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Published in: Tumor Biology 1/2014

01-01-2014 | Research Article

Prognostic significance of VEGF expression in osteosarcoma: a meta-analysis

Authors: Xiao-Wei Yu, Tian-Yi Wu, Xiang Yi, Wei-Ping Ren, Zu-bin Zhou, Yu-qiang Sun, Chang-qing Zhang

Published in: Tumor Biology | Issue 1/2014

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Abstract

Vascular endothelial growth factor (VEGF) is considered as a prime mediator of angiogenesis and has been implicated in carcinogenesis and metastasis. Various studies examined the relationship between VEGF overexpression with the clinical outcome in patients with osteosarcoma but yielded conflicting results. Electronic databases updated to April 2013 were searched to find relevant studies. A meta-analysis was conducted with eligible studies which quantitatively evaluated the relationship between VEGF overexpression and survival of patients with osteosarcoma. Survival data were aggregated and quantitatively analyzed. We performed a meta-analysis of eight studies that evaluated the correlation between VEGF overexpression and survival in patients with osteosarcoma. Combined hazard ratios suggested that VEGF overexpression had an unfavorable impact on overall survival (hazard ratio (HR) = 1.75, 95 % confidence interval (CI): 1.21–2.28) in patients with osteosarcoma for overall populations, 2.37 (1.35–3.39) in Asian studies but not in non-Asian studies (HR = 1.51, 95 % CI: 0.89–2.14). No significant heterogeneity was observed among all studies. VEGF overexpression indicates a poor prognosis for patients with osteosarcoma. However, the prognostic value of VEGF on survival in osteosarcoma patients still needs further large-scale prospective trials to be clarified.
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Metadata
Title
Prognostic significance of VEGF expression in osteosarcoma: a meta-analysis
Authors
Xiao-Wei Yu
Tian-Yi Wu
Xiang Yi
Wei-Ping Ren
Zu-bin Zhou
Yu-qiang Sun
Chang-qing Zhang
Publication date
01-01-2014
Publisher
Springer Netherlands
Published in
Tumor Biology / Issue 1/2014
Print ISSN: 1010-4283
Electronic ISSN: 1423-0380
DOI
https://doi.org/10.1007/s13277-013-1019-1

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