• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Secular trends in outcomes for Fanconi anemia patients who receive transplants: implications for future studies.

作者信息

Rosenberg Philip S, Alter Blanche P, Socié Gerard, Gluckman Eliane

机构信息

Biostatistics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Rockville, MD 20852, USA.

出版信息

Biol Blood Marrow Transplant. 2005 Sep;11(9):672-9. doi: 10.1016/j.bbmt.2005.05.007.

DOI:10.1016/j.bbmt.2005.05.007
PMID:16125637
Abstract

Transplantation protocols for patients with Fanconi anemia are being modified continuously. However, it is unclear how outcomes have changed over time. We determined historical adverse event rates from long-term follow-up of 117 Fanconi anemia patients in the Hôpital Saint Louis transplant cohort, who received low-dose cyclophosphamide- and irradiation-based conditioning, in combination with other modalities, between 1976 and October 2002. In high-risk patients with mismatched donors, the peritransplantation mortality rate during 0 to 6 months declined significantly over time (P = .003), from 28%/month (95% confidence interval [CI], 9%-87%/month) during 1985 to 1989 to 3.3%/month (95% CI, 0.8%-13.3%/month) during 2000 to October 2002. The corresponding proportion of patients who developed severe acute graft-versus-host disease also declined significantly over time (P = .003). In low-risk patients with matched sibling donors, the peritransplantation mortality rate was consistently low, 1.4%/month (95% CI, 0.3%-5.3%/month), during 1990 to October 2002. Sample sizes to detect 2-fold reductions from rates and risks observed since the mid-1990s are larger than recently reported case series. To demonstrate further advances in survival, transplant centers may need to coordinate their protocols and engage in multicenter collaborative studies.

摘要

相似文献

1
Secular trends in outcomes for Fanconi anemia patients who receive transplants: implications for future studies.
Biol Blood Marrow Transplant. 2005 Sep;11(9):672-9. doi: 10.1016/j.bbmt.2005.05.007.
2
Successful prevention of acute graft-versus-host disease using low-dose antithymocyte globulin after mismatched, unrelated, hematopoietic stem cell transplantation for acute myelogenous leukemia.在急性髓系白血病患者接受不匹配、非亲属造血干细胞移植后,使用低剂量抗胸腺细胞球蛋白成功预防急性移植物抗宿主病。
Biol Blood Marrow Transplant. 2009 Jun;15(6):704-17. doi: 10.1016/j.bbmt.2009.02.010. Epub 2009 Apr 9.
3
Unrelated donor bone marrow transplants for severe aplastic anemia with conditioning using total body irradiation and cyclophosphamide.采用全身照射和环磷酰胺进行预处理的无关供者骨髓移植治疗重型再生障碍性贫血。
Biol Blood Marrow Transplant. 2007 Jul;13(7):863-70. doi: 10.1016/j.bbmt.2007.03.013. Epub 2007 May 24.
4
Fludarabine-based cytoreductive regimen and T-cell-depleted grafts from alternative donors for the treatment of high-risk patients with Fanconi anaemia.基于氟达拉滨的细胞减灭方案及来自替代供体的T细胞去除移植物用于治疗高危范可尼贫血患者
Br J Haematol. 2008 Mar;140(6):644-55. doi: 10.1111/j.1365-2141.2007.06975.x.
5
Bone marrow transplantation from matched related donors for patients with Fanconi anemia using low-dose busulfan and cyclophosphamide as conditioning.采用低剂量白消安和环磷酰胺进行预处理,对范可尼贫血患者进行匹配相关供者的骨髓移植。
Pediatr Blood Cancer. 2006 Apr;46(4):496-500. doi: 10.1002/pbc.20286.
6
Favourable long-term outcome after matched sibling transplantation for Fanconi-anemia (FA) and in vivo T-cell depletion.范可尼贫血(FA)同胞匹配移植及体内T细胞清除后的良好长期预后。
Klin Padiatr. 2008 May-Jun;220(3):147-52. doi: 10.1055/s-2008-1065326.
7
Matched sibling donor haematopoietic stem cell transplantation in Fanconi anaemia: an update of the Cincinnati Children's experience.范可尼贫血中匹配同胞供者造血干细胞移植:辛辛那提儿童医院经验的最新情况
Br J Haematol. 2007 Feb;136(4):633-40. doi: 10.1111/j.1365-2141.2006.06460.x.
8
Bone marrow transplants from mismatched related and unrelated donors for severe aplastic anemia.来自不匹配的亲属和非亲属供体的骨髓移植治疗重型再生障碍性贫血。
Bone Marrow Transplant. 2006 Apr;37(7):641-9. doi: 10.1038/sj.bmt.1705299.
9
Matched-related allogeneic stem cell transplantation in Saudi patients with Fanconi anemia: 10 year's experience.沙特范可尼贫血患者的单倍体相合异基因干细胞移植:10年经验
Bone Marrow Transplant. 2008 Aug;42 Suppl 1:S45-S48. doi: 10.1038/bmt.2008.114.
10
Allogeneic bone marrow transplants for Fanconi anemia. A preliminary report from the International Bone Marrow Transplant Registry.范可尼贫血的异基因骨髓移植。来自国际骨髓移植登记处的初步报告。
Bone Marrow Transplant. 1992;10 Suppl 1:53-7.

