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Management of adult Ph-positive acute lymphoblastic leukemia

机译:成人Ph阳性急性淋巴细胞白血病的治疗

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摘要

Philadelphia-positive acute lymphoblastic leukemia (Ph+ ALL) has been regarded for decades as the ALL subgroup with the worse outcome. It represents the most frequent genetic subtype of adult ALL, and increases progressively with age. The introduction of tyrosine kinase inhibitors (TKIs) has enabled to obtain complete hematologic remissions (CHRs) in virtually all patients, including the elderly, to improve disease-free survival and overall survival, as well as to increase the percentage of patients who can undergo an allogeneic stem cell transplant (allo-SCT).
机译:费城阳性急性淋巴细胞白血病(Ph + ALL)几十年来一直被认为是ALL亚组,其预后较差。它代表成年ALL最常见的遗传亚型,并随着年龄的增长而逐渐增加。酪氨酸激酶抑制剂(TKIs)的引入使包括老年人在内的几乎所有患者都能获得完全的血液学缓解(CHR),从而改善无病生存率和总体生存率,并增加可以接受治疗的患者的比例同种异体干细胞移植(allo-SCT)。

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