Adjuvant Chemotherapy in Node-negative Breast Cancer: UPA/PAI-1 Determinations for 163 Cases

被引:0
作者
Venat-Bouvet, Laurence [1 ]
Fermeaux, Veronique [2 ]
Leobon, Sophie [1 ]
Saidi, Nadira [3 ]
Monteil, Jacques [4 ]
Mollard, Joelle [5 ]
Aubard, Yves [5 ]
Jammet, Isabelle [6 ]
Tubiana-Mathieu, Nicole [1 ]
机构
[1] Univ Hosp, Dept Med Oncol, F-87042 Limoges, France
[2] Univ Hosp, Dept Pathol, F-87042 Limoges, France
[3] Univ Hosp, Dept Radiotherapy, F-87042 Limoges, France
[4] Univ Hosp, Dept Nucl Med, F-87042 Limoges, France
[5] Mother & Child Hosp, Dept Gynaecol, Limoges, France
[6] Mother & Child Hosp, Dept Radiol & Med Imaging, Limoges, France
关键词
UPA-PAI-1; molecular biomarkers; adjuvant chemotherapy; node-negative breast cancer; PLASMINOGEN-ACTIVATOR UPA; UROKINASE-TYPE; PROGNOSTIC IMPACT; TYPE-1; INHIBITOR; AMERICAN SOCIETY; PAI-1; MARKERS; TRIAL; PROTEASES; CONSENSUS;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The urokinase-type plasminogen activator (UPA) and its main inhibitor plasminogen activator inhibitor-1 (PAI-1) are involved in tumor interactions with the microenvironment. The UPA/PAI-1 content in tumor tissue can be used to identify populations at low-or high-risk of recurrence of breast cancer, even without other standard prognostic markers. Materials and Methods: The purpose of the present study was to compare adjuvant chemotherapy decisions made by a multi-disciplinary board for 163 node-negative breast cancer cases, based on clinicopathological (CP) and UPA/PAI-1 risk assessment. Results: The UPA/PAI-1 levels identified 37% of the population as being at low risk. Adjuvant chemotherapy indication was spared in high-CP risk in 17%, but maintained in low-CP risk in 33%. Conclusion: The use of UPA/PAI-1 data did not consistently result in a decrease of adjuvant chemotherapy. This study highlighted the difficulties encountered in a local multi-disciplinary board in determining appropriate roles and weights of new prognostic markers (UPA/PAI-1 was not routinely employed in France) when no data are available for assessing their prognostic and predictive power compared to other prognostic factors.
引用
收藏
页码:1213 / 1217
页数:5
相关论文
共 25 条
[1]   Prognostic and predictive value of the urokinase-type plasminogen activator (uPA) and its inhibitors PAI-1 and PAI-2 in operable breast cancer [J].
Cufer, T ;
Borstnar, S ;
Vrhovec, I .
INTERNATIONAL JOURNAL OF BIOLOGICAL MARKERS, 2003, 18 (02) :106-115
[2]  
Duffy MJ, 1996, CLIN CANCER RES, V2, P613
[3]   Urokinase plasminogen activator, a strong independent prognostic factor in breast cancer, analysed in steroid receptor cytosols with a luminometric immunoassay [J].
Ferno, M ;
Bendahl, PO ;
Borg, A ;
Brundell, J ;
Hirschberg, L ;
Olsson, H ;
Killander, D .
EUROPEAN JOURNAL OF CANCER, 1996, 32A (05) :793-801
[4]  
Foekens JA, 2000, CANCER RES, V60, P636
[5]  
FOEKENS JA, 1992, CANCER RES, V52, P6101
[6]   St. Gallen 2011: Summary of the Consensus Discussion [J].
Gnant, Michael ;
Harbeck, Nadia ;
Thomssen, Christoph .
BREAST CARE, 2011, 6 (02) :136-141
[7]   Thresholds for therapies: highlights of the St Gallen International Expert Consensus on the Primary Therapy of Early Breast Cancer 2009 [J].
Goldhirsch, A. ;
Ingle, J. N. ;
Gelber, R. D. ;
Coates, A. S. ;
Thuerlimann, B. ;
Senn, H. -J. .
ANNALS OF ONCOLOGY, 2009, 20 (08) :1319-1329
[8]   Risk group discrimination in node-negative breast cancer using invasion and proliferation markers:: 6-year median follow up [J].
Harbeck, N ;
Dettmar, P ;
Thomssen, C ;
Berger, U ;
Ulm, K ;
Kates, R ;
Höfler, H ;
Jänicke, F ;
Graeff, H ;
Schmitt, M .
BRITISH JOURNAL OF CANCER, 1999, 80 (3-4) :419-426
[9]  
Harbeck N, 1998, ANTICANCER RES, V18, P2187
[10]  
Harbeck N, 2004, J CLIN ONCOL, V22, p8S