The prognostic relevance of urokinase-type plasminogen activator (uPA) in the blood of patients with metastatic breast cancer

被引:29
|
作者
Banys-Paluchowski, Malgorzata [1 ]
Witzel, Isabell [2 ]
Aktas, Bahriye [3 ]
Fasching, Peter A. [4 ]
Hartkopf, Andreas [5 ]
Janni, Wolfgang [6 ]
Kasimir-Bauer, Sabine [7 ]
Pantel, Klaus [8 ]
Schoen, Gerhard [9 ]
Rack, Brigitte [6 ]
Riethdorf, Sabine [8 ]
Solomayer, Erich-Franz [10 ]
Fehm, Tanja [11 ]
Mueller, Volkmar [2 ]
机构
[1] Asklepios Klin Barmbek, Dept Gynecol & Obstet, Hamburg, Germany
[2] Univ Med Ctr Hamburg Eppendorf, Dept Gynecol, Hamburg, Germany
[3] Univ Hosp Leipzig, Dept Obstet & Gynecol, Leipzig, Germany
[4] Friedrich Alexander Univ Erlangen Nuremberg, Univ Hosp Erlangen, Dept Gynecol & Obstet, Comprehens Canc Ctr Erlangen EMN, Erlangen, Germany
[5] Univ Tubingen, Univ Hosp Tubingen, Dept Obstet & Gynecol, Tubingen, Germany
[6] Univ Hosp Ulm, Dept Gynecol & Obstet, Ulm, Germany
[7] Univ Duisburg Essen, Univ Hosp Essen, Dept Obstet & Gynecol, Essen, Germany
[8] Univ Med Ctr Hamburg Eppendorf, Dept Tumour Biol, Hamburg, Germany
[9] Univ Med Ctr Hamburg Eppendorf, Dept Med Biometry & Epidemiol, Hamburg, Germany
[10] Saarland Univ Hosp, Dept Gynecol & Obstet, Homburg, Germany
[11] Heinrich Heine Univ Dusseldorf, Dept Obstet & Gynecol, Dusseldorf, Germany
关键词
CIRCULATING P105 FRACTION; PHASE-III TRIAL; HER-2/NEU PROTOONCOGENE; DISEASE PROGRESSION; AMERICAN SOCIETY; 1ST-LINE THERAPY; INHIBITOR TYPE-1; POOLED ANALYSIS; RECEPTOR SUPAR; TUMOR-TISSUE;
D O I
10.1038/s41598-018-37259-2
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In breast cancer (BC), elevated levels of urokinase-type plasminogen activator (uPA) in tumor tissue have been confirmed as a strong prognostic factor in level-of-evidence-1 studies. The aim of the present study was to evaluate the clinical relevance of uPA levels in serum of metastatic BC patients and to compare uPA with other blood-based biomarkers. 252 patients were enrolled in this prospective, multicentre study. Blood samples were collected before begin of first-line or later-line systemic treatment. Serum uPA was quantified by a commercially available ELISA. Circulating tumor cells (CTCs) were detected using CellSearch; other biomarkers (EGFR, VEGF, HER2, RAS p21, TIMP1, CAIX) by ELISA. Using the ROC analysis, the optimal cut-off value (determined by the Youden index) of serum uPA was 2.52 ng/ml. Using this value, 26% of patients had elevated uPA levels. Patients with visceral metastasis and more than one metastatic site were significantly more likely to present with elevated uPA levels. CTC status, serum HER2, RAS p21, CAIX, TIMP1 and VEGF correlated significantly with uPA levels. Elevated uPA levels predicted shorter overall and progression-free survival in univariate analysis (median OS: 7.5 months [95%-CI 4.5-10.5 months] vs. not reached, p < 0.001; PFS:4.8 [95%CI: 3.1-6.5] vs. 9.1 [7.4-10.8] months, p < 0.001). In multivariate analysis, elevated uPA, presence of >= 5 CTCs, elevated RAS p21, higher grading and higher line of therapy were independent predictors of shorter OS, while elevated CTC counts, higher line of therapy and negative estrogen receptor status were independent predictors of shorter PFS. In conclusion, elevated uPA levels independently predict reduced overall survival and improved prognostication in patients with known CTC status. Whether high serum uPA might identify patients most likely to benefit from therapies targeting uPA, remains to be evaluated in future trials.
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页数:10
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