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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Camilleri-Broët S, Hardy-Bessard AC, Le Tourneau A, Paraiso D, Levrel O, Leduc B, Bain S, Orfeuvre H, Audouin J, and Pujade-Lauraine E
- Subjects
- Adult, Aged, Biomarkers, Tumor metabolism, Cisplatin administration & dosage, Clinical Trials, Phase III as Topic, Cyclophosphamide administration & dosage, Epirubicin administration & dosage, Female, Humans, Immunohistochemistry, Middle Aged, Neoplasms, Glandular and Epithelial pathology, Ovarian Neoplasms pathology, Prognosis, Retrospective Studies, Survival Analysis, Antineoplastic Combined Chemotherapy Protocols therapeutic use, Neoplasms, Glandular and Epithelial drug therapy, Neoplasms, Glandular and Epithelial metabolism, Ovarian Neoplasms drug therapy, Ovarian Neoplasms metabolism, Receptor, ErbB-2 metabolism
- 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
- 2004
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