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Recommendations Summary

ONC: Head and Neck Cancer: Radiation 2007

Click here to see the explanation of recommendation ratings (Strong, Fair, Weak, Consensus, Insufficient Evidence) and labels (Imperative or Conditional). To see more detail on the evidence from which the following recommendations were drawn, use the hyperlinks in the Supporting Evidence Section below.


  • Recommendation(s)

    ONC: Use of Antioxidant Vitamin E Oral Supplement

    Use of vitamin E oral supplements to enhance efficacy, improve tolerance and reduce late-effects of radiation therapy for patients with head/neck cancer is not recommended. While limited evidence supports the use of vitamin E oral supplements to reduce late effects (osteoradionecrosis), there is strong research reporting an increased risk for second primary cancers and decreased survival rate with use of vitamin E in doses greater than or equal to 400 IU (268mg).

    Rating: Weak
    Imperative

    • Risks/Harms of Implementing This Recommendation

      No potential risks or harms are associated with the application of this recommendation.

    • Conditions of Application

      No conditions limit the application of this recommendation.

    • Potential Costs Associated with Application

      No obvious costs are associated with the application of this recommendation.

    • Recommendation Narrative

      • A positive quality RCT (Bairati et al, 2005) of older, stage I and II head and neck cancer patients receiving radiation therapy who continuously supplemented with 400IU per day of a-tocopherol (oral vitamin E) for three years resulted in negative outcomes.  The study indicated use of the supplement may be associated with an increased occurance of second primary cancers and decreased duration of cancer-free survival in this population.
      • A neutral quality before and after time series study (Delanian et al, 2005) with a small, convenience sample found that a combination of pentoxifylline (800mg per day) and vitamin E (1, 000IU per day) boosted with clodronate (1, 600mg per day, 5 days/week) in only the most serious cases, induced mucosal and bone healing in patients with osteoradionecrosis. All patients improved at 6 months, and the investigators were not blinded. 

    • Recommendation Strength Rationale

      • Based on one positive quality RCT, and one neutral quality before and after time series studies, conclusion statements are Grade II and Grade III. 

    • Minority Opinions

      Consensus reached.