ITPA
医学
硫嘌呤甲基转移酶
巯基嘌呤
队列
内科学
白细胞减少症
基因型
药物遗传学
毒性
胃肠病学
肿瘤科
免疫学
遗传学
硫唑嘌呤
生物
基因
丙型肝炎病毒
病毒
疾病
利巴韦林
作者
Paroni O. L. Fan,Kam Tong Leung,Kathy Yuen Yee Chan,Alex Wing Kwan Leung,Grace Kee See Lam,Terry T. W. Chow,Frankie Wai Tsoi Cheng,Liz Y. P. Yuen,Takaya Moriyama,Jun J. Yang,Chi Kong Li
标识
DOI:10.1080/08880018.2021.1973628
摘要
Inter-individual variance in 6-mercaptopurine (6-MP) dose intensity is common in patients with acute lymphoblastic leukemia (ALL). We aimed to evaluate the association of common variants of ABCC4, ITPA, NUDT15, and TPMT with 6-MP dose intensity and toxicity in pediatric ALL patients. In this cohort, 13.8% of patients were intolerant to 6-MP with actual dosage less than 50% of scheduled dose. Twenty percent of patients were found to be heterozygous or homozygous mutated with NUDT15. NUDT15 c.415C > T and the genotype-predicted NUDT15 activity were significantly associated with 6-MP intolerance. TPMT*3C variants were not common in this cohort (2.8%). NUDT15 polymorphisms and genotype predicted NUDT15 activity were significantly associated with 6-MP dose intensity and leukopenia episodes. Combination of ABCC4 and ITPA variants (ABCC4 c.912G > T and ITPA c.94C > A) also showed significant positive association with 6-MP intolerance in Chinese children with ALL. Further study on pharmacogenetic screening for ALL patients to avoid 6-MP induced toxicity is recommended.Supplemental data for this article is available online at https://doi.org/10.1080/08880018.2021.1973628.
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