医学
髓系白血病
伊马替尼
免疫抑制
不利影响
他克莫司
移植
人口
酪氨酸激酶
肾移植
酪氨酸激酶抑制剂
内科学
肿瘤科
慢性粒细胞白血病
白血病
免疫学
癌症
受体
环境卫生
作者
Ahmet Murt,Batuhan Bayram,Umut Yılmaz,Nurhan Seyahi,Ahmet Emre Eşkazan
出处
期刊:
日期:2024-01-01
卷期号:148 (8): 563-568
被引量:2
摘要
Lifelong immunosuppression, cytotoxic effects of some immunosuppressive drugs, and opportunistic oncogenic viruses increase malignancy risks in solid organ recipients. The risk of myeloid neoplasms including chronic myeloid leukemia (CML) is also increased in this patient population. Tyrosine kinase inhibitors (TKIs), the key element of CML therapy, should be used cautiously in transplantation patients as they may interact with calcineurin inhibitors. With this report, a 63-year-old female kidney transplant recipient who developed CML 9 years after kidney transplantation is presented. CML in this patient was treated with a slightly reduced dose of imatinib (300 mg) due to concerns of adverse events including its interaction with tacrolimus. Deep molecular response (DMR) was achieved at 12 months under imatinib treatment. The patient is still in DMR after 30 months of follow-up, and she did not experience any adverse events or acute rejection episodes. CML and the use of TKIs in kidney transplant patients have been discussed with an extensive literature review. In this patient population, TKIs are generally well tolerated with achievement of treatment responses and good prognosis. Graft functions are also well maintained as long as drug interactions are monitored.
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