Comment to “Patients with Concordant Triple-Negative Phenotype between Primary Breast Cancers and Corresponding Metastases Have Poor Prognosis”
نویسندگان
چکیده
http://ejbc.kr | pISSN 1738-6756 eISSN 2092-9900 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/ licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. To the Editor, I read the article by Shin et al. [1] regarding the prognostic impact of discordance between the receptor status of primary breast cancers and corresponding metastases. They concluded that patients with concordant triple-negative phenotype (TNP) had worse long-term outcomes than patients with concordant non-TNP and discordant TNP in a comparison of primary and metastatic breast cancer. As described in the “Methods” section, the cutoff value for estrogen receptor and progesterone receptor positivity was ≥ 10% of tumor cells positive for nuclear staining. However, in the literature, many studies on TNP describe hormone receptor status with different cutoff values [2,3]. Furthermore, the American Society of Clinical Oncology and College of American Pathologists (ASCO/CAP) recommended that a cutoff of 1% positive cells be used to define estrogen receptor-positive status [4]. In conclusion, for better interpretation of studies related to TNP, as in the case of the definition of human epidermal growth factor receptor 2 status, internationally accepted defined cutoff values for hormone receptors are urgently needed.
منابع مشابه
Patients with Concordant Triple-Negative Phenotype between Primary Breast Cancers and Corresponding Metastases Have Poor Prognosis
PURPOSE We investigated the prognostic impact of discordance between the receptor status of primary breast cancers and corresponding metastases. METHODS A total 144 patients with breast cancer and distant metastasis were investigated. The estrogen receptor (ER), progesterone receptor (PR), and human epidermal growth factor receptor 2 (HER2) status of primary tumor and corresponding metastases...
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