2025 / 10 / 06

Oligo Fucoidan Supports Liver Cancer Treatment

This article summarizes clinical research on low molecular weight fucoidan (LMF), also known as Oligo Fucoidan, in liver cancer (hepatocellular carcinoma, HCC) treatment. The study specifically used Oligo Fucoidan supplied by Hi-Q Marine Biotech.

Seaweed-Derived Fucoidan Enhances TACE Therapy

Liver cancer is one of the leading causes of cancer-related deaths worldwide. For patients with unresectable tumors, transarterial chemoembolization (TACE) is a standard treatment. However, TACE is often associated with tumor recurrence and liver function damage.

A randomized, double-blind clinical trial published in Liver International evaluated 82 HCC patients undergoing TACE. Participants received either 4.4 g/day of Hi-Q Marine Biotech’s Oligo Fucoidan or a placebo for six months.

Key Clinical Benefits

  • Improved tumor control:
    The Oligo Fucoidan group achieved a 95.24% disease control rate, compared to 80.00% in the placebo group, with significantly lower tumor progression.
  • Better liver function preservation:
    80.95% of patients taking Oligo Fucoidan maintained Child-Pugh Class A liver function, versus 62.50% in the placebo group.

Why Oligo Fucoidan Works

Oligo Fucoidan from Hi-Q Marine Biotech exhibits anti-inflammatory, antioxidant, anti-angiogenic, and immune-modulating properties, helping reduce oxidative stress and protect healthy liver cells during cancer treatment. The study also confirmed good safety and tolerability, with no increase in serious adverse events.

Conclusion

This clinical study provides evidence that Hi-Q Marine Biotech’s Oligo Fucoidan is a promising adjunct therapy for liver cancer patients receiving TACE, supporting tumor control while protecting liver function.

Disclaimer:
This content is based on a 2025 published clinical study and is for informational purposes only. It does not replace professional medical advice. Patients should consult healthcare professionals before use.

Reference: https://pmc.ncbi.nlm.nih.gov/articles/PMC12442522/