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异基因造血干细胞移植治疗高危细胞遗传学 AML 患儿和青少年:FUS-ERG 阳性病例的结局明显较差。

Allogeneic hematopoietic stem cell transplantation for children and adolescents with high-risk cytogenetic AML: distinctly poor outcomes of FUS-ERG-positive cases.

机构信息

Children's Cancer Center, National Center for Child Health and Development, Tokyo, Japan.

Department of Pediatric Hematology and Oncology Research, National Research Institute for Child Health and Development, Tokyo, Japan.

出版信息

Bone Marrow Transplant. 2019 Mar;54(3):393-401. doi: 10.1038/s41409-018-0273-7. Epub 2018 Jun 29.

Abstract

Allocating patients with acute myeloid leukemia and high-risk cytogenetic abnormalities (HR-AML) for allogeneic hematopoietic stem cell transplantation (allo-HSCT) is part of the standard treatment protocol; however, whether allo-HSCT truly improves the outcomes in these patients is debatable. Data on 169 children and adolescents with HR-AML who received their first allo-HSCT in first or second remission between 2000 and 2015 were extracted from a nationwide, Japanese HSCT registry. The 3-year disease-free survival (DFS) and overall survival (OS) rates were 55.2% (95% CI, 46.8-62.9%) and 69.6% (61.4-76.3%), respectively, for all the HR-AML patients. In univariate analysis, the cytogenetic subgroup had a significant impact on both the DFS (P = 0.011) and OS (P < 0.001) rates. In particular, 14 patients with t(16;21) showed an extremely poor outcome. Additionally, older age at allo-HSCT (10-19 years old, P = 0.025), myeloablative conditioning with total-body irradiation (P = 0.019), and grade II-IV acute graft-versus-host disease (GVHD, P = 0.049) were associated with inferior OS. The donor type and occurrence of chronic GVHD did not affect the outcome. Multivariate analysis revealed t(16;21) to be associated with increased overall mortality (hazard ratio = 4.416, P < 0.001). Because the outcome of patients with certain HR-AML subgroups, such as t(16;21)-positive cases, is extremely poor even with allo-HSCT in remission, a novel therapy is urgently required.

摘要

将伴有高危细胞遗传学异常(HR-AML)的急性髓细胞白血病患者分配进行异体造血干细胞移植(allo-HSCT)是标准治疗方案的一部分;然而,allo-HSCT 是否确实能改善这些患者的预后仍存在争议。从日本全国性的 HSCT 登记处提取了 2000 年至 2015 年间首次缓解期(首次或第二次缓解)接受首次 allo-HSCT 的 169 例儿童和青少年 HR-AML 患者的数据。所有 HR-AML 患者的 3 年无病生存率(DFS)和总生存率(OS)分别为 55.2%(95%CI,46.8-62.9%)和 69.6%(61.4-76.3%)。在单因素分析中,细胞遗传学亚组对 DFS(P=0.011)和 OS(P<0.001)率均有显著影响。特别是 14 例 t(16;21)患者的预后极差。此外,allo-HSCT 时年龄较大(10-19 岁,P=0.025)、全身照射的清髓性预处理(P=0.019)和 2-4 级急性移植物抗宿主病(GVHD,P=0.049)与较差的 OS 相关。供者类型和慢性 GVHD 的发生不影响结果。多因素分析显示 t(16;21)与总死亡率增加相关(危险比=4.416,P<0.001)。由于某些 HR-AML 亚组(如 t(16;21)阳性病例)的患者即使在缓解期进行 allo-HSCT,其预后也极差,因此迫切需要新的治疗方法。

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