Author/Authors :
Nedaeifard, L Hematology Oncology and Bone Marrow Transplantation Research Center - Shariati Hospital - School of Medicine - Medical Sciences/University of Tehran - Tehran, Iran , Iravani, M Hematology Oncology and Bone Marrow Transplantation Research Center - Shariati Hospital - School of Medicine - Medical Sciences/University of Tehran - Tehran, Iran , Alimoghaddam, K Hematology Oncology and Bone Marrow Transplantation Research Center - Shariati Hospital - School of Medicine - Medical Sciences/University of Tehran - Tehran, Iran , Bahar, B Hematology Oncology and Bone Marrow Transplantation Research Center - Shariati Hospital - School of Medicine - Medical Sciences/University of Tehran - Tehran, Iran , Jahani, M Hematology Oncology and Bone Marrow Transplantation Research Center - Shariati Hospital - School of Medicine - Medical Sciences/University of Tehran - Tehran, Iran , Ashouri, A Hematology Oncology and Bone Marrow Transplantation Research Center - Shariati Hospital - School of Medicine - Medical Sciences/University of Tehran - Tehran, Iran , Ghavamzadeh, A Hematology Oncology and Bone Marrow Transplantation Research Center - Shariati Hospital - School of Medicine - Medical Sciences/University of Tehran - Tehran, Iran , Mousavi, A Hematology Oncology and Bone Marrow Transplantation Research Center - Shariati Hospital - School of Medicine - Medical Sciences/University of Tehran - Tehran, Iran , ,
Abstract :
Hematopoietic cell transplantation (HCT) is an accepted treatment for acute myeloid
leukemia (AML) in first remission, the treatment of choice for chronic myeloid leukemia (CML) and
high risk groups of ALL who relapse with conventional chemotherapy. We assessed results of HCT for
pediatric leukemia in our center. A total of 92 children, 63 with diagnose of AML, 23 with ALL and 6
with CML received allogeneic transplantation from HLA full matched siblings (57.6%) and autologous
transplantation (42.4%). Source of hematopoietic cells were peripheral blood 83.7%, bone marrow
15.2% and cord blood 1.6%. The median transplanted nucleated cells were 6.4 ± 4.7 ×108 /Kg (body
weight of patients) and mononuclear cells were 5.5 ± 2.9×108/Kg. The most common conditioning
regimens were cyclophosphamide + busulfan. Prophylaxis regimen for GVHD was cyclosporin ±
methotrexate. GVHD occurred in 50 (54.3%) patients. Eighty five of children had engraftment, 26
(28.6%) relapsed and 57 (62%) are alive. The most common cause of death was relapse (68.6%). Five
years overall survival of patients with AML and ALL were 49% and 44% respectively and disease free
survival of them were 52% and 49%. One year overall survival and disease free survival of CML was
57%. Overall survival increased with increasing age of patients at transplantation time (P = 0.06).
Longer survival significantly related to earlier WBC and platelet recovery (P < 0.0001 and P = 0.006
respectively). Considering acceptable overall and disease free survival of patients after HCT, we
concluded that is a good modality in treatment of leukemia of children.