Objective: Understanding the clinical and genetic characteristics of pediatric acute lymphoblastic leukemia (ALL)<br /> patients may help assigning the appropriate treatment. This study aims to understand patients' characteristics, "real-world"<br /> treatment practice and outcomes of pediatric ALL.

Methods: A cohort of 213 pediatric ALL patients, treated at (King<br /> Faisal Specialist Hospital and Research Center -Jeddah branch) KFSH and RC-J during the period of January 2002 to<br /> December 2015 were analyzed retrospectively. Statistical analyses were performed on patients' demographic, clinical<br /> and genetics characteristics and outcomes of different treatment protocols. Survival was evaluated using Kaplan-Meier<br /> method, and differences in survival were tested using Log-Rank. Significance was set at 0.05 level.

Results: Median<br /> age of the study cohort was 5 years (range 0.5-15 years) with 55.4% of male population. Majority of the patients had<br /> pre-B-cell ALL (88.7%), WBC count <50, 000/μL at diagnosis (76.1%, median = 13.5/μL with a range of 0.51-553.0/<br /> μL) with involvement of central nervous system (CNS) disease in 8.5%patients.Different common chromosomal<br /> anomalies or abnormalities, including t(12, 21) translocation, MLL genre arrangements, trisomy (4, 10, 17)and others,<br /> were detected. Early response to the risk-directed treatment received by the patients (91.1% achieving <5% blast in<br /> the bone marrow) as well as the end of induction outcome (96.2%) was encouraging.

Conclusion: We found that the<br /> patients' clinical characteristics and distribution of genetic abnormalities were similar to those of the western countries.<br /> Our findings show that the earlier gap between the western countries and KSA in terms of survival has been closed and<br /> that competitive outcomes can be achieved with local infrastructure.

Title

Asian Pacific Journal of Cancer Prevention

Publisher

Asian Pacific Organization for Cancer Prevetion

Publisher Country

Iran

Publication Type

Online only

Volume

20

Year

2019

Pages

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