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Nomogram constructed by immunological and inflammatory indicators for predicting prognosis of patients with esophageal squamous cell carcinoma treated with neoadjuvant chemoradiotherapy plus surgery

OBJECTIVES: At present, esophageal squamous cell carcinoma (ESCC) patients accepting neoadjuvant chemoradiotherapy (nCRT) plus surgery lack corresponding prognostic indicators. This study aimed to construct a prognostic prediction model for ESCC patients undergoing nCRT and surgery based on immune a...

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Autores principales: Luo, Yun, Weng, Xue-Fen, Huang, Jia-Tao, Hu, Xue-Hao, Wei, Lai-Feng, Lin, Yi-Wei, Ding, Tian-Yan, Zhang, Biao, Chu, Ling-Yu, Liu, Can-Tong, Peng, Yu-Hui, Xu, Yi-Wei, Wu, Fang-Cai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9373798/
https://www.ncbi.nlm.nih.gov/pubmed/35965555
http://dx.doi.org/10.3389/fonc.2022.882900
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author Luo, Yun
Weng, Xue-Fen
Huang, Jia-Tao
Hu, Xue-Hao
Wei, Lai-Feng
Lin, Yi-Wei
Ding, Tian-Yan
Zhang, Biao
Chu, Ling-Yu
Liu, Can-Tong
Peng, Yu-Hui
Xu, Yi-Wei
Wu, Fang-Cai
author_facet Luo, Yun
Weng, Xue-Fen
Huang, Jia-Tao
Hu, Xue-Hao
Wei, Lai-Feng
Lin, Yi-Wei
Ding, Tian-Yan
Zhang, Biao
Chu, Ling-Yu
Liu, Can-Tong
Peng, Yu-Hui
Xu, Yi-Wei
Wu, Fang-Cai
author_sort Luo, Yun
collection PubMed
description OBJECTIVES: At present, esophageal squamous cell carcinoma (ESCC) patients accepting neoadjuvant chemoradiotherapy (nCRT) plus surgery lack corresponding prognostic indicators. This study aimed to construct a prognostic prediction model for ESCC patients undergoing nCRT and surgery based on immune and inflammation-related indicators. METHODS: We retrospectively analyzed the levels of serum immune- and inflammation-related indicators of ESCC patients before receiving nCRT plus surgery in the training cohort (99 patients) and validation cohort (67 patients), which were collected from 2007 to 2020. Univariate and multivariate Cox survival analyses were conducted to evaluate the indicators to set up a nomogram associated with the patients’ overall survival (OS). The prediction accuracy and discriminative ability of the nomogram were measured by the concordance index (C-index), decision curve, calibration curve, integrated discrimination improvement (IDI), and net reclassification improvement (NRI). RESULTS: Univariate and multivariate Cox analyses demonstrated that immune globin A (IgA) and C-reactive protein (CRP) were independent risk factors. A nomogram based on IgA, CRP, and cTNM stage was established for predicted OS in the training cohort and validated in the validation cohort. The C-index of the nomogram was 0.820 (95% CI: 0.705–0.934), which was higher than that of the cTNM stage (0.655 (95% CI: 0.546–0.764), p < 0.05) in the training cohort, and similar results were observed in the validation cohort (0.832 (95% CI: 0.760–0.903 vs 0.635 (95% CI: 0.509–0.757), p < 0.001). Furthermore, the prediction accuracy and net benefit of the nomogram verified by the calibration curve, decision curve, NRI, and IDI were satisfactory in the training and validation cohorts. CONCLUSION: The newly constructed nomogram concluding serum IgA, CRP, and cTNM stage might be helpful in the prognosis prediction for ESCC patients receiving nCRT plus surgery.
