Ma Hongbing, Liu Ting
Department of Hematology, West China Hospital, Sichuan University, Chengdu, Sichuan 610041, P.R. China.
Oncol Lett. 2016 Jun;11(6):3858-3862. doi: 10.3892/ol.2016.4452. Epub 2016 Apr 18.
Donor cell leukemia (DCL) is a rare complication of hematopoietic stem cell transplantation (HSCT) which occurs in ~5% of all leukemic relapses. In the English literature, >60 cases of DCL have been reported, however, only two cases of DCL following HSCT for the treatment of severe aplastic anemia (SAA) have been described to date. In the present study, the case of a 25 year-old male patient diagnosed with SAA, who underwent a peripheral blood stem cell transplantation (PBSCT) using cells obtained from a sibling with an identical human leukocyte antigen, is presented. The patient developed acute myeloid leukemia with an (8;21)(q22;q22) translocation and an extra copy of the chromosome 8 in donor cells 2.5 years following PBSCT, which was preceded by the development of Graves' disease 1 year following PBSCT. The leukemia achieved complete remission following 1 cycle of priming therapy, 2 cycles of consolidation chemotherapy with daunorubicin and cytarabine and maintenance therapy with interleukin-2 (IL-2). At present, the patient has discontinued IL-2 therapy, and the DCL has been in molecular remission for >3 years. The present case indicates that chemotherapy and IL-2 maintenance therapy are an effective treatment for DCL; hyperthyroidism was relieved following treatment, although hypothyroidism subsequently developed.
供体细胞白血病(DCL)是造血干细胞移植(HSCT)的一种罕见并发症,约占所有白血病复发病例的5%。在英文文献中,已报道了60多例DCL病例,然而,迄今为止,仅描述了2例因治疗重型再生障碍性贫血(SAA)而行HSCT后发生DCL的病例。在本研究中,介绍了一名25岁诊断为SAA的男性患者的病例,该患者接受了使用来自具有相同人类白细胞抗原的同胞的细胞进行的外周血干细胞移植(PBSCT)。该患者在PBSCT后2.5年发生急性髓系白血病,伴有(8;21)(q22;q22)易位,供体细胞中还有一条额外的8号染色体,在PBSCT后1年先出现了格雷夫斯病。白血病在1个周期的诱导治疗、2个周期的柔红霉素和阿糖胞苷巩固化疗以及白细胞介素-2(IL-2)维持治疗后实现了完全缓解。目前,患者已停止IL-2治疗,DCL已处于分子缓解状态超过3年。本病例表明,化疗和IL-2维持治疗是DCL的有效治疗方法;治疗后甲状腺功能亢进得到缓解,尽管随后出现了甲状腺功能减退。