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Prognostic role of systemic immune-inflammation index in solid tumors: a systematic review and meta-analysis
BACKGROUND: Inflammation may play an important role in cancer progression, and a higher systemic immune-inflammation index (SII) has been reported to be a poor prognostic marker in several malignancies. However, the results of published studies are inconsistent. MATERIALS AND METHODS: A systematic r...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5650428/ https://www.ncbi.nlm.nih.gov/pubmed/29088873 http://dx.doi.org/10.18632/oncotarget.18856 |
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author | Zhong, Jie-Hui Huang, Dan-Hui Chen, Zi-Yu |
author_facet | Zhong, Jie-Hui Huang, Dan-Hui Chen, Zi-Yu |
author_sort | Zhong, Jie-Hui |
collection | PubMed |
description | BACKGROUND: Inflammation may play an important role in cancer progression, and a higher systemic immune-inflammation index (SII) has been reported to be a poor prognostic marker in several malignancies. However, the results of published studies are inconsistent. MATERIALS AND METHODS: A systematic review of databases was conducted to search for publications regarding the association between blood SII and clinical outcome in solid tumors with a date up to February 12, 2017. The primary outcome was overall survival (OS) and the secondary outcomes were progression-free survival (PFS) and cancer-specific survival (CSS). Pooled hazard ratios (HRs) and 95% confidence intervals (CIs) were used to assess the strength of the association between blood SII and clinical outcome in solid tumors. RESULTS: A total of 15 articles were included in the analysis. Overall, systemic immune-inflammation index greater than the cutoff predicted poor overall survival (HR = 1.55, 95% CI = 1.27–1.88; P < 0.001). Subgroup analyses revealed that high systemic immune-inflammation index indicated a worse overall survival in hepatocellular carcinoma (P < 0.001), urinary cancers (P < 0.001), gastrointestinal tract cancers (P = 0.02), small cell lung cancer (P < 0.05) and acral melanoma (P < 0.001). Hazard ratio for systemic immune-inflammation index greater than the cutoff for cancer-specific survival was 1.44 (P < 0.05). CONCLUSIONS: Elevated systemic immune-inflammation index is associated with a worse overall survival in many solid tumors. The systemic-inflammation index can act as a powerful prognostic indicator of poor outcome in patients with solid tumors. |
format | Online Article Text |
id | pubmed-5650428 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-56504282017-10-30 Prognostic role of systemic immune-inflammation index in solid tumors: a systematic review and meta-analysis Zhong, Jie-Hui Huang, Dan-Hui Chen, Zi-Yu Oncotarget Meta-Analysis BACKGROUND: Inflammation may play an important role in cancer progression, and a higher systemic immune-inflammation index (SII) has been reported to be a poor prognostic marker in several malignancies. However, the results of published studies are inconsistent. MATERIALS AND METHODS: A systematic review of databases was conducted to search for publications regarding the association between blood SII and clinical outcome in solid tumors with a date up to February 12, 2017. The primary outcome was overall survival (OS) and the secondary outcomes were progression-free survival (PFS) and cancer-specific survival (CSS). Pooled hazard ratios (HRs) and 95% confidence intervals (CIs) were used to assess the strength of the association between blood SII and clinical outcome in solid tumors. RESULTS: A total of 15 articles were included in the analysis. Overall, systemic immune-inflammation index greater than the cutoff predicted poor overall survival (HR = 1.55, 95% CI = 1.27–1.88; P < 0.001). Subgroup analyses revealed that high systemic immune-inflammation index indicated a worse overall survival in hepatocellular carcinoma (P < 0.001), urinary cancers (P < 0.001), gastrointestinal tract cancers (P = 0.02), small cell lung cancer (P < 0.05) and acral melanoma (P < 0.001). Hazard ratio for systemic immune-inflammation index greater than the cutoff for cancer-specific survival was 1.44 (P < 0.05). CONCLUSIONS: Elevated systemic immune-inflammation index is associated with a worse overall survival in many solid tumors. The systemic-inflammation index can act as a powerful prognostic indicator of poor outcome in patients with solid tumors. Impact Journals LLC 2017-06-29 /pmc/articles/PMC5650428/ /pubmed/29088873 http://dx.doi.org/10.18632/oncotarget.18856 Text en Copyright: © 2017 Zhong et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Meta-Analysis Zhong, Jie-Hui Huang, Dan-Hui Chen, Zi-Yu Prognostic role of systemic immune-inflammation index in solid tumors: a systematic review and meta-analysis |
title | Prognostic role of systemic immune-inflammation index in solid tumors: a systematic review and meta-analysis |
title_full | Prognostic role of systemic immune-inflammation index in solid tumors: a systematic review and meta-analysis |
title_fullStr | Prognostic role of systemic immune-inflammation index in solid tumors: a systematic review and meta-analysis |
title_full_unstemmed | Prognostic role of systemic immune-inflammation index in solid tumors: a systematic review and meta-analysis |
title_short | Prognostic role of systemic immune-inflammation index in solid tumors: a systematic review and meta-analysis |
title_sort | prognostic role of systemic immune-inflammation index in solid tumors: a systematic review and meta-analysis |
topic | Meta-Analysis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5650428/ https://www.ncbi.nlm.nih.gov/pubmed/29088873 http://dx.doi.org/10.18632/oncotarget.18856 |
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