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Clinical characteristics and disease-specific prognostic nomogram for primary gliosarcoma: a SEER population-based analysis

Because the study population with gliosarcoma (GSM) is limited, the understanding of this disease is insufficient. In this study, the authors aimed to determine the clinical characteristics and independent prognostic factors influencing the prognosis of GSM patients and to develop a nomogram to pred...

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Autores principales: Feng, Song-Shan, Li, Huang-bao, Fan, Fan, Li, Jing, Cao, Hui, Xia, Zhi-Wei, Yang, Kui, Zhu, Xiao-San, Cheng, Ting-Ting, Cheng, Quan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6656887/
https://www.ncbi.nlm.nih.gov/pubmed/31341246
http://dx.doi.org/10.1038/s41598-019-47211-7
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author Feng, Song-Shan
Li, Huang-bao
Fan, Fan
Li, Jing
Cao, Hui
Xia, Zhi-Wei
Yang, Kui
Zhu, Xiao-San
Cheng, Ting-Ting
Cheng, Quan
author_facet Feng, Song-Shan
Li, Huang-bao
Fan, Fan
Li, Jing
Cao, Hui
Xia, Zhi-Wei
Yang, Kui
Zhu, Xiao-San
Cheng, Ting-Ting
Cheng, Quan
author_sort Feng, Song-Shan
collection PubMed
description Because the study population with gliosarcoma (GSM) is limited, the understanding of this disease is insufficient. In this study, the authors aimed to determine the clinical characteristics and independent prognostic factors influencing the prognosis of GSM patients and to develop a nomogram to predict the prognosis of GSM patients after craniotomy. A total of 498 patients diagnosed with primary GSM between 2004 and 2015 were extracted from the 18 Registries Research Data of the Surveillance, Epidemiology, and End Results (SEER) database. The median disease-specific survival (DSS) was 12.0 months, and the postoperative 0.5-, 1-, and 3-year DSS rates were 71.4%, 46.4% and 9.8%, respectively. We applied both the Cox proportional hazards model and the decision tree model to determine the prognostic factors of primary GSM. The Cox proportional hazards model demonstrated that age at presentation, tumour size, metastasis state and adjuvant chemotherapy (CT) were independent prognostic factors for DSS. The decision tree model suggested that age <71 years and adjuvant CT were associated with a better prognosis for GSM patients. The nomogram generated via the Cox proportional hazards model was developed by applying the rms package in R version 3.5.0. The C-index of internal validation for DSS prediction was 0.67 (95% confidence interval (CI), 0.63 to 0.70). The calibration curve at one year suggested that there was good consistency between the predicted DSS and the actual DSS probability. This study was the first to develop a disease-specific nomogram for predicting the prognosis of primary GSM patients after craniotomy, which can help clinicians immediately and accurately predict patient prognosis and conduct further treatment.
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spelling pubmed-66568872019-07-29 Clinical characteristics and disease-specific prognostic nomogram for primary gliosarcoma: a SEER population-based analysis Feng, Song-Shan Li, Huang-bao Fan, Fan Li, Jing Cao, Hui Xia, Zhi-Wei Yang, Kui Zhu, Xiao-San Cheng, Ting-Ting Cheng, Quan Sci Rep Article Because the study population with gliosarcoma (GSM) is limited, the understanding of this disease is insufficient. In this study, the authors aimed to determine the clinical characteristics and independent prognostic factors influencing the prognosis of GSM patients and to develop a nomogram to predict the prognosis of GSM patients after craniotomy. A total of 498 patients diagnosed with primary GSM between 2004 and 2015 were extracted from the 18 Registries Research Data of the Surveillance, Epidemiology, and End Results (SEER) database. The median disease-specific survival (DSS) was 12.0 months, and the postoperative 0.5-, 1-, and 3-year DSS rates were 71.4%, 46.4% and 9.8%, respectively. We applied both the Cox proportional hazards model and the decision tree model to determine the prognostic factors of primary GSM. The Cox proportional hazards model demonstrated that age at presentation, tumour size, metastasis state and adjuvant chemotherapy (CT) were independent prognostic factors for DSS. The decision tree model suggested that age <71 years and adjuvant CT were associated with a better prognosis for GSM patients. The nomogram generated via the Cox proportional hazards model was developed by applying the rms package in R version 3.5.0. The C-index of internal validation for DSS prediction was 0.67 (95% confidence interval (CI), 0.63 to 0.70). The calibration curve at one year suggested that there was good consistency between the predicted DSS and the actual DSS probability. This study was the first to develop a disease-specific nomogram for predicting the prognosis of primary GSM patients after craniotomy, which can help clinicians immediately and accurately predict patient prognosis and conduct further treatment. Nature Publishing Group UK 2019-07-24 /pmc/articles/PMC6656887/ /pubmed/31341246 http://dx.doi.org/10.1038/s41598-019-47211-7 Text en © The Author(s) 2019 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Feng, Song-Shan
Li, Huang-bao
Fan, Fan
Li, Jing
Cao, Hui
Xia, Zhi-Wei
Yang, Kui
Zhu, Xiao-San
Cheng, Ting-Ting
Cheng, Quan
Clinical characteristics and disease-specific prognostic nomogram for primary gliosarcoma: a SEER population-based analysis
title Clinical characteristics and disease-specific prognostic nomogram for primary gliosarcoma: a SEER population-based analysis
title_full Clinical characteristics and disease-specific prognostic nomogram for primary gliosarcoma: a SEER population-based analysis
title_fullStr Clinical characteristics and disease-specific prognostic nomogram for primary gliosarcoma: a SEER population-based analysis
title_full_unstemmed Clinical characteristics and disease-specific prognostic nomogram for primary gliosarcoma: a SEER population-based analysis
title_short Clinical characteristics and disease-specific prognostic nomogram for primary gliosarcoma: a SEER population-based analysis
title_sort clinical characteristics and disease-specific prognostic nomogram for primary gliosarcoma: a seer population-based analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6656887/
https://www.ncbi.nlm.nih.gov/pubmed/31341246
http://dx.doi.org/10.1038/s41598-019-47211-7
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