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Development and validation of a prognostic model for adult patients with acute myeloid leukaemia

BACKGROUND: The high heterogeneity of acute myeloid leukaemia (AML) reflected in the patient- and disease-related factors accounts for the unsatisfactory prognosis despite the introduction of novel therapeutic approaches and drugs in recent years. METHODS: In the development set (n = 412), parameter...

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Autores principales: Ma, Ting-Ting, Lin, Xiao-Jing, Cheng, Wen-Yan, Xue, Qing, Wang, Shi-Yang, Liu, Fu-Jia, Yan, Han, Zhu, Yong-Mei, Shen, Yang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7689519/
https://www.ncbi.nlm.nih.gov/pubmed/33232873
http://dx.doi.org/10.1016/j.ebiom.2020.103126
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author Ma, Ting-Ting
Lin, Xiao-Jing
Cheng, Wen-Yan
Xue, Qing
Wang, Shi-Yang
Liu, Fu-Jia
Yan, Han
Zhu, Yong-Mei
Shen, Yang
author_facet Ma, Ting-Ting
Lin, Xiao-Jing
Cheng, Wen-Yan
Xue, Qing
Wang, Shi-Yang
Liu, Fu-Jia
Yan, Han
Zhu, Yong-Mei
Shen, Yang
author_sort Ma, Ting-Ting
collection PubMed
description BACKGROUND: The high heterogeneity of acute myeloid leukaemia (AML) reflected in the patient- and disease-related factors accounts for the unsatisfactory prognosis despite the introduction of novel therapeutic approaches and drugs in recent years. METHODS: In the development set (n = 412), parameters including age, hematopoietic cell transplantation-comorbidity index, white blood cell count, hemoglobin, biallelic CEBPA mutations, DNMT3A mutations, FLT3-ITD/NPM1 status, and ELN cytogenetic risk status were identified as independent prognostic factors for overall survival (OS) in the multivariable Cox regression analysis. A nomogram combining these predictors for individual risk estimation was established thereby. FINDINGS: The prognostic model demonstrated promising performance in the development cohort. The calibration plot, C-index (0.74), along with the 1-, 2- and 3-year area under the receiver operating characteristic curve (AUC, 0.76, 0.79, and 0.74, respectively) in the validation set (n = 238) substantiated the robustness of the model. In addition to stratifying young (age ≤ 60 years) and elderly patients (age > 60 years) into three and two risk groups with significant distinct outcomes, the prognostic model succeeded in distinguishing eligible candidates for hematopoietic stem cell transplantation. INTERPRETATION: The prognostic model is capable of survival prediction, risk stratification and helping with therapeutic decision-making with the use of easily acquired variables in daily clinical routine. FUNDING: This work was supported in part by grants from the National Natural Science Foundation of China (81770141), the National Key R&D Program of China (2016YFE0202800), and Shanghai Municipal Education Commission-Gaofeng Clinical Medicine Grant Support (20161406).
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spelling pubmed-76895192020-12-07 Development and validation of a prognostic model for adult patients with acute myeloid leukaemia Ma, Ting-Ting Lin, Xiao-Jing Cheng, Wen-Yan Xue, Qing Wang, Shi-Yang Liu, Fu-Jia Yan, Han Zhu, Yong-Mei Shen, Yang EBioMedicine Research Paper BACKGROUND: The high heterogeneity of acute myeloid leukaemia (AML) reflected in the patient- and disease-related factors accounts for the unsatisfactory prognosis despite the introduction of novel therapeutic approaches and drugs in recent years. METHODS: In the development set (n = 412), parameters including age, hematopoietic cell transplantation-comorbidity index, white blood cell count, hemoglobin, biallelic CEBPA mutations, DNMT3A mutations, FLT3-ITD/NPM1 status, and ELN cytogenetic risk status were identified as independent prognostic factors for overall survival (OS) in the multivariable Cox regression analysis. A nomogram combining these predictors for individual risk estimation was established thereby. FINDINGS: The prognostic model demonstrated promising performance in the development cohort. The calibration plot, C-index (0.74), along with the 1-, 2- and 3-year area under the receiver operating characteristic curve (AUC, 0.76, 0.79, and 0.74, respectively) in the validation set (n = 238) substantiated the robustness of the model. In addition to stratifying young (age ≤ 60 years) and elderly patients (age > 60 years) into three and two risk groups with significant distinct outcomes, the prognostic model succeeded in distinguishing eligible candidates for hematopoietic stem cell transplantation. INTERPRETATION: The prognostic model is capable of survival prediction, risk stratification and helping with therapeutic decision-making with the use of easily acquired variables in daily clinical routine. FUNDING: This work was supported in part by grants from the National Natural Science Foundation of China (81770141), the National Key R&D Program of China (2016YFE0202800), and Shanghai Municipal Education Commission-Gaofeng Clinical Medicine Grant Support (20161406). Elsevier 2020-11-22 /pmc/articles/PMC7689519/ /pubmed/33232873 http://dx.doi.org/10.1016/j.ebiom.2020.103126 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Paper
Ma, Ting-Ting
Lin, Xiao-Jing
Cheng, Wen-Yan
Xue, Qing
Wang, Shi-Yang
Liu, Fu-Jia
Yan, Han
Zhu, Yong-Mei
Shen, Yang
Development and validation of a prognostic model for adult patients with acute myeloid leukaemia
title Development and validation of a prognostic model for adult patients with acute myeloid leukaemia
title_full Development and validation of a prognostic model for adult patients with acute myeloid leukaemia
title_fullStr Development and validation of a prognostic model for adult patients with acute myeloid leukaemia
title_full_unstemmed Development and validation of a prognostic model for adult patients with acute myeloid leukaemia
title_short Development and validation of a prognostic model for adult patients with acute myeloid leukaemia
title_sort development and validation of a prognostic model for adult patients with acute myeloid leukaemia
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7689519/
https://www.ncbi.nlm.nih.gov/pubmed/33232873
http://dx.doi.org/10.1016/j.ebiom.2020.103126
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