Fuji Shigeo
Department of Hematology, Osaka International Cancer Institute.
Rinsho Ketsueki. 2019;60(8):968-972. doi: 10.11406/rinketsu.60.968.
Adult T-cell leukemia-lymphoma (ATL) is a peripheral T-cell lymphoma caused by human T-cell lymphotropic virus type I. Patients with aggressive ATL exhibit poor outcomes, even with dose-dense intensive chemotherapy. Thus, allogeneic hematopoietic stem cell transplantation (allo-HSCT) is considered in all patients eligible for transplant. However, patients with aggressive ATL often have chemo-refractoriness or experience early relapse during chemotherapy. Allo-HSCT is often ineffective in patients with active disease status. Mogamulizumab (Moga) was approved in 2012 in Japan as a potent treatment option for patients with relapsed or refractory ATL. However, there is a major concern that the use of Moga before allo-HSCT could increase the risk of post-transplant complications, such as graft-versus-host disease (GVHD), because Moga depletes regulatory T cells. Here, we would like to describe the possible effects of pre-transplant Moga on post-transplant complications, such as acute GVHD, and to discuss how Moga could be efficiently incorporated in the treatment regimen of patients with aggressive ATL to maximize the expected clinical benefit.
成人T细胞白血病-淋巴瘤(ATL)是一种由I型人类嗜T细胞病毒引起的外周T细胞淋巴瘤。侵袭性ATL患者即便接受剂量密集的强化化疗,预后也较差。因此,所有符合移植条件的患者都应考虑进行异基因造血干细胞移植(allo-HSCT)。然而,侵袭性ATL患者常常对化疗耐药或在化疗期间出现早期复发。对于疾病处于活动状态的患者,allo-HSCT往往无效。莫加莫单抗(Moga)于2012年在日本获批,成为复发或难治性ATL患者的有效治疗选择。然而,一个主要担忧是,在allo-HSCT前使用Moga可能会增加移植后并发症的风险,如移植物抗宿主病(GVHD),因为Moga会消耗调节性T细胞。在此,我们将描述移植前使用Moga对移植后并发症(如急性GVHD)的可能影响,并讨论如何将Moga有效地纳入侵袭性ATL患者的治疗方案中,以实现预期临床获益的最大化。