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[在一名患有治疗相关急性髓系白血病的儿科患者中,使用维多珠单抗和芦可替尼治疗类固醇难治性胃肠道急性移植物抗宿主病]

[Steroid-refractory gastrointestinal acute graft-versus-host disease treated with vedolizumab and ruxolitinib in a pediatric patient with therapy-related acute myeloid leukemia].

作者信息

Nagasawa Shun, Yamada Ai, Kinoshita Mariko, Kamimura Sachiyo, Tanaka Hiroyuki, Nishikawa Takuro, Okamoto Yasuhiro, Moritake Hiroshi

机构信息

Division of Pediatrics, University of Miyazaki.

Department of Diagnostic Pathology, University of Miyazaki Hospital.

出版信息

Rinsho Ketsueki. 2023;64(1):23-29. doi: 10.11406/rinketsu.64.23.

Abstract

A 12-year-old girl developed Philadelphia chromosome-positive acute myeloid leukemia due to therapy-related myelodysplastic syndrome with monosomy 7 following neuroblastoma treatment. She underwent allogenic bone marrow transplantation from a human leukocyte antigens-DR1 locus-mismatched unrelated donor. However, on day 49 post transplantation, she presented with diarrhea due to gastrointestinal acute graft-versus-host disease (aGVHD), and treatments with prednisolone, budesonide rectal foam, and human mesenchymal stem cells were ineffective. Therefore, vedolizumab was administered from day 100, which improved the symptoms from gut stage 3 to gut stage 1. Consequently, prednisolone was withdrawn without any serious adverse effects. However, the symptoms worsened to gut stage 3 again; therefore, ruxolitinib was administered to achieve complete remission. Vedolizumab exhibits gut-selective action without systemic immunosuppressive activity. Hence, vedolizumab administration before other systemic immunosuppressive agents may be recommended in patients with steroid-refractory gastrointestinal aGVHD. Thus far, only a few reports have been published regarding the administration of vedolizumab and ruxolitinib for steroid-refractory gastrointestinal aGVHD in children. Further evidence should be obtained from patients treated with vedolizumab and ruxolitinib to confirm their effectiveness for pediatric steroid-refractory gastrointestinal aGVHD.

摘要

一名12岁女孩在接受神经母细胞瘤治疗后,因治疗相关的骨髓增生异常综合征伴7号染色体单体而发展为费城染色体阳性急性髓系白血病。她接受了来自人类白细胞抗原-DR1位点不匹配的无关供体的异基因骨髓移植。然而,移植后第49天,她因胃肠道急性移植物抗宿主病(aGVHD)出现腹泻,使用泼尼松龙、布地奈德直肠泡沫剂和人间充质干细胞治疗均无效。因此,从第100天开始使用维多珠单抗,症状从肠道3级改善到肠道1级。结果,泼尼松龙停药,未出现任何严重不良反应。然而,症状再次恶化至肠道3级;因此,给予鲁索替尼以实现完全缓解。维多珠单抗具有肠道选择性作用,无全身免疫抑制活性。因此,对于类固醇难治性胃肠道aGVHD患者,可能建议在使用其他全身免疫抑制剂之前使用维多珠单抗。迄今为止,关于维多珠单抗和鲁索替尼用于儿童类固醇难治性胃肠道aGVHD的报道很少。应从接受维多珠单抗和鲁索替尼治疗的患者中获得更多证据,以证实它们对儿童类固醇难治性胃肠道aGVHD的有效性。

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