A Randomised, Double Blind, Placebo-Controlled Pilot Study of Oral Artesunate Therapy for Colorectal Cancer

被引:216
作者
Krishna, Sanjeev [1 ]
Ganapathi, Senthil [2 ]
Ster, Irina Chis [1 ]
Saeed, Mohamed E. M. [3 ]
Cowan, Matt [4 ]
Finlayson, Caroline [1 ]
Kovacsevics, Hajnalka [1 ]
Jansen, Herwig [5 ]
Kremsner, Peter G. [6 ]
Efferth, Thomas [3 ]
Kumar, Devinder [2 ]
机构
[1] Inst Infect & Immun, Dept Pathol, London, England
[2] Univ London, Dept Surg, London SW17 0RE, England
[3] Johannes Gutenberg Univ Mainz, Dept Pharmaceut Biol, D-55128 Mainz, Germany
[4] Surrey & Sussex Healthcare NHS Trust, East Surrey Hosp, Dept Gastroenterol, Redhill RH1 5RH, Sussex, England
[5] Dafra Pharma Nv, B-2300 Turnhout, Belgium
[6] Univ Klinikum Tubingen, Inst Trop Med, D-72074 Tubingen, Germany
关键词
Colorectal cancer; Artesunate; Dihydroartemisinin; Ki67; Neutropaenia; GROWTH-FACTOR RECEPTOR; INTRAVENOUS ARTESUNATE; SEVERE MALARIA; ANTIMALARIAL ARTESUNATE; PROGNOSTIC-SIGNIFICANCE; FALCIPARUM-MALARIA; CELL-LINES; APOPTOSIS; CARCINOMA; INVASION;
D O I
10.1016/j.ebiom.2014.11.010
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Background: Artesunate is an antimalarial agent with broad anti-cancer activity in in vitro and animal experiments and case reports. Artesunate has not been studied in rigorous clinical trials for anticancer effects. Aim: To determine the anticancer effect and tolerability of oral artesunate in colorectal cancer (CRC). Methods: This was a single centre, randomised, double-blind, placebo-controlled trial. Patients planned for curative resection of biopsy confirmed single primary site CRC were randomised (n = 23) by computer-generated code supplied in opaque envelopes to receive preoperatively either 14 daily doses of oral artesunate (200 mg; n = 12) or placebo (n = 11). The primary outcome measure was the proportion of tumour cells undergoing apoptosis (significant if >7% showed Tunel staining). Secondary immunohistochemical outcomes assessed these tumour markers: VEGF, EGFR, c-MYC, CD31, Ki67 and p53, and clinical responses. Findings: 20 patients (artesunate = 9, placebo = 11) completed the trial per protocol. Randomization groups were comparable clinically and for tumour characteristics. Apoptosis in >7% of cells was seen in 67% and 55% of patients in artesunate and placebo groups, respectively. Using Bayesian analysis, the probabilities of an artesunate treatment effect reducing Ki67 and increasing CD31 expression were 0.89 and 0.79, respectively. During a median follow up of 42 months 1 patient in the artesunate and 6 patients in the placebo group developed recurrent CRC. Interpretation: Artesunate has anti-proliferative properties in CRC and is generally well tolerated. (C) 2014 Published by Elsevier B.V.
引用
收藏
页码:82 / 90
页数:9
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