Significance of longitudinal Epstein–Barr virus DNA combined with multipoint tumor response for dynamic risk stratification and treatment adaptation in nasopharyngeal carcinoma
Dynamic therapy response is strongly associated with cancer outcomes. This study aimed to evaluate the significance of longitudinal Epstein–Barr virus (EBV) DNA and radiological tumor regression in risk stratification and response-adaptive treatment in locally-advanced nasopharyngeal carcinoma (LA-N...
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Veröffentlicht in: | Cancer letters 2024-11, Vol.605, p.217276, Article 217276 |
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creator | Liu, Yang Yan, Wenbin Qi, Xiaogai Zhang, Ye Wang, Kai Qu, Yuan Chen, Xuesong Zhang, Jianghu Luo, Jingwei Li, Ye-Xiong Huang, Xiaodong Wu, Runye Wang, Jingbo Yi, Junlin |
description | Dynamic therapy response is strongly associated with cancer outcomes. This study aimed to evaluate the significance of longitudinal Epstein–Barr virus (EBV) DNA and radiological tumor regression in risk stratification and response-adaptive treatment in locally-advanced nasopharyngeal carcinoma (LA-NPC). In total, 1312 patients from two centers were assigned to the training and validation cohorts. Based on the multipoint examination of EBV-DNA and tumor response, four post-induction chemotherapy, four mid-radiotherapy, and four post-radiotherapy subgroups were established. Then seven phenotypes were further generated according to different permutations and combinations. These phenotypes were subsequently congregated into four response clusters, which reflect distinct biological treatment responses. The four response clusters correlated with an evident 5-year progression-free survival in both the training and external validation cohorts (5-year: training cohort 91.1 %, 82.8 %, 30.6 %, and 10.0 %; external validation 94.4 %, 55.6 %, 40.0 %, and 12.7 %) had superior prognostic performance compared to TNM staging and nomogram model (concordance index: training cohort—0.825 vs. 0.603 vs. 0.756 and external validation—0.834 vs. 0.606 vs. 0.789). Importantly, the response clusters exhibited an excellent capability in selecting candidates who can benefit from adjuvant chemotherapy. In conclusion, risk stratification based on the dynamic assessment of both radiological and biological responses can significantly enhance prognostic insights and shed light on individualized treatment modifications in LA-NPCs.
•Using longitudinal cfEBV DNA and tumor response, we identified four response clusters.•The clusters had superior prognostic performance compared to conventional models.•The clusters provided a potential avenue for optimizing real-time treatment selection.•Dynamic treatment response biomarkers enhance prognostic insight and tailored therapy. |
doi_str_mv | 10.1016/j.canlet.2024.217276 |
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•Using longitudinal cfEBV DNA and tumor response, we identified four response clusters.•The clusters had superior prognostic performance compared to conventional models.•The clusters provided a potential avenue for optimizing real-time treatment selection.•Dynamic treatment response biomarkers enhance prognostic insight and tailored therapy.</description><identifier>ISSN: 0304-3835</identifier><identifier>ISSN: 1872-7980</identifier><identifier>EISSN: 1872-7980</identifier><identifier>DOI: 10.1016/j.canlet.2024.217276</identifier><identifier>PMID: 39349290</identifier><language>eng</language><publisher>Ireland: Elsevier B.V</publisher><subject>Adult ; Aged ; DNA, Viral - genetics ; EBV-DNA ; Epstein-Barr Virus Infections - complications ; Epstein-Barr Virus Infections - virology ; Female ; Herpesvirus 4, Human - genetics ; Humans ; Induction Chemotherapy ; Longitudinal tumor response ; Male ; Middle Aged ; Nasopharyngeal carcinoma ; Nasopharyngeal Carcinoma - pathology ; Nasopharyngeal Carcinoma - therapy ; Nasopharyngeal Carcinoma - virology ; Nasopharyngeal Neoplasms - mortality ; Nasopharyngeal Neoplasms - pathology ; Nasopharyngeal Neoplasms - therapy ; Nasopharyngeal Neoplasms - virology ; Neoplasm Staging ; Nomograms ; Prognosis ; Progression-Free Survival ; Risk Assessment ; Risk stratification ; Treatment selection</subject><ispartof>Cancer letters, 2024-11, Vol.605, p.217276, Article 217276</ispartof><rights>2024 Elsevier B.V.