Validation study of a nomogram for predicting probability of low risk of MammaPrint results in women with clinically high-risk breast cancer

Author:

Hwang Young Sol1,Kim Hwa Jung2,Kim Jisun2,Chung Il Yong2,Ko Beom Seok2,Kim Hee Jeong2,Lee Jong Won2,Son Byung Ho2,Ahn Sei-Hyun2,Lee Sae Byul2

Affiliation:

1. University of Ulsan College of Medicine

2. University of Ulsan, Asan Medical Center

Abstract

Abstract Background MammaPrint (MMP) helps clinicians identify the ideal time for adjuvant treatment for patients with early HR+/HER2- breast cancer. We aimed to externally validate a nomogram designed to predict probability of low risk of MMP results and to evaluate the difference in survival outcome between two groups stratified by nomogram score. Methods In this retrospective cohort study, we evaluated 172 patients from Asan Medical Center, Seoul, Korea, who underwent breast cancer surgery and MMP during 2020–2021. We internally validated the nomogram by calculating the area under the curve (AUC) and using calibration. With the data of 1,835 T1-3N0-1M0 HR+/HER2- patients from Asan Medical Center during 2010–2013, we compared the disease-free survival (DFS), overall survival (OS), and breast cancer-specific survival (BCSS) rates by Kaplan-Meier analysis between the two groups divided by nomogram total point (TP) for externally validation. Results The AUC calculated by internal validation of 172 patients was 0.73 (95% confidence interval [CI], 0.77–0.87). The discrimination and calibration of the prediction model were satisfactory following external validation. The high-risk and low-risk groups had different 5-year OS (97.9% vs 98.1%, p = 0.056), DFS (98.6% vs 99.4%, p = 0.008), and BCSS rates (98.6% vs 99.4%, p = 0.002). Conclusions For treatment decision-making among clinically high-risk patients with HR+/HER2- and node-positive disease, the nomogram showed satisfactory performance in predicting patients with low genomic risk. Survival outcome significantly differed between two groups divided by nomogram TP. More studies are needed to validate this model in international cohorts and large prospective cohorts from other institutions.

Publisher

Research Square Platform LLC

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