HER-2 overexpression is an independent marker of poor prognosis of advanced primary ovarian carcinoma:: a multicenter study of the GINECO group

被引:81
作者
Camilleri-Broët, S
Hardy-Bessard, AC
Le Tourneau, A
Paraiso, D
Levrel, O
Leduc, B
Bain, S
Orfeuvre, H
Audouin, J
Pujade-Lauraine, E
机构
[1] UFR Paris 6, Assistance Publ Hop Paris, Hotel Dieu, Serv Anat Pathol, Paris, France
[2] UFR Paris 6, Assistance Publ Hop Paris, Hotel Dieu, Serv Oncol, Paris, France
[3] Hop Fleyriat, Serv Oncohematol, Bourg En Bresse, France
关键词
HER-2; ovarian cancer; prognosis;
D O I
10.1093/annonc/mdh021
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:104 / 112
页数:9
相关论文
共 35 条
[1]   Clinical significance of α-catenin, collagen IV, and Ki-67 expression in epithelial ovarian cancer [J].
Anttila, M ;
Kosma, VM ;
Ji, HX ;
Wei-Ling, X ;
Puolakka, J ;
Juhola, M ;
Saarikoski, S ;
Syrjanen, K .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (08) :2591-2600
[2]   CLONING THE CHROMOSOMAL BREAKPOINT OF T(14-18) HUMAN LYMPHOMAS - CLUSTERING AROUND JH ON CHROMOSOME-14 AND NEAR A TRANSCRIPTIONAL UNIT ON 18 [J].
BAKHSHI, A ;
JENSEN, JP ;
GOLDMAN, P ;
WRIGHT, JJ ;
MCBRIDE, OW ;
EPSTEIN, AL ;
KORSMEYER, SJ .
CELL, 1985, 41 (03) :899-906
[3]  
Ben-Hur H, 1999, EUR J GYNAECOL ONCOL, V20, P249
[4]   Bcl-2 and p53 protein expression, apoptosis, and p53 mutation in human epithelial ovarian cancers [J].
Chan, WY ;
Cheung, KK ;
Schorge, JO ;
Huang, LW ;
Welch, WR ;
Bell, DA ;
Berkowitz, RS ;
Mok, SC .
AMERICAN JOURNAL OF PATHOLOGY, 2000, 156 (02) :409-417
[5]   A prognostic model for ovarian cancer [J].
Clark, TG ;
Stewart, ME ;
Altman, DG ;
Gabra, H ;
Smyth, JF .
BRITISH JOURNAL OF CANCER, 2001, 85 (07) :944-952
[6]   Strong correlation between results of fluorescent in situ hybridization and immunohistochemistry for the assessment of the ERBB2 (HER-2/neu) gene status in breast carcinoma [J].
Couturier, J ;
Vincent-Salomon, A ;
Nicolas, A ;
Beuzeboc, P ;
Mouret, E ;
Zafrani, B ;
Sastre-Garau, X .
MODERN PATHOLOGY, 2000, 13 (11) :1238-1243
[7]  
COX DR, 1972, J R STAT SOC B, V34, P187
[8]   C-ERBB2 GENE AMPLIFICATION AND PROTEIN EXPRESSION IN OVARIAN EPITHELIAL TUMORS - EVALUATION OF THEIR RESPECTIVE PROGNOSTIC-SIGNIFICANCE BY MULTIVARIATE-ANALYSIS [J].
FAJAC, A ;
BENARD, J ;
LHOMME, C ;
REY, A ;
DUVILLARD, P ;
ROCHARD, F ;
BERNAUDIN, JF ;
RIOU, G .
INTERNATIONAL JOURNAL OF CANCER, 1995, 64 (02) :146-151
[9]  
FELIP E, 1995, CANCER, V75, P2147, DOI 10.1002/1097-0142(19950415)75:8<2147::AID-CNCR2820750818>3.0.CO
[10]  
2-8