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A nomogram for predicting hyperprogressive disease after immune checkpoint inhibitor treatment in lung cancer
BACKGROUND: Immune checkpoint inhibitor (ICI) therapy is an emerging type of treatment for lung cancer (LC). However, hyperprogressive disease (HPD) has been observed in patients treated with ICIs that lacks a prognostic prediction model. There is an urgent need for a simple and easily implementable...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9073744/ https://www.ncbi.nlm.nih.gov/pubmed/35529793 http://dx.doi.org/10.21037/tlcr-22-171 |
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author | Cao, Shuhui Zhang, Yao Zhou, Yan Rong, Wenwen Wang, Yue Ling, Xuxinyi Zhang, Lincheng Li, Jingwen Tomita, Yusuke Watanabe, Satoshi Nakada, Takeo Seki, Nobuhiko Hida, Toyoaki Dermime, Said Zhong, Runbo Zhong, Hua |
author_facet | Cao, Shuhui Zhang, Yao Zhou, Yan Rong, Wenwen Wang, Yue Ling, Xuxinyi Zhang, Lincheng Li, Jingwen Tomita, Yusuke Watanabe, Satoshi Nakada, Takeo Seki, Nobuhiko Hida, Toyoaki Dermime, Said Zhong, Runbo Zhong, Hua |
author_sort | Cao, Shuhui |
collection | PubMed |
description | BACKGROUND: Immune checkpoint inhibitor (ICI) therapy is an emerging type of treatment for lung cancer (LC). However, hyperprogressive disease (HPD) has been observed in patients treated with ICIs that lacks a prognostic prediction model. There is an urgent need for a simple and easily implementable predictive model to predict the occurrence of HPD. This study aimed to establish a novel scoring system based on a nomogram for the occurrence of HPD. METHODS: We retrospectively identified 1473 patients with stage III–IV LC or inoperable stage I–II LC (1147 in training set, and 326 in testing set), who had undergone ICI therapy at the Shanghai Chest Hospital between January 2017 and March 2022. Available computed tomography (CT) data from the previous treatment, before ICI administration, and at least 2 months after the first the course of ICI administration is collected to confirm HPD. Data from these patients’ common blood laboratory test results before ICI administration were analyzed by the univariable and multivariable logistic regression analysis, then used to develop nomogram predictive model, and made validation in testing set. RESULTS: A total of 1,055 patients were included in this study (844 in the training set, and 211 in the testing set). In the training set, 93 were HPD and 751were non-HPD. Multivariate logistic regression analyses demonstrated that lactate dehydrogenase [LDH, P<0.001; odds ratio (OR) =0.987; 95% confidence interval (CI): 0.980–0.995], mean corpuscular hemoglobin concentration (MCHC, P=0.038; OR =1.021; 95% CI: 1.003–1.033), and erythrocyte sedimentation rate (ESR, P=0.012; OR =0.989; 95% CI: 0.977–0.997) were significantly different. The prediction model was established and validated based on these 3 variables. The concordance index were 0.899 (95% CI: 0.859–0.918) and 0.924 (95% CI: 0.866–0.983) in training set and testing set, and the calibration curve was acceptable. CONCLUSIONS: This model, which was developed from a laboratory examination of LC patients undergoing ICI treatment, is the first nomogram model to be developed to predict HPD occurrence and exhibited good sensitivity and specificity. |
format | Online Article Text |
id | pubmed-9073744 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-90737442022-05-07 A nomogram for predicting hyperprogressive disease after immune checkpoint inhibitor treatment in lung cancer Cao, Shuhui Zhang, Yao Zhou, Yan Rong, Wenwen Wang, Yue Ling, Xuxinyi Zhang, Lincheng Li, Jingwen Tomita, Yusuke Watanabe, Satoshi Nakada, Takeo Seki, Nobuhiko Hida, Toyoaki Dermime, Said Zhong, Runbo Zhong, Hua Transl Lung Cancer Res Original Article BACKGROUND: Immune checkpoint inhibitor (ICI) therapy is an emerging type of treatment for lung cancer (LC). However, hyperprogressive disease (HPD) has been observed in patients treated with ICIs that lacks a prognostic prediction model. There is an urgent need for a simple and easily implementable predictive model to predict the occurrence of HPD. This study aimed to establish a novel scoring system based on a nomogram for the occurrence of HPD. METHODS: We retrospectively identified 1473 patients with stage III–IV LC or inoperable stage I–II LC (1147 in training set, and 326 in testing set), who had undergone ICI therapy at the Shanghai Chest Hospital between January 2017 and March 2022. Available computed tomography (CT) data from the previous treatment, before ICI administration, and at least 2 months after the first the course of ICI administration is collected to confirm HPD. Data from these patients’ common blood laboratory test results before ICI administration were analyzed by the univariable and multivariable logistic regression analysis, then used to develop nomogram predictive model, and made validation in testing set. RESULTS: A total of 1,055 patients were included in this study (844 in the training set, and 211 in the testing set). In the training set, 93 were HPD and 751were non-HPD. Multivariate logistic regression analyses demonstrated that lactate dehydrogenase [LDH, P<0.001; odds ratio (OR) =0.987; 95% confidence interval (CI): 0.980–0.995], mean corpuscular hemoglobin concentration (MCHC, P=0.038; OR =1.021; 95% CI: 1.003–1.033), and erythrocyte sedimentation rate (ESR, P=0.012; OR =0.989; 95% CI: 0.977–0.997) were significantly different. The prediction model was established and validated based on these 3 variables. The concordance index were 0.899 (95% CI: 0.859–0.918) and 0.924 (95% CI: 0.866–0.983) in training set and testing set, and the calibration curve was acceptable. CONCLUSIONS: This model, which was developed from a laboratory examination of LC patients undergoing ICI treatment, is the first nomogram model to be developed to predict HPD occurrence and exhibited good sensitivity and specificity. AME Publishing Company 2022-04 /pmc/articles/PMC9073744/ /pubmed/35529793 http://dx.doi.org/10.21037/tlcr-22-171 Text en 2022 Translational Lung Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Original Article Cao, Shuhui Zhang, Yao Zhou, Yan Rong, Wenwen Wang, Yue Ling, Xuxinyi Zhang, Lincheng Li, Jingwen Tomita, Yusuke Watanabe, Satoshi Nakada, Takeo Seki, Nobuhiko Hida, Toyoaki Dermime, Said Zhong, Runbo Zhong, Hua A nomogram for predicting hyperprogressive disease after immune checkpoint inhibitor treatment in lung cancer |
title | A nomogram for predicting hyperprogressive disease after immune checkpoint inhibitor treatment in lung cancer |
title_full | A nomogram for predicting hyperprogressive disease after immune checkpoint inhibitor treatment in lung cancer |
title_fullStr | A nomogram for predicting hyperprogressive disease after immune checkpoint inhibitor treatment in lung cancer |
title_full_unstemmed | A nomogram for predicting hyperprogressive disease after immune checkpoint inhibitor treatment in lung cancer |
title_short | A nomogram for predicting hyperprogressive disease after immune checkpoint inhibitor treatment in lung cancer |
title_sort | nomogram for predicting hyperprogressive disease after immune checkpoint inhibitor treatment in lung cancer |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9073744/ https://www.ncbi.nlm.nih.gov/pubmed/35529793 http://dx.doi.org/10.21037/tlcr-22-171 |
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