医学
中止
髓系白血病
内科学
费城染色体
肿瘤科
染色体易位
伊马替尼
重症监护医学
基因
生物化学
化学
作者
Neil P. Shah,Ravi Bhatia,Jessica K. Altman,Maria L. Amaya,Kebede H. Begna,Ellin Berman,Onyee Chan,Joan Clements,Robert H. Collins,Peter Curtin,Daniel J. DeAngelo,Michael W. Drazer,Lori J. Maness,Leland Metheny,Sanjay Mohan,Joseph O. Moore,Vivian G. Oehler,Keith W. Pratz,Iskra Pusic,Michal G. Rose
出处
期刊:Journal of The National Comprehensive Cancer Network
日期:2024-02-01
卷期号:22 (1): 43-69
被引量:52
标识
DOI:10.6004/jnccn.2024.0007
摘要
Chronic myeloid leukemia (CML) is defined by the presence of Philadelphia chromosome resulting from a reciprocal translocation between chromosomes 9 and 22 [t9;22] that gives rise to a BCR::ABL1 fusion gene. CML occurs in 3 different phases (chronic, accelerated, and blast phase) and is usually diagnosed in the chronic phase in developed countries. Tyrosine kinase inhibitor (TKI) therapy is a highly effective treatment option for patients with chronic phase–CML. The primary goal of TKI therapy in patients with chronic phase–CML is to prevent disease progression to accelerated phase–CML or blast phase–CML. Discontinuation of TKI therapy with careful monitoring is feasible in selected patients. This manuscript discusses the recommendations outlined in the NCCN Guidelines for the diagnosis and management of patients with chronic phase–CML.
科研通智能强力驱动
Strongly Powered by AbleSci AI