Early human study Safety and tolerability only 11 recruited, 9 completed
Turkey Tail preparation after breast cancer treatment: phase I study
Nine women completed this early dose-escalation study. It was designed mainly to examine tolerability and immune measures, not whether Turkey Tail prevents recurrence or improves survival.
- What was studied
- Oral Trametes versicolor preparation at 3, 6, or 9 g/day for six weeks after radiation therapy
- Setting
- Not an efficacy study
- Why it ranks here
- The study provides early tolerability information but has no control group and is too small to evaluate cancer outcomes.
Limits and cautions
- Only nine participants completed the study.
- There was no placebo or untreated comparison group.
- Immune changes are not proof of improved cancer outcomes.
Turkey Tail products are not FDA-approved in the United States as a cancer treatment.