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Updated: May 19, 2026

Pre-clinical Evaluation of Tyrosine Kinase Inhibitors for Treatment of Acute Leukemia
Published on: September 18, 2013
Hepatoprotective efficacy of ursodeoxycholic acid in pediatrics acute lymphoblastic leukemia
Mojeb Mohammed Saif1, Samar F Farid, Sahar A Khaleel
1Department of Clinical Pharmacy, Faculty of Pharmacy, Cairo University, Cairo, Egypt. cl.pharm@yahoo.com
Insights
Ursodeoxycholic acid (UDCA) shows potential in protecting liver health during chemotherapy for acute lymphoblastic leukemia (ALL) in children. This pilot study suggests UDCA may reduce liver enzyme elevations, indicating a safer treatment outcome.
Area of Science:
- Pediatric Oncology
- Hepatology
- Pharmacology
Background:
- Drug-induced hepatotoxicity is a concern in cancer treatment.
- Ursodeoxycholic acid (UDCA) is known for its hepatoprotective properties.
- Acute lymphoblastic leukemia (ALL) treatment in children often involves chemotherapy with potential liver side effects.
Purpose of the Study:
- To evaluate the efficacy and safety of UDCA as an adjunct therapy in children with ALL undergoing chemotherapy.
- To assess the impact of UDCA on liver transaminase levels during chemotherapy.
Main Methods:
- Prospective randomized parallel pilot study.
- 39 children with ALL were randomized into two groups.
- One group received chemotherapy with UDCA for 6 months, followed by 3 months of follow-up.
- The control group received chemotherapy without UDCA for 9 months.
Main Results:
- UDCA administration showed a trend toward decreased hepatic transaminase levels.
- This suggests a potentially safer outcome for children with ALL receiving UDCA concurrently with chemotherapy.
- The study was a pilot, necessitating further investigation.
Conclusions:
- UDCA may offer a protective effect against chemotherapy-induced liver injury in pediatric ALL.
- Further large-scale studies are required to confirm the efficacy and safety of UDCA in this patient population.
Abstract:
Ursodeoxycholic acid (UDCA) possesses a hepatoprotective effect in drug-induced hepatotoxicity. In a prospective randomized parallel study, 39 children with acute lymphoblastic leukemia (ALL) were randomized to receive UDCA with chemotherapy for 6 months, then discontinued UDCA and were followed up for 3 months, (UDCA group) (N = 19) or receive chemotherapy without UDCA and followed up for 9 months (control group) (N = 20). In this pilot study, UDCA treatment was associated with a trend toward decreased levels of hepatic transaminases when concomitantly administered with chemotherapy and, therefore, safer outcome in children with ALL. Future studies with a larger sample size are needed to confirm the efficacy and safety of UDCA in this setting.
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