Aoki Jun, Ishiyama Ken, Taniguchi Shuichi, Fukuda Takahiro, Ohashi Kazuteru, Ogawa Hiroyasu, Kanamori Heiwa, Eto Tetsuya, Iwato Koji, Sakamaki Hisashi, Morishima Yasuo, Nagamura Tokiko, Atsuta Yoshiko, Takami Akiyoshi
Department of Hematology, Tokyo Metropolitan Cancer and Infectious Disease Center, Komagome Hospital, Tokyo, Japan; Department of Hematology, Tokyo Metropolitan Otsuka Hospital, Tokyo, Japan; Department of Hematology, Kanagawa Cancer Center, Yokohama, Japan.
Department of Hematology, Tokyo Metropolitan Cancer and Infectious Disease Center, Komagome Hospital, Tokyo, Japan; Department of Hematology, Tokyo Metropolitan Otsuka Hospital, Tokyo, Japan.
Biol Blood Marrow Transplant. 2014 Dec;20(12):2029-33. doi: 10.1016/j.bbmt.2014.09.001. Epub 2014 Sep 6.
Central nervous system (CNS) involvement in adult acute myeloid leukemia (AML) is rare and associated with poor outcomes. Therefore, CNS involvement in AML is an indicator for allogeneic hematopoietic stem cell transplantation (allo-HSCT). However, the impact of CNS involvement in AML on the outcome of allo-HSCT remains unclear. We performed a large-scale nationwide retrospective analysis to elucidate the outcomes of allo-HSCT on AML with CNS involvement (CNS+AML). Clinical data were collected from a registry database of the Japan Society for Hematopoietic Cell Transplantation. CNS involvement was defined as the infiltration of leukemia cells into the CNS or myeloid sarcoma in the CNS identified at any time from diagnosis to transplantation. One hundred fifty-seven patients with CNS+AML underwent allo-HSCT between 2006 and 2011. The estimated overall survival, cumulative incidence of relapse and nonrelapse mortality at 2 years for CNS+AML (51.2%, 30.2%, and 14.5%, respectively) were comparable with those for AML without CNS involvement (48.6%, 27.4%, and 22.0%, respectively). Univariate and multivariate analyses indicated that the development of chronic graft-versus-host disease, disease status, and cytogenetic risk category were independent prognostic factors for overall survival for CNS+AML. These results suggest that allo-HSCT may improve outcomes in patients with CNS+AML.
中枢神经系统(CNS)受累于成人急性髓系白血病(AML)较为罕见,且与不良预后相关。因此,AML中的CNS受累是异基因造血干细胞移植(allo-HSCT)的一个指标。然而,AML中的CNS受累对allo-HSCT结局的影响仍不清楚。我们进行了一项大规模的全国性回顾性分析,以阐明allo-HSCT对伴有CNS受累的AML(CNS+AML)的治疗结局。临床数据来自日本造血细胞移植学会的登记数据库。CNS受累定义为从诊断到移植的任何时间发现白血病细胞浸润至CNS或CNS中的髓系肉瘤。2006年至2011年间,157例CNS+AML患者接受了allo-HSCT。CNS+AML患者2年时的估计总生存率、累积复发率和非复发死亡率(分别为51.2%、30.2%和14.5%)与无CNS受累的AML患者(分别为48.6%、27.4%和22.0%)相当。单因素和多因素分析表明,慢性移植物抗宿主病的发生、疾病状态和细胞遗传学风险类别是CNS+AML患者总生存的独立预后因素。这些结果表明,allo-HSCT可能改善CNS+AML患者的治疗结局。