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Updated: Aug 8, 2026

Pre-clinical Evaluation of Tyrosine Kinase Inhibitors for Treatment of Acute Leukemia
Published on: September 18, 2013
[Evolution of the treatment of acute nonlymphoblastic leukemias in children (1968-1990)]
J J Ortega Aramburu1, T Olive Oliveras, G Javier Manchón
1Servicio de Hematología, Hospital M-Infantil Vall d'Hebrón, Barcelona.
Insights
Pediatric acute non-lymphoblastic leukemia (ANLL) treatment evolved significantly. Intensification therapy followed by bone marrow transplant (BMT) shows improved event-free survival in children with ANLL.
Area of Science:
- Pediatric Hematology Oncology
- Hematopoietic Stem Cell Transplantation
- Pediatric Acute Non-Lymphoblastic Leukemia (ANLL) Treatment
Context:
- Treatment of ANLL in children has evolved over 23 years (1968-1990).
- Advances in pediatric hematological units have improved outcomes.
- Early treatment regimens yielded limited long-term survival.
Purpose:
- To report changes in ANLL treatment over 23 years and recent advances.
- To evaluate the efficacy of intensive chemotherapy and bone marrow transplantation.
- To compare outcomes of different treatment strategies in pediatric ANLL.
Summary:
- Pre-1980 treatment achieved 75% complete remission (CR) but poor survival.
- Intensive chemotherapy (1981-1987) improved CR to 87.5% and 8-year event-free survival (EFS) to 22.5%.
- A 1988 protocol with intensified therapy and bone marrow transplant (BMT) achieved 65% 2-year EFS and 75% post-BMT relapse-free survival.
Impact:
- Intensification therapy followed by BMT (allogeneic or autologous) represents a significant advance.
- Improved EFS and relapse-free survival in pediatric ANLL patients.
- Establishes BMT as a potentially curative option for pediatric ANLL.
Abstract:
Changes in treatment of ANLL in children over 23 years (1968-90) and advances made in the last ten years in a pediatric hematological unit are reported herein. Of 124 patients under 15 years of age, 18 of whom were infants, 118 were evaluable. Of these, 58 were treated before 1980 and, although complete remission (CR) was attained in 75%, the median duration was lower than 12 months and no patient survived in CR more than 6 years. From 1981 to 1987, 40 patients received one or two induction treatments followed by three consolidations and then blocks of sequential intensive chemotherapy for 12-15 months. CR was attained in 87.5% and event-free survival (EFS) was 22.5% at 8 years: 14% for those treated from 1981 to 1983 and 33% for those included in the ANLL-84 protocol. In 1988, a post-remission protocol with intensification therapy (two high-dose ARA-C treatments combined with mitoxantrone in the first and amsacrine in the second) followed by allogeneic or autologous bone marrow transplant (BMT) was initiated. Of 20 patients included, 17 reached CR (85%) and 16 underwent BMT. EFS of the 20 patients was 65% at 2 years and post-BMT relapse-free survival was 75%. These results are compared with those obtained separately with present intensive chemotherapy protocols and with BMT and it is concluded that intensification treatment followed by BMT (allogeneic or autologous) might constitute an advance in the treatment of children with ANLL.
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