Evidence map›Paper›PMID 26137537›Full record

Trial reportEBioMedicine2015

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

Sanjeev Krishna, Senthil Ganapathi, Irina Chis Ster, Mohamed E M Saeed, Matt Cowan, Caroline Finlayson, Hajnalka Kovacsevics, Herwig Jansen, Peter G Kremsner, Thomas Efferth and 1 more

3 registry-linked trialsOpen access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in EBioMedicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 97 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
97citing papers in PubMed, 1 pooled it
5.8field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT03093129 phase2unknown statusnot on this mapstarted 2018, after this paper: background citation

Phase II Randomised, Double Blind, Placebo Controlled Trial of Neoadjuvant Artesunate in Stage II/III Colorectal Cancer in Vietnamese Patients

TypeinterventionalSponsorThe 108 Military Central HospitalRan2018 to 2022Enrolled200ConditionsColorectal CancerArmsartesunate, placebo
NCT07022743 phase2active not recruitingnot on this mapstarted 2025, after this paper: background citation

Improving Treatment Outcomes in Chronic Myeloid Leukaemia Patients Using Imatinib and Artesunate Combination Therapy

TypeinterventionalSponsorObafemi Awolowo UniversityRan2025 to 2026Enrolled75ConditionsChronic Myeloid Leukemia (CML)ArmsImatinib, Artesunate
NCT07095309 phase2not yet recruitingnot on this mapstarted 2025, after this paper: background citation

Phase II Randomised, Double Blind, Placebo Controlled Trial of Neoadjuvant Artesunate in Stage II/III Colorectal Cancer

TypeinterventionalSponsorMetanoic Health Ltd.Ran2025 to 2033Enrolled120ConditionsStage II/III Colon Cancer, Bowel CancerArmsArtesunate, Artesunate matching Placebo
3 · Its place in the literature

Who cites it

97 citing papers in PubMed, 1 synthesis or guideline pooled it, 210 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. The Pro-Metastatic Roles of ROS.Antioxidants (Basel, Switzerland) · 2026
    Review
  5. The Therapeutic Potential of Dihydroartemisinin in Cancer Treatment.International journal of molecular sciences · 2026
    Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Review
  13. Article
  14. Review
  15. Review
  16. Exploring the Therapeutic Potential ofJournal of clinical medicine · 2025
    Review
  17. Review
  18. Review
  19. Article
  20. Review

37 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 5 institutions in 2 countries.

Sanjeev KrishnaInstitute of Infection and Immunity, Department of Pathology, United Kingdom.
Senthil GanapathiDepartment of Surgery, St. George's, University of London, Cranmer Terrace, SW17 0RE, United Kingdom.
Irina Chis SterInstitute of Infection and Immunity, Department of Pathology, United Kingdom.
Mohamed E M SaeedDepartment of Pharmaceutical Biology, Johannes Gutenberg-University, Staudinger Weg 5, 55128 Mainz, Germany.
Matt CowanDepartment of Gastroenterology, Surrey and Sussex Healthcare NHS Trust, East Surrey Hospital, Canada Avenue, Redhill, Sussex RH1 5RH, United Kingdom.
Caroline FinlaysonInstitute of Infection and Immunity, Department of Pathology, United Kingdom.
Hajnalka KovacsevicsInstitute of Infection and Immunity, Department of Pathology, United Kingdom.
Herwig JansenDafra Pharma nv, 2300 Turnhout, Belgium.
Peter G KremsnerInstitut für Tropenmedizin, Universitätsklinikum Tübingen, Wilhelmstraße 27, D-72074 Tübingen, Germany.
Thomas EfferthDepartment of Pharmaceutical Biology, Johannes Gutenberg-University, Staudinger Weg 5, 55128 Mainz, Germany.
Devinder KumarDepartment of Surgery, St. George's, University of London, Cranmer Terrace, SW17 0RE, United Kingdom.
Centre for Immunity, Infection and Evolution · GBJohannes Gutenberg University Mainz · DESt George's, University of London · GBEast Surrey Hospital · GBUniversitätsklinikum Tübingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundArtesunate 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.

aimTo determine the anticancer effect and tolerability of oral artesunate in colorectal cancer (CRC).

methodsThis 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.

findings20 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.

interpretationArtesunate has anti-proliferative properties in CRC and is generally well tolerated.

Indexed as

Administration, OralAgedArtemisininsArtesunateBiomarkers, TumorCarcinoembryonic AntigenColorectal NeoplasmsDemographyDouble-Blind MethodFemaleHumansImmunohistochemistryKi-67 AntigenMalePilot ProjectsPlacebosArtemisininsArtesunateBiomarkers, TumorCarcinoembryonic AntigenKi-67 AntigenPlacebosArtesunateColorectal cancerDihydroartemisininKi67Neutropaenia

Identifiers

PMID26137537
PMCPMC4484515
OpenAlexW2163182602

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.