Prognostic impact of proliferation associated factors MIBI (Ki-67) and S-phase in node-negative breast cancer

被引:68
作者
Dettmar, P
Harbeck, N
Thomssen, C
Pache, L
Ziffer, P
Fizi, K
Janicke, F
Nathrath, W
Schmitt, M
Graeff, H
Hofler, H
机构
[1] TECH UNIV MUNICH,INST ALLGEMEINE PATHOL & PATHOL ANAT,D-81675 MUNICH,GERMANY
[2] TECH UNIV MUNICH,FRAUENKLIN & POLIKLIN,D-81675 MUNICH,GERMANY
关键词
proliferation; MIBI (Ki-67); S-phase; node-negative breast cancer; prognosis;
D O I
10.1038/bjc.1997.261
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MIB1 proliferation rate (MIB1-PR) and total S-phase fraction (SPF) were retrospectively determined in formalin-fixed, paraffin-embedded sections of 90 primary node-negative breast carcinomas. None of the patients had received adjuvant systemic therapy. Median follow-up in patients still alive at the time of analysis was 37.5 months (16-72 months). Immunostaining of Ki-67 antigen was pet-formed using the monoclonal antibody MIB1 and the APAAP technique. An adjacent 50-mu m paraffin section was used for flow cytometric S-phase determination. Results were compared to established clinicopathological prognostic factors. MIBI-PR was significantly correlated to grading (P = 0.018); SPF was significantly correlated with tumour size (P = 0.041) and inversely with steroid hormone receptor status (P = 0.03). A significant correlation between MIBI-PR and SPF was found in aneuploid (P = 0.025) but not in diploid tumours (P = 0.164). In univariate analysis, both MIB1-PR (optimized cut-off of 25%) and SPF (optimized cut-off of 8%) were significant prognostic factors for disease-free survival (DFS) (MIB1-PR, P = 0.0224; SPF, P = 0.0028). in multivariate analysis, however, only SPF remained significant; it was the strongest prognostic factor for DFS (P = 0.0073), stronger than MIB1-PR or established clinicopathological prognostic factors. We thus conclude that MIBI-PR and SPF provide additional prognostic information in node-negative breast cancer. However, in our study, flow cytometrically determined SPF had the greater prognostic impact.
引用
收藏
页码:1525 / 1533
页数:9
相关论文
共 50 条
  • [31] KALLIONIEMI OP, 1988, CANCER, V62, P2183, DOI 10.1002/1097-0142(19881115)62:10<2183::AID-CNCR2820621019>3.0.CO
  • [32] 2-B
  • [33] KAMEL OW, 1989, AM J PATHOL, V134, P107
  • [34] LELLE RJ, 1986, TUMORDIAGN THER, V7, P181
  • [35] LELLE RJ, 1987, CANCER, V59, P83, DOI 10.1002/1097-0142(19870101)59:1<83::AID-CNCR2820590119>3.0.CO
  • [36] 2-I
  • [37] MCDIVITT RW, 1986, CANCER, V57, P269, DOI 10.1002/1097-0142(19860115)57:2<269::AID-CNCR2820570214>3.0.CO
  • [38] 2-D
  • [39] NODE-NEGATIVE BREAST-CANCER - PROGNOSTIC SUBGROUPS DEFINED BY TUMOR SIZE AND FLOW-CYTOMETRY
    OREILLY, SM
    CAMPLEJOHN, RS
    BARNES, DM
    MILLIS, RR
    RUBENS, RD
    RICHARDS, MA
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1990, 8 (12) : 2040 - 2046
  • [40] ASSESSMENT OF NUCLEOLAR ORGANIZER REGIONS BY AUTOMATIC IMAGE-ANALYSIS IN BREAST-CANCER - CORRELATION WITH DNA CONTENT, PROLIFERATION RATE, RECEPTOR STATUS AND HISTOPATHOLOGICAL GRADING
    RUSCHOFF, J
    NEUMANN, K
    CONTRACTOR, H
    PLATE, K
    THOMAS, C
    [J]. JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 1990, 116 (05) : 480 - 485