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Immunization-based scores as independent prognostic predictors in soft tissue sarcoma patients
Background: The purpose of this study was to examine and compare the prognostic value of different immunization-based scoring systems in patients with soft tissue sarcoma (STS). Methods: We conducted a retrospective study evaluating a cohort of 165 patients diagnosed with STS between July 2007 and J...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Ivyspring International Publisher
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5370504/ https://www.ncbi.nlm.nih.gov/pubmed/28367240 http://dx.doi.org/10.7150/jca.17356 |
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author | Jiang, Shan-Shan Jiang, Long Weng, De-Sheng Li, Yuan-fang Pan, Qiu-Zhong Zhao, Jing-Jing Tang, Yan Zhou, Zhi-Wei Xia, Jian-Chuan |
author_facet | Jiang, Shan-Shan Jiang, Long Weng, De-Sheng Li, Yuan-fang Pan, Qiu-Zhong Zhao, Jing-Jing Tang, Yan Zhou, Zhi-Wei Xia, Jian-Chuan |
author_sort | Jiang, Shan-Shan |
collection | PubMed |
description | Background: The purpose of this study was to examine and compare the prognostic value of different immunization-based scoring systems in patients with soft tissue sarcoma (STS). Methods: We conducted a retrospective study evaluating a cohort of 165 patients diagnosed with STS between July 2007 and July 2014. The relative Glasgow prognostic score (GPS) of these patients was calculated using 3 different systems: the traditional GPS system (tGPS), the modified GPS system 1 (m1GPS), and the modified GPS system 2 (m2GPS). Then, we evaluated the relationships between each GPS system and clinicopathological characteristics. The mean follow-up for survivors in the cohort was 73.7 months as of March 2015. Results: The most favorable overall survival (OS) rate was associated with the score 0 groups, and the poorest progression-free survival (PFS) rate was associated with the score 2 groups, regardless of which system was used to calculate the score. Specifically, the m1GPS provided the greatest accuracy in predicting OS and PFS. Moreover, the same effect was observed in a separate analysis restricted to patients with metastases. Remarkably, in patients with a score of 2 as measured by all 3 systems, local treatment resulted in a poorer prognosis compared to patients with a score of 2 who did not receive local treatment. Conclusion: The GPS is a valuable prognostic marker and has the capability to predict the appropriate treatment strategy for STS patients with metastases. The modified GPS systems demonstrated superior prognostic and predictive value compared with the traditional GPS system. |
format | Online Article Text |
id | pubmed-5370504 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-53705042017-03-31 Immunization-based scores as independent prognostic predictors in soft tissue sarcoma patients Jiang, Shan-Shan Jiang, Long Weng, De-Sheng Li, Yuan-fang Pan, Qiu-Zhong Zhao, Jing-Jing Tang, Yan Zhou, Zhi-Wei Xia, Jian-Chuan J Cancer Research Paper Background: The purpose of this study was to examine and compare the prognostic value of different immunization-based scoring systems in patients with soft tissue sarcoma (STS). Methods: We conducted a retrospective study evaluating a cohort of 165 patients diagnosed with STS between July 2007 and July 2014. The relative Glasgow prognostic score (GPS) of these patients was calculated using 3 different systems: the traditional GPS system (tGPS), the modified GPS system 1 (m1GPS), and the modified GPS system 2 (m2GPS). Then, we evaluated the relationships between each GPS system and clinicopathological characteristics. The mean follow-up for survivors in the cohort was 73.7 months as of March 2015. Results: The most favorable overall survival (OS) rate was associated with the score 0 groups, and the poorest progression-free survival (PFS) rate was associated with the score 2 groups, regardless of which system was used to calculate the score. Specifically, the m1GPS provided the greatest accuracy in predicting OS and PFS. Moreover, the same effect was observed in a separate analysis restricted to patients with metastases. Remarkably, in patients with a score of 2 as measured by all 3 systems, local treatment resulted in a poorer prognosis compared to patients with a score of 2 who did not receive local treatment. Conclusion: The GPS is a valuable prognostic marker and has the capability to predict the appropriate treatment strategy for STS patients with metastases. The modified GPS systems demonstrated superior prognostic and predictive value compared with the traditional GPS system. Ivyspring International Publisher 2017-02-25 /pmc/articles/PMC5370504/ /pubmed/28367240 http://dx.doi.org/10.7150/jca.17356 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Research Paper Jiang, Shan-Shan Jiang, Long Weng, De-Sheng Li, Yuan-fang Pan, Qiu-Zhong Zhao, Jing-Jing Tang, Yan Zhou, Zhi-Wei Xia, Jian-Chuan Immunization-based scores as independent prognostic predictors in soft tissue sarcoma patients |
title | Immunization-based scores as independent prognostic predictors in soft tissue sarcoma patients |
title_full | Immunization-based scores as independent prognostic predictors in soft tissue sarcoma patients |
title_fullStr | Immunization-based scores as independent prognostic predictors in soft tissue sarcoma patients |
title_full_unstemmed | Immunization-based scores as independent prognostic predictors in soft tissue sarcoma patients |
title_short | Immunization-based scores as independent prognostic predictors in soft tissue sarcoma patients |
title_sort | immunization-based scores as independent prognostic predictors in soft tissue sarcoma patients |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5370504/ https://www.ncbi.nlm.nih.gov/pubmed/28367240 http://dx.doi.org/10.7150/jca.17356 |
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