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High Intersystem Variability for the Prediction of Additional Axillary Non-Sentinel Lymph Node Involvement in Individual Patients with Sentinel Node-Positive Breast Cancer
Authors:Ingrid van den Hoven MD  Gerrit P. Kuijt MD  Adri C. Voogd PhD  Rudi M. H. Roumen MD   PhD
Affiliation:Department of General Surgery, Máxima Medical Centre, Veldhoven, The Netherlands. i.vandenhoven@mmc.nl
Abstract:

Purpose

To compare the outcomes of the available systems that predict the risk of non-sentinel lymph node (non-SLN) metastasis and to evaluate the variability within a group of SLN-positive breast cancer patients.

Methods

Predicted probabilities and scores for non-SLN metastasis were calculated with nine predictive systems for 120 SLN-positive patients who underwent a completion axillary lymph node dissection. The number of patients was calculated that were considered low risk or had a probability of ??10% by at least one of the systems. For each nomogram, a box plot was constructed. All patients with a predicted probability of ??10% according to the Memorial Sloan-Kettering Cancer Center (MSKCC) nomogram were selected, and a comparison was made with the probabilities predicted by the other systems.

Results

Nearly two-thirds (64.2%, n?=?77) of patients with SLN-positive breast cancer were allocated to a low-risk or low-probability group by at least one of the predictive systems. No patients were uniformly classified as low risk by all nine prediction models. At the group level, a considerable variation in the distribution of the predicted probabilities was observed. At the individual level, calculation of the predicted probabilities for the selected patients who were considered low risk (??10%) according to the MSKCC nomogram, showed even larger variations, ranging from 4 to 94%.

Conclusions

This study shows that there is an unacceptably high variability in individual predictions when the predictive systems that are currently available are used to predict non-SLN metastasis in patients with SLN-positive breast cancer.
Keywords:
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