Department of Pediatrics, Kagoshima University Graduate School of Medical and Dental Sciences, 8-35-1 Sakuragaoka, Kagoshima, 890-8544, Japan.
Department of Pediatrics, Fujita Health University Hospital, 1-98 Dengakugakubo Kutsukake-cho, Toyoake-city, Aichi, 470-1192, Japan.
Bone Marrow Transplant. 2019 Sep;54(9):1489-1498. doi: 10.1038/s41409-019-0461-0. Epub 2019 Feb 4.
Allogeneic hematopoietic stem cell transplantation (HSCT) can be used to treat children with refractory acute myeloid leukemia (AML). This retrospective analysis aimed to describe the outcomes and risk factors in such children. Data were collected through the nation-wide registry program in Japan. A total of 417 AML (median age: 13 years) patients 20 years or younger at HSCT, between January 2001 and December 2015, were included. A total of 314 patients died, and the median follow-up duration of the survivors was 1052 days. The most frequent cause of death was leukemia progression (58%). The 3-year overall survival (OS) rate was 23% (95% confidence interval [CI]: 19-28%). Chronic GVHD was associated with improved 3-year OS (47%, 95% CI, 36-57%, hazard ratio: 0.603, p = 0.001). Low performance status, presence of more than 25% of marrow blasts, presence of blasts in the blood at transplantation, FAB (other than M1 or M2), male donors, and number of transplantations ≥ 2 were adverse pre-HSCT variables. Patients with 0, 1-2, 3-4, 5, and 6-7 pre-HSCT variables had 3-year OS rates of 52%, 32%, 19%, 8, and 0%, respectively. Our findings may help experts decide if HSCT should be performed in such cases.
异基因造血干细胞移植(HSCT)可用于治疗难治性急性髓系白血病(AML)患儿。本回顾性分析旨在描述此类患儿的结局和相关风险因素。研究数据来自日本全国性注册研究项目。共纳入 417 例年龄 20 岁及以下、于 2001 年 1 月至 2015 年 12 月期间接受 HSCT 的 AML 患儿(中位年龄:13 岁)。共有 314 例患儿死亡,幸存者的中位随访时间为 1052 天。最常见的死亡原因为白血病进展(58%)。3 年总生存率(OS)为 23%(95%置信区间[CI]:19-28%)。慢性移植物抗宿主病(GVHD)与 3 年 OS 改善相关(47%,95%CI:36-57%,风险比:0.603,p=0.001)。低体能状态、骨髓原始细胞比例超过 25%、移植时血液中存在原始细胞、FAB 分型(非 M1 或 M2)、供者为男性以及移植次数≥2 是 HSCT 前的不良预后因素。HSCT 前存在 0、1-2、3-4、5 和 6-7 个不良预后因素的患儿 3 年 OS 率分别为 52%、32%、19%、8%和 0%。本研究结果可能有助于专家判断此类患儿是否应进行 HSCT。