Developing Targeted Therapies for T Cell Acute Lymphoblastic Leukemia/Lymphoma

被引:2
作者
DuVall, Adam S. S. [1 ]
Wesevich, Austin [1 ]
Larson, Richard A. A. [1 ]
机构
[1] Univ Chicago, Dept Med, Sect Hematol Oncol, Chicago, IL 60637 USA
基金
英国科研创新办公室;
关键词
Acute lymphoblastic leukemia; T cell acute lymphoblastic leukemia; Developmental therapeutics; JAK/STAT PATHWAY INHIBITION; GLUCOCORTICOID RESISTANCE; ACTIVATION; MUTATIONS; PHOSPHORYLATES; PROLIFERATION; CHEMOTHERAPY; REQUIREMENT; COMBINATION; SENSITIVITY;
D O I
10.1007/s11899-023-00706-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose of ReviewLargely, treatment advances in relapsed and/or refractory acute lymphoblastic leukemia (ALL) have been made in B cell disease leaving T cell ALL reliant upon high-intensity chemotherapy. Recent advances in the understanding of the biology of T-ALL and the improvement in immunotherapies have led to new therapeutic pathways to target and exploit. Here, we review the more promising pathways that are able to be targeted and other therapeutic possibilities for T-ALL.Recent FindingsPreclinical models and early-phase clinical trials have shown promising results in some case in the treatment of T-ALL. Targeting many different pathways could lead to the next advancement in the treatment of relapsed and/or refractory disease. Recent advances in cellular therapies have also shown promise in this space.When reviewing the literature as a whole, targeting important pathways and antigens likely will lead to the next advancement in T-ALL survival since intensifying chemotherapy.
引用
收藏
页码:217 / 225
页数:9
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