Immunotherapy in pediatric B-cell acute lymphoblastic leukemia

被引:21
|
作者
Wyatt, Kirk D. [1 ]
Bram, Richard J. [1 ,2 ]
机构
[1] Mayo Clin, Dept Pediat & Adolescent Med, Div Pediat Hematol Oncol, 200 First St SW, Rochester, MN 55905 USA
[2] Mayo Clin, Dept Immunol, 200 First St SW, Rochester, MN 55905 USA
关键词
MINIMAL RESIDUAL DISEASE; NON-HODGKIN-LYMPHOMA; TERM-FOLLOW-UP; MARROW-TRANSPLANTATION; BODY IRRADIATION; ADULT PATIENTS; HOST-DISEASE; YOUNG-ADULTS; BONE-MARROW; SINGLE-ARM;
D O I
10.1016/j.humimm.2019.01.011
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Advances in multi-agent chemotherapy and supportive care have dramatically improved survival of children with B-cell acute lymphoblastic leukemia (B-ALL); however, patients with relapsed and refractory disease continue to represent a therapeutic challenge. Hematopoietic stem cell transplant was the first immunotherapeutic approach to be used in the treatment of patients with relapsed or refractory disease. However, novel therapies such as bispecific antibodies that engage T-cells and chimeric antigen receptor T-cells (CAR-T) therapy have emerged as novel FDA-approved options that have the potential to become the new standard of care for these difficult-to-treat leukemias. With multiple immunotherapeutic agents in the drug development pipeline, it is important for cancer researchers and oncologists to be familiar with these agents, including their mechanism of action, side effects and efficacy. In this paper, we review the role of the human immune system in the development and treatment of childhood ALL and provide an overview of current and upcoming immunotherapeutic treatment approaches.
引用
收藏
页码:400 / 408
页数:9
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