International Multicenter Tool to Predict the Risk of Nonsentinel Node Metastases in Breast Cancer

被引:68
作者
Meretoja, Tuomo J. [1 ]
Leidenius, Marjut H. K. [1 ]
Heikkila, Paivi S. [2 ]
Boross, Gabor [3 ]
Sejben, Istvan [4 ]
Regitnig, Peter [5 ]
Luschin-Ebengreuth, Gero [6 ]
Zgajnar, Janez [7 ]
Perhavec, Andraz [7 ]
Gazic, Barbara [8 ]
Lazar, Gyorgy [9 ]
Takacs, Tibor [9 ]
Voros, Andras [10 ]
Saidan, Zuhair A. [11 ]
Nadeem, Rana M. [11 ]
Castellano, Isabella [12 ]
Sapino, Anna [12 ]
Bianchi, Simonetta [13 ]
Vezzosi, Vania [13 ]
Barranger, Emmanuel [14 ]
Lousquy, Ruben [14 ]
Arisio, Riccardo [15 ]
Foschini, Maria Pia [16 ]
Imoto, Shigeru [17 ]
Kamma, Hiroshi [18 ]
Tvedskov, Tove F. [19 ]
Kroman, Niels [19 ]
Jensen, Maj-Brit [20 ]
Audisio, Riccardo A. [21 ]
Cserni, Gabor [4 ,10 ]
机构
[1] Univ Helsinki, Cent Hosp, Breast Surg Unit, FI-00029 Helsinki, Finland
[2] Univ Helsinki, Cent Hosp, Dept Pathol, FI-00029 Helsinki, Finland
[3] Bacs Kiskun Cty Teaching Hosp, Dept Surg, Kecskemet, Hungary
[4] Bacs Kiskun Cty Teaching Hosp, Dept Pathol, Kecskemet, Hungary
[5] Med Univ Graz, Dept Pathol, Graz, Austria
[6] Med Univ Graz, Dept Obstet & Gynecol, Graz, Austria
[7] Inst Oncol, Dept Surg Oncol, Ljubljana, Slovenia
[8] Inst Oncol, Dept Pathol, Ljubljana, Slovenia
[9] Univ Szeged, Dept Surg, Szeged, Hungary
[10] Univ Szeged, Dept Pathol, Szeged, Hungary
[11] Lancashire Teaching Hosp, Dept Breast Surg, Chorley, Lancs, England
[12] Univ Turin, Dept Biomed Sci & Human Oncol, Breast Unit, Azienda Osped Univ San Giovanni Battista Torino, I-10124 Turin, Italy
[13] Univ Florence, Dept Med & Surg Crit Care, Sect Pathol Anat, Florence, Italy
[14] Lariboisiere Hosp, Dept Gynecol & Obstet, Paris, France
[15] St Anna Hosp, OIRM, Dept Pathol, Turin, Italy
[16] Univ Bologna, Dept Biomed Sci & Neuromotory Disorders, Bellaria Hosp, Sect Anat Pathol, Bologna, Italy
[17] Kyorin Univ, Sch Med, Dept Breast Surg, Tokyo, Japan
[18] Kyorin Univ, Sch Med, Dept Pathol, Tokyo, Japan
[19] Copenhagen Univ Hosp, Dept Breast Surg, Copenhagen, Denmark
[20] Copenhagen Univ Hosp, Danish Breast Canc Cooperat Grp, Copenhagen, Denmark
[21] St Helens Teaching Hosp, Dept Surg, St Helens, Merseyside, England
来源
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE | 2012年 / 104卷 / 24期
基金
芬兰科学院;
关键词
SENTINEL LYMPH-NODE; SCORING SYSTEM; WOMEN; INVOLVEMENT; BIOPSY; MICROMETASTASES; NOMOGRAM; DISEASE; MODELS;
D O I
10.1093/jnci/djs455
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Axillary treatment of breast cancer patients is undergoing a paradigm shift, as completion axillary lymph node dissections (ALNDs) are being questioned in the treatment of patients with tumor-positive sentinel nodes. This study aims to develop a novel multi-institutional predictive tool to calculate patient-specific risk of residual axillary disease after tumor-positive sentinel node biopsy. Breast cancer patients with a tumor-positive sentinel node and a completion ALND from five European centers formed the original patient series (N 1000). Statistically significant variables predicting nonsentinel node involvement were identified in logistic regression analysis. A multivariable predictive model was developed and validated by area under the receiver operating characteristics curve (AUC), first internally in 500 additional patients and then externally in 1068 patients from other centers. All statistical tests were two-sided. Nine tumor- and sentinel nodespecific variables were identified as statistically significant factors predicting nonsentinel node involvement in logistic regression analysis. A resulting predictive model applied to the internal validation series resulted in an AUC of 0.714 (95% confidence interval [CI] 0.665 to 0.763). For the external validation series, the AUC was 0.719 (95% CI 0.689 to 0.750). The model was well calibrated in the external validation series. We present a novel, international, multicenter, predictive tool to assess the risk of additional axillary metastases after tumor-positive sentinel node biopsy in breast cancer. The predictive model performed well in internal and external validation but needs to be further studied in each center before application to clinical use. J Natl Cancer Inst 2012;104:1888-1896
引用
收藏
页码:1888 / 1896
页数:9
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