Nakata Keiichi, Fuji Shigeo, Koike Midori, Tada Yuma, Masaie Hiroaki, Yoshida Hitoshi, Watanabe Eri, Kobayashi Seiichiro, Tojo Arinobu, Uchimaru Kaoru, Ishikawa Jun
Department of Hematology, Osaka International Cancer Institute, Osaka, Japan.
Department of IMSUT Clinical Flow Cytometry Laboratory, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
Blood Cell Ther. 2020 Feb 25;3(1):6-10. doi: 10.31547/bct-2019-012.
Adult T-cell leukemia-lymphoma (ATL) is a rare type of mature T cell lymphoma caused by human T-lymphotropic virus type 1 (HTLV-1) with dismal outcome with conventional chemotherapy. A humanized anti-CC chemokine receptor 4 (CCR4) monoclonal antibody, mogamulizumab (MOG), has been shown to be effective for CCR4-positive ATL. However, MOG administration before allogeneic hematopoietic stem cell transplantation (allo-HSCT) was reported to be associated with an increased risk of severe acute graft-versus-host disease (aGVHD) after allo-HSCT due to reduction of donor-derived regulatory T cells (Tregs). We herein present a patient with ATL who underwent allo-HSCT after MOG administration without developing severe GVHD while referring to serum MOG concentration. The clinical course of our case suggests that it might be possible to determine the appropriate timing of allo-HSCT with monitoring of residual MOG level while avoiding the detrimental effect of MOG on post-transplant clinical outcome without increasing the risk of relapse/progression.
成人T细胞白血病-淋巴瘤(ATL)是一种由1型人类嗜T淋巴细胞病毒(HTLV-1)引起的罕见成熟T细胞淋巴瘤,采用传统化疗预后不佳。一种人源化抗CC趋化因子受体4(CCR4)单克隆抗体莫加莫单抗(MOG)已被证明对CCR4阳性的ATL有效。然而,据报道,在异基因造血干细胞移植(allo-HSCT)前使用MOG会因供体来源的调节性T细胞(Tregs)减少而增加allo-HSCT后严重急性移植物抗宿主病(aGVHD)的风险。我们在此报告一例ATL患者,在使用MOG后接受了allo-HSCT,且未发生严重GVHD,同时参考了血清MOG浓度。我们病例的临床过程表明,在监测残留MOG水平的同时确定allo-HSCT的合适时机可能是可行的,既能避免MOG对移植后临床结果的不利影响,又不会增加复发/进展的风险。