Azathioprine-associated severe myelosuppression: Indication of routine determination of thiopurine S-methyltransferase variant?

作者：Ngo S; Sauvetre G; Vittecoq O; Levesque H; Marie I^*

来源：Revue de Medecine Interne, 2011, 32(6): 373-376.

DOI：10.1016/j.revmed.2010.09.006

• Azathioprine
• Myelosuppression
• Severe myelosuppression
• Thiopurine S-methyltransferase genotype
• Prophylaxis
• Pharmacogenetics

Introduction. - Myelotoxicity is a well-known adverse effect of azathioprine, leading mainly to leukopenia. Other azathioprine associated hematological adverse effects are uncommon.
Case report. - We report a 49-year-old woman with rheumatoid arthritis and acquired hemophilia, who presented a severe myelosuppression occurring 3 weeks after an increase of her azathioprine regimen (at a daily dose of 150 mg). The patient had a heterozygous mutation of the thiopurine S-methyltransferase gene (TPMT*3A). Azathioprine therapy was discontinued and she recovered at 3 weeks. The patient had no relapse of pancytopenia after a 1 year follow-up.
Conclusion. - Routine measurement of TPMT activity or determination of TPMT variant allele may be useful tests, in order to identify the subgroup of patients who are at risk to develop azathioprine induced severe myelosuppression.

• 出版日期2011-6