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Updated: Aug 13, 2026

Pre-clinical Evaluation of Tyrosine Kinase Inhibitors for Treatment of Acute Leukemia
Published on: September 19, 2013
[Alpha interferon in children with Philadelphia chromosome-positive chronic myeloid-leukaemia]
Raihane Ben Lakhal1, Lamia Aissaoui, Ramzi Jeddi
1Service d'hématologie de l'hôpital Aziza Othmana, Place du gouvernement la Kasba, Tunis.
Insights
Alpha interferon demonstrated therapeutic efficacy in pediatric patients with chronic myeloid leukemia (CML), showing a complete hematologic response. This treatment was generally well-tolerated, offering a potential alternative to bone marrow transplantation for children with CML.
Area of Science:
- Hematology
- Pediatric Oncology
- Pharmacology
Background:
- Chronic myeloid leukemia (CML) in pediatric patients requires effective and tolerable treatment options.
- Hydroxyurea was used as an initial therapy for all patients.
- Alpha interferon was administered after a median of 8 months of hydroxyurea treatment.
Observation:
- Five pediatric patients with CML were treated with alpha interferon between 1990 and 1999.
- Treatment involved alpha interferon at 5 million units/m2.
- Patients were followed up for therapeutic efficacy and toxicity.
Findings:
- All patients achieved a complete hematologic response six months after initiating alpha interferon therapy.
- The median overall survival was 66 months, with three patients still alive.
- Common side effects included mild symptoms like asthenia and fever; myelosuppression occurred in two patients.
Implications:
- Alpha interferon is well-tolerated in pediatric CML patients and may serve as an alternative to bone marrow transplantation for those in the chronic phase without a donor.
- Further evaluation of novel agents like STI 571 is warranted for pediatric CML treatment.
Abstract:
The present work focuses on the therapeutic efficacy and the toxicity of alpha interferon in patients younger than age 18 years. 5 patients younger than 18 years were treated and followed up between 1990 and 1999 at the department of haematology (Aziza Othmana Hospital) Hydroxyurea was given as initial treatment to all patients. After a median period of 8 months, these patients received alpha interferon (5 millions units/m2 once). Six months after the beginning of the alpha interferon a complete hematologic response was obtained in all patients. The median overall survival was of 66 months: 3 patients are still alive (2 patients in an advanced stage and one patient in chronic phase) and 2 patients died after transformation. The most common reported side effects of alpha interferon were asthenia, weight loss, fever, myalgia, chills and headaches--these toxic manifestations were mild and were noticed in all our patients. Myelosuppression was noted in two patients. Interferon is well tolerated in patients younger than age years 18 old, with CML. It may offer an alternative to bone marrow transplantation in children in the chronic phase of CML without histocompatible donor. The role of new agents such as STI 571 needs to be evaluated as well.
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