Preoperative plasma soluble urokinase plasminogen activator receptor as a prognostic marker in rectal cancer patients.: An EORTC-receptor and Biomarker Group collaboration

被引:26
作者
Riisbro, R
Christensen, IJ
Nielsen, HJ
Brünner, N
Nilbert, A
Fernebro, E
机构
[1] Copenhagen Univ Hosp, Finsen Lab, Copenhagen, Denmark
[2] Hvidovre Univ Hosp, Dept Surg Gastroenterol, Hvidovre, Denmark
[3] Royal Vet & Agr Univ, Inst Vet Pathobiol, Frederiksberg, Denmark
[4] Univ Hosp, Jubileum Inst, Dept Oncol, Lund, Sweden
关键词
rectal cancer; soluble urokinase plasminogen receptor; suPAR; prognosis;
D O I
10.1177/172460080502000203
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
Background and aims: Since approximately 30% of patients with Dukes' stage B colorectal cancer will experience disease recurrence within five years of primary treatment, current staging of patients with early colorectal cancer apparently fails to adequately predict patient outcome. It has previously been shown that the preoperative plasma concentration of soluble urokinase plasminogen activator receptor (suPAR) is associated with the survival of patients with early colorectal cancer. In this study we sought to confirm the independent prognostic value of suPAR in rectal cancer. Methods: suPAR was retrospectively determined by two different versions of a suPAR ELISA in preoperatively collected plasma samples from a Swedish (n=354) and a Danish (n=255) cohort of rectal cancer patients. Results: In both cohorts the suPAR concentration was significantly higher in Dukes' stage D patients than in Dukes' stage A-C patients (p < 0.0001). Among Dukes' stage A-C patients, no differences in median suPAR values were seen. In univariate analysis, continuous suPAR was found to be associated with survival (p < 0.0001 in both cohorts). Of particular interest was that similar results were obtained for Dukes' stage A and B patients when analyzed separately. In multivariate analysis, continuous suPAR was found in both cohorts to be independent of Dukes' stage. Conclusions: This study confirms that the preoperative concentration of plasma suPAR contains independent prognostic information on patients with rectal cancer. This result was independent of the two different versions of an in-house suPAR ELISA used to perform the analyses. The next step. in the evaluation of suPAR as a prognostic parameter in rectal cancer will be to launch an appropriately dimensioned prospective study where the benefit of applying preoperative plasma suPAR measurement to clinical decision-making regarding adjuvant therapy is assessed.
引用
收藏
页码:93 / 102
页数:10
相关论文
共 18 条
[1]  
Andreasen PA, 1997, INT J CANCER, V72, P1, DOI 10.1002/(SICI)1097-0215(19970703)72:1<1::AID-IJC1>3.0.CO
[2]  
2-Z
[3]  
BEHRENDT N, 1998, FIBRINOLYSIS PROTEOL, V108, P1987
[4]   Recurrence and survival after mesorectal excision for rectal cancer [J].
Bülow, S ;
Christensen, IJ ;
Harling, H ;
Kronborg, O ;
Fenger, C ;
Nielsen, HJ .
BRITISH JOURNAL OF SURGERY, 2003, 90 (08) :974-980
[5]   THE UROKINASE RECEPTOR - PROTEIN-STRUCTURE AND ROLE IN PLASMINOGEN ACTIVATION AND CANCER INVASION [J].
DANO, K ;
BEHRENDT, N ;
BRUNNER, N ;
ELLIS, V ;
PLOUG, M ;
PYKE, C .
FIBRINOLYSIS, 1994, 8 :189-203
[6]   Total mesorectal excision - The new golden standard of surgery for rectal cancer [J].
Enker, WE .
ANNALS OF MEDICINE, 1997, 29 (02) :127-133
[7]   Prognostic importance of the soluble plasminogen activator receptor; suPAR, in plasma from rectal cancer patients [J].
Fernebro, E ;
Madsen, RR ;
Fernö, M ;
Brünner, N ;
Bendahl, PO ;
Christensen, IJ ;
Johnson, A ;
Nilbert, M .
EUROPEAN JOURNAL OF CANCER, 2001, 37 (04) :486-491
[8]  
GANESH S, 1994, CANCER RES, V54, P4065
[9]   Tumor marker utility grading system: A framework to evaluate clinical utility of tumor markers [J].
Hayes, DF ;
Bast, RC ;
Desch, CE ;
Fritsche, H ;
Kemeny, NE ;
Jessup, JM ;
Locker, GY ;
MacDonald, JS ;
Mennel, RG ;
Norton, L ;
Ravdin, P ;
Taube, S ;
Winn, RJ .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1996, 88 (20) :1456-1466
[10]  
HOYERHANSEN G, 1992, J BIOL CHEM, V267, P18224