Prognostic significance of several biomarkers in epithelial ovarian cancer: a meta-analysis of published studies

Objective Abnormal expression of several biomarkers might predict disease prognosis and response to chemotherapy in patients with epithelial ovarian cancer (EOC). However, the published data are inconsistent. Methods Eligible studies that investigated the association between survival or response to...

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Veröffentlicht in:Journal of cancer research and clinical oncology 2013-08, Vol.139 (8), p.1257-1277
Hauptverfasser: Xu, Linjuan, Cai, Jing, Yang, Qiang, Ding, Hui, Wu, Liying, Li, Tao, Wang, Zehua
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container_issue 8
container_start_page 1257
container_title Journal of cancer research and clinical oncology
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creator Xu, Linjuan
Cai, Jing
Yang, Qiang
Ding, Hui
Wu, Liying
Li, Tao
Wang, Zehua
description Objective Abnormal expression of several biomarkers might predict disease prognosis and response to chemotherapy in patients with epithelial ovarian cancer (EOC). However, the published data are inconsistent. Methods Eligible studies that investigated the association between survival or response to platinum-based chemotherapy in EOC and the expression status of Bcl-2, EGFR, GST, LRP, p16, p21, P-gp and TNF-α were identified by an electronic search of PubMed and Embase. The measures of interest were hazard ratio (HR) for survival or risk ratio for chemotherapy response. A meta-analysis was performed using the fixed-effect or random-effect models. Results The number of eligible studies analyzed was 27 for Bcl-2, 22 for EGFR, 29 for GST, 12 for LRP, 16 for p16, 22 for p21, 27 for P-gp and three for TNF-α. A meta-analysis showed that high EGFR and P-gp expression was associated with poor overall survival (OS) (pooled adjusted HR = 1.826 and HR = 1.822). Only high GST expression was associated with improved OS (HR = 0.780). Furthermore, high p16 and P-gp expression was associated with poor progression-free survival (PFS) (HR = 1.550 and HR = 2.136). High GST expression was associated with improved PFS (HR = 0.689). Among these factors, only LRP, P-gp and TNF-α were associated with response to platinum-based chemotherapy. Conclusions The markers we analyzed are unlikely to be useful as predictors of prognosis and response to platinum-based chemotherapy in EOC patients in clinical practice.
doi_str_mv 10.1007/s00432-013-1435-z
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However, the published data are inconsistent. Methods Eligible studies that investigated the association between survival or response to platinum-based chemotherapy in EOC and the expression status of Bcl-2, EGFR, GST, LRP, p16, p21, P-gp and TNF-α were identified by an electronic search of PubMed and Embase. The measures of interest were hazard ratio (HR) for survival or risk ratio for chemotherapy response. A meta-analysis was performed using the fixed-effect or random-effect models. Results The number of eligible studies analyzed was 27 for Bcl-2, 22 for EGFR, 29 for GST, 12 for LRP, 16 for p16, 22 for p21, 27 for P-gp and three for TNF-α. A meta-analysis showed that high EGFR and P-gp expression was associated with poor overall survival (OS) (pooled adjusted HR = 1.826 and HR = 1.822). Only high GST expression was associated with improved OS (HR = 0.780). Furthermore, high p16 and P-gp expression was associated with poor progression-free survival (PFS) (HR = 1.550 and HR = 2.136). High GST expression was associated with improved PFS (HR = 0.689). Among these factors, only LRP, P-gp and TNF-α were associated with response to platinum-based chemotherapy. Conclusions The markers we analyzed are unlikely to be useful as predictors of prognosis and response to platinum-based chemotherapy in EOC patients in clinical practice.</description><identifier>ISSN: 0171-5216</identifier><identifier>EISSN: 1432-1335</identifier><identifier>DOI: 10.1007/s00432-013-1435-z</identifier><identifier>PMID: 23595127</identifier><identifier>CODEN: JCROD7</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Antineoplastic agents ; Antineoplastic Agents - therapeutic use ; Biological and medical sciences ; Biomarkers ; Biomarkers, Tumor - analysis ; Cancer Research ; Carcinoma, Ovarian Epithelial ; Female genital diseases ; Gynecology. Andrology. 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High GST expression was associated with improved PFS (HR = 0.689). Among these factors, only LRP, P-gp and TNF-α were associated with response to platinum-based chemotherapy. Conclusions The markers we analyzed are unlikely to be useful as predictors of prognosis and response to platinum-based chemotherapy in EOC patients in clinical practice.</description><subject>Antineoplastic agents</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Biomarkers</subject><subject>Biomarkers, Tumor - analysis</subject><subject>Cancer Research</subject><subject>Carcinoma, Ovarian Epithelial</subject><subject>Female genital diseases</subject><subject>Gynecology. Andrology. 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However, the published data are inconsistent. Methods Eligible studies that investigated the association between survival or response to platinum-based chemotherapy in EOC and the expression status of Bcl-2, EGFR, GST, LRP, p16, p21, P-gp and TNF-α were identified by an electronic search of PubMed and Embase. The measures of interest were hazard ratio (HR) for survival or risk ratio for chemotherapy response. A meta-analysis was performed using the fixed-effect or random-effect models. Results The number of eligible studies analyzed was 27 for Bcl-2, 22 for EGFR, 29 for GST, 12 for LRP, 16 for p16, 22 for p21, 27 for P-gp and three for TNF-α. A meta-analysis showed that high EGFR and P-gp expression was associated with poor overall survival (OS) (pooled adjusted HR = 1.826 and HR = 1.822). Only high GST expression was associated with improved OS (HR = 0.780). Furthermore, high p16 and P-gp expression was associated with poor progression-free survival (PFS) (HR = 1.550 and HR = 2.136). High GST expression was associated with improved PFS (HR = 0.689). Among these factors, only LRP, P-gp and TNF-α were associated with response to platinum-based chemotherapy. Conclusions The markers we analyzed are unlikely to be useful as predictors of prognosis and response to platinum-based chemotherapy in EOC patients in clinical practice.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>23595127</pmid><doi>10.1007/s00432-013-1435-z</doi><tpages>21</tpages></addata></record>
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subjects Antineoplastic agents
Antineoplastic Agents - therapeutic use
Biological and medical sciences
Biomarkers
Biomarkers, Tumor - analysis
Cancer Research
Carcinoma, Ovarian Epithelial
Female genital diseases
Gynecology. Andrology. Obstetrics
Hematology
Humans
Internal Medicine
Medical sciences
Medicine
Medicine & Public Health
Meta-analysis
Multiple tumors. Solid tumors. Tumors in childhood (general aspects)
Neoplasms, Glandular and Epithelial - drug therapy
Neoplasms, Glandular and Epithelial - metabolism
Neoplasms, Glandular and Epithelial - mortality
Oncology
Ovarian cancer
Ovarian Neoplasms - drug therapy
Ovarian Neoplasms - metabolism
Ovarian Neoplasms - mortality
Pharmacology. Drug treatments
Prognosis
Review
Studies
Treatment Outcome
Tumors
title Prognostic significance of several biomarkers in epithelial ovarian cancer: a meta-analysis of published studies
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