Department of Hematology, Toyama Red Cross Hospital, Toyama, Japan.
Division of Diagnostic Pathology, Toyama Red Cross Hospital, Toyama, Japan.
J Clin Exp Hematop. 2022;62(3):175-180. doi: 10.3960/jslrt.22014.
We report a case of donor-derived diffuse large B-cell lymphoma (DLBCL), which developed 5 years after stem cell transplantation from a human leukocyte antigen (HLA)-haploidentical donor for acute myeloid leukemia (AML). A 51-year-old male was diagnosed with AML with variant KMT2A translocation involving t(6;11)(q13;q23). After 12 cycles of azacitidine treatment, fluorescence in situ hybridization (FISH) for KMT2A split signal indicated that 94% of his bone marrow (BM) cells were positive. He underwent peripheral blood stem cell transplantation (PBSCT) from his HLA-haploidentical son. The preconditioning regimen consisted of fludarabine, busulfan, melphalan, and antithymocyte globulin (ATG). The graft-versus-host disease (GVHD) prophylaxis consisted of tacrolimus and short-term methotrexate. On day 28, KMT2A FISH analysis indicated that he had achieved a complete response (CR). He continued to receive tacrolimus for the limited type of cutaneous chronic GVHD. Five years after the transplantation, positron emission tomography/computed tomography (PET/CT) showed an abdominal tumor. The tumor was diagnosed as DLBCL without Epstein-Barr virus. BM aspiration revealed the infiltration of lymphoma cells with t(8;14)(q24;q32). Chimerism analysis showed that both the peripheral blood (PB) and abdominal lymphoma cells were of donor origin. After 4 cycles of salvage chemotherapy, PET/CT showed that a CR had been achieved. He underwent a second PBSCT from an HLA-identical unrelated donor. The preconditioning regimen and GVHD prophylaxis were the same as those for the first PBSCT without ATG. The patient's PB revealed complete second donor-type chimerism, and the patient has maintained a CR since the second transplantation.
我们报告了一例 5 年前因急性髓系白血病(AML)接受 HLA 单倍体相合供者造血干细胞移植后发生供体来源弥漫性大 B 细胞淋巴瘤(DLBCL)的病例。一名 51 岁男性被诊断为 AML,伴 KMT2A 易位,涉及 t(6;11)(q13;q23)。接受 12 周期阿扎胞苷治疗后,KMT2A 分裂信号荧光原位杂交(FISH)显示其骨髓(BM)细胞中有 94%呈阳性。他接受了来自 HLA 单倍体相合儿子的外周血造血干细胞移植(PBSCT)。预处理方案包括氟达拉滨、白消安、马法兰和抗胸腺细胞球蛋白(ATG)。移植物抗宿主病(GVHD)预防方案包括他克莫司和短期甲氨蝶呤。第 28 天,KMT2A FISH 分析显示他已达到完全缓解(CR)。他继续接受他克莫司治疗局限性皮肤慢性 GVHD。移植后 5 年,正电子发射断层扫描/计算机断层扫描(PET/CT)显示腹部肿瘤。肿瘤诊断为无 EBV 的 DLBCL。BM 抽吸显示淋巴瘤细胞浸润伴 t(8;14)(q24;q32)。嵌合分析显示外周血(PB)和腹部淋巴瘤细胞均来源于供者。4 周期挽救化疗后,PET/CT 显示 CR 已达到。他接受了来自 HLA 完全相合无关供者的第二次 PBSCT。预处理方案和 GVHD 预防方案与第一次 PBSCT 相同,不使用 ATG。患者的 PB 显示完全的第二次供者型嵌合体,自第二次移植以来,患者一直保持 CR。