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Correlation between expression of EGFR and the prognosis of patients with cervical carcinoma

Authors
 Young Tae Kim  ;  Sang Won Park  ;  Jae Wook Kim 
Citation
 GYNECOLOGIC ONCOLOGY, Vol.87(1) : 84-89, 2002 
Journal Title
GYNECOLOGIC ONCOLOGY
ISSN
 0090-8258 
Issue Date
2002
MeSH
Adult ; Aged ; Cohort Studies ; Disease-Free Survival ; Enzyme-Linked Immunosorbent Assay ; ErbB Receptors/biosynthesis* ; Female ; Humans ; Middle Aged ; Multivariate Analysis ; Predictive Value of Tests ; Prognosis ; Prospective Studies ; Uterine Cervical Neoplasms/metabolism* ; Uterine Cervical Neoplasms/pathology
Keywords
EGFR ; cervical cancer ; enzyme immunoassay ; prognosis
Abstract
Objective. Overexpressionof epidermal growth factor receptor (EGFR) gene has been detected in a large number of human tumors, in most of which the association between overexpression of EGFR and poor prognosis of the disease has been reported. However, the prognostic role of EGFR oncoprotein in cervical carcinoma remains controversial. The current study aimed to determine the prognostic value of EGFR in patients with cervical cancer.

Methods. We measured EGFR oncoprotein with an enzyme-linked immunosorbent assay (ELISA). Results were correlated to clinical data.

Results. The presence of measurable levels of EGFR in the tumor was found in all of the explored tumors. The levels varied widely from 31 to 2874 fmol/mg protein with a median at 582 fmol/mg protein, and Q1, Q2, and Q3 quartiles were 156, 562, and 1047, respectively. Overexpression of EGFR was associated with an impaired prognosis with respect to disease-free interval (P = 0.03) and overall survival (P = 0.04). Multivariate analysis revealed that tumor EGFR provided prognostic information with respect to disease-free interval (P = 0.002) and overall survival (P = 0.005) independently of the two established prognosticators, FIGO stage and lesion size.

Conclusion. Our results are consistent with the concept that EGFR confers prognostic information in addition to that provided by the established clinicopathologic parameters of FIGO stage and lesion size.
Full Text
http://www.sciencedirect.com/science/article/pii/S0090825802968034?np=y
DOI
10.1006/gyno.2002.6803
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Obstetrics and Gynecology (산부인과학교실) > 1. Journal Papers
Yonsei Authors
Kim, Young Tae(김영태) ORCID logo https://orcid.org/0000-0002-7347-1052
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/143614
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