1. HER-2 overexpression is an independent marker of poor prognosis of advanced primary ovarian carcinoma: a multicenter study of the GINECO group
- Author
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S. Bain, B. Leduc, Sophie Camilleri-Broët, A Le Tourneau, Josée Audouin, H. Orfeuvre, O. Levrel, D. Paraiso, Anne-Claire Hardy-Bessard, and Eric Pujade-Lauraine
- Subjects
Oncology ,Adult ,medicine.medical_specialty ,Pathology ,Combination therapy ,Receptor, ErbB-2 ,Population ,Internal medicine ,Ovarian carcinoma ,Antineoplastic Combined Chemotherapy Protocols ,medicine ,Carcinoma ,Biomarkers, Tumor ,Humans ,Neoplasms, Glandular and Epithelial ,education ,Cyclophosphamide ,Survival analysis ,Aged ,Epirubicin ,Retrospective Studies ,Ovarian Neoplasms ,education.field_of_study ,business.industry ,Cancer ,Hematology ,Middle Aged ,medicine.disease ,Prognosis ,Immunohistochemistry ,Survival Analysis ,Clinical trial ,Clinical Trials, Phase III as Topic ,Female ,Cisplatin ,Ovarian cancer ,business - Abstract
Background Despite numerous studies, no biological marker has been identified that accurately predicts prognosis of advanced ovarian cancer. Tumors from a homogeneous population of 117 patients with a stage III/IV ovarian cancer, enrolled in a multicenter prospective GINECO clinical trial were analyzed retrospectively. Patients and methods All patients received the same platinum-based combination therapy and were followed-up for a median of 68 months. Tumor expression of Ki67, BCL-2, BAX, P53 or c-erbB-2 proteins was evaluated immunohistochemically on paraffin-embedded tissues and their prognostic impact analyzed. Results The median rate of Ki67-positive nuclear area was 30%. BCL-2, BAX and P53 proteins were expressed in 52, 54 and 71% of the tumors, respectively, while HER-2 protein was overexpressed in 16%. Only HER-2 overexpression was significantly associated with shorter progression-free survival and overall survival. According to our multivariate analysis, the HER-2 prognostic impact was independent of classical clinical prognostic factors. Conclusion HER-2 appeared to influence the outcome of advanced ovarian cancer patients included in a clinical trial with prolonged follow-up, thereby suggesting that HER-2 is a potential target for treatment of this cancer.
- Published
- 2003