范科尼贫血
医学
造血干细胞移植
骨髓衰竭
救世主兄弟
全身照射
氟达拉滨
环磷酰胺
外科
贫血
干细胞
移植物抗宿主病
内科学
移植
胃肠病学
造血
化疗
化学
DNA修复
基因
生物
生物化学
遗传学
作者
Ahmad Alhuraiji,Hazza Al-Zahrani,Fahad Al Mohareb,Naeem Chaudhri,Fahad Alsharif,Mohamed Sy,Walid Rasheed,Ghuzayel Aldawsari,Syed Osman Ahmed,Mahmoud Aljurf
出处
期刊:Experimental and Clinical Transplantation
[Baskent University Publishers]
日期:2016-12-01
卷期号:14 (6)
被引量:1
标识
DOI:10.6002/ect.2015.0364
摘要
Fanconi anemia is a congenital bone marrow failure syndrome that is associated with congenital anomalies and increased risk of cancer. Hematopoietic stem cell transplant is a potentially curative modality for bone marrow failure in Fanconi anemia patients. Here, we report our center's experience regarding adolescent and young adult patients with Fanconi anemia and hematopoietic stem cell transplant.We conducted a retrospective patient record analyses of patients who presented at our center from 1988 to 2014. We included patients greater than 14 years old with confirmed Fanconi anemia based on positive chromosome breakage study and who underwent hematopoietic stem cell transplant at our institution.Our study group comprised 12 patients with Fanconi anemia who underwent hematopoietic stem cell transplant at our institution. The median age was 20 years (range, 14-31 y) with a female predominance of 83%. Low-dose cyclophosphamide (20-80 mg/kg)-based conditioning regimens were used with different combinations that included fludarabine, antithymocyte globulin, or total body irradiation. All patients had HLA-matched sibling grafts. In all patients, stem cell source was the bone marrow. All patients showed engraftment. Four patients (33%) developed acute graft-versus-host disease. Three patients (25%) died early before day 100 after hematopoietic stem cell transplant due to infectious complications, with 1 patient having steroid refractory acute graft-versus-host disease. Overall survival was 75% at a median follow-up of 43 months. All patients who survived are well and remained transfusion independent without evidence of secondary malignancy.Our findings support the feasibility of reduced intensity conditioning allogeneic hematopoietic stem cell transplant in older and more heavily pretreated patients with Fanconi anemia, especially for those who are engrafted.
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