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spelling pubmed-93737982022-08-13 Nomogram constructed by immunological and inflammatory indicators for predicting prognosis of patients with esophageal squamous cell carcinoma treated with neoadjuvant chemoradiotherapy plus surgery Luo, Yun Weng, Xue-Fen Huang, Jia-Tao Hu, Xue-Hao Wei, Lai-Feng Lin, Yi-Wei Ding, Tian-Yan Zhang, Biao Chu, Ling-Yu Liu, Can-Tong Peng, Yu-Hui Xu, Yi-Wei Wu, Fang-Cai Front Oncol Oncology OBJECTIVES: At present, esophageal squamous cell carcinoma (ESCC) patients accepting neoadjuvant chemoradiotherapy (nCRT) plus surgery lack corresponding prognostic indicators. This study aimed to construct a prognostic prediction model for ESCC patients undergoing nCRT and surgery based on immune and inflammation-related indicators. METHODS: We retrospectively analyzed the levels of serum immune- and inflammation-related indicators of ESCC patients before receiving nCRT plus surgery in the training cohort (99 patients) and validation cohort (67 patients), which were collected from 2007 to 2020. Univariate and multivariate Cox survival analyses were conducted to evaluate the indicators to set up a nomogram associated with the patients’ overall survival (OS). The prediction accuracy and discriminative ability of the nomogram were measured by the concordance index (C-index), decision curve, calibration curve, integrated discrimination improvement (IDI), and net reclassification improvement (NRI). RESULTS: Univariate and multivariate Cox analyses demonstrated that immune globin A (IgA) and C-reactive protein (CRP) were independent risk factors. A nomogram based on IgA, CRP, and cTNM stage was established for predicted OS in the training cohort and validated in the validation cohort. The C-index of the nomogram was 0.820 (95% CI: 0.705–0.934), which was higher than that of the cTNM stage (0.655 (95% CI: 0.546–0.764), p < 0.05) in the training cohort, and similar results were observed in the validation cohort (0.832 (95% CI: 0.760–0.903 vs 0.635 (95% CI: 0.509–0.757), p < 0.001). Furthermore, the prediction accuracy and net benefit of the nomogram verified by the calibration curve, decision curve, NRI, and IDI were satisfactory in the training and validation cohorts. CONCLUSION: The newly constructed nomogram concluding serum IgA, CRP, and cTNM stage might be helpful in the prognosis prediction for ESCC patients receiving nCRT plus surgery. Frontiers Media S.A. 2022-07-29 /pmc/articles/PMC9373798/ /pubmed/35965555 http://dx.doi.org/10.3389/fonc.2022.882900 Text en Copyright © 2022 Luo, Weng, Huang, Hu, Wei, Lin, Ding, Zhang, Chu, Liu, Peng, Xu and Wu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Luo, Yun
Weng, Xue-Fen
Huang, Jia-Tao
Hu, Xue-Hao
Wei, Lai-Feng
Lin, Yi-Wei
Ding, Tian-Yan
Zhang, Biao
Chu, Ling-Yu
Liu, Can-Tong
Peng, Yu-Hui
Xu, Yi-Wei
Wu, Fang-Cai
Nomogram constructed by immunological and inflammatory indicators for predicting prognosis of patients with esophageal squamous cell carcinoma treated with neoadjuvant chemoradiotherapy plus surgery
title Nomogram constructed by immunological and inflammatory indicators for predicting prognosis of patients with esophageal squamous cell carcinoma treated with neoadjuvant chemoradiotherapy plus surgery
title_full Nomogram constructed by immunological and inflammatory indicators for predicting prognosis of patients with esophageal squamous cell carcinoma treated with neoadjuvant chemoradiotherapy plus surgery
title_fullStr Nomogram constructed by immunological and inflammatory indicators for predicting prognosis of patients with esophageal squamous cell carcinoma treated with neoadjuvant chemoradiotherapy plus surgery
title_full_unstemmed Nomogram constructed by immunological and inflammatory indicators for predicting prognosis of patients with esophageal squamous cell carcinoma treated with neoadjuvant chemoradiotherapy plus surgery
title_short Nomogram constructed by immunological and inflammatory indicators for predicting prognosis of patients with esophageal squamous cell carcinoma treated with neoadjuvant chemoradiotherapy plus surgery
title_sort nomogram constructed by immunological and inflammatory indicators for predicting prognosis of patients with esophageal squamous cell carcinoma treated with neoadjuvant chemoradiotherapy plus surgery
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9373798/
https://www.ncbi.nlm.nih.gov/pubmed/35965555
http://dx.doi.org/10.3389/fonc.2022.882900
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