Bcl-2 as a predictor of chemosensitivity and prognosis in primary epithelial ovarian cancer

Citation
Y. Mano et al., Bcl-2 as a predictor of chemosensitivity and prognosis in primary epithelial ovarian cancer, EUR J CANC, 35(8), 1999, pp. 1214-1219
Citations number
23
Categorie Soggetti
Oncology,"Onconogenesis & Cancer Research
Journal title
EUROPEAN JOURNAL OF CANCER
ISSN journal
09598049 → ACNP
Volume
35
Issue
8
Year of publication
1999
Pages
1214 - 1219
Database
ISI
SICI code
0959-8049(199908)35:8<1214:BAAPOC>2.0.ZU;2-S
Abstract
This retrospective study of ovarian cancer aimed to elucidate whether expre ssion of apoptosis-related proteins, bcl-2, p53 or MDM-2, is associated wit h resistance to chemotherapy, especially cisplatin (CDDP) based chemotherap y. Expression of bcl-2, p53 and MDM-2, was assessed by immunohistochemical staining of tumour tissues collected at initial surgery prior to treatment with CDDP-based chemotherapy. Among 66 patients with advanced ovarian cance r with measurable tumour following surgery and evaluable for response to ch emotherapy, 42, 45 and 56% were positive for bcl-2, p53 and MDM-2, respecti vely. Significantly fewer tumours of patients who had a complete response t o chemotherapy (CR) showed positivity for bcl-2 (2/20) than for p53 (6/20) and MDM-2 (8/20, P < 0.001). There was an inverse correlation between bcl-2 staining and initial response to chemotherapy, especially in serous and en dometrial adenocarcinomas. In patients with stage III-IV, serous or endomet rioid adenocarcinomas, significantly poorer survival was seen for those wit h bcl-2 positive tumours than those with negative bcl-2 staining (P= 0.0064 ). p53 and MDM-2 were not correlated with initial response to chemotherapy. Multivariate analysis revealed that bcl-2, residual tumour size and histol ogy were significant independent prognostic factors. These results suggest that bcl-2 can be a possible predictor of response to chemotherapy and prog nosis in patients with advanced ovarian carcinoma. (C) 1999 Elsevier Scienc e Ltd. All rights reserved.