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Prognostic significance of the systemic immune‐inflammation index in pancreatic carcinoma patients: a meta-analysis

Background: Systemic immune-inflammation index (SII) is a prognostic indicator for several malignancies, including pancreatic carcinoma; however, there is no consensus on its significance. In the current study, a systematic meta-analysis was used to explore the correlation between SII and prognosis...

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Autores principales: Li, Xiaocheng, Lin, Huapeng, Ouyang, Renbin, Yang, Yaowei, Peng, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8329648/
https://www.ncbi.nlm.nih.gov/pubmed/34286342
http://dx.doi.org/10.1042/BSR20204401
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author Li, Xiaocheng
Lin, Huapeng
Ouyang, Renbin
Yang, Yaowei
Peng, Jing
author_facet Li, Xiaocheng
Lin, Huapeng
Ouyang, Renbin
Yang, Yaowei
Peng, Jing
author_sort Li, Xiaocheng
collection PubMed
description Background: Systemic immune-inflammation index (SII) is a prognostic indicator for several malignancies, including pancreatic carcinoma; however, there is no consensus on its significance. In the current study, a systematic meta-analysis was used to explore the correlation between SII and prognosis in pancreatic carcinoma patients. Methods: PubMed, Embase and Cochrane Library databases were screened from inception to May 2020. Studies describing the prognostic role of SII in pancreatic carcinoma were then retrieved. The pooled hazard ratio (HR) and 95% confidence interval (CI) was calculated using random- or fixed-effects models to determine the correlation between SII and prognosis. Results: A total of four studies, comprising 1749 patients, met the inclusion criteria of the study and were therefore included in this meta-analysis. The meta-analysis showed that high SII indicated was correlated with worse overall survival (OS) in patients with pancreatic carcinoma (HR: 1.43, 95% CI: 1.24–1.65, P<0.001). These findings were validated through subgroup analyses, stratified by the American Joint Committee on Cancer (AJCC) stage. In addition, patients with high SII showed poorer cancer-specific survival (HR: 2.32, 95% CI: 1.55–3.48, P<0.001). However, analysis showed no significant correlations between SII and disease-free and relapse-free survival (RFS). Conclusion: These findings indicate that SII is a potential non-invasive and a promising tool for predicting clinical outcomes of pancreatic carcinoma patients. However, the current research did not explore whether neoadjuvant therapy has an effect on the prognostic value of SII. Further studies using adequate designs and larger sample sizes are required to validate these findings.
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spelling pubmed-83296482021-08-11 Prognostic significance of the systemic immune‐inflammation index in pancreatic carcinoma patients: a meta-analysis Li, Xiaocheng Lin, Huapeng Ouyang, Renbin Yang, Yaowei Peng, Jing Biosci Rep Cancer Background: Systemic immune-inflammation index (SII) is a prognostic indicator for several malignancies, including pancreatic carcinoma; however, there is no consensus on its significance. In the current study, a systematic meta-analysis was used to explore the correlation between SII and prognosis in pancreatic carcinoma patients. Methods: PubMed, Embase and Cochrane Library databases were screened from inception to May 2020. Studies describing the prognostic role of SII in pancreatic carcinoma were then retrieved. The pooled hazard ratio (HR) and 95% confidence interval (CI) was calculated using random- or fixed-effects models to determine the correlation between SII and prognosis. Results: A total of four studies, comprising 1749 patients, met the inclusion criteria of the study and were therefore included in this meta-analysis. The meta-analysis showed that high SII indicated was correlated with worse overall survival (OS) in patients with pancreatic carcinoma (HR: 1.43, 95% CI: 1.24–1.65, P<0.001). These findings were validated through subgroup analyses, stratified by the American Joint Committee on Cancer (AJCC) stage. In addition, patients with high SII showed poorer cancer-specific survival (HR: 2.32, 95% CI: 1.55–3.48, P<0.001). However, analysis showed no significant correlations between SII and disease-free and relapse-free survival (RFS). Conclusion: These findings indicate that SII is a potential non-invasive and a promising tool for predicting clinical outcomes of pancreatic carcinoma patients. However, the current research did not explore whether neoadjuvant therapy has an effect on the prognostic value of SII. Further studies using adequate designs and larger sample sizes are required to validate these findings. Portland Press Ltd. 2021-08-02 /pmc/articles/PMC8329648/ /pubmed/34286342 http://dx.doi.org/10.1042/BSR20204401 Text en © 2021 The Author(s). https://creativecommons.org/licenses/by/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Cancer
Li, Xiaocheng
Lin, Huapeng
Ouyang, Renbin
Yang, Yaowei
Peng, Jing
Prognostic significance of the systemic immune‐inflammation index in pancreatic carcinoma patients: a meta-analysis
title Prognostic significance of the systemic immune‐inflammation index in pancreatic carcinoma patients: a meta-analysis
title_full Prognostic significance of the systemic immune‐inflammation index in pancreatic carcinoma patients: a meta-analysis
title_fullStr Prognostic significance of the systemic immune‐inflammation index in pancreatic carcinoma patients: a meta-analysis
title_full_unstemmed Prognostic significance of the systemic immune‐inflammation index in pancreatic carcinoma patients: a meta-analysis
title_short Prognostic significance of the systemic immune‐inflammation index in pancreatic carcinoma patients: a meta-analysis
title_sort prognostic significance of the systemic immune‐inflammation index in pancreatic carcinoma patients: a meta-analysis
topic Cancer
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8329648/
https://www.ncbi.nlm.nih.gov/pubmed/34286342
http://dx.doi.org/10.1042/BSR20204401
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