0000-0002-3849-964X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ccell.2024.09.008$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39406186$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shang, Xiaobin</creatorcontrib><creatorcontrib>Xie, Yongjie</creatorcontrib><creatorcontrib>Yu, Jinpu</creatorcontrib><creatorcontrib>Zhang, Chen</creatorcontrib><creatorcontrib>Zhao, Gang</creatorcontrib><creatorcontrib>Liang, Fei</creatorcontrib><creatorcontrib>Liu, Liang</creatorcontrib><creatorcontrib>Zhang, Weihong</creatorcontrib><creatorcontrib>Li, Runmei</creatorcontrib><creatorcontrib>Yu, Wenwen</creatorcontrib><creatorcontrib>Yue, Jie</creatorcontrib><creatorcontrib>Chen, Chuangui</creatorcontrib><creatorcontrib>Duan, Xiaofeng</creatorcontrib><creatorcontrib>Ma, Zhao</creatorcontrib><creatorcontrib>Chen, Zuoyu</creatorcontrib><creatorcontrib>Xiong, Yanjuan</creatorcontrib><creatorcontrib>Yang, Fan</creatorcontrib><creatorcontrib>Xiao, Jianyu</creatorcontrib><creatorcontrib>Zhang, Rui</creatorcontrib><creatorcontrib>Liu, Pengpeng</creatorcontrib><creatorcontrib>Cheng, Yanan</creatorcontrib><creatorcontrib>Cao, Fuliang</creatorcontrib><creatorcontrib>Guo, Feng</creatorcontrib><creatorcontrib>Liu, Guoyan</creatorcontrib><creatorcontrib>Meng, Bin</creatorcontrib><creatorcontrib>Zhou, Dejun</creatorcontrib><creatorcontrib>Sun, Yan</creatorcontrib><creatorcontrib>Ren, Xiubao</creatorcontrib><creatorcontrib>Yu, Jun</creatorcontrib><creatorcontrib>Hao, Jihui</creatorcontrib><creatorcontrib>Jiang, Hongjing</creatorcontrib><title>A prospective study of neoadjuvant pembrolizumab plus chemotherapy for resectable esophageal squamous cell carcinoma: The Keystone-001 trial</title><title>Cancer cell</title><addtitle>Cancer Cell</addtitle><description>In this phase II study, 47 patients with locally advanced, resectable esophageal squamous cell carcinoma (ESCC) received three cycles of pembrolizumab plus chemotherapy, followed by Da Vinci robot-assisted surgery. The primary endpoints were safety and major pathological response (MPR). Key secondary endpoints included complete pathological response (pCR) and survival. No grade ≥3 adverse events or surgical delays occurred during neoadjuvant therapy. Among 46 patients studied for efficacy, the MPR and pCR rates were 72% and 41%, respectively. After a median follow-up of 27.2 months, the 2-year overall survival (OS) and disease-free survival (DFS) rates were 91% and 89%, respectively. Expansion of TRGC2+ NKT cells in peripheral blood correlated with neoadjuvant treatment effectiveness, which was validated by in vitro organoid experiments and external cancer datasets, and its functional classification and mechanism of action were further explored. These findings show preoperative pembrolizumab plus chemotherapy is a promising therapeutic strategy for resectable ESCC.
