Muto Tomoya, Takeuchi Masahiro, Yamazaki Atsuko, Sugita Yasumasa, Tsukamoto Shokichi, Sakai Shio, Takeda Yusuke, Mimura Naoya, Ohwada Chikako, Sakaida Emiko, Aotsuka Nobuyuki, Iseki Tohru, Nakaseko Chiaki
Department of Hematology, Chiba University Hospital, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670, Japan.
Int J Hematol. 2015 Jul;102(1):86-92. doi: 10.1007/s12185-015-1779-z. Epub 2015 Mar 11.
Acute myeloid leukemia (AML) with mixed lineage leukemia-eleven-nineteen lysine-rich leukemia (MLL-ELL) is a rare subtype of MLL-rearranged AML. The outcome of allogeneic hematopoietic stem cell transplantation (allo-HSCT) for patients with this disease remains unknown. In the present study, we retrospectively investigated the efficacy of allo-HSCT in eight adult MLL-ELL-positive AML patients. Although all eight patients achieved first complete remission (CR1), three (37.5 %) patients experienced relapse after induction therapy. Five (62.5 %) patients underwent allo-HSCT during CR1, whereas two (25.0 %) underwent allo-HSCT during disease relapse, and one (12.5 %) during CR2. All three patients who received allo-HSCT beyond CR1 died due to AML progression after allo-HSCT. Of the five patients who received allo-HSCT during CR1, three (60.0 %) remained alive at study conclusion. The overall survival rate at five years was 50.0 %. Intriguingly, clonally expanded non-leukemic cells expressing MLL-ELL during consolidation therapy were found to be eradicated after allo-HSCT during the monitoring of minimal residual disease in one patient; this indicates that allo-HSCT is efficacious for eliminating pre-leukemic cells resistant to chemotherapy. In conclusion, allo-HSCT soon after CR1 represents a promising therapeutic option for adult AML patients with MLL-ELL, although the outcome of allo-HSCT for patients beyond CR1 was dismal.
伴有混合谱系白血病-11-19赖氨酸丰富白血病(MLL-ELL)的急性髓系白血病(AML)是MLL重排AML的一种罕见亚型。同种异体造血干细胞移植(allo-HSCT)治疗该疾病患者的疗效尚不清楚。在本研究中,我们回顾性调查了8例成年MLL-ELL阳性AML患者接受allo-HSCT的疗效。尽管所有8例患者均实现首次完全缓解(CR1),但3例(37.5%)患者在诱导治疗后复发。5例(62.5%)患者在CR1期间接受了allo-HSCT,而2例(25.0%)在疾病复发期间接受了allo-HSCT,1例(12.5%)在CR2期间接受了allo-HSCT。所有在CR1之后接受allo-HSCT的3例患者均因allo-HSCT后AML进展而死亡。在CR1期间接受allo-HSCT的5例患者中,3例(60.0%)在研究结束时仍存活。五年总生存率为50.0%。有趣的是,在一名患者的微小残留病监测中发现,巩固治疗期间表达MLL-ELL的克隆性扩增非白血病细胞在allo-HSCT后被清除;这表明allo-HSCT对于消除对化疗耐药的白血病前期细胞是有效的。总之,CR1后尽早进行allo-HSCT对于成年MLL-ELL阳性AML患者是一种有前景的治疗选择,尽管CR1之后患者接受allo-HSCT的结果不佳。