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Bone marrow transplantation for beta-thalassemia

被引：47
作者：
Giardini, C
Lucarelli, G
机构：
[1] Azienda Ospedaliera S Salvatore, Div Ematol, Pesaro, Italy
[2] Azienda Ospedliera S Salvatore, Ctr Trapianto Midollo Osseo, Pesaro, Italy
来源：
HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA | 1999年 / 13卷 / 05期
关键词：
D O I：
10.1016/S0889-8588(05)70109-X
中图分类号：
R73 [肿瘤学];
学科分类号：
100214 ;
摘要：
Bone marrow transplantation in thalassemia represents the only form of radical cure of this disease. Patients younger than 17 years are divided into three classes of risk according to the presence or absence of portal fibrosis, hepatomegaly, and history of adequate chelation treatment. Patients older than 16 years are categorized as adult thalassemics. Survival and event-free survival are 93% and 91% for Class 1, 87% and 83% for Class 2, and 79% and 58% for Class 3, respectively. Adult patient survival is 66% and event-free survival is 62%.
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收藏
页码：1059 / +
页数：7
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