| Literature DB >> 27079770 |
Heinrich Pohl1, Maritha J Kotze2, Kathleen A Grant2,3, Lize van der Merwe4,5, Fredrieka M Pienaar6, Justus P Apffelstaedt1, Ettienne J Myburgh1,7.
Abstract
The aim of the study was to evaluate the impact of MammaPrint on treatment decision-making in patients with breast cancer. Clinicopathologic information of all breast cancer patients referred for MammaPrint testing in South Africa was collected from 2007 until 2014. A total of 107 patients (109 tumors) with estrogen receptor/progesterone receptor positive and human epidermal growth factor receptor-2 negative tumors were selected with tumors ≥10 mm, or when 1-3 nodes were involved without extra-nodal extension. None of the clinical indicators correlated significantly with the MammaPrint risk classification, which changed the decision for adjuvant chemotherapy in 52% of patients. Of 60 patients who were clinically high risk, 62% had a low-risk MammaPrint result and of the 47 clinically low -risk patients 40% had a high-risk MammaPrint result. This study indicates that MammaPrint could reduce the need for adjuvant chemotherapy by 17% using the selection criteria stipulated. The significant impact on treatment decisions confirmed the clinical utility of MammaPrint independent of standard clinicopathologic risk factors as supported by long-term clinical outcome studies.Entities:
Keywords: Mammaprint; adjuvant chemotherapy; breast cancer; genomic profiling; impact
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Year: 2016 PMID: 27079770 DOI: 10.1111/tbj.12605
Source DB: PubMed Journal: Breast J ISSN: 1075-122X Impact factor: 2.431