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1
Incident cancers and late mortality in Australian children treated by allogeneic stem cell transplantation for non-malignant diseases.澳大利亚接受异基因干细胞移植治疗非恶性疾病的儿童的新发癌症和晚期死亡率。
Pediatr Blood Cancer. 2017 Jan;64(1):197-202. doi: 10.1002/pbc.26219. Epub 2016 Sep 26.
2
Four decades of stem cell transplantation for Fanconi anaemia in the Netherlands.荷兰范可尼贫血症的四十年干细胞移植历程。
Br J Haematol. 2016 Sep;174(6):952-61. doi: 10.1111/bjh.14165. Epub 2016 Jul 29.
3
Long-term Survival, Organ Function, and Malignancy after Hematopoietic Stem Cell Transplantation for Fanconi Anemia.范可尼贫血患者造血干细胞移植后的长期生存、器官功能及恶性肿瘤情况
Biol Blood Marrow Transplant. 2016 Jul;22(7):1257-1263. doi: 10.1016/j.bbmt.2016.03.007. Epub 2016 Mar 11.
4
Allogeneic hematopoietic stem cell transplantation in Fanconi anemia: the European Group for Blood and Marrow Transplantation experience.异基因造血干细胞移植治疗范可尼贫血:欧洲血液和骨髓移植学会经验。
Blood. 2013 Dec 19;122(26):4279-86. doi: 10.1182/blood-2013-01-479733. Epub 2013 Oct 21.
5
Late effects among pediatric patients followed for nearly 4 decades after transplantation for severe aplastic anemia.近 40 年随访的重型再生障碍性贫血患儿移植后晚期效应。
Blood. 2011 Aug 4;118(5):1421-8. doi: 10.1182/blood-2011-02-334953. Epub 2011 Jun 7.
6
Long-term survival and late deaths after allogeneic hematopoietic cell transplantation.异基因造血细胞移植后的长期生存和晚期死亡。
J Clin Oncol. 2011 Jun 1;29(16):2230-9. doi: 10.1200/JCO.2010.33.7212. Epub 2011 Apr 4.
7
Life expectancy in patients surviving more than 5 years after hematopoietic cell transplantation.造血细胞移植后生存超过 5 年的患者的预期寿命。
J Clin Oncol. 2010 Feb 20;28(6):1011-6. doi: 10.1200/JCO.2009.25.6693. Epub 2010 Jan 11.
8
The outcome of children with Fanconi anemia given hematopoietic stem cell transplantation and the influence of fludarabine in the conditioning regimen: a report from the Italian pediatric group.接受造血干细胞移植的范可尼贫血患儿的治疗结果及氟达拉滨在预处理方案中的影响:来自意大利儿科组的报告
Haematologica. 2007 Oct;92(10):1381-8. doi: 10.3324/haematol.11436.
9
Outcome of patients with acquired aplastic anemia given first line bone marrow transplantation or immunosuppressive treatment in the last decade: a report from the European Group for Blood and Marrow Transplantation (EBMT).过去十年中接受一线骨髓移植或免疫抑制治疗的获得性再生障碍性贫血患者的结局:欧洲血液和骨髓移植组(EBMT)的报告
Haematologica. 2007 Jan;92(1):11-8. doi: 10.3324/haematol.10075.
10
Unrelated donor bone marrow transplantation for the treatment of Fanconi anemia.无关供者骨髓移植治疗范科尼贫血。
Blood. 2007 Mar 1;109(5):2256-62. doi: 10.1182/blood-2006-07-036657. Epub 2006 Oct 12.

儿童骨髓衰竭综合征和重型再生障碍性贫血异基因骨髓移植后的晚期死亡率。

Late Mortality after Allogeneic Bone Marrow Transplantation in Childhood for Bone Marrow Failure Syndromes and Severe Aplastic Anemia.

机构信息

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.

出版信息

Biol Blood Marrow Transplant. 2019 Apr;25(4):749-755. doi: 10.1016/j.bbmt.2018.12.063. Epub 2018 Dec 20.

DOI:10.1016/j.bbmt.2018.12.063
PMID:30578940
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9990882/
Abstract

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.

摘要

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。