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Abstract
Endocrine therapy is a key modality in the management of breast cancer, with current options for postmenopausal women including tamoxifen, aromatase inhibitors and fulvestrant. Unfortunately, in spite of these advances, many women still relapse or progress on endocrine therapy. Given that resistance (de novo or acquired resistance) is a major limiting factor in the use of endocrine therapy, additional endocrine therapies with novel methods of action are required. Steroid sulfatase, which is responsible for the conversion of estrone sulfate to estrone, as well as dehydroepiandrosterone sulfate to dehydroepiandrosterone, has been implicated in endocrine resistance. In this article, we summarize the preclinical and clinical data to support the potential role of steroid sulfatase in breast cancer, as well as the current data on the first available steroid sulfatase inhibitor named irosustat (STX64; 667 Coumate; BN83495), and discuss its potential clinical development.
Financial & competing interests disclosure
Irosustat is owned by Ipsen; Prof R. Charles Coombes has received research funding and consultancy fees from Ipsen. Carlo Palmieri and R. Charles Coombes wish to acknowledge grant support from Cancer Reasearch UK and the Imperial College Healthcare Charity. The Division of Cancer at Imperial College London/Imperial College Healthcare NHS Trust is an Experimental Cancer Medicine Centre (ECMC), which is supported by funds from Cancer Research UK and the Department of Health. The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed.
No writing assistance was utilized in the production of this manuscript.