医学
淋巴细胞白血病
造血干细胞移植
肿瘤科
移植
疾病
前线
费城染色体
化疗
干细胞
内科学
重症监护医学
免疫学
白血病
生物
政治学
基因
遗传学
法学
染色体易位
作者
Zia Ur Rahman,Partow Kebriaei
标识
DOI:10.1016/j.clml.2023.06.007
摘要
The therapeutic landscape of Philadelphia chromosome positive acute lymphoblastic leukemia (ALL) for adults has dramatically changed over the past 2 decades; the emergence of newer generations of tyrosine kinase inhibitors and incorporation of targeted immunotherapies into front-line therapy have significantly improved outcomes to the point where an argument can be made that this entity may no longer be considered a high-risk ALL subgroup. In this review article, we discuss different front-line regimens (both intensive and deintensified regimens including chemotherapy-free regimens). We also review disease monitoring strategies, discuss the role of allogeneic hematopoietic stem cell transplantation, and discuss the rapidly changing therapeutic landscape for patients with relapsed disease.
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