Pediatric Oncology and Hematology, Skåne University Hospital, Lund, Sweden; Department of Clinical Sciences, Lund University, Lund, Sweden.
Institute for Cancer Outcomes and Survivorship, University of Alabama at Birmingham, Birmingham, Alabama.
Biol Blood Marrow Transplant. 2019 Apr;25(4):749-755. doi: 10.1016/j.bbmt.2018.12.063. Epub 2018 Dec 20.
Children with bone marrow failure syndromes and severe aplastic anemia (SAA) are treated with allogeneic blood or marrow transplantation (BMT). However, there is a paucity of studies examining late mortality risk after allogeneic BMT performed in childhood for bone marrow failure syndromes and SAA and evaluating how this risk differs between these diseases. We investigated cause-specific late mortality in 2-year survivors of allogeneic BMT for bone marrow failure syndromes and SAA performed before age 22years between 1974 and 2010 at 2 US transplantation centers. Vital status information was collected from medical records, the National Death Index, and Accurint databases. Overall survival was calculated using Kaplan-Meier techniques. The standardized mortality ratio (SMR) was calculated using age- sex-, and calendar-specific mortality rates from the Centers for Disease Control and Prevention. Among the 2-year survivors of bone marrow failure syndromes (n = 120) and SAA (n = 147), there were 15 and 19 deaths, respectively, yielding an overall survival of 86.4% for bone marrow failure syndromes and 93.1% for SAA at 15years post-BMT. Compared with the general population, patients with bone marrow failure syndromes were at a higher risk for premature death (SMR, 22.7; 95% CI, 13.1 to 36.2) compared with those with SAA (SMR, 4.5; 95% CI, 2.8 to 7.0) (P < .0001). The elevated relative risk persisted at ≥15years after BMT for both diseases. The hazard of all-cause late mortality was 2.9-fold (95% CI, 1.1 to 7.3) higher in patients with bone marrow failure syndromes compared with those with SAA. The high late mortality risk in recipients of allogeneic BMT in childhood for bone marrow failure syndromes calls for intensified life-long follow-up.
患有骨髓衰竭综合征和严重再生障碍性贫血 (SAA) 的儿童接受异基因血液或骨髓移植 (BMT) 治疗。然而,对于儿童时期因骨髓衰竭综合征和 SAA 而进行的异基因 BMT 后晚期死亡率风险的研究很少,并且评估这些疾病之间的风险差异。我们调查了在 1974 年至 2010 年间在美国 2 个移植中心接受异基因 BMT 的 2 岁幸存者的特定病因的晚期死亡率,这些患者的年龄均小于 22 岁,患有骨髓衰竭综合征和 SAA。通过病历、国家死亡索引和 Accurint 数据库收集生存状态信息。使用 Kaplan-Meier 技术计算总生存率。使用疾病预防控制中心的年龄、性别和日历特异性死亡率计算标准化死亡率比 (SMR)。在骨髓衰竭综合征 (n=120) 和 SAA (n=147) 的 2 岁幸存者中,分别有 15 例和 19 例死亡,BMT 后 15 年的总生存率分别为骨髓衰竭综合征 86.4%和 SAA 93.1%。与普通人群相比,骨髓衰竭综合征患者的早逝风险更高 (SMR,22.7;95%CI,13.1 至 36.2),而 SAA 患者的早逝风险则较低 (SMR,4.5;95%CI,2.8 至 7.0) (P<0.0001)。这一相对风险在 BMT 后至少 15 年仍然存在。与 SAA 相比,骨髓衰竭综合征患者的全因晚期死亡率的危险比为 2.9 倍 (95%CI,1.1 至 7.3)。骨髓衰竭综合征患儿接受异基因 BMT 的晚期死亡率高,需要加强终身随访。