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Two decades of experience in a combined adult/pediatric allogeneic hematopoietic stem cell transplantation center in Algiers, Algeria

医学 造血干细胞移植 移植 血液学 再生障碍性贫血 人口 儿科 地中海贫血 内科学 范科尼贫血 骨髓 生物 环境卫生 生物化学 DNA修复 基因
作者
Malek Benakli,Redhouane Ahmed Nacer,Farih Mehdid,Rachida Belhadj,Amina Talbi,Nadia Rahmoune,Christian Niederwieser,Mounira Baazizi,Sabrina Akhrouf,Dina Ait Ouali,Hanane Bouarab,Sara Zerkout,Imene Abderahim,Farida Harieche,Rose‐Marie Hamladji
出处
期刊:Annals of Hematology [Springer Science+Business Media]
卷期号:99 (3): 619-625 被引量:3
标识
DOI:10.1007/s00277-020-03914-w
摘要

Hematopoietic stem cell transplantation (HSCT) has evolved from an experimental to a successful treatment modality reaching worldwide 80.000 HSCT/year. Distribution and trends of HSCT, however, remain heterogeneous. Activities range from none to more than 511/10 million population between countries and regions. Here, we report on a successful autologous and allogeneic HSCT program for adult and pediatric patients started two decades ago in Northern Africa. From 1998 to December 2017, a total of 2828 HSCT was performed of which 2059 were allo-HSCT (1474 adults and 585 children). The activities were analyzed according to indication, donor type, stem cell source, and trends over time. There was a significant difference in indications according to age. Adult patients were transplanted more often for hematological malignancies. In children, the indications were distributed equally between malignant and non-malignant diseases. Overall activities increased substantially in AML and to a lower extent in ALL and CLL despite sharp reduction of activity in CML after 2005. Finally, a higher transplantation rate (33/10 million population) was reached as compared to most regions of the world except Europe and USA/Canada. Overall survival in children with AML was 56.0% at 15 years, in adults 61.3% at 5 years, and in patients with CML 55.5% at 15 years without difference between reduced intensity condition (RIC) and myeloablative conditioning (MAC). Patients with Ph+ ALL had the lowest survival reaching 26.7% at 5 years. Highest survival was observed in patients with aplastic anemia, Fanconi anemia, and thalassemia reaching 77.3%, 73.5%, and 75.7% at 15 years respectively. Long distances and late referral remain a challenge for this large country.

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