Barsan Valentin, Ramakrishna Sneha, Davis Kara L
Bass Center for Childhood Cancer and Blood Disorders, Center for Cancer Cell Therapy, Department of Pediatrics, Stanford University, 265 Campus Drive, G2065, Stanford, CA, 94305-5435, USA.
Curr Oncol Rep. 2020 Jan 29;22(2):11. doi: 10.1007/s11912-020-0875-2.
Immunotherapy for the treatment of acute lymphoblastic leukemia (ALL) broadens therapeutic options beyond chemotherapy and targeted therapy. Here, we review the use of monoclonal antibody-based drugs and cellular therapies to treat ALL. We discuss the challenges facing the field regarding the optimal timing and sequencing of these therapies in relation to other treatment options as well as considerations of cost effectiveness.
By early identification of patients at risk for leukemic relapse, monoclonal antibody and cellular immunotherapies can be brought to the forefront of treatment options. Novel CAR design and manufacturing approaches may enhance durable patient response. Multiple clinical trials are now underway to evaluate the sequence and timing of monoclonal antibody, cellular therapy, and/or stem cell transplantation. The biologic and clinical contexts in which immunotherapies have advanced the treatment of ALL confer optimism that more patients will achieve durable remissions. Immunotherapy treatments in ALL will expand through rationally targeted approaches alongside advances in CAR T cell therapy design and clinical experience.
用于治疗急性淋巴细胞白血病(ALL)的免疫疗法拓宽了化疗和靶向治疗之外的治疗选择。在此,我们综述基于单克隆抗体的药物和细胞疗法在治疗ALL中的应用。我们讨论了该领域在这些疗法与其他治疗选择的最佳时机和顺序方面面临的挑战,以及成本效益的考量。
通过早期识别有白血病复发风险的患者,单克隆抗体和细胞免疫疗法可成为治疗选择的前沿。新型嵌合抗原受体(CAR)设计和制造方法可能增强患者的持久反应。目前正在进行多项临床试验,以评估单克隆抗体、细胞疗法和/或干细胞移植的顺序和时机。免疫疗法推动ALL治疗取得进展的生物学和临床背景让人乐观地认为,更多患者将实现持久缓解。ALL中的免疫疗法治疗将通过合理的靶向方法以及CAR T细胞疗法设计和临床经验的进步而得到扩展。