Impact of steroid receptors, pS2 and cathepsin D on the outcome of N+ postmenopausal breast cancer patients treated with tamoxifen

被引:8
作者
Dittadi, R
Biganzoli, E
Boracchi, P
Salbe, C
Mione, R
Gatti, C
Gion, M
机构
[1] Osped Civile, Ctr Study Biol Markers Malignancy, Venezia, Italy
[2] Ist Nazl Studio & Cura Tumori, Div Med Stat & Biometry, I-20133 Milano, Italy
[3] Univ Milan, Inst Med Stat & Biometry, I-20122 Milan, Italy
[4] Osped Civile, Ctr Oncol, Div Radiotherapy, Venezia, Italy
关键词
breast cancer; cathepsin D; pS2; steroid receptors; continuous variables;
D O I
10.1177/172460089801300106
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
In spite of the complexity of the biological basis of the hormonal regulation of breast cancer clinical studies tend to simplify the information by mainly categorizing continuous variables related to hormonal status and not considering the interactions between variables. The present study was planned to examine the presence of an interaction between cathepsin D (Cath-D) and pS2 in patients treated with adjuvant tamoxifen in a homogeneous subset of node-positive postmenopausal patients and to evaluate the contribution of the interaction to the predictive ability of the model. Steroid receptors (ER and PgR) were measured in cytosol using the dextran-coated charcoal method, while Cath-D and pS2 were determined using commercially available immunoradiometric assays. The prognostic role of each variable and their joint effect were investigated using a Cox regression model. Biological variables were analyzed as continuous and when their prognostic relationship did not seem linear a restricted cubic spline regression smoothing approach was adopted. The logarithm of hazard showed a linear relationship with the log(ER), while it i) remained almost constant up to about 20 fmol/mg and subsequently decreased for PgR; ii) was almost constant up to about 50 pmol/mg and subsequently, decreased for Cath-D; iii) decreased for increasing log(value) up to about 33 ng/mg and subsequently, increased for pS2. In the multivariate analysis both PgR and the interaction between pS2 and Cath-D retained a significant prognostic role. For low values of pS2, the prognosis worsened with the increase in Cath-D levels and this relationship reversed for high values of pS2. From the results of the present study we can conclude that i) a significant interaction between Cath-D and pS2 was found in this case series; ii) the prognostic relationships should not be underestimated in clinical decision making; iii) a predictive score obtained considering the contribution of PgR, pS2 and Cath-D could be useful for clinical use.
引用
收藏
页码:30 / 41
页数:12
相关论文
共 39 条
[1]  
Akaike H., 1973, 2 INT S INFORM THEOR, P199
[2]   REVIEW OF SURVIVAL ANALYSES PUBLISHED IN CANCER JOURNALS [J].
ALTMAN, DG ;
DESTAVOLA, BL ;
LOVE, SB ;
STEPNIEWSKA, KA .
BRITISH JOURNAL OF CANCER, 1995, 72 (02) :511-518
[3]   DANGERS OF USING OPTIMAL CUTPOINTS IN THE EVALUATION OF PROGNOSTIC FACTORS [J].
ALTMAN, DG ;
LAUSEN, B ;
SAUERBREI, W ;
SCHUMACHER, M .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1994, 86 (11) :829-835
[4]   Specific oncological contribution of cathepsin D and pS2 in human breast cancer: Their relationship with TNM status, estradiol receptors, epidermal growth factor receptor and neu amplification [J].
Bolufer, P ;
Torregrosa, MD ;
Gomez, L ;
Munarriz, B ;
Lopez, JA ;
Asins, E ;
Espinoza, S ;
Vera, F ;
Vazquez, C ;
Guillem, V .
CLINICA CHIMICA ACTA, 1996, 247 (1-2) :89-103
[5]   ESTROGENS AND GROWTH-FACTORS INDUCE THE MESSENGER-RNA OF THE 52K-PRO-CATHEPSIN-D SECRETED BY BREAST-CANCER CELLS [J].
CAVAILLES, V ;
AUGEREAU, P ;
GARCIA, M ;
ROCHEFORT, H .
NUCLEIC ACIDS RESEARCH, 1988, 16 (05) :1903-1919
[6]   CATHEPSIN-D GENE IS CONTROLLED BY A MIXED PROMOTER, AND ESTROGENS STIMULATE ONLY TATA-DEPENDENT TRANSCRIPTION IN BREAST-CANCER CELLS [J].
CAVAILLES, V ;
AUGEREAU, P ;
ROCHEFORT, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (01) :203-207
[7]  
CAZIN JL, 1993, INT J ONCOL, V2, P1081
[8]   SYNTHETIC ANTIESTROGENS MODULATE INDUCTION OF PS2 AND CATHEPSIN-D MESSENGER-RIBONUCLEIC-ACID BY GROWTH-FACTORS AND ADENOSINE-3',5'-MONOPHOSPHATE IN MCF7 CELLS [J].
CHALBOS, D ;
PHILIPS, A ;
GALTIER, F ;
ROCHEFORT, H .
ENDOCRINOLOGY, 1993, 133 (02) :571-576
[9]  
CLARK GM, 1993, CANCER-AM CANCER SOC, V71, P2157, DOI 10.1002/1097-0142(19930315)71:6+<2157::AID-CNCR2820711606>3.0.CO
[10]  
2-O