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A Randomised, Double Blind, Placebo-Controlled Pilot Study of Oral Artesunate Therapy for Colorectal Cancer.
Krishna, Sanjeev; Ganapathi, Senthil; Ster, Irina Chis; Saeed, Mohamed E M; Cowan, Matt; Finlayson, Caroline; Kovacsevics, Hajnalka; Jansen, Herwig; Kremsner, Peter G; Efferth, Thomas; Kumar, Devinder.
Afiliação
  • Krishna S; Institute of Infection and Immunity, Department of Pathology, United Kingdom.
  • Ganapathi S; Department of Surgery, St. George's, University of London, Cranmer Terrace, SW17 0RE, United Kingdom.
  • Ster IC; Institute of Infection and Immunity, Department of Pathology, United Kingdom.
  • Saeed ME; Department of Pharmaceutical Biology, Johannes Gutenberg-University, Staudinger Weg 5, 55128 Mainz, Germany.
  • Cowan M; Department of Gastroenterology, Surrey and Sussex Healthcare NHS Trust, East Surrey Hospital, Canada Avenue, Redhill, Sussex RH1 5RH, United Kingdom.
  • Finlayson C; Institute of Infection and Immunity, Department of Pathology, United Kingdom.
  • Kovacsevics H; Institute of Infection and Immunity, Department of Pathology, United Kingdom.
  • Jansen H; Dafra Pharma nv, 2300 Turnhout, Belgium.
  • Kremsner PG; Institut für Tropenmedizin, Universitätsklinikum Tübingen, Wilhelmstraße 27, D-72074 Tübingen, Germany.
  • Efferth T; Department of Pharmaceutical Biology, Johannes Gutenberg-University, Staudinger Weg 5, 55128 Mainz, Germany.
  • Kumar D; Department of Surgery, St. George's, University of London, Cranmer Terrace, SW17 0RE, United Kingdom.
EBioMedicine ; 2(1): 82-90, 2015 Jan.
Article em En | MEDLINE | ID: mdl-26137537
ABSTRACT

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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Artemisininas Tipo de estudo: Clinical_trials / Guideline Limite: Aged / Female / Humans / Male Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Artemisininas Tipo de estudo: Clinical_trials / Guideline Limite: Aged / Female / Humans / Male Idioma: En Ano de publicação: 2015 Tipo de documento: Article