</rights><rights>Copyright © 2024 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c241t-9fcecc9677c696cea55a43fbba73e27e87913ca287e3118f46e031b4bee061bf3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0304383524006712$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,65309</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39349290$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Yang</creatorcontrib><creatorcontrib>Yan, Wenbin</creatorcontrib><creatorcontrib>Qi, Xiaogai</creatorcontrib><creatorcontrib>Zhang, Ye</creatorcontrib><creatorcontrib>Wang, Kai</creatorcontrib><creatorcontrib>Qu, Yuan</creatorcontrib><creatorcontrib>Chen, Xuesong</creatorcontrib><creatorcontrib>Zhang, Jianghu</creatorcontrib><creatorcontrib>Luo, Jingwei</creatorcontrib><creatorcontrib>Li, Ye-Xiong</creatorcontrib><creatorcontrib>Huang, Xiaodong</creatorcontrib><creatorcontrib>Wu, Runye</creatorcontrib><creatorcontrib>Wang, Jingbo</creatorcontrib><creatorcontrib>Yi, Junlin</creatorcontrib><title>Significance of longitudinal Epstein–Barr virus DNA combined with multipoint tumor response for dynamic risk stratification and treatment adaptation in nasopharyngeal carcinoma</title><title>Cancer letters</title><addtitle>Cancer Lett</addtitle><description>Dynamic therapy response is strongly associated with cancer outcomes. This study aimed to evaluate the significance of longitudinal Epstein–Barr virus (EBV) DNA and radiological tumor regression in risk stratification and response-adaptive treatment in locally-advanced nasopharyngeal carcinoma (LA-NPC). In total, 1312 patients from two centers were assigned to the training and validation cohorts. Based on the multipoint examination of EBV-DNA and tumor response, four post-induction chemotherapy, four mid-radiotherapy, and four post-radiotherapy subgroups were established. Then seven phenotypes were further generated according to different permutations and combinations. These phenotypes were subsequently congregated into four response clusters, which reflect distinct biological treatment responses. The four response clusters correlated with an evident 5-year progression-free survival in both the training and external validation cohorts (5-year: training cohort 91.1 %, 82.8 %, 30.6 %, and 10.0 %; external validation 94.4 %, 55.6 %, 40.0 %, and 12.7 %) had superior prognostic performance compared to TNM staging and nomogram model (concordance index: training cohort—0.825 vs. 0.603 vs. 0.756 and external validation—0.834 vs. 0.606 vs. 0.789). Importantly, the response clusters exhibited an excellent capability in selecting candidates who can benefit from adjuvant chemotherapy. In conclusion, risk stratification based on the dynamic assessment of both radiological and biological responses can significantly enhance prognostic insights and shed light on individualized treatment modifications in LA-NPCs.
•Using longitudinal cfEBV DNA and tumor response, we identified four response clusters.•The clusters had superior prognostic performance compared to conventional models.•The clusters provided a potential avenue for optimizing real-time treatment selection.•Dynamic treatment response biomarkers enhance prognostic insight and tailored therapy.