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1991 - 2012年伊朗儿童造血干细胞移植

Hematopoietic SCT in Iranian children 1991-2012.

作者信息

Hamidieh A A, Behfar M, Babaki A E S, Jalali A, Hosseini A-S, Jahani M, Alimoghaddam K, Ghavamzadeh A

机构信息

Hematology-Oncology and Stem Cell Transplantation Research Center/Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Bone Marrow Transplant. 2015 Apr;50(4):517-22. doi: 10.1038/bmt.2014.299. Epub 2015 Jan 19.

DOI:10.1038/bmt.2014.299
PMID:25599168
Abstract

This study presents the pediatric hematopoietic SCT (HSCT) activity in Iran between 1991 and 2012. Overall, 1105 fifteen-year-old or younger patients have undergone HSCT (975 allogeneic and 130 autologous). Annual HSCTs have been increasing steadily since 2007. HLA-matched siblings and other related donors were the main source of HSCs, although since 2008 a national HLA registry has been established to fill the gap for patients lacking a related donor. Inherited abnormalities of RBCs (45.88%), leukemias (27.6%) and BM failure syndromes (11.94%) constituted the majority of HSCTs during this period. Two-year overall survival and disease-free survival rates for all patients were 74.2% (95% confidence interval (CI): 71.6-77) and 66.3% (95% CI: 63.5-69.3), respectively. Leading cause of death in allogeneic group was TRM (165 deaths) and relapse caused the majority of deaths in the autologous group (39 deaths). All HSCTs from the beginning have been performed exclusively with TBI-free-conditioning regimens, which provides unique data for comparison with activities of other centers. Encouraging survival rates provide a basis for future studies on the extensive applicability of TBI-free-conditioning regimens in pediatric HSCT.

摘要

本研究展示了1991年至2012年间伊朗儿科造血干细胞移植(HSCT)的情况。总体而言,1105名15岁及以下患者接受了HSCT(975例为异基因移植,130例为自体移植)。自2007年以来,每年的HSCT数量一直在稳步增加。HLA匹配的同胞及其他相关供者是造血干细胞的主要来源,不过自2008年起已建立了全国性HLA登记处,以填补缺乏相关供者患者的缺口。在此期间,红细胞遗传性异常(45.88%)、白血病(27.6%)和骨髓衰竭综合征(11.94%)构成了HSCT的大多数。所有患者的两年总生存率和无病生存率分别为74.2%(95%置信区间(CI):71.6 - 77)和66.3%(95%CI:63.5 -

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Eur J Haematol. 2014 Apr;92(4):331-6. doi: 10.1111/ejh.12244. Epub 2014 Jan 10.
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Challenges and opportunities for international cooperative studies in pediatric hematopoeitic cell transplantation: priorities of the Westhafen Intercontinental Group.儿科造血细胞移植国际合作研究的挑战与机遇:威斯特法伦洲际组的优先事项。
Biol Blood Marrow Transplant. 2013 Sep;19(9):1279-87. doi: 10.1016/j.bbmt.2013.07.006. Epub 2013 Jul 21.
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急性髓系白血病患者异基因造血干细胞移植中的感染情况调查
Int J Organ Transplant Med. 2018;9(3):112-116. Epub 2018 Aug 1.
Outcomes of haematopoietic stem cell transplantation for inherited metabolic disorders: a report from the Australian and New Zealand Children's Haematology Oncology Group and the Australasian Bone Marrow Transplant Recipient Registry.
遗传性代谢疾病造血干细胞移植的结果:来自澳大利亚和新西兰儿童血液肿瘤学组及澳大拉西亚骨髓移植受者登记处的报告。
Pediatr Transplant. 2013 Sep;17(6):582-8. doi: 10.1111/petr.12109. Epub 2013 Jun 27.
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Hematopoietic stem cell transplantation with a reduced-intensity conditioning regimen in pediatric patients with Griscelli syndrome type 2.采用减低剂量预处理方案对2型格里塞利综合征患儿进行造血干细胞移植。
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