Ishii Hiroto, Yokoyama Hiroki, Katsube Atsushi, Gunji Tadahiro, Saito Takeshi, Yano Shingo
Division of Clinical Oncology and Hematology, Department of Internal Medicine, The Jikei University School of Medicine, Tokyo, Japan.
Blood Cell Ther. 2021 Nov 25;4(4):88-91. doi: 10.31547/bct-2021-006.
Posttransplant treatment is performed to treat hematopoietic diseases but can lead to allogeneic-specific complications in addition to those seen in a non-transplant setting. Immunomodulatory drugs (IMiDs) activate cytotoxic T cells and suppress regulatory T cells. The optimal timing and optimal dose of IMiDs after allogeneic transplantation (allo-HSCT) to reduce complications and increase antitumor efficacy are difficult to determine because the degree of recovery of donor immune cells varies depending on the time after allo-HSCT. We experienced a patient with allo-HSCT who developed severe late acute graft-versus-host disease (GVHD) of the lower intestinal tract after receiving pomalidomide as a posttransplant therapy eight months after allo-HSCT. It is possible that pomalidomide induced acute GVHD by altering the activity of donor immune cells. This first case report highlights that the use of pomalidomide after allo-HSCT may lead to severe late acute GVHD. When pomalidomide is used after allo-HSCT, it is desirable to start with a small dose and gradually increase the dose while monitoring cytokine and lymphocyte subsets for the onset of GVHD.
移植后治疗用于治疗造血系统疾病,但除了在非移植情况下出现的并发症外,还可能导致同种异体特异性并发症。免疫调节药物(IMiDs)可激活细胞毒性T细胞并抑制调节性T细胞。由于供体免疫细胞的恢复程度因异基因造血干细胞移植(allo-HSCT)后的时间而异,因此难以确定allo-HSCT后使用IMiDs的最佳时机和最佳剂量,以减少并发症并提高抗肿瘤疗效。我们遇到一名接受allo-HSCT的患者,在allo-HSCT八个月后接受泊马度胺作为移植后治疗后,出现了严重的晚期下肠道急性移植物抗宿主病(GVHD)。泊马度胺可能通过改变供体免疫细胞的活性诱导急性GVHD。这例首例病例报告强调,allo-HSCT后使用泊马度胺可能导致严重的晚期急性GVHD。当allo-HSCT后使用泊马度胺时,最好从小剂量开始,逐渐增加剂量,同时监测细胞因子和淋巴细胞亚群,以观察GVHD的发生。