Gut · 2002 · 150 citations · 11 references
PharmacyPharmacologyPharmacotherapyGastrointestinal PharmacotherapyImmunopathologyInflammationCrohn Disease PharmacotherapyGastrointestinal InflammationGastrointestinal ToxicityGastrointestinal Toxicity ManagementInflammatory Bowel DiseaseAzathioprine PharmacogeneticsAzathioprine UseDrug Dose IndividualizationInflammatory Bowel Disease TherapyMercaptopurine PharmacogeneticsThiopurine MetabolismThiopurine Methyltransferase PharmacogeneticsThiopurine Therapy
Thiopurine S-methyltransferase (TPMT) deficient patients develop life threatening haematotoxicity (for example, pancytopenia) when treated with a standard dose of azathioprine (AZA) and 6-mercaptopurine (6-MP) due to excessive accumulation of cytotoxic metabolites. At present, it is generally recommended that these patients should not receive AZA or 6-MP treatment for inflammatory bowel disease. We report for the first time that Crohn's disease patients with TPMT deficiency can be successfully treated with AZA. We illustrate this with three cases where treatment has been successful and toxicity has been avoided by carefully titrating the drug dose. Thus very low TPMT activity demands pharmacogenetically guided dosing.
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Christoph Gasché, Jürgen Schölmerich, Geert D’Haens et al. · Inflammatory Bowel Diseases · 2000 · 1.1K citations · Full text
Possible carcinogenic effect of 6-mercaptopurine on bone marrow stem cells
Jens Bo Thomsen, Henrik Schr�der, Jón Kristinsson et al. · Cancer · 1999 · 172 citations · Full text