PROGESTERONE-RECEPTOR LEVELS INDEPENDENTLY PREDICT SURVIVAL IN ENDOMETRIAL ADENOCARCINOMA

被引:27
|
作者
NYHOLM, HCJ
CHRISTENSEN, IJ
NIELSEN, AL
机构
[1] UNIV COPENHAGEN, HVIDOVRE HOSP, DEPT OBSTET & GYNECOL, COPENHAGEN, DENMARK
[2] RIGSHOSP, FINSEN LAB, DK-2100 COPENHAGEN, DENMARK
[3] BISPEBJERG HOSP, DEPT PATHOL, DK-2400 COPENHAGEN, DENMARK
关键词
D O I
10.1006/gyno.1995.9964
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Estrogen receptor (ER) and progesterone receptor (PR) contents were determined by biochemical (dextran charcoal-coated (DCC) assay) and immunohistochemical (ICA) methods in biopsies from 145 primary endometrial adenocarcinomas and those with eligible receptor measurements were analyzed with respect to correlations to cancer-specific survival in a multivariate analysis including histopathological characteristics. Median patient follow-up time was 67 months with 18 cancer deaths, The PR-DCC and ER-DCC values were dichotomized according to levels previously found by us to correspond to the best agreement between receptor status as determined by the DCC and ICA methods (130 fmol/mg cytosol protein for ER, 114 fmol/mg for PR), Using these thresholds, we found by multivariate analysis that ''high'' PR-DCC levels (>114 fmol/mg) correlated significantly (P = 0.004) with survival, independent of stage risk group (Ia + b vs Ic-IV), Patient age and histologic grade were prognostic factors in a univariate setting, but these parameters were eliminated in the multivariate model, While the PR-ICA scores also correlated significantly and independently with survival, the predictive effect of PR-ICA positivity alone could not be statistically evaluated due to the number of cases with eligible ICA values, However, we suggest that owing to a close correlation between DCC and ICA results, PR-ICA status may provide significant prognostic information when DCC measurements are not available. (C) 1995 Academic Press, Inc.
引用
收藏
页码:347 / 351
页数:5
相关论文
共 50 条
  • [1] HETEROGENEITY AND PROGESTERONE-RECEPTOR DISTRIBUTION IN ENDOMETRIAL ADENOCARCINOMA
    MORTEL, R
    ZAINO, R
    SATYASWAROOP, PG
    CANCER, 1984, 53 (01) : 113 - 116
  • [2] HETEROGENEITY OF PROGESTERONE-RECEPTOR DISTRIBUTION IN HUMAN ENDOMETRIAL ADENOCARCINOMA
    ZAINO, RJ
    CLARKE, CL
    MORTEL, R
    SATYASWAROOP, PG
    CANCER RESEARCH, 1988, 48 (07) : 1889 - 1895
  • [3] THE PREDICTIVE VALUE OF PROGESTERONE-RECEPTOR LEVELS IN ENDOMETRIAL CANCER
    INGRAM, SS
    ROSENMAN, J
    HEATH, R
    MORGAN, TM
    MOORE, D
    VARIA, M
    INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1989, 17 (01): : 21 - 27
  • [4] HISTOLOGICAL-EVALUATION OF INVITRO RESPONSES OF ENDOMETRIAL ADENOCARCINOMA TO PROGESTINS AND THEIR RELATION TO PROGESTERONE-RECEPTOR LEVELS
    HOLINKA, CF
    DELIGDISCH, L
    GURPIDE, E
    CANCER RESEARCH, 1984, 44 (01) : 293 - 296
  • [5] ENDOMETRIAL ADENOCARCINOMA - PROGNOSTIC-SIGNIFICANCE OF ESTROGEN AND PROGESTERONE-RECEPTOR ANALYSIS
    NOVOTNY, D
    SEGRETTI, E
    SOPER, J
    FLOWERS, J
    MCCARTY, K
    LABORATORY INVESTIGATION, 1988, 58 (01) : A67 - A67
  • [6] ENDOMETRIAL ADENOCARCINOMA - PROGNOSTIC-SIGNIFICANCE OF ESTROGEN AND PROGESTERONE-RECEPTOR ANALYSIS
    NOVOTNY, D
    SEGRETTI, E
    SOPER, J
    FLOWERS, J
    MCCARTY, K
    MODERN PATHOLOGY, 1988, 1 (01) : A67 - A67
  • [7] CLINICAL-SIGNIFICANCE OF NUCLEAR PROGESTERONE-RECEPTOR (PR) CONCENTRATIONS IN ENDOMETRIAL ADENOCARCINOMA
    RAKAR, S
    RAINER, S
    LENASI, H
    HUDNIKPLEVNIK, T
    ANTICANCER RESEARCH, 1986, 6 (03) : 378 - 378
  • [8] THE INFLUENCE OF MALIGNANT TRANSFORMATION ON THE PROGESTERONE-RECEPTOR CONTENT IN ENDOMETRIAL ADENOCARCINOMA - PRELIMINARY-REPORT
    LENASI, H
    RAKAR, S
    RAINER, S
    HUDNIKPLEVNIK, T
    ZDRAVSTVENI VESTNIK, 1986, 55 (06): : 271 - 274
  • [9] PROGESTERONE-RECEPTOR HETEROGENEITY AND ENDOMETRIAL TUMOR DIFFERENTIATION
    CHENG, C
    BUI, C
    CAUCHI, M
    CANCER LETTERS, 1988, 43 (03) : 215 - 218
  • [10] CHARACTERIZATION OF THE PROGESTERONE-RECEPTOR IN HUMAN ENDOMETRIAL CARCINOMA
    CLARKE, CL
    FEIL, PD
    SATYASWAROOP, PG
    PROCEEDINGS OF THE AMERICAN ASSOCIATION FOR CANCER RESEARCH, 1985, 26 (MAR): : 202 - 202