医学
帕纳替尼
尼罗替尼
博舒替尼
达沙替尼
费城染色体
Blinatumoab公司
伊马替尼
嵌合抗原受体
肿瘤科
化疗
酪氨酸激酶
内科学
免疫学
白血病
淋巴细胞白血病
髓系白血病
免疫疗法
癌症
受体
染色体易位
化学
基因
生物化学
作者
Musa Yılmaz,Hagop M. Kantarjian,Farhad Ravandi‐Kashani,Nicholas J. Short
出处
期刊:PubMed
日期:2018-03-01
卷期号:16 (3): 216-223
被引量:28
摘要
Philadelphia chromosome-positive (Ph+) acute lymphoblastic leukemia (ALL) accounts for approximately one-fourth of cases of adult ALL. It typically presents with an aggressive clinical course, responds poorly to standard chemotherapy, and carries a high risk for relapse. The landscape of Ph+ ALL therapy has changed favorably since the development of tyrosine kinase inhibitors (TKIs). With the successful incorporation of TKIs into chemotherapy regimens, remissions occur more frequently and patients live longer. Imatinib was the first TKI that targeted the BCR-ABL1 oncoprotein in Ph+ ALL. Since then, nilotinib, dasatinib, bosutinib, and ponatinib have been developed. Despite the significant progress that has been made in inducing remission, frequent relapses remain a challenge, especially among those with resistant BCR-ABL1 mutations. Still, the therapeutic armamentarium of ALL therapy is expanding at a breathtaking pace today compared with a decade ago. Novel drugs, such as potent later-generation TKIs, antibody-drug conjugates, bispecific monoclonal antibodies, and chimeric antigen receptor T-cell therapies, are being developed and investigated in patients with Ph+ ALL. In this review, we summarize the current treatment options for Ph+ ALL and highlight the therapies that may become the standard of care in the near future.
科研通智能强力驱动
Strongly Powered by AbleSci AI