2022年Ph+ ALL:是否有最佳方案?

IF 2.9 3区 教育学 Q1 EDUCATION, SCIENTIFIC DISCIPLINES
Matthew J Wieduwilt
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引用次数: 2

摘要

在酪氨酸激酶抑制剂(TKIs)出现之前,费城染色体阳性(Ph+)急性淋巴细胞白血病(ALL)预后非常差,TKIs可以阻断BCR-ABL1癌蛋白的活性。随着TKI疗效和同种异体造血细胞移植(HCT)的提高,生存率在过去30年中有所提高,化疗和同种异体造血细胞移植的作用正在发生变化。更好的风险分层,第三代TKI ponatinib的应用,以及使用CD19-CD3双功能t细胞抗体blinatumumab代替化疗的免疫疗法,使得Ph+ ALL的治疗更耐受,也可以说更有效,特别是对于大多数Ph+ ALL患者的老年患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ph+ ALL in 2022: is there an optimal approach?

Philadelphia chromosome-positive (Ph+) acute lymphoblastic leukemia (ALL) carried a very poor prognosis prior to the advent of tyrosine kinase inhibitors (TKIs) that block the activity of the BCR-ABL1 oncoprotein. With improvements in TKI efficacy and allogeneic hematopoietic cell transplantation (HCT), survival has improved over the past 3 decades, and the role of chemotherapy and allogeneic HCT is now changing. Better risk stratification, the application of the third-generation TKI ponatinib, and the use of immunotherapy with the CD19-CD3 bifunctional T-cell engaging antibody blinatumomab in place of chemotherapy has made therapy for Ph+ ALL more tolerable and arguably more efficacious, especially for older patients who comprise most patients with Ph+ ALL.

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来源期刊
Hematology. American Society of Hematology. Education Program
Hematology. American Society of Hematology. Education Program EDUCATION, SCIENTIFIC DISCIPLINES-HEMATOLOGY
CiteScore
4.70
自引率
3.30%
发文量
0
期刊介绍: Hematology, the ASH Education Program, is published annually by the American Society of Hematology (ASH) in one volume per year.
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