Vermylen C, Cornu G
Department of Pediatric Hematology, Cliniques Saint Luc, University of Louvain, Brussels, Belgium.
Curr Opin Hematol. 1997 Nov;4(6):377-80. doi: 10.1097/00062752-199704060-00003.
Hematopoietic stem cell transplantation is the only therapy able to cure sickle cell anemia at the present time. So far, transplantations have been undertaken in approximatively 140 sickle cell patients all over the world, with good results. The selection of patients for transplantation remains a subject of dilemma because of the unpredictable course of the disease and the lack of valuable prognostic markers. The selection criteria accepted so far concern young patients under the age of 16, with a morbid course of the disease and having a HLA-compatible sibling. In Belgium, patients going back to their country of origin were also considered for transplantation. For 100 patients who underwent transplantation in Europe, the current Kaplan-Meier estimates of overall survival, event-free survival, and disease-free survival rates are 90%, 79%, and 81%, respectively. Benefits and side effects are analyzed.
造血干细胞移植是目前唯一能够治愈镰状细胞贫血的疗法。迄今为止,全球约140例镰状细胞病患者接受了移植,效果良好。由于疾病进程不可预测且缺乏有价值的预后标志物,移植患者的选择仍然是一个两难的问题。目前公认的选择标准是年龄在16岁以下、疾病进程严重且有人类白细胞抗原(HLA)相匹配同胞的年轻患者。在比利时,回到原籍国的患者也被考虑进行移植。在欧洲接受移植的100例患者中,目前采用Kaplan-Meier法估计的总生存率、无事件生存率和无病生存率分别为90%、79%和81%。文中分析了其益处和副作用。