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Intrapleural Perfusion With Staphylococcal Enterotoxin C for Malignant Pleural Effusion: A Clustered Systematic Review and Meta-Analysis

INTRODUCTION: The staphylococcal enterotoxin C (SEC), a commercially available bio-product from Staphylococcus aureus (S. aureus), has been widely used to control MPE. OBJECTIVES: We designed and performed a new systematic review (SR) and meta-analysis to clarify the perfusion protocols with SEC, de...

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Autores principales: Jiang, Hong, Yang, Xue-Mei, Wang, Cheng-Qiong, Xu, Jiao, Huang, Jun, Feng, Ji-Hong, Chen, Xiao-Fan, Chen, Kai, Zhan, Lin, Xiao, Xue, Xiao, Zheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9081816/
https://www.ncbi.nlm.nih.gov/pubmed/35547209
http://dx.doi.org/10.3389/fmed.2022.816973
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author Jiang, Hong
Yang, Xue-Mei
Wang, Cheng-Qiong
Xu, Jiao
Huang, Jun
Feng, Ji-Hong
Chen, Xiao-Fan
Chen, Kai
Zhan, Lin
Xiao, Xue
Xiao, Zheng
author_facet Jiang, Hong
Yang, Xue-Mei
Wang, Cheng-Qiong
Xu, Jiao
Huang, Jun
Feng, Ji-Hong
Chen, Xiao-Fan
Chen, Kai
Zhan, Lin
Xiao, Xue
Xiao, Zheng
author_sort Jiang, Hong
collection PubMed
description INTRODUCTION: The staphylococcal enterotoxin C (SEC), a commercially available bio-product from Staphylococcus aureus (S. aureus), has been widely used to control MPE. OBJECTIVES: We designed and performed a new systematic review (SR) and meta-analysis to clarify the perfusion protocols with SEC, determine their clinical effectiveness and safety, and reveal the indication and optimum usage for achieving the desired responses. METHODOLOGY: All randomized controlled trials (RCTs) about SEC for MPE were collected from electronic databases (from inception until July 2021), and clustered into multiple logical topics. After evaluating their methodological quality, we pooled the data from each topic using the meta-analysis or descriptive analysis, and summarized the evidence quality using the grading of recommendation assessment, development, and evaluation (GRADE) approach. RESULTS: All 114 studies were clustered into SEC perfusion alone or plus chemical agents. The SEC alone showed a better complete response (CR), a lower pleurodesis failure, and adverse drug reactions (ADRs), and a higher fever than cisplatin (DDP) alone. The SEC and chemical agents developed 10 perfusion protocols. Among them, only SEC and DDP perfusion showed a better CR, a lower failure, disease progression and ADRs, and a higher fever than DDP alone. The SEC (100–200 ng per time, one time a week for one to four times) with DDP (30–40 mg, or 50–60 mg each time) significantly improved clinical responses for patients with moderate to large volume, Karnofsky performance status (KPS) scores ≥40, ≥50, or ≥60, and anticipated survival time (AST) ≥2 or 3 months. Most results were moderate to low quality. CONCLUSION: Current pieces of evidence indicate that super-antigen SEC is a pleurodesis agent, which provides an attractive alternative to existing palliative modalities for patients with MPE. Among 10 protocols, the SEC and DDP perfusion is a most commonly used, which shows a significant improvement in clinical responses with low ADRs. These findings also provide a possible indication and optimal usage for SEC and DDP perfusion.
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spelling pubmed-90818162022-05-10 Intrapleural Perfusion With Staphylococcal Enterotoxin C for Malignant Pleural Effusion: A Clustered Systematic Review and Meta-Analysis Jiang, Hong Yang, Xue-Mei Wang, Cheng-Qiong Xu, Jiao Huang, Jun Feng, Ji-Hong Chen, Xiao-Fan Chen, Kai Zhan, Lin Xiao, Xue Xiao, Zheng Front Med (Lausanne) Medicine INTRODUCTION: The staphylococcal enterotoxin C (SEC), a commercially available bio-product from Staphylococcus aureus (S. aureus), has been widely used to control MPE. OBJECTIVES: We designed and performed a new systematic review (SR) and meta-analysis to clarify the perfusion protocols with SEC, determine their clinical effectiveness and safety, and reveal the indication and optimum usage for achieving the desired responses. METHODOLOGY: All randomized controlled trials (RCTs) about SEC for MPE were collected from electronic databases (from inception until July 2021), and clustered into multiple logical topics. After evaluating their methodological quality, we pooled the data from each topic using the meta-analysis or descriptive analysis, and summarized the evidence quality using the grading of recommendation assessment, development, and evaluation (GRADE) approach. RESULTS: All 114 studies were clustered into SEC perfusion alone or plus chemical agents. The SEC alone showed a better complete response (CR), a lower pleurodesis failure, and adverse drug reactions (ADRs), and a higher fever than cisplatin (DDP) alone. The SEC and chemical agents developed 10 perfusion protocols. Among them, only SEC and DDP perfusion showed a better CR, a lower failure, disease progression and ADRs, and a higher fever than DDP alone. The SEC (100–200 ng per time, one time a week for one to four times) with DDP (30–40 mg, or 50–60 mg each time) significantly improved clinical responses for patients with moderate to large volume, Karnofsky performance status (KPS) scores ≥40, ≥50, or ≥60, and anticipated survival time (AST) ≥2 or 3 months. Most results were moderate to low quality. CONCLUSION: Current pieces of evidence indicate that super-antigen SEC is a pleurodesis agent, which provides an attractive alternative to existing palliative modalities for patients with MPE. Among 10 protocols, the SEC and DDP perfusion is a most commonly used, which shows a significant improvement in clinical responses with low ADRs. These findings also provide a possible indication and optimal usage for SEC and DDP perfusion. Frontiers Media S.A. 2022-04-25 /pmc/articles/PMC9081816/ /pubmed/35547209 http://dx.doi.org/10.3389/fmed.2022.816973 Text en Copyright © 2022 Jiang, Yang, Wang, Xu, Huang, Feng, Chen, Chen, Zhan, Xiao and Xiao. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Medicine
Jiang, Hong
Yang, Xue-Mei
Wang, Cheng-Qiong
Xu, Jiao
Huang, Jun
Feng, Ji-Hong
Chen, Xiao-Fan
Chen, Kai
Zhan, Lin
Xiao, Xue
Xiao, Zheng
Intrapleural Perfusion With Staphylococcal Enterotoxin C for Malignant Pleural Effusion: A Clustered Systematic Review and Meta-Analysis
title Intrapleural Perfusion With Staphylococcal Enterotoxin C for Malignant Pleural Effusion: A Clustered Systematic Review and Meta-Analysis
title_full Intrapleural Perfusion With Staphylococcal Enterotoxin C for Malignant Pleural Effusion: A Clustered Systematic Review and Meta-Analysis
title_fullStr Intrapleural Perfusion With Staphylococcal Enterotoxin C for Malignant Pleural Effusion: A Clustered Systematic Review and Meta-Analysis
title_full_unstemmed Intrapleural Perfusion With Staphylococcal Enterotoxin C for Malignant Pleural Effusion: A Clustered Systematic Review and Meta-Analysis
title_short Intrapleural Perfusion With Staphylococcal Enterotoxin C for Malignant Pleural Effusion: A Clustered Systematic Review and Meta-Analysis
title_sort intrapleural perfusion with staphylococcal enterotoxin c for malignant pleural effusion: a clustered systematic review and meta-analysis
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9081816/
https://www.ncbi.nlm.nih.gov/pubmed/35547209
http://dx.doi.org/10.3389/fmed.2022.816973
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