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High/positive expression of ERCC1 predicts poor treatment response and survival prognosis in nasopharyngeal carcinoma: A systematic meta-analysis from 21 studies

BACKGROUND: Excision repair cross-complementation group 1 (ERCC1) protein is a member of the nucleotide excision repair (NER) system, which plays an important role in DNA damage repair. Recently, its predictive and prognostic value in nasopharyngeal carcinoma (NPC) has been investigated by several s...

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Autores principales: Yang, Lin, Wei, Wenjie, Zhou, Lei, Wang, Jing, Hu, Guangyuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6571253/
https://www.ncbi.nlm.nih.gov/pubmed/31124943
http://dx.doi.org/10.1097/MD.0000000000015641
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author Yang, Lin
Wei, Wenjie
Zhou, Lei
Wang, Jing
Hu, Guangyuan
author_facet Yang, Lin
Wei, Wenjie
Zhou, Lei
Wang, Jing
Hu, Guangyuan
author_sort Yang, Lin
collection PubMed
description BACKGROUND: Excision repair cross-complementation group 1 (ERCC1) protein is a member of the nucleotide excision repair (NER) system, which plays an important role in DNA damage repair. Recently, its predictive and prognostic value in nasopharyngeal carcinoma (NPC) has been investigated by several studies. However, their results remain controversial. OBJECTIVES: In an attempt to address this issue, we conducted the present comprehensive meta-analysis. DATA SOURCES: Studies published until November 2017 were searched. Finally, total 21 literatures involving 22 cohorts and 2921 NPC patients fulfilled the inclusion criteria. RESULTS: The pooled results showed that high/positive expression of ERCC1 predicted poor objective response rate (ORR) [odds ratio (OR) = 2.83; 95% confidence interval (CI) = 2.11–3.80; P <.001], overall survival (OS) [hazard ratio (HR) = 1.77; 95% CI = 1.48–2.12; P <.001], and disease-free survival (DFS) (HR = 1.60; 95% CI = 1.43–1.79; P <.001) in NPC. Low heterogeneity was detected among these studies (ORR: I(2) = 0.0%, P = .776; DFS: I(2) = 38.7%, P = .148; OS: I(2) = 0.0%; P = .530). The results of sensitivity analyses and publication bias verified the reliability of our findings. CONCLUSIONS: This study suggested ERCC1 as a potential predictive and prognostic biomarker for the treatment response and survival prognosis of NPC patients.
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spelling pubmed-65712532019-07-22 High/positive expression of ERCC1 predicts poor treatment response and survival prognosis in nasopharyngeal carcinoma: A systematic meta-analysis from 21 studies Yang, Lin Wei, Wenjie Zhou, Lei Wang, Jing Hu, Guangyuan Medicine (Baltimore) Research Article BACKGROUND: Excision repair cross-complementation group 1 (ERCC1) protein is a member of the nucleotide excision repair (NER) system, which plays an important role in DNA damage repair. Recently, its predictive and prognostic value in nasopharyngeal carcinoma (NPC) has been investigated by several studies. However, their results remain controversial. OBJECTIVES: In an attempt to address this issue, we conducted the present comprehensive meta-analysis. DATA SOURCES: Studies published until November 2017 were searched. Finally, total 21 literatures involving 22 cohorts and 2921 NPC patients fulfilled the inclusion criteria. RESULTS: The pooled results showed that high/positive expression of ERCC1 predicted poor objective response rate (ORR) [odds ratio (OR) = 2.83; 95% confidence interval (CI) = 2.11–3.80; P <.001], overall survival (OS) [hazard ratio (HR) = 1.77; 95% CI = 1.48–2.12; P <.001], and disease-free survival (DFS) (HR = 1.60; 95% CI = 1.43–1.79; P <.001) in NPC. Low heterogeneity was detected among these studies (ORR: I(2) = 0.0%, P = .776; DFS: I(2) = 38.7%, P = .148; OS: I(2) = 0.0%; P = .530). The results of sensitivity analyses and publication bias verified the reliability of our findings. CONCLUSIONS: This study suggested ERCC1 as a potential predictive and prognostic biomarker for the treatment response and survival prognosis of NPC patients. Wolters Kluwer Health 2019-05-24 /pmc/articles/PMC6571253/ /pubmed/31124943 http://dx.doi.org/10.1097/MD.0000000000015641 Text en Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle Research Article
Yang, Lin
Wei, Wenjie
Zhou, Lei
Wang, Jing
Hu, Guangyuan
High/positive expression of ERCC1 predicts poor treatment response and survival prognosis in nasopharyngeal carcinoma: A systematic meta-analysis from 21 studies
title High/positive expression of ERCC1 predicts poor treatment response and survival prognosis in nasopharyngeal carcinoma: A systematic meta-analysis from 21 studies
title_full High/positive expression of ERCC1 predicts poor treatment response and survival prognosis in nasopharyngeal carcinoma: A systematic meta-analysis from 21 studies
title_fullStr High/positive expression of ERCC1 predicts poor treatment response and survival prognosis in nasopharyngeal carcinoma: A systematic meta-analysis from 21 studies
title_full_unstemmed High/positive expression of ERCC1 predicts poor treatment response and survival prognosis in nasopharyngeal carcinoma: A systematic meta-analysis from 21 studies
title_short High/positive expression of ERCC1 predicts poor treatment response and survival prognosis in nasopharyngeal carcinoma: A systematic meta-analysis from 21 studies
title_sort high/positive expression of ercc1 predicts poor treatment response and survival prognosis in nasopharyngeal carcinoma: a systematic meta-analysis from 21 studies
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6571253/
https://www.ncbi.nlm.nih.gov/pubmed/31124943
http://dx.doi.org/10.1097/MD.0000000000015641
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