Boddu Prajwal, Kantarjian Hagop, Garcia-Manero Guillermo, Allison James, Sharma Padmanee, Daver Naval
a Department of Leukemia , The University of Texas M. D. Anderson Cancer Center , Houston , TX , USA.
b Immunotherapy Platform , The University of Texas M. D. Anderson Cancer Center , Houston , TX , USA.
Leuk Lymphoma. 2018 Apr;59(4):790-802. doi: 10.1080/10428194.2017.1344905. Epub 2017 Jul 6.
The development of immune checkpoint inhibitors represents a major breakthrough in the field of cancer therapeutics. Pursuant to their success in melanoma and numerous solid tumor malignancies, these agents are being investigated in hematological malignancies including acute myelogenous leukemia (AML) and myelodysplastic syndromes (MDS). Although AML/MDS have traditionally been considered to be less immunogenic than solid tumor malignancies, recent pre-clinical models suggest a therapeutic role for immune checkpoint inhibition in these diseases. CTLA-4 inhibition may be especially effective in treating late post-allogeneic stem cell transplant relapse of AML in patients with limited or no graft versus host disease. Immune checkpoint inhibition, specifically PD-1 inhibition, demonstrated limited single agent efficacy in patients with relapsed AML and with MDS post-hypomethylating therapy. Rationally designed combinations of PD-1 inhibitors with standard anti-leukemic therapy are needed. Hypomethylating agents such as azacitidine, up-regulate PD-1, PD-L1, and PD-L2 in patients with AML/MDS and up-regulation of these genes was associated with the emergence of resistance. The combination of azacitidine and PD-1/PD-L1 inhibition may be a potential mechanism to prevent or overcome resistance to 5-azacitidine. A number of such combinations are being evaluated in clinical trials with early encouraging results. Immune checkpoint inhibition is also an attractive option to improve relapse-free survival or eliminate minimal residual disease post induction and consolidation by enhancing T-cell surveillance in patients with high-risk AML. The ongoing clinical trials with checkpoint inhibitors in AML/MDS will improve our understanding of the immunobiology of these diseases and guide us to the most appropriate application of these agents in the therapy of AML/MDS.
免疫检查点抑制剂的发展是癌症治疗领域的一项重大突破。鉴于其在黑色素瘤和众多实体瘤恶性肿瘤治疗中的成功,这些药物正在血液系统恶性肿瘤中进行研究,包括急性髓性白血病(AML)和骨髓增生异常综合征(MDS)。尽管传统上认为AML/MDS的免疫原性低于实体瘤恶性肿瘤,但最近的临床前模型表明免疫检查点抑制在这些疾病中具有治疗作用。CTLA-4抑制在治疗移植物抗宿主病有限或无移植物抗宿主病的AML患者异基因干细胞移植后晚期复发中可能特别有效。免疫检查点抑制,特别是PD-1抑制,在复发AML患者和低甲基化治疗后的MDS患者中显示出有限的单药疗效。需要合理设计PD-1抑制剂与标准抗白血病治疗的联合方案。阿扎胞苷等低甲基化药物可上调AML/MDS患者的PD-1、PD-L1和PD-L2,这些基因的上调与耐药性的出现有关。阿扎胞苷与PD-1/PD-L1抑制的联合可能是预防或克服对5-阿扎胞苷耐药的潜在机制。一些此类联合方案正在临床试验中进行评估,早期结果令人鼓舞。免疫检查点抑制也是通过增强高危AML患者的T细胞监测来提高无复发生存率或消除诱导和巩固后微小残留病的一个有吸引力的选择。正在进行的AML/MDS中检查点抑制剂的临床试验将提高我们对这些疾病免疫生物学的理解,并指导我们在AML/MDS治疗中最恰当地应用这些药物。