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Percent change in apparent diffusion coefficient and plasma EBV DNA after induction chemotherapy identifies distinct prognostic response phenotypes in advanced nasopharyngeal carcinoma

BACKGROUND: To evaluate the prognostic value of the apparent diffusion coefficient (ADC) derived from diffusion-weighted magnetic resonance imaging (MRI) and monitor the early treatment response to induction chemotherapy (IC) with plasma EBV DNA in locoregionally advanced nasopharyngeal carcinoma (L...

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Autores principales: Liu, Li-Ting, Guo, Shan-Shan, Li, Hui, Lin, Chao, Sun, Rui, Chen, Qiu-Yan, Liang, Yu-Jing, Tang, Qing-Nan, Sun, Xue-Song, Tang, Lin-Quan, Xie, Chuan-Miao, Mai, Hai-Qiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8662833/
https://www.ncbi.nlm.nih.gov/pubmed/34886807
http://dx.doi.org/10.1186/s12885-021-09063-1
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author Liu, Li-Ting
Guo, Shan-Shan
Li, Hui
Lin, Chao
Sun, Rui
Chen, Qiu-Yan
Liang, Yu-Jing
Tang, Qing-Nan
Sun, Xue-Song
Tang, Lin-Quan
Xie, Chuan-Miao
Mai, Hai-Qiang
author_facet Liu, Li-Ting
Guo, Shan-Shan
Li, Hui
Lin, Chao
Sun, Rui
Chen, Qiu-Yan
Liang, Yu-Jing
Tang, Qing-Nan
Sun, Xue-Song
Tang, Lin-Quan
Xie, Chuan-Miao
Mai, Hai-Qiang
author_sort Liu, Li-Ting
collection PubMed
description BACKGROUND: To evaluate the prognostic value of the apparent diffusion coefficient (ADC) derived from diffusion-weighted magnetic resonance imaging (MRI) and monitor the early treatment response to induction chemotherapy (IC) with plasma EBV DNA in locoregionally advanced nasopharyngeal carcinoma (LA-NPC). RESULTS: A total of 307 stage III-IVb NPC patients were prospectively enrolled. All patients underwent MRI examinations to calculate ADC and plasma EBV DNA measurements pretreatment and post-IC. The participants’ ADC value of 92.5% (284/307) increased post-IC. A higher percent change in ADC value (ΔADC%(high) group) post-IC was associated with a higher 5-year OS rate (90.7% vs 74.9%, p < 0.001) than those in the ΔADC%(low) group. Interestingly, ΔADC% was closely related to the response measured by RECIST 1.1 (p < 0.001) and plasma EBV DNA level (p = 0.037). The AUC significantly increased when post-IC plasma EBV DNA was added to ΔADC% to predict treatment failure. Thus, based on ΔADC% and plasma EBV DNA, we further divided the participants into three new prognostic response phenotypes (early response, intermediate response, and no response) that correlated with disparate risks of death (p = 0.001), disease progression (p < 0.001), distant metastasis (p < 0.001), and locoregional relapse (p < 0.001). CONCLUSION: The percentage change in ADC post-IC is indicative of treatment response and clinical outcome. ΔADC% and plasma EBV DNA-based response phenotypes may provide potential utility for early termination of treatment and allow guiding risk-adapted therapeutic strategies for LA-NPC. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-021-09063-1.
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spelling pubmed-86628332021-12-10 Percent change in apparent diffusion coefficient and plasma EBV DNA after induction chemotherapy identifies distinct prognostic response phenotypes in advanced nasopharyngeal carcinoma Liu, Li-Ting Guo, Shan-Shan Li, Hui Lin, Chao Sun, Rui Chen, Qiu-Yan Liang, Yu-Jing Tang, Qing-Nan Sun, Xue-Song Tang, Lin-Quan Xie, Chuan-Miao Mai, Hai-Qiang BMC Cancer Research BACKGROUND: To evaluate the prognostic value of the apparent diffusion coefficient (ADC) derived from diffusion-weighted magnetic resonance imaging (MRI) and monitor the early treatment response to induction chemotherapy (IC) with plasma EBV DNA in locoregionally advanced nasopharyngeal carcinoma (LA-NPC). RESULTS: A total of 307 stage III-IVb NPC patients were prospectively enrolled. All patients underwent MRI examinations to calculate ADC and plasma EBV DNA measurements pretreatment and post-IC. The participants’ ADC value of 92.5% (284/307) increased post-IC. A higher percent change in ADC value (ΔADC%(high) group) post-IC was associated with a higher 5-year OS rate (90.7% vs 74.9%, p < 0.001) than those in the ΔADC%(low) group. Interestingly, ΔADC% was closely related to the response measured by RECIST 1.1 (p < 0.001) and plasma EBV DNA level (p = 0.037). The AUC significantly increased when post-IC plasma EBV DNA was added to ΔADC% to predict treatment failure. Thus, based on ΔADC% and plasma EBV DNA, we further divided the participants into three new prognostic response phenotypes (early response, intermediate response, and no response) that correlated with disparate risks of death (p = 0.001), disease progression (p < 0.001), distant metastasis (p < 0.001), and locoregional relapse (p < 0.001). CONCLUSION: The percentage change in ADC post-IC is indicative of treatment response and clinical outcome. ΔADC% and plasma EBV DNA-based response phenotypes may provide potential utility for early termination of treatment and allow guiding risk-adapted therapeutic strategies for LA-NPC. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-021-09063-1. BioMed Central 2021-12-09 /pmc/articles/PMC8662833/ /pubmed/34886807 http://dx.doi.org/10.1186/s12885-021-09063-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Liu, Li-Ting
Guo, Shan-Shan
Li, Hui
Lin, Chao
Sun, Rui
Chen, Qiu-Yan
Liang, Yu-Jing
Tang, Qing-Nan
Sun, Xue-Song
Tang, Lin-Quan
Xie, Chuan-Miao
Mai, Hai-Qiang
Percent change in apparent diffusion coefficient and plasma EBV DNA after induction chemotherapy identifies distinct prognostic response phenotypes in advanced nasopharyngeal carcinoma
title Percent change in apparent diffusion coefficient and plasma EBV DNA after induction chemotherapy identifies distinct prognostic response phenotypes in advanced nasopharyngeal carcinoma
title_full Percent change in apparent diffusion coefficient and plasma EBV DNA after induction chemotherapy identifies distinct prognostic response phenotypes in advanced nasopharyngeal carcinoma
title_fullStr Percent change in apparent diffusion coefficient and plasma EBV DNA after induction chemotherapy identifies distinct prognostic response phenotypes in advanced nasopharyngeal carcinoma
title_full_unstemmed Percent change in apparent diffusion coefficient and plasma EBV DNA after induction chemotherapy identifies distinct prognostic response phenotypes in advanced nasopharyngeal carcinoma
title_short Percent change in apparent diffusion coefficient and plasma EBV DNA after induction chemotherapy identifies distinct prognostic response phenotypes in advanced nasopharyngeal carcinoma
title_sort percent change in apparent diffusion coefficient and plasma ebv dna after induction chemotherapy identifies distinct prognostic response phenotypes in advanced nasopharyngeal carcinoma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8662833/
https://www.ncbi.nlm.nih.gov/pubmed/34886807
http://dx.doi.org/10.1186/s12885-021-09063-1
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