A phase I and pharmacokinetic study of silybin-phytosome in prostate cancer patients

Investigational New Drugs - Tập 25 - Trang 139-146 - 2006
Thomas W. Flaig1, Daniel L. Gustafson2, Lih-Jen Su1, Joseph A. Zirrolli2, Frances Crighton3, Gail S. Harrison1, A. Scott Pierson1, Rajesh Agarwal2, L. Michael Glodé1
1Department of Medicine, Division of Medical Oncology, University of Colorado at Denver and Health Sciences Center, Denver, USA
2Department of Pharmaceutical Sciences, School of Pharmacy, University of Colorado at Denver and Health Sciences Center, Denver, USA
3Urologic Oncology, University of Colorado Hospital, Denver, USA

Tóm tắt

Silibinin is a polyphenolic flavonoid isolated from milk thistle with anti-neoplastic activity in several in vitro and in vivo models of cancer, including prostate cancer. Silybin-phytosome is a commercially available formulation containing silibinin. This trial was designed to assess the toxicity of high-dose silybin-phytosome and recommend a phase II dose. Silybin-phytosome was administered orally to prostate cancer patients, giving 2.5–20 g daily, in three divided doses. Each course was 4 weeks in duration. Thirteen patients received a total of 91 courses of silybin-phytosome. Baseline patient characteristics included: median age of 70 years, median baseline prostate specific antigen (PSA) of 4.3 ng/ml, and a median ECOG performance status of 0. The most prominent adverse event was hyperbilirubinemia, with grade 1–2 bilirubin elevations in 9 of the 13 patients. The only grade 3 toxicity observed was elevation of alanine aminotransferase (ALT) in one patient; no grade 4 toxicity was noted. No objective PSA responses were observed. We conclude that 13 g of oral silybin-phytosome daily, in 3 divided doses, appears to be well tolerated in patients with advanced prostate cancer and is the recommended phase II dose. Asymptomatic liver toxicity is the most commonly seen adverse event.

Tài liệu tham khảo

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