C-ERBB-2 PROTEIN EXPRESSION IN NODE NEGATIVE BREAST-CANCER

被引:44
作者
RICHNER, J
GERBER, HA
LOCHER, GW
GOLDHIRSCH, A
GELBER, RD
GULLICK, WJ
BERGER, MS
GRONER, B
HYNES, NE
机构
[1] LUDWIG INST CANC RES,BERN,SWITZERLAND
[2] UNIV BERN,DEPT PATHOL,CH-3000 BERN,SWITZERLAND
[3] UNIV BERN,DEPT OBSTET GYNECOL,CH-3000 BERN,SWITZERLAND
[4] HARVARD UNIV,SCH MED,DANA FARBER CANC INST,BOSTON,MA 02115
[5] HAMMERSMITH HOSP,IMPERIAL CANC RES FUND,ONCOL GRP,LONDON W12 0HS,ENGLAND
[6] HOSP UNIV PENN,PHILADELPHIA,PA 19104
关键词
Breast cancer; Immunohistochemistry; Oncogenes; Prognostic factors;
D O I
10.1093/oxfordjournals.annonc.a057745
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We investigated the expression of c-erbB-2 protein in two matched groups of breast cancer patients, one with and one without relapse. 37 patients with relapse were compared with 42 patients without recurrence for time of observation, adjuvant treatment, age, menopausal status and estrogen receptor content. Paraffin-embedded sections were stained with the polyclonal antibody 21 N, raised against a synthetic peptide from the predicted sequence of the c-erbB-2 protein. The staining of c-erbB-2 was measured on a scale of 0 to 3+. C-erbB-2 staining was negative in 16 (38%) patients in the relapse-free group, and in 8 (22%) of the patients with metastases. Neither disease-free survival (DFS) nor overall survival (OS) were dependent upon the extent of c-erbB-2 expression. An analysis by estrogen receptor (ER) status (i.e. positive or negative) and by c-erbB-2 expression (i.e. positive or negative) revealed that patients with ER-positive primaries and negative c-erbB-2 have the longest disease-free survival (DFS) and overall survival (OS). We conclude that c-erbB-2 expression might be clinically useful only if other prognostic variables (e.g. estrogen receptor content in the tumor) are also considered. © 1990 Kluwer Academic Publishers.
引用
收藏
页码:263 / 268
页数:6
相关论文
共 38 条
[1]   REDUCTION TO HOMOZYGOSITY OF GENES ON CHROMOSOME-11 IN HUMAN-BREAST NEOPLASIA [J].
ALI, IU ;
LIDEREAU, R ;
THEILLET, C ;
CALLAHAN, R .
SCIENCE, 1987, 238 (4824) :185-188
[2]   AN IMMUNOHISTOCHEMICAL EVALUATION OF C-ERB-2 EXPRESSION IN HUMAN-BREAST CARCINOMA [J].
BARNES, DM ;
LAMMIE, GA ;
MILLIS, RR ;
GULLICK, WL ;
ALLEN, DS ;
ALTMAN, DG .
BRITISH JOURNAL OF CANCER, 1988, 58 (04) :448-452
[3]  
BERGER MS, 1988, CANCER RES, V48, P1238
[4]  
BETTELHEIM R, 1984, BRIT J CANCER, V50, P771, DOI 10.1038/bjc.1984.255
[5]  
Bonadonna G, 1989, Important Adv Oncol, P151
[6]   PROTOONCOGENE ABNORMALITIES IN HUMAN-BREAST CANCER - CORRELATIONS WITH ANATOMIC FEATURES AND CLINICAL COURSE OF DISEASE [J].
CLINE, MJ ;
BATTIFORA, H ;
YOKOTA, J .
JOURNAL OF CLINICAL ONCOLOGY, 1987, 5 (07) :999-1006
[7]   TYROSINE KINASE RECEPTOR WITH EXTENSIVE HOMOLOGY TO EGF RECEPTOR SHARES CHROMOSOMAL LOCATION WITH NEU ONCOGENE [J].
COUSSENS, L ;
YANGFENG, TL ;
LIAO, YC ;
CHEN, E ;
GRAY, A ;
MCGRATH, J ;
SEEBURG, PH ;
LIBERMANN, TA ;
SCHLESSINGER, J ;
FRANCKE, U ;
LEVINSON, A ;
ULLRICH, A .
SCIENCE, 1985, 230 (4730) :1132-1139
[8]   GENETIC ALTERATION OF THE C-MYC PROTOONCOGENE (MYC) IN HUMAN PRIMARY BREAST CARCINOMAS [J].
ESCOT, C ;
THEILLET, C ;
LIDEREAU, R ;
SPYRATOS, F ;
CHAMPEME, MH ;
GEST, J ;
CALLAHAN, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (13) :4834-4838
[9]   A RANDOMIZED CLINICAL-TRIAL EVALUATING SEQUENTIAL METHOTREXATE AND FLUOROURACIL IN THE TREATMENT OF PATIENTS WITH NODE-NEGATIVE BREAST-CANCER WHO HAVE ESTROGEN-RECEPTOR-NEGATIVE TUMORS [J].
FISHER, B ;
REDMOND, C ;
DIMITROV, NV ;
BOWMAN, D ;
LEGAULTPOISSON, S ;
WICKERHAM, DL ;
WOLMARK, N ;
FISHER, ER ;
MARGOLESE, R ;
SUTHERLAND, C ;
GLASS, A ;
FOSTER, R ;
CAPLAN, R .
NEW ENGLAND JOURNAL OF MEDICINE, 1989, 320 (08) :473-478
[10]  
FISHER ER, 1984, CANCER-AM CANCER SOC, V53, P712