Related Experiment Videos
Systemic exposure to mercaptopurine as a prognostic factor in acute lymphocytic leukemia in children
1Division of Clinical Pharmacology, Hospital for Sick Children, Toronto, ON, Canada.
Insights
Low systemic exposure to mercaptopurine (MP) in children with acute lymphocytic leukemia (ALL) is linked to a higher risk of relapse. Tailoring MP doses based on individual pharmacokinetics is crucial for improving treatment outcomes in ALL maintenance therapy.
Area of Science:
- Pediatric Oncology
- Pharmacology
- Clinical Pharmacology
Background:
- Acute lymphocytic leukemia (ALL) in children has high remission rates but significant relapse rates.
- Maintenance therapy for childhood ALL commonly involves oral mercaptopurine (MP) and methotrexate.
- Variability in oral MP bioavailability raises concerns about its impact on relapse risk.
Purpose of the Study:
- To investigate the association between systemic MP exposure and relapse risk in pediatric ALL patients undergoing maintenance therapy.
- To determine if lower MP exposure increases the likelihood of relapse in children with ALL.
Main Methods:
- Prospective study of 23 children with ALL on maintenance therapy.
- Patients categorized into low-risk (n=11) and standard-risk (n=12) relapse groups.
- Measured mercaptopurine area under the concentration-time curve (AUC) and total daily systemic exposure.
Main Results:
- Relapsed patients exhibited significantly lower MP AUC (1636 vs. 2424 nmol/L*min) and total daily systemic exposure (104,043 vs. 168,862 nmol/L*min) compared to non-relapsed patients (P<0.005).
- Lower MP exposure (AUC < 1971 nmol/L*min) was associated with a poorer prognosis (P<0.01).
- Higher systemic exposure (>137,970 nmol/L*min) correlated with a better prognosis (P<0.005).
Conclusions:
- Suboptimal systemic exposure to oral mercaptopurine during maintenance therapy negatively impacts prognosis in childhood ALL.
- Pharmacokinetic profiling of MP at the start of maintenance therapy is recommended.
- Individualized MP dosing to achieve adequate systemic exposure is essential for improving outcomes in pediatric ALL.
Background:
Despite a success rate of more than 90 percent in inducing remission in children with acute lymphocytic leukemia, 30 to 40 percent of such children relapse. Maintenance therapy during remission usually includes oral mercaptopurine and methotrexate. Recently, wide variability in the bioavailability of oral mercaptopurine has been demonstrated, and there is concern that this may affect the risk of relapse.
Methods:
To investigate whether lower systemic exposure to mercaptopurine may increase the risk of relapse in acute lymphocytic leukemia, we prospectively studied 23 children receiving maintenance therapy. On the basis of disease features, 11 were classified as being at low risk of relapse, and 12 at standard risk. Those who relapsed (n = 10) did not differ from those who did not in their mean age, hemoglobin level, mean daily dose of mercaptopurine and weekly dose of methotrexate, or the total number of days during which mercaptopurine and methotrexate therapy was interrupted.
Results:
There was a significant difference in the mean (+/- SEM) area under the mercaptopurine concentration-time curve achieved by a dose of 1 mg of mercaptopurine per square meter of body-surface area: 1636 +/- 197 nmol per liter x minutes in those who relapsed, as compared with 2424 +/- 177 nmol per liter x minutes in those who did not (P less than 0.005). This caused a significantly lower total daily systemic exposure to mercaptopurine in those who relapsed (104,043 +/- 12,812 nmol per liter x minutes) than in those who did not (168,862 +/- 18,830 nmol per liter x minutes) (P less than 0.005). An identical tendency prevailed when patients at low risk and patients at standard risk were analyzed separately. Kaplan-Meier analysis revealed that children in whom an area under the curve of less than 1971 nmol per liter x minutes was achieved by a dose of 1 mg of mercaptopurine per square meter had a significantly poorer prognosis than those with larger areas under the curve (P less than 0.01). Similarly, those with a total daily systemic exposure of more than 137,970 nmol per liter x minutes had a significantly better prognosis than those with a lower exposure (P less than 0.005).
Conclusions:
Low systemic exposure to oral mercaptopurine during maintenance therapy for acute lymphocytic leukemia in childhood adversely affects prognosis. Children should be studied at the beginning of maintenance therapy to establish the pharmacokinetics of mercaptopurine, and the dose should be tailored to achieve an appropriate systemic exposure.