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Increased D-dimer level was a poor predictor of neuroblastoma, especially in the high-risk group

PURPOSE: D-dimer levels are associated with tumor progression and prognosis in various cancers. However, there are few research about the relationship between D-dimer and neuroblastoma (NB). This study assessed the relationships of D-dimer levels with clinical features and overall survival (OS) in p...

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Autores principales: Ma, Yue, Li, Changchun, Zhao, Zhenzhen, Yang, Chao, Zhou, Jianwu, Peng, Liang, Deng, Xiaobin, Wang, Shan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10010962/
https://www.ncbi.nlm.nih.gov/pubmed/36915082
http://dx.doi.org/10.1186/s12957-023-02974-2
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author Ma, Yue
Li, Changchun
Zhao, Zhenzhen
Yang, Chao
Zhou, Jianwu
Peng, Liang
Deng, Xiaobin
Wang, Shan
author_facet Ma, Yue
Li, Changchun
Zhao, Zhenzhen
Yang, Chao
Zhou, Jianwu
Peng, Liang
Deng, Xiaobin
Wang, Shan
author_sort Ma, Yue
collection PubMed
description PURPOSE: D-dimer levels are associated with tumor progression and prognosis in various cancers. However, there are few research about the relationship between D-dimer and neuroblastoma (NB). This study assessed the relationships of D-dimer levels with clinical features and overall survival (OS) in patients with NB. METHODS: Information about the clinical features of 365 patients and the prognosis of 301 patients was collected. The relationship between D-dimer levels and clinical features or OS was analyzed. We constructed the risk score based on Cox regression analysis and verified the predictive efficacy of the model through ROC curve and calibration curve. RESULTS: The results showed that D-dimer levels were significantly increased in patients with nonmediastinal tumor, tumor larger than 10 cm, stage 3–4 disease, bone marrow metastasis, unfavorable histology, bone metastasis, NMYC amplification, and the high-risk group (all P < 0.05). The Kaplan–Meier survival analysis showed that there were significant differences in 3- and 5-year OS (87.4% vs. 32.3%, 79.3% vs. 32.3%, P < 0.0001) between the low D-dimer and high D-dimer groups. In the high-risk group, the OS of high D-dimer was significantly lower than that of low D-dimer (P < 0.0001). All cases were divided into the training cohort (N = 211) and the validation cohort (N = 90). Multivariate analysis further suggested that D-dimer level, bone metastasis, and NMYC status were independent prognostic factors for OS (all P < 0.05). Based on the above three factors, we constructed the risk score in the training cohort. Survival analysis showed that compared with the other groups, the group with 11 scores had the worst prognosis (3-year OS 0%, P < 0.0001). The time-dependent ROC analysis and calibration curve indicated that the risk score had good accuracy. CONCLUSIONS: Patients with high D-dimer levels tended to have unfavorable clinical characteristics and poor prognosis.
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spelling pubmed-100109622023-03-14 Increased D-dimer level was a poor predictor of neuroblastoma, especially in the high-risk group Ma, Yue Li, Changchun Zhao, Zhenzhen Yang, Chao Zhou, Jianwu Peng, Liang Deng, Xiaobin Wang, Shan World J Surg Oncol Research PURPOSE: D-dimer levels are associated with tumor progression and prognosis in various cancers. However, there are few research about the relationship between D-dimer and neuroblastoma (NB). This study assessed the relationships of D-dimer levels with clinical features and overall survival (OS) in patients with NB. METHODS: Information about the clinical features of 365 patients and the prognosis of 301 patients was collected. The relationship between D-dimer levels and clinical features or OS was analyzed. We constructed the risk score based on Cox regression analysis and verified the predictive efficacy of the model through ROC curve and calibration curve. RESULTS: The results showed that D-dimer levels were significantly increased in patients with nonmediastinal tumor, tumor larger than 10 cm, stage 3–4 disease, bone marrow metastasis, unfavorable histology, bone metastasis, NMYC amplification, and the high-risk group (all P < 0.05). The Kaplan–Meier survival analysis showed that there were significant differences in 3- and 5-year OS (87.4% vs. 32.3%, 79.3% vs. 32.3%, P < 0.0001) between the low D-dimer and high D-dimer groups. In the high-risk group, the OS of high D-dimer was significantly lower than that of low D-dimer (P < 0.0001). All cases were divided into the training cohort (N = 211) and the validation cohort (N = 90). Multivariate analysis further suggested that D-dimer level, bone metastasis, and NMYC status were independent prognostic factors for OS (all P < 0.05). Based on the above three factors, we constructed the risk score in the training cohort. Survival analysis showed that compared with the other groups, the group with 11 scores had the worst prognosis (3-year OS 0%, P < 0.0001). The time-dependent ROC analysis and calibration curve indicated that the risk score had good accuracy. CONCLUSIONS: Patients with high D-dimer levels tended to have unfavorable clinical characteristics and poor prognosis. BioMed Central 2023-03-14 /pmc/articles/PMC10010962/ /pubmed/36915082 http://dx.doi.org/10.1186/s12957-023-02974-2 Text en © The Author(s) 2023 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
Ma, Yue
Li, Changchun
Zhao, Zhenzhen
Yang, Chao
Zhou, Jianwu
Peng, Liang
Deng, Xiaobin
Wang, Shan
Increased D-dimer level was a poor predictor of neuroblastoma, especially in the high-risk group
title Increased D-dimer level was a poor predictor of neuroblastoma, especially in the high-risk group
title_full Increased D-dimer level was a poor predictor of neuroblastoma, especially in the high-risk group
title_fullStr Increased D-dimer level was a poor predictor of neuroblastoma, especially in the high-risk group
title_full_unstemmed Increased D-dimer level was a poor predictor of neuroblastoma, especially in the high-risk group
title_short Increased D-dimer level was a poor predictor of neuroblastoma, especially in the high-risk group
title_sort increased d-dimer level was a poor predictor of neuroblastoma, especially in the high-risk group
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10010962/
https://www.ncbi.nlm.nih.gov/pubmed/36915082
http://dx.doi.org/10.1186/s12957-023-02974-2
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