微小残留病
髓系白血病
造血干细胞移植
医学
移植
疾病
肿瘤科
干细胞
残余物
白血病
内科学
癌症研究
免疫学
生物
遗传学
算法
计算机科学
作者
Úna Bhreathnach,Dearbhla Doherty,Karen Murphy,Catherine M. Flynn,Stephen E. Langabeer
标识
DOI:10.1016/j.leukres.2022.106823
摘要
• Therapy-related AML with the t(8;16) is uncommon and associated with a poor prognosis. • Hematopoietic allogeneic stem cell transplantation remains the only curative option. • KAT6A-CREBBP transcript identification is necessary for measurable residual disease. • RT-qPCR monitoring confirms the efficacy of allogeneic stem cell transplantation. • In t(8;16) AML, measurable residual disease peri-transplant may influence prognosis.
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