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Pui, Ching‐Hon

Mayo Clinic

St. Jude Children's Research Hospital

Citations 1

Clinical Pharmacogenetics Implementation Consortium Guideline for Thiopurine Dosing Based on TPMT and N
Relling, Mary V. , Schwab, Matthias , Whirl‐Carrillo, Michelle , Suarez‐Kurtz, Guilherme , Pui, Ching‐Hon, Stein, Charles, Moyer, Ann M. , Evans, William E. , Klein, Teri E. , Antillon‐Klussmann, Federico Guillermo, Caudle, Kelly E. , Yeoh, Allen Eng Juh , Antillón‐Klussmann, Federico , Yang, Jun J.J. , Whirl-Carrillo, Michelle , Klein, Teri E , Yeoh, Allen E J , Pui, Ching-Hon , Kato, Motohiro , Schmiegelow, Kjeld , Schwab, Matthias

Clinical Pharmacology & Therapeutics | November 17, 2018 | Volume: 105 | Issue: 5 | Pages: 1095-1105

10.1002/cpt.1304 Get It

Thiopurine methyltransferase (TPMT) activity exhibits a monogenic codominant inheritance and catabolizes thiopurines. TPMT variant alleles are associated with low enzyme activity and pronounced pharmacologic effects of thiopurines. Loss‐of‐function alleles in the NUDT15 gene are common in Asians and Hispanics and reduce the degradation of active thiopurine nucleotide metabolites, also predisposing to myelosuppression. We provide recommendations for adjusting starting doses of azathioprine, mercaptopurine, and thioguanine based on TPMT and NUDT15 genotypes (updates on www.cpicpgx.org ).