AE-941, a multifunctional antiangiogenic compound: trials in renal cell carcinoma

Ronald M Bukowski1

  • 1Experimental Therapeutics Program, The Cleveland Clinic Taussig Cancer Center, Cleveland, OH 44195, USA. bukowsr@cc.ccf.org

Insights

AE-941, derived from shark cartilage, shows promise in treating renal cell carcinoma by inhibiting angiogenesis. Early trials suggest improved survival, leading to a large Phase III study in metastatic clear cell kidney cancer.

Area of Science:

  • Oncology
  • Molecular Biology
  • Pharmacology

Background:

  • Renal cell carcinoma (RCC) therapy is challenging, with limited success for current treatments like IL-2 and IFN.
  • Molecular abnormalities in clear cell RCC, including chromosome 3p alterations and von Hippel-Lindau (VHL) gene hypermethylation, are linked to tumor angiogenesis.
  • The VHL protein's role in angiogenesis suggests that targeting this pathway could be a novel therapeutic strategy for RCC.

Purpose of the Study:

  • To evaluate the efficacy and safety of AE-941 (Neovostat), an angiogenesis inhibitor derived from shark cartilage, in patients with metastatic clear cell renal cell carcinoma.
  • To explore the potential of AE-941 as a novel therapeutic agent for RCC, addressing the unmet need for more effective treatments.

Main Methods:

  • AE-941's in vitro and in vivo activities were identified, including modulation of matrix proteases, inhibition of vascular endothelial growth factor (VEGF) binding, induction of endothelial cell apoptosis, and stimulation of angiostatin production.
  • Preclinical studies in murine models demonstrated AE-941's antitumour effects on primary tumors and metastases.
  • A large, multi-institutional, randomized Phase III trial was conducted in over 300 patients with metastatic clear cell RCC, with AE-941 administered orally.

Main Results:

  • Preliminary trials in RCC patients indicated responses to AE-941, with higher doses potentially correlating with improved survival.
  • Preclinical studies showed AE-941's effectiveness against primary tumors and metastases in various murine models.
  • AE-941 demonstrated an excellent toxicity profile in oral administration.

Conclusions:

  • AE-941 exhibits multiple mechanisms of action that inhibit angiogenesis and possess antitumour activity.
  • Preliminary clinical data suggest AE-941 may offer a survival benefit in patients with metastatic clear cell RCC.
  • The ongoing Phase III trial is expected to provide definitive data on the clinical effectiveness of AE-941 for this challenging malignancy.

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