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Cetuximab for esophageal cancer: an updated meta-analysis of randomized controlled trials

BACKGROUND: Increasing evidence indicates that cetuximab (CET) combined with chemoradiotherapy may be effective for patients with esophageal cancer. However, the recent results are still contradictory and no consensus has yet been reached on this issue. To evaluate the clinical effects and safety of...

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Autores principales: Huang, Ze-Hao, Ma, Xiao-Wen, Zhang, Jing, Li, Xiao, Lai, Na-Lin, Zhang, Sheng-Xiao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6258395/
https://www.ncbi.nlm.nih.gov/pubmed/30477458
http://dx.doi.org/10.1186/s12885-018-5040-z
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author Huang, Ze-Hao
Ma, Xiao-Wen
Zhang, Jing
Li, Xiao
Lai, Na-Lin
Zhang, Sheng-Xiao
author_facet Huang, Ze-Hao
Ma, Xiao-Wen
Zhang, Jing
Li, Xiao
Lai, Na-Lin
Zhang, Sheng-Xiao
author_sort Huang, Ze-Hao
collection PubMed
description BACKGROUND: Increasing evidence indicates that cetuximab (CET) combined with chemoradiotherapy may be effective for patients with esophageal cancer. However, the recent results are still contradictory and no consensus has yet been reached on this issue. To evaluate the clinical effects and safety of CET, we conducted an updated meta-analysis by retrieving published data up to June 2018. METHODS: A comprehensive literature search was performed in several electronic databases, including PubMed, Embase, the Cochrane Library, CNKI database and Chinese Biomedicine Database using subject terms and free terms. Pooled odds ratios (ORs) with 95% confidence intervals (CIs) were calculated to determine the efficiency and safety of CET. RESULTS: This meta-analysis included 10 randomized controlled trials (RCTs). Five RCTs reported localized esophageal cancer and other five RCTs reported metastatic esophageal cancer. For these patients with localized esophageal cancer, CET could not significantly improve the response rate, overall survival and progression-free survival (PFS, 1–5 years). But CET treatment might increase the incidences of diarrhea (OR = 2.07; CI = 1.01–4.25) and rash (OR = 16.91; CI = 3.20–89.42). For other patients with metastatic esophageal cancer, the addition of CET significantly increased the response rate (OR = 3.34; CI = 1.90–5.88), disease control rate (OR = 2.92; CI = 1.49–5.71) and 2-year overall survival (OR = 2.78; CI = 1.20–6.46) compared with the control group. However, CET could not improve the 1-year overall survival and might make patients with metastatic esophageal cancer more susceptible to rash (OR = 5.50; CI = 2.14–14.14). No significant differences in other adverse effects were found between the two groups. CONCLUSIONS: Our findings suggested that adding CET to multimodal therapy significantly improved response rate and disease control rate for patients with metastatic esophageal cancer rather than patients with localized esophageal cancer. CET might be a safe therapeutic choice, but CET failed to significantly improve the overall survival and PFS for patients with localized or metastatic esophageal cancer.
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spelling pubmed-62583952018-11-29 Cetuximab for esophageal cancer: an updated meta-analysis of randomized controlled trials Huang, Ze-Hao Ma, Xiao-Wen Zhang, Jing Li, Xiao Lai, Na-Lin Zhang, Sheng-Xiao BMC Cancer Research Article BACKGROUND: Increasing evidence indicates that cetuximab (CET) combined with chemoradiotherapy may be effective for patients with esophageal cancer. However, the recent results are still contradictory and no consensus has yet been reached on this issue. To evaluate the clinical effects and safety of CET, we conducted an updated meta-analysis by retrieving published data up to June 2018. METHODS: A comprehensive literature search was performed in several electronic databases, including PubMed, Embase, the Cochrane Library, CNKI database and Chinese Biomedicine Database using subject terms and free terms. Pooled odds ratios (ORs) with 95% confidence intervals (CIs) were calculated to determine the efficiency and safety of CET. RESULTS: This meta-analysis included 10 randomized controlled trials (RCTs). Five RCTs reported localized esophageal cancer and other five RCTs reported metastatic esophageal cancer. For these patients with localized esophageal cancer, CET could not significantly improve the response rate, overall survival and progression-free survival (PFS, 1–5 years). But CET treatment might increase the incidences of diarrhea (OR = 2.07; CI = 1.01–4.25) and rash (OR = 16.91; CI = 3.20–89.42). For other patients with metastatic esophageal cancer, the addition of CET significantly increased the response rate (OR = 3.34; CI = 1.90–5.88), disease control rate (OR = 2.92; CI = 1.49–5.71) and 2-year overall survival (OR = 2.78; CI = 1.20–6.46) compared with the control group. However, CET could not improve the 1-year overall survival and might make patients with metastatic esophageal cancer more susceptible to rash (OR = 5.50; CI = 2.14–14.14). No significant differences in other adverse effects were found between the two groups. CONCLUSIONS: Our findings suggested that adding CET to multimodal therapy significantly improved response rate and disease control rate for patients with metastatic esophageal cancer rather than patients with localized esophageal cancer. CET might be a safe therapeutic choice, but CET failed to significantly improve the overall survival and PFS for patients with localized or metastatic esophageal cancer. BioMed Central 2018-11-26 /pmc/articles/PMC6258395/ /pubmed/30477458 http://dx.doi.org/10.1186/s12885-018-5040-z Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Huang, Ze-Hao
Ma, Xiao-Wen
Zhang, Jing
Li, Xiao
Lai, Na-Lin
Zhang, Sheng-Xiao
Cetuximab for esophageal cancer: an updated meta-analysis of randomized controlled trials
title Cetuximab for esophageal cancer: an updated meta-analysis of randomized controlled trials
title_full Cetuximab for esophageal cancer: an updated meta-analysis of randomized controlled trials
title_fullStr Cetuximab for esophageal cancer: an updated meta-analysis of randomized controlled trials
title_full_unstemmed Cetuximab for esophageal cancer: an updated meta-analysis of randomized controlled trials
title_short Cetuximab for esophageal cancer: an updated meta-analysis of randomized controlled trials
title_sort cetuximab for esophageal cancer: an updated meta-analysis of randomized controlled trials
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6258395/
https://www.ncbi.nlm.nih.gov/pubmed/30477458
http://dx.doi.org/10.1186/s12885-018-5040-z
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