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Estrogen receptor-negative progesterone receptor-positive breast cancer – “Nobody's land“ or just an artifact?

•ER(−)/PgR(+) breast cancers have distinct clinical course and response to treatment when compared to other breast cancer types.•A portion of ER(−)/PgR(+) breast cancers is an artifact.•Since these cancers respond to both chemotherapy and endocrine therapy, both should be considered in their treatme...

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Bibliographic Details
Published in:Cancer treatment reviews 2018-06, Vol.67, p.78-87
Main Authors: Kunc, Michał, Biernat, Wojciech, Senkus-Konefka, Elżbieta
Format: Article
Language:English
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Summary:•ER(−)/PgR(+) breast cancers have distinct clinical course and response to treatment when compared to other breast cancer types.•A portion of ER(−)/PgR(+) breast cancers is an artifact.•Since these cancers respond to both chemotherapy and endocrine therapy, both should be considered in their treatment schedules.•It is necessary to increase the knowledge and improve guidelines regarding this phenotype. The estrogen receptor α (ER) and the progesterone receptor (PgR) are one of the most important prognostic and predictive immunohistochemical markers in breast cancer. Breast cancers may express various profiles of hormone receptors: ER(+)/PgR(+), ER(−)/PgR(−), ER(+)/PgR(−) and ER(−)/PgR(+). The existence of the latter profile is a matter of controversy since PgR expressions is induced by ER-dependent pathways in breast cancer cells. One of the most extensively propagated hypotheses trying to explain the origin of ER(−)/PgR(+) breast cancers claims that they are technical artifacts dependent on the immunohistochemical procedure. On the other hand, in recent years there is a growing body of evidence, suggesting that such cancers create a unique group with distinct molecular and clinical features. In the following review, we present background theories on the ER(−)/PgR(+) breast cancer origin and their epidemiological and clinicopathological characteristics, including the predictive and prognostic significance of these rare tumors.
ISSN:0305-7372
1532-1967
DOI:10.1016/j.ctrv.2018.05.005