Abstract
We thank Yélamos et al. for their interest in our nicotinamide chemoprevention studies.1 Some of their comments are pertinent, while others are based on a flawed interpretation of our data.
Zhao2 previously commented on (nonsignificant) numerical differences in the frequency of adverse-event term groupings (mucocutaneous infections) between the placebo and nicotinamide groups in our ONTRAC chemoprevention study (Oral Nicotinamide To Reduce Actinic Cancer).3 As stated previously, chance remains a highly plausible explanation for the numerically higher mucocutaneous infections in the nicotinamide arm and also, for example, for the numerically lower respiratory infections observed in the nicotinamide arm.4
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