Prognostic impact of in vivo soluble cell adhesion molecules in metastatic renal cell carcinoma

被引:27
作者
Hoffmann, R
Franzke, A
Buer, J
Sel, S
Oevermann, K
Duensing, A
Probst, M
Duensing, S
Kirchner, H
Ganser, A
Atzpodien, J
机构
[1] Med Hsch Hannover, Dept Hematol & Oncol, D-30625 Hannover, Germany
[2] Med Hsch Hannover, Dept Pathol, D-30625 Hannover, Germany
[3] Natl Biotechnol Ctr, OBF, Dept Cell Biol & Immunbiol, Braunschweig, Germany
关键词
renal carcinoma; soluble adhesion molecules; predictor;
D O I
10.1038/sj.bjc.6690277
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The purpose of the study was to determine prognostic significance of pretreatment serum levels of different molecules involved in cell to cell interactions along with other clinical parameters in patients with metastatic renal cell carcinoma. sICAM-1, sVCAM-1 and sELAM-1 serum levels were determined by ELISA assays in sera from 99 patients with histologically confirmed progressive metastatic renal cell carcinoma prior to initiation of systemic therapy. Kaplan-Meier survival analysis, log-rank statistics and two-proportional Cox regression analyses were employed to identify risk factors and to demonstrate statistical independence. In univariate analyses, the following pretreatment risk factors could be identified: serum sICAM-1 level > 360 ng ml(-1) erythrocyte sedimentation rate > 70 mm h(-1), serum C-reactive protein level > 8 mg l(-1), serum lactic dehydrogenase level > 240 U/ I and neutrophil count > 6000 mu(1-1). Multivariate analyses demonstrated statistical independence for serum sICAM-1 level, erythrocyte sedimentation rate (ESR) and serum C-reactive protein (CRP) level as pretreatment predictors of overall patient survival. The prognostic significance of sICAM-1 might indicate a role of this molecule for tumour progression, potentially in association with the abrogation of anti-tumour immune responses. The possibility of defining a pretreatment risk model based on sIcAM-1 level, ESR and CRP also warrants further investigation, with regard to a possible linkage between acute phase proteins and sICAM-1 levels.
引用
收藏
页码:1742 / 1745
页数:4
相关论文
共 33 条
[1]   MOLECULAR ANALYSIS OF ANTIGEN-INDEPENDENT ADHESION FORCES BETWEEN T-LYMPHOCYTES AND B-LYMPHOCYTES [J].
AMBLARD, F ;
AUFFRAY, C ;
SEKALY, R ;
FISCHER, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (09) :3628-3632
[2]   IN-VIVO DISTRIBUTION OF INTEGRINS IN RENAL-CELL CARCINOMA - INTEGRIN-PHENOTYPE ALTERATION IN DIFFERENT DEGREES OF TUMOR DIFFERENTIATION AND VLA-2 INVOLVEMENT IN TUMOR-METASTASIS [J].
ANASTASSIOU, G ;
DUENSING, S ;
STEINHOFF, G ;
KIRCHNER, H ;
GANSER, A ;
ATZPODIEN, J .
CANCER BIOTHERAPY, 1995, 10 (04) :287-292
[3]   HOME THERAPY WITH RECOMBINANT INTERLEUKIN-2 AND INTERFERON-ALPHA-2B IN ADVANCED HUMAN MALIGNANCIES [J].
ATZPODIEN, J ;
KORFER, A ;
FRANKS, CR ;
POLIWODA, H ;
KIRCHNER, H .
LANCET, 1990, 335 (8704) :1509-1512
[4]  
BECKER JC, 1993, J IMMUNOL, V151, P7224
[5]   INTERCELLULAR-ADHESION MOLECULE-1 (ICAM-1) HAS A CENTRAL ROLE IN CELL CELL CONTACT-MEDIATED IMMUNE-MECHANISMS [J].
BOYD, AW ;
WAWRYK, SO ;
BURNS, GF ;
FECONDO, JV .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (09) :3095-3099
[6]   CD54/ICAM-1 IS A COSTIMULATOR OF NK CELL-MEDIATED CYTOTOXICITY [J].
CHONG, ASF ;
BOUSSY, IA ;
JIANG, XL ;
LAMAS, M ;
GRAF, LH .
CELLULAR IMMUNOLOGY, 1994, 157 (01) :92-105
[7]   SOLUBLE ICAM-1 IN HODGKINS-DISEASE - A PROMISING INDEPENDENT PREDICTIVE MARKER FOR SURVIVAL [J].
CHRISTIANSEN, I ;
ENBLAD, G ;
KALKNER, KM ;
GIDLOF, C ;
GLIMELIUS, B ;
TOTTERMAN, TH .
LEUKEMIA & LYMPHOMA, 1995, 19 (3-4) :243-251
[8]   Elevated serum levels of soluble ICAM-1 in non-Hodgkin's lymphomas correlate with tumour burden, disease activity and other prognostic markers [J].
Christiansen, I ;
Gidlof, C ;
Kalkner, KM ;
Hagberg, H ;
Bennmarker, H ;
Totterman, T .
BRITISH JOURNAL OF HAEMATOLOGY, 1996, 92 (03) :639-646
[9]   INHIBITION OF INTERCELLULAR-ADHESION MOLECULE 1-DEPENDENT BIOLOGICAL-ACTIVITIES BY A SYNTHETIC PEPTIDE ANALOG [J].
FECONDO, JV ;
KENT, SBH ;
BOYD, AW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (07) :2879-2882
[10]   MECHANISMS OF SELECTIVE KILLING OF NEUROBLASTOMA-CELLS BY NATURAL-KILLER-CELLS AND LYMPHOKINE-ACTIVATED KILLER-CELLS - POTENTIAL FOR RESIDUAL DISEASE ERADICATION [J].
FOREMAN, NK ;
RILL, DR ;
COUSTANSMITH, E ;
DOUGLASS, EC ;
BRENNER, MK .
BRITISH JOURNAL OF CANCER, 1993, 67 (05) :933-938