</description><subject>Adult</subject><subject>Aged</subject><subject>DNA, Viral - genetics</subject><subject>EBV-DNA</subject><subject>Epstein-Barr Virus Infections - complications</subject><subject>Epstein-Barr Virus Infections - virology</subject><subject>Female</subject><subject>Herpesvirus 4, Human - genetics</subject><subject>Humans</subject><subject>Induction Chemotherapy</subject><subject>Longitudinal tumor response</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Nasopharyngeal carcinoma</subject><subject>Nasopharyngeal Carcinoma - pathology</subject><subject>Nasopharyngeal Carcinoma - therapy</subject><subject>Nasopharyngeal Carcinoma - virology</subject><subject>Nasopharyngeal Neoplasms - mortality</subject><subject>Nasopharyngeal Neoplasms - pathology</subject><subject>Nasopharyngeal Neoplasms - therapy</subject><subject>Nasopharyngeal Neoplasms - virology</subject><subject>Neoplasm Staging</subject><subject>Nomograms</subject><subject>Prognosis</subject><subject>Progression-Free Survival</subject><subject>Risk Assessment</subject><subject>Risk stratification</subject><subject>Treatment selection</subject><issn>0304-3835</issn><issn>1872-7980</issn><issn>1872-7980</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kUFu1TAQhi0Eoo_CDRDyks172HESJxuk0pYWqYIFsLYmzuR1HokdbKeoO-7ATTgSJ8ElhSWr0Wj-f_4ZfYw9l2InhaxfHXYW3IhpV4ii3BVSF7p-wDay0cVWt414yDZCiXKrGlUdsScxHoQQVamrx-xItapsi1Zs2M-PtHc0UN5lkfuBj97tKS09ORj5-RwTkvv1_ccbCIHfUFgiP3t_wq2fOnLY82-Urvm0jIlmTy7xtEw-8IBx9i4iH3LT3zqYyPJA8QuPKUD6k5fIOw6u5ykgpAmzGXqY0zogxx1EP19DuHV7zLdYCJacn-ApezTAGPHZfT1mn9-efzq93F59uHh3enK1tUUp07YdLFrb1lrbuq0tQlVBqYauA62w0NjoVioLRaNRSdkMZY1Cya7sEEUtu0Eds5fr3jn4rwvGZCaKFscRHPolmuyStaqUFFlarlIbfIwBBzMHmvLpRgpzR8sczErL3NEyK61se3GfsHQT9v9Mf_FkwetVgPnPG8JgoiXMpHoKaJPpPf0_4TdXMK61</recordid><startdate>20241128</startdate><enddate>20241128</enddate><creator>Liu, Yang</creator><creator>Yan, Wenbin</creator><creator>Qi, Xiaogai</creator><creator>Zhang, Ye</creator><creator>Wang, Kai</creator><creator>Qu, Yuan</creator><creator>Chen, Xuesong</creator><creator>Zhang, Jianghu</creator><creator>Luo, Jingwei</creator><creator>Li, Ye-Xiong</creator><creator>Huang, Xiaodong</creator><creator>Wu, Runye</creator><creator>Wang, Jingbo</creator><creator>Yi, Junlin</creator><general>Elsevier B.V</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></search><sort><creationdate>20241128</creationdate><title>Significance of longitudinal Epstein–Barr virus DNA combined with multipoint tumor response for dynamic risk stratification and treatment adaptation in nasopharyngeal carcinoma</title><author>Liu, Yang ; Yan, Wenbin ; Qi, Xiaogai ; Zhang, Ye ; Wang, Kai ; Qu, Yuan ; Chen, Xuesong ; Zhang, Jianghu ; Luo, Jingwei ; Li, Ye-Xiong ; Huang, Xiaodong ; Wu, Runye ; Wang, Jingbo ; Yi, Junlin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c241t-9fcecc9677c696cea55a43fbba73e27e87913ca287e3118f46e031b4bee061bf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adult</topic><topic>Aged</topic><topic>DNA, Viral - genetics</topic><topic>EBV-DNA</topic><topic>Epstein-Barr Virus Infections - complications</topic><topic>Epstein-Barr Virus Infections - virology</topic><topic>Female</topic><topic>Herpesvirus 4, Human - genetics</topic><topic>Humans</topic><topic>Induction Chemotherapy</topic><topic>Longitudinal tumor response</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Nasopharyngeal carcinoma</topic><topic>Nasopharyngeal Carcinoma - pathology</topic><topic>Nasopharyngeal Carcinoma - therapy</topic><topic>Nasopharyngeal Carcinoma - virology</topic><topic>Nasopharyngeal Neoplasms - mortality</topic><topic>Nasopharyngeal Neoplasms - pathology</topic><topic>Nasopharyngeal Neoplasms - therapy</topic><topic>Nasopharyngeal Neoplasms - virology</topic><topic>Neoplasm Staging</topic><topic>Nomograms</topic><topic>Prognosis</topic><topic>Progression-Free Survival</topic><topic>Risk Assessment</topic><topic>Risk stratification</topic><topic>Treatment selection</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Yang</creatorcontrib><creatorcontrib>Yan, Wenbin</creatorcontrib><creatorcontrib>Qi, Xiaogai</creatorcontrib><creatorcontrib>Zhang, Ye</creatorcontrib><creatorcontrib>Wang, Kai</creatorcontrib><creatorcontrib>Qu, Yuan</creatorcontrib><creatorcontrib>Chen, Xuesong</creatorcontrib><creatorcontrib>Zhang, Jianghu</creatorcontrib><creatorcontrib>Luo, Jingwei</creatorcontrib><creatorcontrib>Li, Ye-Xiong</creatorcontrib><creatorcontrib>Huang, Xiaodong</creatorcontrib><creatorcontrib>Wu, Runye</creatorcontrib><creatorcontrib>Wang, Jingbo</creatorcontrib><creatorcontrib>Yi, Junlin</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 letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Yang</au><au>Yan, Wenbin</au><au>Qi, Xiaogai</au><au>Zhang, Ye</au><au>Wang, Kai</au><au>Qu, Yuan</au><au>Chen, Xuesong</au><au>Zhang, Jianghu</au><au>Luo, Jingwei</au><au>Li, Ye-Xiong</au><au>Huang, Xiaodong</au><au>Wu, Runye</au><au>Wang, Jingbo</au><au>Yi, Junlin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Significance of longitudinal Epstein–Barr virus DNA combined with multipoint tumor response for dynamic risk stratification and treatment adaptation in nasopharyngeal carcinoma</atitle><jtitle>Cancer letters</jtitle><addtitle>Cancer Lett</addtitle><date>2024-11-28</date><risdate>2024</risdate><volume>605</volume><spage>217276</spage><pages>217276-</pages><artnum>217276</artnum><issn>0304-3835</issn><issn>1872-7980</issn><eissn>1872-7980</eissn><abstract>Dynamic therapy response is strongly associated with cancer outcomes. This study aimed to evaluate the significance of longitudinal Epstein–Barr virus (EBV) DNA and radiological tumor regression in risk stratification and response-adaptive treatment in locally-advanced nasopharyngeal carcinoma (LA-NPC). In total, 1312 patients from two centers were assigned to the training and validation cohorts. Based on the multipoint examination of EBV-DNA and tumor response, four post-induction chemotherapy, four mid-radiotherapy, and four post-radiotherapy subgroups were established. Then seven phenotypes were further generated according to different permutations and combinations. These phenotypes were subsequently congregated into four response clusters, which reflect distinct biological treatment responses. The four response clusters correlated with an evident 5-year progression-free survival in both the training and external validation cohorts (5-year: training cohort 91.1 %, 82.8 %, 30.6 %, and 10.0 %; external validation 94.4 %, 55.6 %, 40.0 %, and 12.7 %) had superior prognostic performance compared to TNM staging and nomogram model (concordance index: training cohort—0.825 vs. 0.603 vs. 0.756 and external validation—0.834 vs. 0.606 vs. 0.789). Importantly, the response clusters exhibited an excellent capability in selecting candidates who can benefit from adjuvant chemotherapy. In conclusion, risk stratification based on the dynamic assessment of both radiological and biological responses can significantly enhance prognostic insights and shed light on individualized treatment modifications in LA-NPCs.
•Using longitudinal cfEBV DNA and tumor response, we identified four response clusters.•The clusters had superior prognostic performance compared to conventional models.•The clusters provided a potential avenue for optimizing real-time treatment selection.•Dynamic treatment response biomarkers enhance prognostic insight and tailored therapy.</abstract><cop>Ireland</cop><pub>Elsevier B.V</pub><pmid>39349290</pmid><doi>10.1016/j.canlet.2024.217276</doi></addata></record> |
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subjects | Adult Aged DNA, Viral - genetics EBV-DNA Epstein-Barr Virus Infections - complications Epstein-Barr Virus Infections - virology Female Herpesvirus 4, Human - genetics Humans Induction Chemotherapy Longitudinal tumor response Male Middle Aged Nasopharyngeal carcinoma Nasopharyngeal Carcinoma - pathology Nasopharyngeal Carcinoma - therapy Nasopharyngeal Carcinoma - virology Nasopharyngeal Neoplasms - mortality Nasopharyngeal Neoplasms - pathology Nasopharyngeal Neoplasms - therapy Nasopharyngeal Neoplasms - virology Neoplasm Staging Nomograms Prognosis Progression-Free Survival Risk Assessment Risk stratification Treatment selection |
title | Significance of longitudinal Epstein–Barr virus DNA combined with multipoint tumor response for dynamic risk stratification and treatment adaptation in nasopharyngeal carcinoma |
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