Drug and biomarker tissue levels in a randomized presurgical trial on exemestane alternative schedules

Author:

Serrano Davide1ORCID,Johansson Harriet1,Bertelsen Bjørn-Erik2ORCID,Gandini Sara1,Mellgren Gunnar23,Thomas Parijatham4,Crew Katherine D5,Kumar Nagi B6,Macis Debora1,Aristarco Valentina1,Guerrieri-Gonzaga Aliana1,Lazzeroni MatteoORCID,D’Amico Mauro7,Buttiron-Webber Tania7,Briata Irene Maria7,Spinaci Stefano8,Galimberti Viviana1,Vornik Lana A4,Villar-Sanchez Eduardo4,Brown Powel H4,Heckman-Stoddard Brandy M9,Szabo Eva9,Bonanni Bernardo1,DeCensi Andrea710

Affiliation:

1. Division of Cancer Prevention and Genetics, European Institute of Oncology IRCCS , Milan, Italy

2. Hormone Laboratory, Department of Medical Biochemistry and Pharmacology, Haukeland University Hospital , Bergen, Norway

3. Department of Clinical Science, University of Bergen , Bergen, Norway

4. Department of Clinical Cancer Prevention, University of Texas, MD Anderson Cancer Center , Houston, TX, USA

5. Clinical Breast Cancer Prevention Program, Columbia University Irving Medical Center , New York, NY, USA

6. Departments Cancer Epidemiology, Genitourinary and Breast Oncology, Moffitt Cancer Center, University of South Florida , Tampa, FL, USA

7. Medical Oncology, Ospedali Galliera , Genoa, Italy

8. Breast Unit, Ospedale Villa Scassi ASL3 , Genoa, Italy

9. Division of Cancer Prevention, NCI , Bethesda, MD, USA

10. Wolfson Institute of Population Health, Queen Mary University of London , UK

Abstract

Abstract The drug’s activity at the target tissue could help to define the minimal effective dose to promote cancer preventive therapy. Here we present exemestane and sex hormone concentrations within breast tissue from a presurgical study of alternative exemestane schedules. Postmenopausal women candidates for breast surgery for estrogen receptor-positive breast cancer were randomly assigned to exemestane 25 mg once daily (QD), 25 mg 3 times/week (TIW), or 25 mg per week (QW) for 4-6 weeks before surgery. Drug and sex hormones were analyzed from homogenized frozen tissue using a QTRAP 6500+ LC-MS/MS System. Tissue drug concentrations were detectable only in the QD arm with higher concentrations in nonmalignant tissue. Estradiol was nearly suppressed in all groups in the nonmalignant tissue (QD vs TIW P = .364 and QD vs QW P = .693). In contrast, a dose-response trend was observed in cancer tissue. Based on estradiol suppression in nonmalignant tissue, lower exemestane schedules should be explored for breast cancer preventive therapy.

Funder

NCI

Publisher

Oxford University Press (OUP)

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