Pooled analysis of prognostic impact of urokinase-type plasminogen activator and its inhibitor PAI-1 8377 breast cancer patients

被引:467
作者
Look, MP
van Putten, WLJ
Duffy, MJ
Harbeck, N
Christensen, IJ
Thomssen, C
Kates, R
Spyratos, F
Fernö, M
Eppenberger-Castori, S
Sweep, CGJF
Ulm, K
Peyrat, JP
Martin, PM
Magdelenat, H
Brünner, N
Duggan, C
Lisboa, BW
Bendahl, PO
Quillien, V
Daver, A
Ricolleau, G
Meijer-van Gelder, E
Manders, P
Fiets, WE
Blankenstein, MA
Broët, P
Romain, S
Daxenbichler, G
Windbichler, G
Cufer, T
Borstnar, S
Kueng, W
Beex, LVAM
Klijn, JGM
O'Higgins, N
Eppenberger, U
Jänicke, F
Schmitt, M
Foekens, JA
机构
[1] Rotterdam Canc Inst, Daniel Den Hoed Klin, Dept Med Oncol, Rotterdam, Netherlands
[2] Rotterdam Canc Inst, Daniel Den Hoed Klin, Dept Stat, Rotterdam, Netherlands
[3] St Vincents Univ Hosp, Dublin, Ireland
[4] Tech Univ Munich, Klinikum Rechts Isar, Frauenklin, D-8000 Munich, Germany
[5] Finsen Lab, DK-2100 Copenhagen, Denmark
[6] Univ Hamburg, Klinikum Eppendorf, Hamburg, Germany
[7] Lab Biol Tissulaire, St Cloud, France
[8] Univ Lund Hosp, Dept Oncol, S-22185 Lund, Sweden
[9] Stiftung Tumorbank, Basel, Switzerland
[10] Univ Basel Hosp, Dept Res, CH-4031 Basel, Switzerland
[11] Univ Nijmegen Hosp, Dept Chem Endocrinol, NL-6500 HB Nijmegen, Netherlands
[12] Ctr Oscar Lambret, Lab Oncol Mol Humaine, F-59020 Lille, France
[13] Lab Transfert Oncol Biol, Marseille, France
[14] Inst Curie, F-75231 Paris, France
[15] Ctr Eugene Marquis, Biol Lab, Rennes, France
[16] Ctr Paul Papin, Angers, France
[17] Ctr Rene Gauducheau, St Herblain, France
[18] Univ Utrecht, Med Ctr, Utrecht, Netherlands
[19] Univ Innsbruck, Klin Frauenheilkunde, Innsbruck, Austria
[20] Inst Oncol, Ljubljana, Slovenia
[21] Univ Coll Dublin, Dublin 2, Ireland
来源
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE | 2002年 / 94卷 / 02期
关键词
D O I
10.1093/jnci/94.2.116
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Urokinase-type plasminogen activator (uPA) and its inhibitor (PAI-1) play essential roles in tumor invasion and metastasis. High levels of both uPA and PAT-1 are associated with poor prognosis in breast cancer patients. To confirm the prognostic value of uPA and PAI-1 in primary breast cancer, we reanalyzed individual patient data provided by members of the European Organization for Research and Treatment of Cancer-Receptor and Biomarker Group (EORTC-RBG). Methods: The study included 18 datasets involving 8377 breast cancer patients. During follow-up (median 79 months), 35% of the patients relapsed and 27% died. Levels of uPA and PAI-1 in tumor tissue extracts were determined by different immunoassays; values were ranked within each dataset and divided by the number of patients in that dataset to produce fractional ranks that could be compared directly across datasets. Associations of ranks of uPA and PAI-1 levels with relapse-free survival (RFS) and overall survival (OS) were analyzed by Cox multivariable regression analysis stratified by dataset, including the following traditional prognostic variables: age, menopausal status, lymph node status, tumor size, histologic grade, and steroid hormone-receptor status. All P values were two-sided. Results: Apart from lymph node status, high levels of uPA and PAI-1 were the strongest predictors of both poor RFS and poor OS in the analyses of all patients. Moreover, in both lymph node-positive and lymph nodenegative patients, higher uPA and PAI-1 values were independently associated with poor RFS and poor OS. For (untreated) lymph node-negative patients in particular, uPA and PAI-1 included together showed strong prognostic ability (all P<.001). Conclusions: This pooled analysis of the EORTC-RBG datasets confirmed the strong and independent prognostic value of uPA and PAI-1 in primary breast cancer. For patients with lymph node-negative breast cancer, uPA and PAI-1 measurements in primary tumors may be especially useful for designing individualized treatment strategies.
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页码:116 / 128
页数:13
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