[Display omitted]
•Neoadjuvant pembrolizumab + chemotherapy was explored in resectable stage III ESCC•Quality of life and nutritional status improved following neoadjuvant therapy•After a median follow-up of 27.2 months, the 2-year overall survival rate was 91%•TRGC2+ NKT cells in peripheral blood are a potential response biomarker
Shang et al. demonstrate the efficacy and safety of neoadjuvant pembrolizumab plus chemotherapy for patients with locally advanced, resectable esophageal squamous cell carcinoma in a phase II clinical trial. They identify TRGC2+ NKT cells as potential biomarkers of response using single-cell RNA-seq in peripheral blood.</description><subject>Adult</subject><subject>Aged</subject><subject>Antibodies, Monoclonal, Humanized - administration & dosage</subject><subject>Antibodies, Monoclonal, Humanized - therapeutic use</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Disease-Free Survival</subject><subject>esophageal</subject><subject>Esophageal Neoplasms - drug therapy</subject><subject>Esophageal Neoplasms - pathology</subject><subject>Esophageal Squamous Cell Carcinoma - drug therapy</subject><subject>Esophageal Squamous Cell Carcinoma - mortality</subject><subject>Esophageal Squamous Cell Carcinoma - pathology</subject><subject>Esophageal Squamous Cell Carcinoma - surgery</subject><subject>Esophageal Squamous Cell Carcinoma - therapy</subject><subject>Female</subject><subject>Humans</subject><subject>immune checkpoint inhibitor</subject><subject>locally advanced</subject><subject>major pathological response</subject><subject>Male</subject><subject>Middle Aged</subject><subject>neoadjuvant therapy</subject><subject>Neoadjuvant Therapy - methods</subject><subject>NKT cell subsets</subject><subject>Prospective Studies</subject><subject>robotic-assisted surgery</subject><subject>single-cell RNA-seq</subject><subject>squamous cell cancer</subject><subject>TRGC2</subject><issn>1535-6108</issn><issn>1878-3686</issn><issn>1878-3686</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9Uclu2zAQJYoGievkCwoUPPYiZaiFJgv0EBhdggTIJTkTFDWsaUiiTEoGnG_IR4eu0x5zmjm8N_MWQj4zyBkwfr3NjcGuywsoqhxkDiA-kAUTK5GVXPCPaa_LOuMMxAX5FOMWEout5Dm5KGUFnAm-IC83dAw-jmgmt0cap7k9UG_pgF6323mvh4mO2DfBd-557nVDx26O1Gyw99MGgx4P1PpAA8Z0QjcdUox-3Og_qDsad7Pu_RGfhFKjg3GD7_U3-rhBeoeHOPkBs6SLTsHp7pKcWd1FvHqbS_L088fj-nd2__Drdn1znxkmgWWmKASvWwG2xqKwljUNSmgbXpfcIhiwTFaF1AxqNFVbc6lrQAsWBCCzVbkkX093k_XdjHFSvYtHiTrZnqMqGVvBqpRSJmh5gpqUUgxo1Rhcr8NBMVDHGtRW_a1BHWtQIFWqIbG-vD2Ymx7b_5x_uSfA9xMAk829w6CicTgYbF1IOarWu3cfvAK-NJzB</recordid><startdate>20241014</startdate><enddate>20241014</enddate><creator>Shang, Xiaobin</creator><creator>Xie, Yongjie</creator><creator>Yu, Jinpu</creator><creator>Zhang, Chen</creator><creator>Zhao, Gang</creator><creator>Liang, Fei</creator><creator>Liu, Liang</creator><creator>Zhang, Weihong</creator><creator>Li, Runmei</creator><creator>Yu, Wenwen</creator><creator>Yue, Jie</creator><creator>Chen, Chuangui</creator><creator>Duan, Xiaofeng</creator><creator>Ma, Zhao</creator><creator>Chen, Zuoyu</creator><creator>Xiong, Yanjuan</creator><creator>Yang, Fan</creator><creator>Xiao, Jianyu</creator><creator>Zhang, Rui</creator><creator>Liu, Pengpeng</creator><creator>Cheng, Yanan</creator><creator>Cao, Fuliang</creator><creator>Guo, Feng</creator><creator>Liu, Guoyan</creator><creator>Meng, Bin</creator><creator>Zhou, Dejun</creator><creator>Sun, Yan</creator><creator>Ren, Xiubao</creator><creator>Yu, Jun</creator><creator>Hao, Jihui</creator><creator>Jiang, Hongjing</creator><general>Elsevier Inc</general><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/0000-0002-3849-964X</orcidid></search><sort><creationdate>20241014</creationdate><title>A prospective study of neoadjuvant pembrolizumab plus chemotherapy for resectable esophageal squamous cell carcinoma: The Keystone-001 trial</title><author>Shang, Xiaobin ; Xie, Yongjie ; Yu, Jinpu ; Zhang, Chen ; Zhao, Gang ; Liang, Fei ; Liu, Liang ; Zhang, Weihong ; Li, Runmei ; Yu, Wenwen ; Yue, Jie ; Chen, Chuangui ; Duan, Xiaofeng ; Ma, Zhao ; Chen, Zuoyu ; Xiong, Yanjuan ; Yang, Fan ; Xiao, Jianyu ; Zhang, Rui ; Liu, Pengpeng ; Cheng, Yanan ; Cao, Fuliang ; Guo, Feng ; Liu, Guoyan ; Meng, Bin ; Zhou, Dejun ; Sun, Yan ; Ren, Xiubao ; Yu, Jun ; Hao, Jihui ; Jiang, Hongjing</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1901-c22865d80f5e22ff1bbe90db6536fe0c0f19429a105ec4d569a50ef0f080e1f43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Antibodies, Monoclonal, Humanized - administration & dosage</topic><topic>Antibodies, Monoclonal, Humanized - therapeutic use</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Disease-Free Survival</topic><topic>esophageal</topic><topic>Esophageal Neoplasms - drug therapy</topic><topic>Esophageal Neoplasms - pathology</topic><topic>Esophageal Squamous Cell Carcinoma - drug therapy</topic><topic>Esophageal Squamous Cell Carcinoma - mortality</topic><topic>Esophageal Squamous Cell Carcinoma - pathology</topic><topic>Esophageal Squamous Cell Carcinoma - surgery</topic><topic>Esophageal Squamous Cell Carcinoma - therapy</topic><topic>Female</topic><topic>Humans</topic><topic>immune checkpoint inhibitor</topic><topic>locally advanced</topic><topic>major pathological response</topic><topic>Male</topic><topic>Middle Aged</topic><topic>neoadjuvant therapy</topic><topic>Neoadjuvant Therapy - methods</topic><topic>NKT cell subsets</topic><topic>Prospective Studies</topic><topic>robotic-assisted surgery</topic><topic>single-cell RNA-seq</topic><topic>squamous cell cancer</topic><topic>TRGC2</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shang, Xiaobin</creatorcontrib><creatorcontrib>Xie, Yongjie</creatorcontrib><creatorcontrib>Yu, Jinpu</creatorcontrib><creatorcontrib>Zhang, Chen</creatorcontrib><creatorcontrib>Zhao, Gang</creatorcontrib><creatorcontrib>Liang, Fei</creatorcontrib><creatorcontrib>Liu, Liang</creatorcontrib><creatorcontrib>Zhang, Weihong</creatorcontrib><creatorcontrib>Li, Runmei</creatorcontrib><creatorcontrib>Yu, Wenwen</creatorcontrib><creatorcontrib>Yue, Jie</creatorcontrib><creatorcontrib>Chen, Chuangui</creatorcontrib><creatorcontrib>Duan, Xiaofeng</creatorcontrib><creatorcontrib>Ma, Zhao</creatorcontrib><creatorcontrib>Chen, Zuoyu</creatorcontrib><creatorcontrib>Xiong, Yanjuan</creatorcontrib><creatorcontrib>Yang, Fan</creatorcontrib><creatorcontrib>Xiao, Jianyu</creatorcontrib><creatorcontrib>Zhang, Rui</creatorcontrib><creatorcontrib>Liu, Pengpeng</creatorcontrib><creatorcontrib>Cheng, Yanan</creatorcontrib><creatorcontrib>Cao, Fuliang</creatorcontrib><creatorcontrib>Guo, Feng</creatorcontrib><creatorcontrib>Liu, Guoyan</creatorcontrib><creatorcontrib>Meng, Bin</creatorcontrib><creatorcontrib>Zhou, Dejun</creatorcontrib><creatorcontrib>Sun, Yan</creatorcontrib><creatorcontrib>Ren, Xiubao</creatorcontrib><creatorcontrib>Yu, Jun</creatorcontrib><creatorcontrib>Hao, Jihui</creatorcontrib><creatorcontrib>Jiang, Hongjing</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>Cancer cell</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shang, Xiaobin</au><au>Xie, Yongjie</au><au>Yu, Jinpu</au><au>Zhang, Chen</au><au>Zhao, Gang</au><au>Liang, Fei</au><au>Liu, Liang</au><au>Zhang, Weihong</au><au>Li, Runmei</au><au>Yu, Wenwen</au><au>Yue, Jie</au><au>Chen, Chuangui</au><au>Duan, Xiaofeng</au><au>Ma, Zhao</au><au>Chen, Zuoyu</au><au>Xiong, Yanjuan</au><au>Yang, Fan</au><au>Xiao, Jianyu</au><au>Zhang, Rui</au><au>Liu, Pengpeng</au><au>Cheng, Yanan</au><au>Cao, Fuliang</au><au>Guo, Feng</au><au>Liu, Guoyan</au><au>Meng, Bin</au><au>Zhou, Dejun</au><au>Sun, Yan</au><au>Ren, Xiubao</au><au>Yu, Jun</au><au>Hao, Jihui</au><au>Jiang, Hongjing</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A prospective study of neoadjuvant pembrolizumab plus chemotherapy for resectable esophageal squamous cell carcinoma: The Keystone-001 trial</atitle><jtitle>Cancer cell</jtitle><addtitle>Cancer