| Literature DB >> 32996592 |
Oukseub Lee1, Melissa Pilewskie2, Scott Karlan3, Mary B Tull4, Kelly Benante1, Yanfei Xu1, Luis Blanco5, Irene Helenowski4, Masha Kocherginsky4, Shivangi Yadav1, Omid Hosseini1, Nora Hansen1, Kevin Bethke1, Miguel Muzzio6, Melissa A Troester7, Eileen Dimond8, Marjorie Perloff8, Brandy Heckman-Stoddard8, Seema A Khan1.
Abstract
Oral breast cancer prevention medications entail systemic exposure, limiting acceptance by high-risk women. Delivery through the breast skin, although an attractive alternative, requires demonstration of drug distribution throughout the breast. We conducted a randomized double-blind, placebo-controlled phase II clinical trial comparing telapristone acetate, a progesterone receptor antagonist, administered orally (12 mg/day) or transdermally (12 mg/breast) for 4 ± 1 weeks to women planning mastectomy. Plasma and tissue concentrations, measured at five locations in the mastectomy specimen using liquid chromatography tandem mass spectrometry were compared. In 60 evaluable subjects, median drug concentration (ng/g tissue) was 103 (interquartile range (IQR): 46.3-336) in the oral vs. 2.82 (IQR: 1.4-5.5) in the transdermal group. Despite poor dermal permeation, within-breast drug distribution pattern was identical in both groups (R2 = 0.88, P = 0.006), demonstrating that transdermally and orally delivered drug is distributed similarly through the breast, and is strongly influenced by tissue adiposity (P < 0.0001). Other skin-penetrant drugs should be tested for breast cancer prevention.Entities:
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Year: 2020 PMID: 32996592 PMCID: PMC8388824 DOI: 10.1002/cpt.2041
Source DB: PubMed Journal: Clin Pharmacol Ther ISSN: 0009-9236 Impact factor: 6.875