Outcomes of pediatric acute myeloid leukemia treatment in Western Kenya
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Updated: Oct 12, 2025

Pre-clinical Evaluation of Tyrosine Kinase Inhibitors for Treatment of Acute Leukemia
Published on: September 18, 2013
Romy E van Weelderen1,2, Festus Njuguna3, Kim Klein1,4
1Pediatric Oncology, Emma Children's Hospital, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Insights
Pediatric acute myeloid leukemia (AML) survival is poor in Kenya, with 2-year survival rates of 4-7%. Improving supportive care and reducing treatment delays are crucial for better outcomes in low-income countries.
Area of Science:
- Pediatric Oncology
- Hematology
- Global Health
Background:
- Pediatric acute myeloid leukemia (AML) presents significant treatment challenges in low- and middle-income countries (LMICs).
- Survival rates for pediatric AML are notably lower in LMICs compared to high-income countries (HICs).
Purpose of the Study:
- To evaluate treatment outcomes for Kenyan children diagnosed with AML.
- To assess the influence of sociodemographic and clinical factors on pediatric AML outcomes in Kenya.
Main Methods:
- Retrospective study of medical records at Moi Teaching and Referral Hospital (MTRH), Eldoret, Kenya (2010-2018).
- Analysis of sociodemographic, clinical characteristics, and treatment protocols including chemotherapy (doxorubicin, cytarabine, etoposide) and supportive care.
- Inclusion of 73 children with AML, with data on symptom duration, diagnosis time, and treatment initiation.
Main Results:
- The 2-year event-free and overall survival probabilities were 4% and 7%, respectively.
- Complete remission was achieved by 33% of patients who started chemotherapy, with a 56% relapse rate among them.
- High rates of treatment abandonment (22%) and early death (46%) were observed. Median symptom duration was 1 month, with diagnosis 6 days and treatment 16 days post-admission.
Conclusions:
- Survival for Kenyan children with AML is extremely low, significantly lagging behind HICs.
- Enhancing supportive care, optimizing treatment protocols, and reducing delays in diagnosis and treatment initiation are critical for improving survival rates.
Background:
Pediatric acute myeloid leukemia (AML) is a challenging disease to treat in low- and middle-income countries (LMICs). Literature suggests that survival in LMICs is poorer compared with survival in high-income countries (HICs).
Aims:
This study evaluates the outcomes of Kenyan children with AML and the impact of sociodemographic and clinical characteristics on outcome.
Methods And Results:
A retrospective medical records study was performed at Moi Teaching and Referral Hospital (MTRH) in Eldoret, Kenya, between January 2010 and December 2018. Sociodemographic and clinical characteristics, and treatment outcomes were evaluated. Chemotherapy included two "3 + 7" induction courses with doxorubicin and cytarabine and two "3 + 5" consolidation courses with etoposide and cytarabine. Supportive care included antimicrobial prophylaxis with cotrimoxazole and fluconazole, and blood products, if available. Seventy-three children with AML were included. The median duration of symptoms before admission at MTRH was 1 month. The median time from admission at MTRH to diagnosis was 6 days and to the start of AML treatment 16 days. Out of the 55 children who were started on chemotherapy, 18 (33%) achieved complete remission, of whom 10 (56%) relapsed. The abandonment rate was 22% and the early death rate was 46%. The 2-year probabilities of event-free survival and overall survival were 4% and 7%, respectively. None of the sociodemographic and clinical characteristics were significantly associated with outcome.
Conclusion:
Survival of Kenyan children with AML is dismal and considerably lower compared with survival in HICs. Strategies to improve survival should be put in place including better supportive care, optimization of the treatment protocol, and reduction of the abandonment rate and time lag to diagnosis with sooner start of treatment.
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