淋巴细胞白血病
疾病
化疗
医学
微小残留病
费城染色体
重症监护医学
年轻人
肿瘤科
儿科
内科学
遗传学
白血病
生物
基因
染色体易位
作者
Madelyn Burkart,Shira Dinner
出处
期刊:Blood Reviews
[Elsevier BV]
日期:2024-04-25
卷期号:66: 101208-101208
被引量:2
标识
DOI:10.1016/j.blre.2024.101208
摘要
There have been major paradigm shifts in the treatment of Philadelphia chromosome negative (Ph-) acute lymphoblastic leukemia (ALL) in the last decade with the introduction of new immunotherapies and targeted agents, adoption of pediatric-type chemotherapy protocols in younger adults as well as chemotherapy light approaches in older adults and the incorporation of measurable residual disease (MRD) testing to inform clinical decision making. With this, treatment outcomes in adult Ph- ALL have improved across all age groups. However, a subset of patients will still develop relapsed disease, which can be challenging to treat and associated with poor outcomes. Here we review the treatment of Ph- ALL in both younger and older adults, including the latest advancements and future directions.
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