Impact of epidermal growth factor receptor expression on disease-free survival and rate of pelvic relapse in patients with advanced cancer of the cervix treated with chemoradiotherapy
- PMID: 20859196
- DOI: 10.1097/COC.0b013e3181e84634
Impact of epidermal growth factor receptor expression on disease-free survival and rate of pelvic relapse in patients with advanced cancer of the cervix treated with chemoradiotherapy
Abstract
Objectives: To determine the impact of the expression of epidermal growth factor receptor (EGFR) on disease-free survival (DFS) and on pelvic relapse in patients with advanced cancer of the cervix receiving concurrent chemoradiotherapy.
Methods: In 112 consecutive patients with advanced cancer of the cervix (11 stage IB2-IIA, 25 IIB, 63 IIIB, 13 IVA) treated with chemoradiotherapy between December 1994 and September 2004, the expression of EGFR using histoimmunochemistry was measured and used in univariate and multivariate analysis, along with variables such as age, International Federation of Gynecology and Obstetrics Staging System for Epithelial Ovarian Cancer (FIGO) stage, histology, Eastern Cooperative Oncology Group (ECOG), tumor size, and ganglia involvement diagnosed with computerized axial tomography, treatment with cisplatin to evaluate its impact on DFS and pelvic relapse.
Results: Of the 112 biopsies, 32 (28.6%) were negative or slightly positive (EGFR±) and 80 (71.4%) were moderate or intensely positive (EGFR++/+++). The overexpression of EGFR (++/+++) was significantly associated with an epidermoid histology (P < 0.0001), with a higher rate of pelvis relapse and a decreased DFS (hazard ratio [HR]: 2.31 [1.08-4.96]; P = 0.03). Overall, treatment with cisplatin increased DFS (HR: 0.51 [0.26-0.97]; P = 0.04).
Conclusions: Patients with tumors of the cervix and overexpression of the EGFR++/+++ show a higher probability of pelvic relapses and a decreased disease-free survival. The poor prognosis of these tumors may be a consequence of an increase in radio-resistance.
Similar articles
-
Clinical behaviors and outcomes for adenocarcinoma or adenosquamous carcinoma of cervix treated by radical hysterectomy and adjuvant radiotherapy or chemoradiotherapy.Int J Radiat Oncol Biol Phys. 2012 Oct 1;84(2):420-7. doi: 10.1016/j.ijrobp.2011.12.013. Epub 2012 Feb 24. Int J Radiat Oncol Biol Phys. 2012. PMID: 22365621
-
Outcomes of chemoradiotherapy in cervical cancer--the Western Australian experience.Int J Radiat Oncol Biol Phys. 2012 Mar 15;82(4):1431-8. doi: 10.1016/j.ijrobp.2011.04.047. Epub 2011 Jun 2. Int J Radiat Oncol Biol Phys. 2012. PMID: 21640504
-
Pelvic irradiation with concurrent chemotherapy versus pelvic and para-aortic irradiation for high-risk cervical cancer: an update of radiation therapy oncology group trial (RTOG) 90-01.J Clin Oncol. 2004 Mar 1;22(5):872-80. doi: 10.1200/JCO.2004.07.197. J Clin Oncol. 2004. PMID: 14990643 Clinical Trial.
-
Adenosquamous histology predicts a poor outcome for patients with advanced-stage, but not early-stage, cervical carcinoma.Cancer. 2003 May 1;97(9):2196-202. doi: 10.1002/cncr.11371. Cancer. 2003. PMID: 12712471 Review.
-
Cervical cancer: combined modality therapy.Cancer J. 2001 Jul-Aug;7 Suppl 1:S47-50. Cancer J. 2001. PMID: 11504285 Review.
Cited by
-
Validation of Potential Protein Markers Predicting Chemoradioresistance in Early Cervical Cancer by Immunohistochemistry.Front Oncol. 2021 Jul 19;11:665595. doi: 10.3389/fonc.2021.665595. eCollection 2021. Front Oncol. 2021. PMID: 34350111 Free PMC article.
-
Chemoradiotherapy response prediction model by proteomic expressional profiling in patients with locally advanced cervical cancer.Gynecol Oncol. 2020 May;157(2):437-443. doi: 10.1016/j.ygyno.2020.02.017. Epub 2020 Feb 24. Gynecol Oncol. 2020. PMID: 32107047 Free PMC article.
-
Prognostic significance of the co-expression of EGFR and HER2 in adenocarcinoma of the uterine cervix.PLoS One. 2017 Aug 31;12(8):e0184123. doi: 10.1371/journal.pone.0184123. eCollection 2017. PLoS One. 2017. PMID: 28859123 Free PMC article.
-
Prognostic Impact of Epidermal Growth Factor Receptor Overexpression in Patients with Cervical Cancer: A Meta-Analysis.PLoS One. 2016 Jul 20;11(7):e0158787. doi: 10.1371/journal.pone.0158787. eCollection 2016. PLoS One. 2016. PMID: 27438047 Free PMC article.
-
Emerging biological treatments for uterine cervical carcinoma.J Cancer. 2014 Jan 5;5(2):86-97. doi: 10.7150/jca.7963. eCollection 2014. J Cancer. 2014. PMID: 24494026 Free PMC article. Review.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Research Materials
Miscellaneous
