Endogenous plasma and salivary uracil to dihydrouracil ratios and DPYD genotyping as predictors of severe fluoropyrimidine toxicity in patients with gastrointestinal malignancies
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The limited sensibility of DPYD genotyping significantly limits its clinical use.

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Plasma and salivary DPD tests can detect patients at risk of severe toxicity.

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Salivary [UH2]/[U] ratio performed better than plasma.

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Salivary test had 85.7% sensitivity and 76.9% specificity to predict severe toxicity.

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