引用本文的文献

1
A self-repair history: compensatory effect of a variant on the c.2778+83C>G splicing mutation.一段自我修复历程:一个变异对c.2778+83C>G剪接突变的补偿作用。
Front Genet. 2023 Jul 20;14:1209138. doi: 10.3389/fgene.2023.1209138. eCollection 2023.
2
Busulfan Pharmacokinetics and Precision Dosing: Are Patients with Fanconi Anemia Different?白消安药代动力学和精准用药:范可尼贫血患者是否不同?
Biol Blood Marrow Transplant. 2019 Dec;25(12):2416-2421. doi: 10.1016/j.bbmt.2019.07.014. Epub 2019 Jul 18.
3
Radiation-free, alternative-donor HCT for Fanconi anemia patients: results from a prospective multi-institutional study.
范可尼贫血患者的无辐射、替代供体造血细胞移植:一项前瞻性多机构研究的结果
Blood. 2017 Apr 20;129(16):2308-2315. doi: 10.1182/blood-2016-09-743112. Epub 2017 Feb 8.
4
Late effects in patients with Fanconi anemia following allogeneic hematopoietic stem cell transplantation from alternative donors.范可尼贫血患者接受来自替代供体的异基因造血干细胞移植后的晚期效应。
Bone Marrow Transplant. 2016 Jul;51(7):938-44. doi: 10.1038/bmt.2016.32. Epub 2016 Mar 21.
5
Neonatal manifestations of inherited bone marrow failure syndromes.遗传性骨髓衰竭综合征的新生儿表现。
Semin Fetal Neonatal Med. 2016 Feb;21(1):57-65. doi: 10.1016/j.siny.2015.12.003. Epub 2015 Dec 24.
6
Twenty years of the Italian Fanconi Anemia Registry: where we stand and what remains to be learned.意大利范可尼贫血登记处二十年:我们所处的位置以及仍有待了解的内容。
Haematologica. 2016 Mar;101(3):319-27. doi: 10.3324/haematol.2015.133520. Epub 2015 Dec 3.
7
Fanconi Anemia with MDS RAEB-2 Rapidly Progressing to AML in a 5-Year-Old Boy.一名5岁男孩患范可尼贫血合并MDS-RAEB-2,迅速进展为急性髓系白血病。
Indian J Hematol Blood Transfus. 2014 Sep;30(Suppl 1):379-82. doi: 10.1007/s12288-014-0424-y. Epub 2014 Jul 1.
8
Fanconi anemia.范科尼贫血
Hematol Oncol Clin North Am. 2009 Apr;23(2):193-214. doi: 10.1016/j.hoc.2009.01.008.
9
HLA-matched related donor hematopoietic cell transplantation in 43 patients with Fanconi anemia conditioned with 60 mg/kg of cyclophosphamide.43例范可尼贫血患者接受60mg/kg环磷酰胺预处理后进行人白细胞抗原匹配的相关供者造血细胞移植。
Biol Blood Marrow Transplant. 2007 Dec;13(12):1455-60. doi: 10.1016/j.bbmt.2007.08.004. Epub 2007 Oct 18.