A Phase I Study of the Chinese Herbal Medicine PHY906 as a Modulator of Irinotecan-based Chemotherapy in Patients with Advanced Colorectal Cancer

伊立替康 医学 耐受性 结直肠癌 养生 药理学 安慰剂 内科学 药代动力学 丸(消化) 化疗 肿瘤科 癌症 不利影响 病理 替代医学
作者
Shivaani Kummar,Mehmet Sitki Copur,Michal G. Rose,Scott Wadler,Joe Stephenson,Mark Allen O’Rourke,Wayne D. Brenckman,Robert D. Tilton,Shwu-Huey Liu,Zaoli Jiang,Tah-Mun Su,Yung-Chi Cheng,Edward Chu
出处
期刊:Clinical Colorectal Cancer [Elsevier BV]
卷期号:10 (2): 85-96 被引量:112
标识
DOI:10.1016/j.clcc.2011.03.003
摘要

PHY906 is a novel Chinese herbal preparation that has been used in the Orient for over 1800 years to treat a wide range of gastrointestinal side effects including diarrhea, abdominal cramps, vomiting, fever, and headache. Preclinical and clinical studies were conducted to further investigate the biologic and clinical activities of this herbal medicine. To ensure standardization and maintain interbatch reliability of PHY906, high performance liquid chromatography (HPLC) was used to establish a "chemical fingerprint" of PHY906. In vivo preclinical studies using the murine Colon 39 tumor model showed that PHY906 protected against the weight loss associated with irinotecan treatment. In the presence of PHY906, mice were able to tolerate otherwise lethal doses of irinotecan. Significantly improved antitumor activity and overall survival were observed in animals treated with the combination of irinotecan and PHY906 versus irinotecan alone. The combination of PHY906 with irinotecan, 5-fluorouracil (5-FU), and leucovorin (LV) also resulted in at least additive antitumor activity with no increased host toxicity. Based on these in vivo studies, a phase I multicenter, double-blind, randomized, placebo-controlled, dose escalation, cross-over study of PHY906 as a modulator of the weekly, bolus regimen of irinotecan, 5-FU, and LV (IFL) in the first-line treatment of patients with advanced colorectal cancer (CRC) was conducted. The specific objectives of this clinical trial were to determine the safety and tolerability of PHY906 when administered concomitantly with the bolus, weekly IFL regimen. Treatment with PHY906 did not alter the pharmacokinetics of 5-FU, irinotecan, or the irinotecan metabolite SN-38.
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