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Published research on Artemisinin

4 peer-reviewed publications on Artemisinin in oncology research, clinical work first, then laboratory studies. Each entry reports what the authors stated; follow the link for the full paper.

This page is a reading list of peer-reviewed publications, compiled for information. It is not a statement of indications, a recommendation or medical advice. Results from cell and animal studies do not translate into clinical use. Medsuvac products are supplied for their registered purposes; clinical decisions belong to a qualified physician.
  1. Clinical trial

    Prospective open uncontrolled phase I study to define a well-tolerated dose of oral artesunate as add-on therapy in patients with metastatic breast cancer (ARTIC M33/2)

    von Hagens C et al., Breast Cancer Research and Treatment, 2017

    In 23 metastatic breast cancer patients, oral artesunate as add-on therapy for four weeks was reported to be safe and well tolerated, with dose-limiting adverse events not exceeding 33 percent at any dose level.

  2. Clinical trial

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

    Krishna S et al., EBioMedicine, 2015

    In 20 colorectal cancer patients who completed this pilot trial, preoperative oral artesunate was reported to show anti-proliferative effects (Bayesian probability 0.89 of reduced Ki67) and was generally well tolerated, with 1 recurrence in the artesunate group versus 6 in the placebo group over a median 42-month follow-up.

  3. Review

    From ancient herb to modern drug: Artemisia annua and artemisinin for cancer therapy

    Efferth T et al., Seminars in Cancer Biology, 2017

    This overview of two decades of literature reported that artemisinin and its derivatives (dihydroartemisinin, artesunate, artemether, arteether) acted against cancer cells through oxidative stress, DNA damage, multiple cell death modes and inhibition of angiogenesis and signalling pathways, with case reports and pilot phase I/II trials indicating clinical activity and hepatotoxicity cases noted in combination with complementary medicines.

  4. In vitro

    Artemisinin derivatives induce iron-dependent cell death (ferroptosis) in tumor cells

    Ooko E et al., Phytomedicine, 2015

    Across the NCI panel of 60 tumour cell lines, expression of 20 iron-related genes correlated with cytotoxicity of ten artemisinin derivatives, and the ferroptosis inhibitor ferrostatin-1 and the iron chelator deferoxamine reduced the cytotoxicity of dihydroartemisinin, indicating ferroptosis as the cell death mode.