Cell</addtitle><date>2024-10-14</date><risdate>2024</risdate><volume>42</volume><issue>10</issue><spage>1747</spage><epage>1763.e7</epage><pages>1747-1763.e7</pages><issn>1535-6108</issn><issn>1878-3686</issn><eissn>1878-3686</eissn><abstract>In this phase II study, 47 patients with locally advanced, resectable esophageal squamous cell carcinoma (ESCC) received three cycles of pembrolizumab plus chemotherapy, followed by Da Vinci robot-assisted surgery. The primary endpoints were safety and major pathological response (MPR). Key secondary endpoints included complete pathological response (pCR) and survival. No grade ≥3 adverse events or surgical delays occurred during neoadjuvant therapy. Among 46 patients studied for efficacy, the MPR and pCR rates were 72% and 41%, respectively. After a median follow-up of 27.2 months, the 2-year overall survival (OS) and disease-free survival (DFS) rates were 91% and 89%, respectively. Expansion of TRGC2+ NKT cells in peripheral blood correlated with neoadjuvant treatment effectiveness, which was validated by in vitro organoid experiments and external cancer datasets, and its functional classification and mechanism of action were further explored. These findings show preoperative pembrolizumab plus chemotherapy is a promising therapeutic strategy for resectable ESCC.
[Display omitted]
•Neoadjuvant pembrolizumab + chemotherapy was explored in resectable stage III ESCC•Quality of life and nutritional status improved following neoadjuvant therapy•After a median follow-up of 27.2 months, the 2-year overall survival rate was 91%•TRGC2+ NKT cells in peripheral blood are a potential response biomarker
Shang et al. demonstrate the efficacy and safety of neoadjuvant pembrolizumab plus chemotherapy for patients with locally advanced, resectable esophageal squamous cell carcinoma in a phase II clinical trial. They identify TRGC2+ NKT cells as potential biomarkers of response using single-cell RNA-seq in peripheral blood.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>39406186</pmid><doi>10.1016/j.ccell.2024.09.008</doi><orcidid>https://orcid.org/0000-0002-3849-964X</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1535-6108 |
ispartof | Cancer cell, 2024-10, Vol.42 (10), p.1747-1763.e7 |
issn | 1535-6108 1878-3686 1878-3686 |
language | eng |
recordid | cdi_proquest_miscellaneous_3117073999 |
source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | Adult Aged Antibodies, Monoclonal, Humanized - administration & dosage Antibodies, Monoclonal, Humanized - therapeutic use Antineoplastic Combined Chemotherapy Protocols - therapeutic use Disease-Free Survival esophageal Esophageal Neoplasms - drug therapy Esophageal Neoplasms - pathology Esophageal Squamous Cell Carcinoma - drug therapy Esophageal Squamous Cell Carcinoma - mortality Esophageal Squamous Cell Carcinoma - pathology Esophageal Squamous Cell Carcinoma - surgery Esophageal Squamous Cell Carcinoma - therapy Female Humans immune checkpoint inhibitor locally advanced major pathological response Male Middle Aged neoadjuvant therapy Neoadjuvant Therapy - methods NKT cell subsets Prospective Studies robotic-assisted surgery single-cell RNA-seq squamous cell cancer TRGC2 |
title | A prospective study of neoadjuvant pembrolizumab plus chemotherapy for resectable esophageal squamous cell carcinoma: The Keystone-001 trial |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-18T02%3A17%3A49IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20prospective%20study%20of%20neoadjuvant%20pembrolizumab%20plus%20chemotherapy%20for%20resectable%20esophageal%20squamous%20cell%20carcinoma:%20The%20Keystone-001%20trial&rft.jtitle=Cancer%20cell&rft.au=Shang,%20Xiaobin&rft.date=2024-10-14&rft.volume=42&rft.issue=10&rft.spage=1747&rft.epage=1763.e7&rft.pages=1747-1763.e7&rft.issn=1535-6108&rft.eissn=1878-3686&rft_id=info:doi/10.1016/j.ccell.2024.09.008&rft_dat=%3Cproquest_cross%3E3117073999%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=3117073999&rft_id=info:pmid/39406186&rft_els_id=S1535610824003568&rfr_iscdi=true |