医学
髓系白血病
疾病
肿瘤科
干细胞
酪氨酸激酶
入射(几何)
靶向治疗
髓样
内科学
进行性疾病
免疫学
微小残留病
酪氨酸激酶抑制剂
白血病
移植
癌症研究
免疫疗法
介绍(产科)
慢性淋巴细胞白血病
达沙替尼
生物信息学
临床试验
伊布替尼
造血干细胞移植
出处
期刊:Blood
[Elsevier BV]
日期:2025-12-02
卷期号:147 (4): 369-378
被引量:1
标识
DOI:10.1182/blood.2024026510
摘要
Advanced phases of Philadelphia chromosome-positive chronic myeloid leukemia (CML), classically encompassing de novo presentation of accelerated-phase disease and blast-phase disease (myeloid and lymphoid "blast crisis") and progression to these from antecedent chronic-phase disease, have diminished in incidence but remain a challenge. Despite continued development of additional and novel kinase inhibitors of BCR::ABL1, global limitations on access to diagnostics and therapy persist and account for continued incidence of advanced disease at initial presentation and progressive disease. Evolution in defining risk through clinical and molecular characterization should increase ability to identify emerging advanced disease, minimize progression, and improve treatment of resistant chronic-phase and blast-phase diseases. While BCR::ABL1 tyrosine kinase inhibition remains central in advanced disease, combination therapy with conventional and novel chemotherapy, immunotherapy, and allogeneic stem cell transplant provide best long-term outcomes.
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